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CT Caskey
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14
Lee, Cheng Chi
12
Gibbs, Richard
11
Belmont, John
10
Chamberlain, Jeffrey
9
Clemens, Paula
9
Grompe, Markus
9
Morsy, MA
9
Muzny, Donna
7
Pizzuti, Antonio
7
Timchenko, Lubov
7
Nelson, David
7
Liu, Qingyun
7
Craigen, William
7
Austin, Christopher
6
Ashizawa, Tetsuo
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All Publications
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2001: Gerhold D; Lu M; Xu J; Austin C; Caskey C T; Rushmore T
Monitoring expression of genes involved in drug metabolism and toxicology using DNA microarrays.
Physiological genomics 2001;5(4):161-70.
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2000: Howard A D; Wang R; Pong S S; Mellin T N; Strack A; Guan X M; Zeng Z; Williams D L; Feighner S D; Nunes C N; Murphy B; Stair J N; Yu H; Jiang Q; Clements M K; Tan C P; McKee K K; Hreniuk D L; McDonald T P; Lynch K R; Evans J F; Austin C P; Caskey C T; Van der Ploeg L H; Liu Q
Identification of receptors for neuromedin U and its role in feeding.
Nature 2000;406(6791):70-4.
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2000: Bai C; Connolly B; Metzker M L; Hilliard C A; Liu X; Sandig V; Soderman A; Galloway S M; Liu Q; Austin C P; Caskey C T
Overexpression of M68/DcR3 in human gastrointestinal tract tumors independent of gene amplification and its location in a four-gene cluster.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(3):1230-5.
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2000: Sandig V; Youil R; Bett A J; Franlin L L; Oshima M; Maione D; Wang F; Metzker M L; Savino R; Caskey C T
Optimization of the helper-dependent adenovirus system for production and potency in vivo.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(3):1002-7.
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1999: Chen F; Figueroa D J; Marmorstein A D; Zhang Q; Petrukhin K; Caskey C T; Austin C P
Retina-specific nuclear receptor: A potential regulator of cellular retinaldehyde-binding protein expressed in retinal pigment epithelium and Müller glial cells.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(26):15149-54.
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1999: Liu Q; Pong S S; Zeng Z; Zhang Q; Howard A D; Williams D L; Davidoff M; Wang R; Austin C P; McDonald T P; Bai C; George S R; Evans J F; Caskey C T
Identification of urotensin II as the endogenous ligand for the orphan G-protein-coupled receptor GPR14.
Biochemical and biophysical research communications 1999;266(1):174-8.
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1999: Allikmets R; Seddon J M; Bernstein P S; Hutchinson A; Atkinson A; Sharma S; Gerrard B; Li W; Metzker M L; Wadelius C; Caskey C T; Dean M; Petrukhin K
Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies.
Human genetics 1999;104(6):449-53.
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1999: Lynch K R; O'Neill G P; Liu Q; Im D S; Sawyer N; Metters K M; Coulombe N; Abramovitz M; Figueroa D J; Zeng Z; Connolly B M; Bai C; Austin C P; Chateauneuf A; Stocco R; Greig G M; Kargman S; Hooks S B; Hosfield E; Williams D L; Ford-Hutchinson A W; Caskey C T; Evans J F
Characterization of the human cysteinyl leukotriene CysLT1 receptor.
Nature 1999;399(6738):789-93.
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1999: Austin C P; Holder D J; Ma L; Mixson L A; Caskey C T
Mapping of hKCa3 to chromosome 1q21 and investigation of linkage of CAG repeat polymorphism to schizophrenia.
Molecular psychiatry 1999;4(3):261-6.
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1999: Gerhold D; Rushmore T; Caskey C T
DNA chips: promising toys have become powerful tools.
Trends in biochemical sciences 1999;24(5):168-73.
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1999: Chen F; Zhang Q; McDonald T; Davidoff M J; Bailey W; Bai C; Liu Q; Caskey C T
Identification of two hERR2-related novel nuclear receptors utilizing bioinformatics and inverse PCR.
Gene 1999;228(1-2):101-9.
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1999: Morsy M A; Caskey C T
Expanded-capacity adenoviral vectors--the helper-dependent vectors.
Molecular medicine today 1999;5(1):18-24.
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1998: Harvey D M; Caskey C T
Inducible control of gene expression: prospects for gene therapy.
Current opinion in chemical biology 1998;2(4):512-8.
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1998: Brown S D; Twells R C; Hey P J; Cox R D; Levy E R; Soderman A R; Metzker M L; Caskey C T; Todd J A; Hess J F
Isolation and characterization of LRP6, a novel member of the low density lipoprotein receptor gene family.
Biochemical and biophysical research communications 1998;248(3):879-88.
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1998: Petrukhin K; Koisti M J; Bakall B; Li W; Xie G; Marknell T; Sandgren O; Forsman K; Holmgren G; Andreasson S; Vujic M; Bergen A A; McGarty-Dugan V; Figueroa D; Austin C P; Metzker M L; Caskey C T; Wadelius C
Identification of the gene responsible for Best macular dystrophy.
Nature genetics 1998;19(3):241-7.
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1998: Morsy M A; Gu M; Motzel S; Zhao J; Lin J; Su Q; Allen H; Franlin L; Parks R J; Graham F L; Kochanek S; Bett A J; Caskey C T
An adenoviral vector deleted for all viral coding sequences results in enhanced safety and extended expression of a leptin transgene.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(14):7866-71.
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1998: McDonald T; Wang R; Bailey W; Xie G; Chen F; Caskey C T; Liu Q
Identification and cloning of an orphan G protein-coupled receptor of the glycoprotein hormone receptor subfamily.
Biochemical and biophysical research communications 1998;247(2):266-70.
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1998: Morsy M A; Gu M C; Zhao J Z; Holder D J; Rogers I T; Pouch W J; Motzel S L; Klein H J; Gupta S K; Liang X; Tota M R; Rosenblum C I; Caskey C T
Leptin gene therapy and daily protein administration: a comparative study in the ob/ob mouse.
Gene therapy 1998;5(1):8-18.
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1998: Liu Q; Bai C; Chen F; Wang R; MacDonald T; Gu M; Zhang Q; Morsy M A; Caskey C T
Uncoupling protein-3: a muscle-specific gene upregulated by leptin in ob/ob mice.
Gene 1998;207(1):1-7.
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1997: Caskey C T
Medical genetics.
JAMA : the journal of the American Medical Association 1997;277(23):1869-70.
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1997: Morsy M A; Caskey C T
Safe gene vectors made simpler.
Nature biotechnology 1997;15(1):17.
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1996: Timchenko L T; Caskey C T
Trinucleotide repeat disorders in humans: discussions of mechanisms and medical issues.
The FASEB journal : official publication of the Federation of American Societies for Experimental Biology 1996;10(14):1589-97.
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1996: Alford R L; Ashizawa T; Jankovic J; Caskey C T; Richards C S
Molecular detection of new mutations, resolution of ambiguous results and complex genetic counseling issues in Huntington disease.
American journal of medical genetics 1996;66(3):281-6.
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1996: Timchenko L T; Miller J W; Timchenko N A; DeVore D R; Datar K V; Lin L; Roberts R; Caskey C T; Swanson M S
Identification of a (CUG)n triplet repeat RNA-binding protein and its expression in myotonic dystrophy.
Nucleic acids research 1996;24(22):4407-14.
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1996: Clemens P R; Kochanek S; Sunada Y; Chan S; Chen H H; Campbell K P; Caskey C T
In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genes.
Gene therapy 1996;3(11):965-72.
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1996: Zhao Z; Yazdani A; Shen Y; Sun Z; Bailey J; Caskey C T; Lee C C
Molecular dissection of a cosmid from a gene-rich region in 17q21 and characterization of a candidate gene for alpha-N-acetylglucosaminidase with two cDNA isoforms.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(9):686-90.
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1996: Ashizawa T; Monckton D G; Vaishnav S; Patel B J; Voskova A; Caskey C T
Instability of the expanded (CTG)n repeats in the myotonin protein kinase gene in cultured lymphoblastoid cell lines from patients with myotonic dystrophy.
Genomics 1996;36(1):47-53.
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1996: Zhao Z; Lee C C; Monckton D G; Yazdani A; Coolbaugh M I; Li X; Bailey J; Shen Y; Caskey C T
Characterization and genomic mapping of genes and pseudogenes of a new human protein tyrosine phosphatase.
Genomics 1996;35(1):172-81.
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1996: Kochanek S; Clemens P R; Mitani K; Chen H H; Chan S; Caskey C T
A new adenoviral vector: Replacement of all viral coding sequences with 28 kb of DNA independently expressing both full-length dystrophin and beta-galactosidase.
Proceedings of the National Academy of Sciences of the United States of America 1996;93(12):5731-6.
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1996: Morsy M A; Zhao J Z; Ngo T T; Warman A W; O'Brien W E; Graham F L; Caskey C T
Patient selection may affect gene therapy success. Dominant negative effects observed for ornithine transcarbamylase in mouse and human hepatocytes.
The Journal of clinical investigation 1996;97(3):826-32.
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1996: Timchenko L T; Timchenko N A; Caskey C T; Roberts R
Novel proteins with binding specificity for DNA CTG repeats and RNA CUG repeats: implications for myotonic dystrophy.
Human molecular genetics 1996;5(1):115-21.
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1996: Caskey C T; Swanson M S; Timchenko L T
Myotonic dystrophy: discussion of molecular mechanism.
Cold Spring Harbor symposia on quantitative biology 1996;61():607-14.
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1996: DeMarchi J M; Caskey C T; Richards C S
Population-specific screening by mutation analysis for diseases frequent in Ashkenazi Jews.
Human mutation 1996;8(2):116-25.
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1996: Shumaker J M; Metspalu A; Caskey C T
Mutation detection by solid phase primer extension.
Human mutation 1996;7(4):346-54.
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1995: Clemens P R; Krause T L; Chan S; Korb K E; Graham F L; Caskey C T
Recombinant truncated dystrophin minigenes: construction, expression, and adenoviral delivery.
Human gene therapy 1995;6(11):1477-85.
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1995: Blackburn M R; Wakamiya M; Caskey C T; Kellems R E
Tissue-specific rescue suggests that placental adenosine deaminase is important for fetal development in mice.
The Journal of biological chemistry 1995;270(41):23891-4.
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1995: Rossiter B J; Caskey C T
Presymptomatic testing for genetic diseases of later life. Pharmacoepidemiological considerations.
Drugs & aging 1995;7(2):117-30.
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1995: Mitani K; Wakamiya M; Hasty P; Graham F L; Bradley A; Caskey C T
Gene targeting in mouse embryonic stem cells with an adenoviral vector.
Somatic cell and molecular genetics 1995;21(4):221-31.
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1995: Timchenko L; Nastainczyk W; Schneider T; Patel B; Hofmann F; Caskey C T
Full-length myotonin protein kinase (72 kDa) displays serine kinase activity.
Proceedings of the National Academy of Sciences of the United States of America 1995;92(12):5366-70.
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1995: Hammond H A; Redman J B; Caskey C T
In utero paternity testing following alleged sexual assault. A comparison of DNA-based methods.
JAMA : the journal of the American Medical Association 1995;273(22):1774-7.
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1995: Zhao Z; Lee C C; Baldini A; Caskey C T
A human homologue of the Drosophila polarity gene frizzled has been identified and mapped to 17q21.1.
Genomics 1995;27(2):370-3.
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1995: Mitani K; Graham F L; Caskey C T; Kochanek S
Rescue, propagation, and partial purification of a helper virus-dependent adenovirus vector.
Proceedings of the National Academy of Sciences of the United States of America 1995;92(9):3854-8.
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1995: Zhao Z; Lee C C; Jiralerspong S; Juyal R C; Lu F; Baldini A; Greenberg F; Caskey C T; Patel P I
The gene for a human microfibril-associated glycoprotein is commonly deleted in Smith-Magenis syndrome patients.
Human molecular genetics 1995;4(4):589-97.
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1995: Alford R L; Redman J B; O'Brien W E; Caskey C T
Lesch-Nyhan syndrome: carrier and prenatal diagnosis.
Prenatal diagnosis 1995;15(4):329-38.
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1995: Panzer S; Kuhl D P; Caskey C T
Unstable triplet repeat sequences: a source of cancer mutations?
Stem cells (Dayton, Ohio) 1995;13(2):146-57.
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1995: Timchenko L; Monckton D G; Caskey C T
Myotonic dystrophy: an unstable CTG repeat in a protein kinase gene.
Seminars in cell biology 1995;6(1):13-9.
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1995: Rossiter B J; Caskey C T
Impact of the human genome project on medical practice.
Annals of surgical oncology 1995;2(1):14-25.
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1995: Wong L J; Ashizawa T; Monckton D G; Caskey C T; Richards C S
Somatic heterogeneity of the CTG repeat in myotonic dystrophy is age and size dependent.
American journal of human genetics 1995;56(1):114-22.
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1995: Monckton D G; Wong L J; Ashizawa T; Caskey C T
Somatic mosaicism, germline expansions, germline reversions and intergenerational reductions in myotonic dystrophy males: small pool PCR analyses.
Human molecular genetics 1995;4(1):1-8.
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1994: Pearlman J A; Powaser P A; Elledge S J; Caskey C T
Troponin T is capable of binding dystrophin via a leucine zipper.
FEBS letters 1994;354(2):183-6.
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1994: Mitani K; Graham F L; Caskey C T
Transduction of human bone marrow by adenoviral vector.
Human gene therapy 1994;5(8):941-8.
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1994: Alford R L; Hammond H A; Coto I; Caskey C T
Rapid and efficient resolution of parentage by amplification of short tandem repeats.
American journal of human genetics 1994;55(1):190-5.
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1994: Hammond H A; Jin L; Zhong Y; Caskey C T; Chakraborty R
Evaluation of 13 short tandem repeat loci for use in personal identification applications.
American journal of human genetics 1994;55(1):175-89.
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1994: Ashizawa T; Wong L J; Richards C S; Caskey C T; Jankovic J
CAG repeat size and clinical presentation in Huntington's disease.
Neurology 1994;44(6):1137-43.
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1994: Chakraborty R; Zhong Y; de Andrade M; Clemens P R; Fenwick R G; Caskey C T
Linkage disequilibria among (CA)n polymorphisms in the human dystrophin gene and their implications in carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophies.
Genomics 1994;21(3):567-70.
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1994: Wehnert M S; Matson R S; Rampal J B; Coassin P J; Caskey C T
A rapid scanning strip for tri- and dinucleotide short tandem repeats.
Nucleic acids research 1994;22(9):1701-4.
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1994: Timchenko L; Caskey C T
The "eRF" clone corresponds to tryptophanyl-tRNA synthetase, not mammalian release factor.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(7):2777-80.
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1994: Faustinella F; Kwon H; Serrano F; Belmont J W; Caskey C T; Aguilar-Cordova E
A new family of murine retroviral vectors with extended multiple cloning sites for gene insertion.
Human gene therapy 1994;5(3):307-12.
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1994: Alford R L; Caskey C T
DNA analysis in forensics, disease and animal/plant identification.
Current opinion in biotechnology 1994;5(1):29-33.
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1994: Wu X; Wakamiya M; Vaishnav S; Geske R; Montgomery C; Jones P; Bradley A; Caskey C T
Hyperuricemia and urate nephropathy in urate oxidase-deficient mice.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(2):742-6.
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1994: DeMarchi J M; Beaudet A L; Caskey C T; Richards C S
Experience of an academic reference laboratory using automation for analysis of cystic fibrosis mutations.
Archives of pathology & laboratory medicine 1994;118(1):26-32.
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1994: Clemens P R; Caskey C T
Gene therapy prospects for Duchenne muscular dystrophy.
European neurology 1994;34(4):181-5.
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1994: Alford R L; Rossiter B J; Caskey C T
DNA diagnosis in monogenic diseases.
International journal of technology assessment in health care 1994;10(4):628-43.
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1994: Morsy M A; Caskey C T
Ornithine transcarbamylase deficiency: a model for gene therapy.
Advances in experimental medicine and biology 1994;368():145-54.
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1993: Pizzuti A; Gennarelli M; Novelli G; Colosimo A; Lo Cicero S; Caskey C T; Dallapiccola B
Human elongation factor EF-1 beta: cloning and characterization of the EF1 beta 5a gene and assignment of EF-1 beta isoforms to chromosomes 2,5,15 and X.
Biochemical and biophysical research communications 1993;197(1):154-62.
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1993: Morsy M A; Mitani K; Clemens P; Caskey C T
Progress toward human gene therapy.
JAMA : the journal of the American Medical Association 1993;270(19):2338-45.
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1993: Pizzuti A; Friedman D L; Caskey C T
The myotonic dystrophy gene.
Archives of neurology 1993;50(11):1173-9.
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1993: Caskey C T
Presymptomatic diagnosis: a first step toward genetic health care.
Science (New York, N.Y.) 1993;262(5130):48-9.
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1993: Morsy M A; Alford E L; Bett A; Graham F L; Caskey C T
Efficient adenoviral-mediated ornithine transcarbamylase expression in deficient mouse and human hepatocytes.
The Journal of clinical investigation 1993;92(3):1580-6.
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1993: Panzer S W; Hammond H A; Stephens L; Chai A; Caskey C T
Trinucleotide repeat polymorphism at D6S366.
Human molecular genetics 1993;2(9):1511.
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1993: Wehnert M; Reiner O; Caskey C T
Four STR polymorphisms map to a 500 kb region between DXS15 and DXS134.
Human molecular genetics 1993;2(9):1503.
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1993: Rossiter B J; Caskey C T
The human genome project.
Clinical obstetrics and gynecology 1993;36(3):466-75.
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1993: Reiner O; Carrozzo R; Shen Y; Wehnert M; Faustinella F; Dobyns W B; Caskey C T; Ledbetter D H
Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats.
Nature 1993;364(6439):717-21.
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1993: Kuhl D P; Caskey C T
Trinucleotide repeats and genome variation.
Current opinion in genetics & development 1993;3(3):404-7.
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1993: Lee C C; Pons F; Jones P G; Bies R D; Schlang A M; Leger J J; Caskey C T
Mdx transgenic mouse: restoration of recombinant dystrophin to the dystrophic muscle.
Human gene therapy 1993;4(3):273-81.
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1993: Caskey C T
Molecular medicine. A spin-off from the helix.
JAMA : the journal of the American Medical Association 1993;269(15):1986-92.
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1993: Redman J B; Fenwick R G; Fu Y H; Pizzuti A; Caskey C T
Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring.
JAMA : the journal of the American Medical Association 1993;269(15):1960-5.
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1993: Mitani K; Wakamiya M; Caskey C T
Long-term expression of retroviral-transduced adenosine deaminase in human primitive hematopoietic progenitors.
Human gene therapy 1993;4(1):9-16.
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1993: Mitani K; Clemens P R; Moseley A B; Caskey C T
Gene transfer therapy for heritable disease: cell and expression targeting.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences 1993;339(1288):217-24.
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1993: Moseley A B; Caskey C T
Prospects for human gene therapy.
Genetic engineering 1993;15():213-23.
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1992: Rossiter B J; Caskey C T
The human genome project and clinical medicine.
Oncology (Williston Park, N.Y.) 1992;6(11):61-8, 71; discussion 71, 75-6.
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1992: Ashizawa T; Dubel J R; Dunne P W; Dunne C J; Fu Y H; Pizzuti A; Caskey C T; Boerwinkle E; Perryman M B; Epstein H F
Anticipation in myotonic dystrophy. II. Complex relationships between clinical findings and structure of the GCT repeat.
Neurology 1992;42(10):1877-83.
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1992: Caskey C T
Antisense and differentiation.
Annals of the New York Academy of Sciences 1992;660():154-8.
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1992: Clemens P R; Ward P A; Caskey C T; Bulman D E; Fenwick R G
Premature chain termination mutation causing Duchenne muscular dystrophy.
Neurology 1992;42(9):1775-82.
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1992: Sutcliffe J S; Nelson D L; Zhang F; Pieretti M; Caskey C T; Saxe D; Warren S T
DNA methylation represses FMR-1 transcription in fragile X syndrome.
Human molecular genetics 1992;1(6):397-400.
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1992: Bies R D; Caskey C T; Fenwick R
An intact cysteine-rich domain is required for dystrophin function.
The Journal of clinical investigation 1992;90(2):666-72.
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1992: Sutcliffe J S; Zhang F; Caskey C T; Nelson D L; Warren S T
PCR amplification and analysis of yeast artificial chromosomes.
Genomics 1992;13(4):1303-6.
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1992: Rossiter B J; Stirpe N S; Caskey C T
Report of the MDA Gene Therapy Conference, Tucson, Arizona, September 27-28, 1991.
Neurology 1992;42(7):1413-8.
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1992: Pizzuti A; Pieretti M; Fenwick R G; Gibbs R A; Caskey C T
A transposon-like element in the deletion-prone region of the dystrophin gene.
Genomics 1992;13(3):594-600.
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1992: Kilimann M W; Pizzuti A; Grompe M; Caskey C T
Point mutations and polymorphisms in the human dystrophin gene identified in genomic DNA sequences amplified by multiplex PCR.
Human genetics 1992;89(3):253-8.
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1992: Caskey C T; Pizzuti A; Fu Y H; Fenwick R G; Nelson D L
Triplet repeat mutations in human disease.
Science (New York, N.Y.) 1992;256(5058):784-9.
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1992: Caskey C T; Rossiter B J
9th Ernst Klenk Lecture. Molecular medicine.
Biological chemistry Hoppe-Seyler 1992;373(4):159-70.
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1992: Bies R D; Phelps S F; Cortez M D; Roberts R; Caskey C T; Chamberlain J S
Human and murine dystrophin mRNA transcripts are differentially expressed during skeletal muscle, heart, and brain development.
Nucleic acids research 1992;20(7):1725-31.
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1992: Grompe M; Pieretti M; Caskey C T; Ballabio A
The sulfatase gene family: cross-species PCR cloning using the MOPAC technique.
Genomics 1992;12(4):755-60.
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1992: Edwards A; Hammond H A; Jin L; Caskey C T; Chakraborty R
Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups.
Genomics 1992;12(2):241-53.
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1992: Grompe M; Jones S N; Loulseged H; Caskey C T
Retroviral-mediated gene transfer of human ornithine transcarbamylase into primary hepatocytes of spf and spf-ash mice.
Human gene therapy 1992;3(1):35-44.
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1992: Caskey C T; Rossiter B J
The human genome project. Purpose and potential.
The Journal of pharmacy and pharmacology 1992;44 Suppl 1():198-204.
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1992: Wu X W; Muzny D M; Lee C C; Caskey C T
Two independent mutational events in the loss of urate oxidase during hominoid evolution.
Journal of molecular evolution 1992;34(1):78-84.
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1992: Grompe M; Rao N; Elder F F; Caskey C T; Greenberg F
45,X/46,X,+r(X) can have a distinct phenotype different from Ullrich-Turner syndrome.
American journal of medical genetics 1992;42(1):39-43.
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1991: Jones S N; Jones P G; Ibarguen H; Caskey C T; Craigen W J
Induction of the Cyp1a-1 dioxin-responsive enhancer in transgenic mice.
Nucleic acids research 1991;19(23):6547-51.
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1991: Huang T H; Hejtmancik J F; Edwards A; Pettigrew A L; Herrera C A; Hammond H A; Caskey C T; Zoghbi H Y; Ledbetter D H
Linkage of the gene for an X-linked mental retardation disorder to a hypervariable (AGAT)n repeat motif within the human hypoxanthine phosphoribosyltransferase (HPRT) locus (Xq26).
American journal of human genetics 1991;49(6):1312-9.
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1991: Edwards A; Caskey C T
Genetic marker technology.
Current opinion in biotechnology 1991;2(6):818-22.
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1991: Clemens P R; Fenwick R G; Chamberlain J S; Gibbs R A; de Andrade M; Chakraborty R; Caskey C T
Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms.
American journal of human genetics 1991;49(5):951-60.
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1991: Caskey C T
American Society of Human Genetics presidential address, October 18, 1990.
American journal of human genetics 1991;49(5):911-6.
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1991: Caskey C T
Physician-laboratory interface in X-chromosome mapping.
Hospital practice (Office ed.) 1991;26(10):131-8, 141-2, 144.
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1991: Edwards A; Civitello A; Hammond H A; Caskey C T
DNA typing and genetic mapping with trimeric and tetrameric tandem repeats.
American journal of human genetics 1991;49(4):746-56.
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1991: Taylor L D; Krizman D B; Jankovic J; Hayani A; Steuber P C; Greenberg F; Fenwick R G; Caskey C T
9p monosomy in a patient with Gilles de la Tourette's syndrome.
Neurology 1991;41(9):1513-5.
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1991: Pettigrew A L; Greenberg F; Caskey C T; Ledbetter D H
Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13.
Human genetics 1991;87(4):452-6.
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1991: Pieretti M; Zhang F P; Fu Y H; Warren S T; Oostra B A; Caskey C T; Nelson D L
Absence of expression of the FMR-1 gene in fragile X syndrome.
Cell 1991;66(4):817-22.
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1991: Nelson D L; Ballabio A; Victoria M F; Pieretti M; Bies R D; Gibbs R A; Maley J A; Chinault A C; Webster T D; Caskey C T
Alu-primed polymerase chain reaction for regional assignment of 110 yeast artificial chromosome clones from the human X chromosome: identification of clones associated with a disease locus.
Proceedings of the National Academy of Sciences of the United States of America 1991;88(14):6157-61.
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1991: Chamberlain J S; Farwell N J; Chamberlain J R; Cox G A; Caskey C T
PCR analysis of dystrophin gene mutation and expression.
Journal of cellular biochemistry 1991;46(3):255-9.
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1991: Caskey C T
A genome approach to the human X chromosome.
Current opinion in genetics & development 1991;1(1):20-4.
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1991: Rossiter B J; Fuscoe J C; Muzny D M; Fox M; Caskey C T
The Chinese hamster HPRT gene: restriction map, sequence analysis, and multiplex PCR deletion screen.
Genomics 1991;9(2):247-56.
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1991: Scarpa M; Cournoyer D; Muzny D M; Moore K A; Belmont J W; Caskey C T
Characterization of recombinant helper retroviruses from Moloney-based vectors in ecotropic and amphotropic packaging cell lines.
Virology 1991;180(2):849-52.
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1991: Grompe M; Caskey C T; Fenwick R G
Improved molecular diagnostics for ornithine transcarbamylase deficiency.
American journal of human genetics 1991;48(2):212-22.
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1991: Rossiter B J; Caskey C T
Molecular studies of human genetic disease.
The FASEB journal : official publication of the Federation of American Societies for Experimental Biology 1991;5(1):21-7.
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1991: Lee C C; Pearlman J A; Chamberlain J S; Caskey C T
Expression of recombinant dystrophin and its localization to the cell membrane.
Nature 1991;349(6307):334-6.
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1991: Moore K A; Scarpa M; Kooyer S; Utter A; Caskey C T; Belmont J W
Evaluation of lymphoid-specific enhancer addition or substitution in a basic retrovirus vector.
Human gene therapy 1991;2(4):307-15.
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1991: Grompe M; Mitani K; Lee C C; Jones S N; Caskey C T
Gene therapy in man and mice: adenosine deaminase deficiency, ornithine transcarbamylase deficiency, and Duchenne muscular dystrophy.
Advances in experimental medicine and biology 1991;309B():51-6.
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1991: Cournoyer D; Scarpa M; Mitani K; Moore K A; Markowitz D; Bank A; Belmont J W; Caskey C T
Gene transfer of adenosine deaminase into primitive human hematopoietic progenitor cells.
Human gene therapy 1991;2(3):203-13.
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1990: Cournoyer D; Scarpa M; Caskey C T
Gene therapy.
Current opinion in biotechnology 1990;1(2):196-208.
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1990: Rossiter B J; Muzny D M; Hampson I; Caskey C T; Fox M
Induced reversion of a spontaneous point mutation within the Chinese hamster HPRT gene to the wild-type sequence.
Mutagenesis 1990;5(6):605-8.
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1990: Grompe M; Jones S N; Caskey C T
Molecular detection and correction of ornithine transcarbamylase deficiency.
Trends in genetics : TIG 1990;6(10):335-9.
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1990: Jones S N; Grompe M; Munir M I; Veres G; Craigen W J; Caskey C T
Ectopic correction of ornithine transcarbamylase deficiency in sparse fur mice.
The Journal of biological chemistry 1990;265(24):14684-90.
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1990: Corbo L; Maley J A; Nelson D L; Caskey C T
Direct cloning of human transcripts with HnRNA from hybrid cell lines.
Science (New York, N.Y.) 1990;249(4969):652-5.
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1990: Rossiter B J; Caskey C T
Molecular scanning methods of mutation detection.
The Journal of biological chemistry 1990;265(22):12753-6.
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1990: Munir M I; Rossiter B J; Caskey C T
Antisense RNA production in transgenic mice.
Somatic cell and molecular genetics 1990;16(4):383-94.
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1990: Stout J T; Caskey C T
Antisense RNA inhibition of HPRT synthesis.
Somatic cell and molecular genetics 1990;16(4):369-82.
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1990: Gibbs R A; Nguyen P N; Edwards A; Civitello A B; Caskey C T
Multiplex DNA deletion detection and exon sequencing of the hypoxanthine phosphoribosyltransferase gene in Lesch-Nyhan families.
Genomics 1990;7(2):235-44.
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1990: Craigen W J; Lee C C; Caskey C T
Recent advances in peptide chain termination.
Molecular microbiology 1990;4(6):861-5.
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1990: Ballabio A; Ranier J E; Chamberlain J S; Zollo M; Caskey C T
Screening for steroid sulfatase (STS) gene deletions by multiplex DNA amplification.
Human genetics 1990;84(6):571-3.
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1990: Lee C C; Craigen W J; Muzny D M; Harlow E; Caskey C T
Cloning and expression of a mammalian peptide chain release factor with sequence similarity to tryptophanyl-tRNA synthetases.
Proceedings of the National Academy of Sciences of the United States of America 1990;87(9):3508-12.
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1990: Edwards A; Voss H; Rice P; Civitello A; Stegemann J; Schwager C; Zimmermann J; Erfle H; Caskey C T; Ansorge W
Automated DNA sequencing of the human HPRT locus.
Genomics 1990;6(4):593-608.
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1990: Cournoyer D; Scarpa M; Jones S N; Moore K A; Belmont J W; Caskey C T
Gene therapy: a new approach for the treatment of genetic disorders.
Clinical pharmacology and therapeutics 1990;47(1):1-11.
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1989: Wu X W; Lee C C; Muzny D M; Caskey C T
Urate oxidase: primary structure and evolutionary implications.
Proceedings of the National Academy of Sciences of the United States of America 1989;86(23):9412-6.
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1989: Nelson D L; Ledbetter S A; Corbo L; Victoria M F; Ramírez-Solis R; Webster T D; Ledbetter D H; Caskey C T
Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sources.
Proceedings of the National Academy of Sciences of the United States of America 1989;86(17):6686-90.
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1989: Grompe M; Muzny D M; Caskey C T
Scanning detection of mutations in human ornithine transcarbamoylase by chemical mismatch cleavage.
Proceedings of the National Academy of Sciences of the United States of America 1989;86(15):5888-92.
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1989: Baumbach L L; Chamberlain J S; Ward P A; Farwell N J; Caskey C T
Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophies.
Neurology 1989;39(4):465-74.
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1989: Gibbs R A; Nguyen P N; Caskey C T
Detection of single DNA base differences by competitive oligonucleotide priming.
Nucleic acids research 1989;17(7):2437-48.
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1989: Gibbs R A; Nguyen P N; McBride L J; Koepf S M; Caskey C T
Identification of mutations leading to the Lesch-Nyhan syndrome by automated direct DNA sequencing of in vitro amplified cDNA.
Proceedings of the National Academy of Sciences of the United States of America 1989;86(6):1919-23.
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1989: MacGregor G R; Caskey C T
Construction of plasmids that express E. coli beta-galactosidase in mammalian cells.
Nucleic acids research 1989;17(6):2365.
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1989: Chapman V M; Miller D R; Armstrong D; Caskey C T
Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice.
Proceedings of the National Academy of Sciences of the United States of America 1989;86(4):1292-6.
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1989: Ward P A; Hejtmancik J F; Witkowski J A; Baumbach L L; Gunnell S; Speer J; Hawley P; Tantravahi U; Caskey C T
Prenatal diagnosis of Duchenne muscular dystrophy: prospective linkage analysis and retrospective dystrophin cDNA analysis.
American journal of human genetics 1989;44(2):270-81.
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1989: Gibbs R A; Caskey C T
The application of recombinant DNA technology for genetic probing in epidemiology.
Annual review of public health 1989;10():27-48.
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1989: Edwards A; Gibbs R A; Nguyen P N; Ansorge W; Caskey C T
Automated DNA sequencing methods for detection and analysis of mutations: applications to the Lesch-Nyhan syndrome.
Transactions of the Association of American Physicians 1989;102():185-94.
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1989: Lee C C; Wu X W; Caskey C T
Cloning the full-length cDNA for the porcine urate oxidase by the MOPAC generated probe.
Advances in experimental medicine and biology 1989;253A():499-505.
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1989: Moore K A; Fletcher F A; Alford R L; Villalon D K; Hawkins D H; MacGregor G R; Caskey C T; Belmont J W
Expression vectors for human adenosine deaminase gene therapy.
Genome / National Research Council Canada = Génome / Conseil national de recherches Canada 1989;31(2):832-9.
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1988: Chamberlain J S; Gibbs R A; Ranier J E; Nguyen P N; Caskey C T
Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification.
Nucleic acids research 1988;16(23):11141-56.
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1988: Belmont J W; MacGregor G R; Wager-Smith K; Fletcher F A; Moore K A; Hawkins D; Villalon D; Chang S M; Caskey C T
Expression of human adenosine deaminase in murine hematopoietic cells.
Molecular and cellular biology 1988;8(12):5116-25.
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1988: Lee C C; Kohara Y; Akiyama K; Smith C L; Craigen W J; Caskey C T
Rapid and precise mapping of the Escherichia coli release factor genes by two physical approaches.
Journal of bacteriology 1988;170(10):4537-41.
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1988: Caskey C T; Gibbs R A; Witkowski J A; Hejtmancik J F
Diagnosis of human heritable defects by recombinant DNA methods.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences 1988;319(1194):353-60.
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1988: Yang T P; Stout J T; Konecki D S; Patel P I; Alford R L; Caskey C T
Spontaneous reversion of novel Lesch-Nyhan mutation by HPRT gene rearrangement.
Somatic cell and molecular genetics 1988;14(3):293-303.
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1988: Chamberlain J S; Pearlman J A; Muzny D M; Gibbs R A; Ranier J E; Caskey C T; Reeves A A
Expression of the murine Duchenne muscular dystrophy gene in muscle and brain.
Science (New York, N.Y.) 1988;239(4846):1416-8.
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1988: Lee C C; Wu X W; Gibbs R A; Cook R G; Muzny D M; Caskey C T
Generation of cDNA probes directed by amino acid sequence: cloning of urate oxidase.
Science (New York, N.Y.) 1988;239(4845):1288-91.
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1988: Scherer S E; Veres G; Caskey C T
The genetic structure of mouse ornithine transcarbamylase.
Nucleic acids research 1988;16(4):1593-601.
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1988: Fletcher F A; Moore K A; MacGregor G R; Belmont J W; Caskey C T
Human gene expression in murine hemopoietic cells in vivo.
Advances in experimental medicine and biology 1988;241():123-7.
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1987: Chamberlain J S; Grant S G; Reeves A A; Mullins L J; Stephenson D A; Hoffman E P; Monaco A P; Kunkel L M; Caskey C T; Chapman V M
Regional localization of the murine Duchenne muscular dystrophy gene on the mouse X chromosome.
Somatic cell and molecular genetics 1987;13(6):671-8.
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1987: Mullins L J; Veres G; Caskey C T; Chapman V
Differential methylation of the ornithine carbamoyl transferase gene on active and inactive mouse X chromosomes.
Molecular and cellular biology 1987;7(11):3916-22.
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1987: Craigen W J; Caskey C T
The function, structure and regulation of E. coli peptide chain release factors.
Biochimie 1987;69(10):1031-41.
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1987: Yang T P; Caskey C T
Nuclease sensitivity of the mouse HPRT gene promoter region: differential sensitivity on the active and inactive X chromosomes.
Molecular and cellular biology 1987;7(8):2994-8.
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1987: Veres G; Gibbs R A; Scherer S E; Caskey C T
The molecular basis of the sparse fur mouse mutation.
Science (New York, N.Y.) 1987;237(4813):415-7.
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1987: Chamberlain J S; VanTuinen P; Reeves A A; Philip B A; Caskey C T
Isolation of cDNA clones for the catalytic gamma subunit of mouse muscle phosphorylase kinase: expression of mRNA in normal and mutant Phk mice.
Proceedings of the National Academy of Sciences of the United States of America 1987;84(9):2886-90.
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1987: Chang S M; Wager-Smith K; Tsao T Y; Henkel-Tigges J; Vaishnav S; Caskey C T
Construction of a defective retrovirus containing the human hypoxanthine phosphoribosyltransferase cDNA and its expression in cultured cells and mouse bone marrow.
Molecular and cellular biology 1987;7(2):854-63.
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1987: Caskey C T
Lesch-Nyhan syndrome: mutation, prevention, and therapy.
Research publications - Association for Research in Nervous and Mental Disease 1987;65():187-94.
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1986: Belmont J W; Henkel-Tigges J; Chang S M; Wager-Smith K; Kellems R E; Dick J E; Magli M C; Phillips R A; Bernstein A; Caskey C T
Expression of human adenosine deaminase in murine haematopoietic progenitor cells following retroviral transfer.
Nature 1986;322(6077):385-7.
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1986: Veres G; Craigen W J; Caskey C T
The 5' flanking region of the ornithine transcarbamylase gene contains DNA sequences regulating tissue-specific expression.
The Journal of biological chemistry 1986;261(17):7588-91.
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1986: Chang S M; Tsao T Y; Patel P I; Chinault A C; Melton D W; Caskey C T
Expression of human and mouse HPRT minigenes.
Advances in experimental medicine and biology 1986;195 Pt A():231-6.
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1986: Patel P I; Yang T P; Stout J T; Konecki D S; Chinault A C; Caskey C T
Mutational diversity at the human HPRT locus.
Progress in clinical and biological research 1986;209A():457-63.
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1986: Nelson D L; Chang S M; Henkel-Tigges J; Wager-Smith K; Belmont J W; Caskey C T
Gene replacement therapy for inborn errors of purine metabolism.
Cold Spring Harbor symposia on quantitative biology 1986;51 Pt 2():1065-71.
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1986: Belmont J W; Henkel-Tigges J; Wager-Smith K; Chang S M; Caskey C T
Towards gene therapy for adenosine deaminase deficiency.
Annals of clinical research 1986;18(5-6):322-6.
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1985: Stout J T; Jackson L G; Caskey C T
First trimester diagnosis of Lesch-Nyhan syndrome: applications to other disorders of purine metabolism.
Prenatal diagnosis 1985;5(3):183-9.
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1984: Yang T P; Patel P I; Chinault A C; Stout J T; Jackson L G; Hildebrand B M; Caskey C T
Molecular evidence for new mutation at the hprt locus in Lesch-Nyhan patients.
Nature 1984;310(5976):412-4.
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1984: Melton D W; Konecki D S; Brennand J; Caskey C T
Structure, expression, and mutation of the hypoxanthine phosphoribosyltransferase gene.
Proceedings of the National Academy of Sciences of the United States of America 1984;81(7):2147-51.
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1984: Chinault A C; Brennand J; Konecki D S; Nussbaum R L; Caskey C T
Characterization and use of cloned sequences of the hypoxanthine-guanine phosphoribosyltransferase gene.
Advances in experimental medicine and biology 1984;165 Pt A():411-5.
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1983: Brennand J; Konecki D S; Caskey C T
Expression of human and Chinese hamster hypoxanthine-guanine phosphoribosyltransferase cDNA recombinants in cultured Lesch-Nyhan and Chinese hamster fibroblasts.
The Journal of biological chemistry 1983;258(16):9593-6.
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1982: Konecki D S; Brennand J; Fuscoe J C; Caskey C T; Chinault A C
Hypoxanthine-guanine phosphoribosyltransferase genes of mouse and Chinese hamster: construction and sequence analysis of cDNA recombinants.
Nucleic acids research 1982;10(21):6763-75.
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1982: Brennand J; Chinault A C; Konecki D S; Melton D W; Caskey C T
Cloned cDNA sequences of the hypoxanthine/guanine phosphoribosyltransferase gene from a mouse neuroblastoma cell line found to have amplified genomic sequences.
Proceedings of the National Academy of Sciences of the United States of America 1982;79(6):1950-4.
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1981: Melton D W; Konecki D S; Ledbetter D H; Hejtmancik J F; Caskey C T
In vitro translation of hypoxanthine/guanine phosphoribosyltransferase mRNA: characterization of a mouse neuroblastoma cell line that has elevated levels of hypoxanthine/guanine phosphoribosyltransferase protein.
Proceedings of the National Academy of Sciences of the United States of America 1981;78(11):6977-80.
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