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Kirby Smith

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Rebecca Deering Brose; Gao-xiang Dong; JEFFREY KEEFER; Martina C McGuinness; Shirley Purvis; Tonya Schneidereith; Gloria Shin; Forrest Spencer; Kirby D Smith
Activation of the stress proteome as a mechanism for small molecule therapeutics.
Rebecca Deering Brose; Dimitrios Avramopoulos; Kirby D Smith
SOD2 as a potential modifier of X-linked adrenoleukodystrophy clinical phenotypes.
P S Duggan; Andrew Siegel; David M Blass; H Bok; J T Coyle; Ruth R Faden; J Finkel; John D Gearhart; H T Greely; ARGYE HILLIS-TRUPE; Ahmet Hoke; Richard T Johnson; Michael V Johnston; J Kahn; Douglas A Kerr; P King; J Kurtzberg; S M Liao; JOHN MCDONALD; Guy M McKhann; K B Nelson; Mahendra S Rao; A Regenberg; Kirby D Smith; D Solter; Hongjun Song; Jeremy Sugarman; R J Traystman; A Vescovi; J Yanofski; W Young; Debra J H Mathews
Unintended changes in cognition, mood, and behavior arising from cell-based interventions for neurological conditions: ethical challenges.

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2012: Rebecca Deering Brose; Gao-xiang Dong; JEFFREY KEEFER; Martina C McGuinness; Shirley Purvis; Tonya Schneidereith; Gloria Shin; Forrest Spencer; Kirby D Smith
Activation of the stress proteome as a mechanism for small molecule therapeutics.
Human molecular genetics 2012;21(19):4237-52.
2012: Rebecca Deering Brose; Dimitrios Avramopoulos; Kirby D Smith
SOD2 as a potential modifier of X-linked adrenoleukodystrophy clinical phenotypes.
Journal of neurology 2012;259(7):1440-7.
2009: P S Duggan; Andrew Siegel; David M Blass; H Bok; J T Coyle; Ruth R Faden; J Finkel; John D Gearhart; H T Greely; ARGYE HILLIS-TRUPE; Ahmet Hoke; Richard T Johnson; Michael V Johnston; J Kahn; Douglas A Kerr; P King; J Kurtzberg; S M Liao; JOHN MCDONALD; Guy M McKhann; K B Nelson; Mahendra S Rao; A Regenberg; Kirby D Smith; D Solter; Hongjun Song; Jeremy Sugarman; R J Traystman; A Vescovi; J Yanofski; W Young; Debra J H Mathews
Unintended changes in cognition, mood, and behavior arising from cell-based interventions for neurological conditions: ethical challenges.
The American journal of bioethics : AJOB 2009;9(5):31-6.
2009: Alan Regenberg; Debra J H Mathews; David M Blass; Hilary Bok; Joseph T Coyle; Patrick Duggan; Ruth R Faden; Julia Finkel; John D Gearhart; ARGYE HILLIS-TRUPE; Ahmet Hoke; Richard T Johnson; Michael V Johnston; Jeffrey Kahn; Douglas A Kerr; Patricia King; Joanne Kurtzberg; S Matthew Liao; JOHN MCDONALD; Guy M McKhann; Karin B Nelson; Mahendra S Rao; Andrew Siegel; Kirby D Smith; Davor Solter; Hongjun Song; Jeremy Sugarman; Angelo Vescovi; Wise Young; Henry T Greely; Richard J Traystman
The role of animal models in evaluating reasonable safety and efficacy for human trials of cell-based interventions for neurologic conditions.
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism 2009;29(1):1-9.
2008: Debra J H Mathews; Jeremy Sugarman; Hilary Bok; David M Blass; J T Coyle; P Duggan; J Finkel; H T Greely; ARGYE HILLIS-TRUPE; Ahmet Hoke; Richard T Johnson; Michael V Johnston; J Kahn; Douglas A Kerr; J Kurtzberg; S Matthew Liao; JOHN MCDONALD; Guy M McKhann; K B Nelson; Mahendra S Rao; A Regenberg; Andrew Siegel; Kirby D Smith; Davor Solter; Hongjun Song; A Vescovi; W Young; John D Gearhart; Ruth R Faden
Cell-based interventions for neurologic conditions: ethical challenges for early human trials.
Neurology 2008;71(4):288-93.
2007: Jyh-Feng Lu; EMILY BARRON-CASELLA; Rebecca Deering; Ann Heinzer; Ann B Moser; Karen L deMesy Bentley; Gary S Wand; Martina C McGuinness; Zhengtong Pei; Paul A Watkins; Aurora Pujol; Kirby D Smith; James M Powers
The role of peroxisomal ABC transporters in the mouse adrenal gland: the loss of Abcd2 (ALDR), Not Abcd1 (ALD), causes oxidative damage.
Laboratory investigation; a journal of technical methods and pathology 2007;87(3):261-72.
2006: JEFFREY KEEFER; Tonya A Schneidereith; Abbie Mays; Shirley H Purvis; George J Dover; Kirby D Smith
Role of cyclic nucleotides in fetal hemoglobin induction in cultured CD34+ cells.
Experimental hematology 2006;34(9):1151-61.
2005: James M Powers; Zhengtong Pei; Ann Heinzer; Rebecca Deering; Ann B Moser; Hugo W Moser; Paul A Watkins; Kirby D Smith
Adreno-leukodystrophy: oxidative stress of mice and men.
Journal of neuropathology and experimental neurology 2005;64(12):1067-79.
2004: Zhenzhen Jia; Zhengtong Pei; Yuanyuan Li; Liumei Wei; Kirby D Smith; Paul A Watkins
X-linked adrenoleukodystrophy: role of very long-chain acyl-CoA synthetases.
Molecular genetics and metabolism 2004;83(1-2):117-27.
2003: Zhengtong Pei; Nadia A Oey; Maartje M Zuidervaart; Zhenzhen Jia; Yuanyuan Li; Steven J Steinberg; Kirby D Smith; Paul A Watkins
The acyl-CoA synthetase "bubblegum" (lipidosin): further characterization and role in neuronal fatty acid beta-oxidation..
The Journal of biological chemistry 2003;278(47):47070-8.
2003: Ann Heinzer; Paul A Watkins; Jyh-Feng Lu; Stephan Kemp; Ann B Moser; Yuan Yuan Li; Stephanie J Mihalik; James M Powers; Kirby D Smith
A very long-chain acyl-CoA synthetase-deficient mouse and its relevance to X-linked adrenoleukodystrophy.
Human molecular genetics 2003;12(10):1145-54.
2003: Ann Heinzer; Martina C McGuinness; Jyh-Feng Lu; O Colin Stine; Heming Wei; Mark Van der Vlies; Gao-xiang Dong; James Powers; Paul A Watkins; Kirby D Smith
Mouse models and genetic modifiers in X-linked adrenoleukodystrophy.
Advances in experimental medicine and biology 2003;544():75-93.
2003: Martina C McGuinness; Jyh-Feng Lu; H-P Zhang; Gao-xiang Dong; Ann Heinzer; Paul A Watkins; J Powers; Kirby D Smith
Role of ALDP (ABCD1) and mitochondria in X-linked adrenoleukodystrophy.
Molecular and cellular biology 2003;23(2):744-53.
2002: Xiaoling Li; Eveline Baumgart; Gao-xiang Dong; James C Morrell; Gerardo Jimenez-Sanchez; David Valle; Kirby D Smith; Stephen J Gould
PEX11alpha is required for peroxisome proliferation in response to 4-phenylbutyrate but is dispensable for peroxisome proliferator-activated receptor alpha-mediated peroxisome proliferation.
Molecular and cellular biology 2002;22(23):8226-40.
2002: Ann Heinzer; Stephan Kemp; Jyh-Feng Lu; Paul A Watkins; Kirby D Smith
Mouse very long-chain acyl-CoA synthetase in X-linked adrenoleukodystrophy.
The Journal of biological chemistry 2002;277(32):28765-73.
2002: Stephanie J Mihalik; Steven J Steinberg; Zhengtong Pei; Joseph Park; Do G Kim; Ann Heinzer; Georges Dacremont; Ronald J A Wanders; Dean Cuebas; Kirby D Smith; Paul A Watkins
Participation of two members of the very long-chain acyl-CoA synthetase family in bile acid synthesis and recycling.
The Journal of biological chemistry 2002;277(27):24771-9.
2002: Deyanira Corzo; William Gibson; Kisha Johnson; Grant Mitchell; Guy LePage; Gerald F Cox; Robin Casey; Carolyn Zeiss; Heidi Tyson; Garry R Cutting; Gerald V Raymond; Kirby D Smith; Paul A Watkins; Ann B Moser; Hugo W Moser; Steven J Steinberg
Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders.
American journal of human genetics 2002;70(6):1520-31.
2001: M Ito; Benjamin M Blumberg; David J Mock; Andrew D Goodman; Ann B Moser; H W Moser; Kirby D Smith; James M Powers
Potential environmental and host participants in the early white matter lesion of adreno-leukodystrophy: morphologic evidence for CD8 cytotoxic T cells, cytolysis of oligodendrocytes, and CD1-mediated lipid antigen presentation.
Journal of neuropathology and experimental neurology 2001;60(10):1004-19.
2001: Martina C McGuinness; H P Zhang; Kirby D Smith
Evaluation of pharmacological induction of fatty acid beta-oxidation in X-linked adrenoleukodystrophy.
Molecular genetics and metabolism 2001;74(1-2):256-63.
2001: Yen-Pei C Chang; Roberto Littera; R Garau; Kirby D Smith; George J Dover; S Iannelli; Enrico Cacace; Licinio Contu
The role of heterocellular hereditary persistence of fetal haemoglobin in beta(0)-thalassaemia intermedia.
British journal of haematology 2001;114(4):899-906.
2001: Lena Bezman; Ann B Moser; Gerald V Raymond; P Rinaldo; Paul A Watkins; Kirby D Smith; Nancy Kass; Hugo W Moser
Adrenoleukodystrophy: incidence, new mutation rate, and results of extended family screening.
Annals of neurology 2001;49(4):512-7.
2000: Steven J Steinberg; J Morgenthaler; Ann Heinzer; Kirby D Smith; Paul A Watkins
Very long-chain acyl-CoA synthetases. Human "bubblegum" represents a new family of proteins capable of activating very long-chain fatty acids.
The Journal of biological chemistry 2000;275(45):35162-9.
2000: Martina C McGuinness; H Wei; Kirby D Smith
Therapeutic developments in peroxisome biogenesis disorders.
Expert opinion on investigational drugs 2000;9(9):1985-92.
2000: MB Lachtermacher; H N Seuanez; Hugo W Moser; Kirby D Smith
One-step multiplex PCR strategy for identification of mutations by SSCP and DNA sequencing.
BioTechniques 2000;29(2):234-6.
2000: H Wei; Stephan Kemp; Martina C McGuinness; Ann B Moser; Kirby D Smith
Pharmacological induction of peroxisomes in peroxisome biogenesis disorders.
Annals of neurology 2000;47(3):286-96.
2000: Paul A Watkins; Jyh-Feng Lu; Lelita T Braiterman; Steven J Steinberg; Kirby D Smith
Disruption of a yeast very-long-chain acyl-CoA synthetase gene simulates the cellular phenotype of X-linked adrenoleukodystrophy.
Cell biochemistry and biophysics 2000;32 Spring():333-7.
2000: MB Lachtermacher; H N Seuánez; Ann B Moser; Hugo W Moser; Kirby D Smith
Determination of 30 X-linked adrenoleukodystrophy mutations, including 15 not previously described.
Human mutation 2000;15(4):348-53.
1999: Kirby D Smith; Stephan Kemp; Lelita T Braiterman; Jyh-Feng Lu; H M Wei; M Geraghty; Gail Stetten; J S Bergin; Jonathan Pevsner; Paul A Watkins
X-linked adrenoleukodystrophy: genes, mutations, and phenotypes.
Neurochemical research 1999;24(4):521-35.
1999: H W Moser; Stephan Kemp; Kirby D Smith
Mutational analysis and the pathogenesis of variant X-linked adrenoleukodystrophy phenotypes.
Archives of neurology 1999;56(3):273-5.
1999: Lelita T Braiterman; Paul A Watkins; Ann B Moser; Kirby D Smith
Peroxisomal very long chain fatty acid beta-oxidation activity is determined by the level of adrenodeukodystrophy protein (ALDP) expression.
Molecular genetics and metabolism 1999;66(2):91-9.
1999: AW Bergen; C Y Wang; J Tsai; K Jefferson; C Dey; Kirby D Smith; S C Park; S J Tsai; David Goldman
An Asian-Native American paternal lineage identified by RPS4Y resequencing and by microsatellite haplotyping.
Annals of human genetics 1999;63(Pt 1):63-80.
1999: M C McGuinness; Kirby D Smith
Cerebral inflammation in X-linked adrenoleukodystrophy.
Archivum immunologiae et therapiae experimentalis 1999;47(5):281-7.
1998: Stephan Kemp; H M Wei; Jyh-Feng Lu; Lelita T Braiterman; Martina C McGuinness; Ann B Moser; Paul A Watkins; Kirby D Smith
Gene redundancy and pharmacological gene therapy: implications for X-linked adrenoleukodystrophy.
Nature medicine 1998;4(11):1261-8.
1998: Paul A Watkins; Jyh-Feng Lu; Steven J Steinberg; Stephen J Gould; Kirby D Smith; Lelita T Braiterman
Disruption of the Saccharomyces cerevisiae FAT1 gene decreases very long-chain fatty acyl-CoA synthetase activity and elevates intracellular very long-chain fatty acid concentrations.
The Journal of biological chemistry 1998;273(29):18210-9.
1998: Lelita T Braiterman; S Zheng; Paul A Watkins; M T Geraghty; G Johnson; Martina C McGuinness; Ann B Moser; Kirby D Smith
Suppression of peroxisomal membrane protein defects by peroxisomal ATP binding cassette (ABC) proteins.
Human molecular genetics 1998;7(2):239-47.
1997: Jyh-Feng Lu; Ann M Lawler; Paul A Watkins; James M Powers; Ann B Moser; Hugo W Moser; Kirby D Smith
A mouse model for X-linked adrenoleukodystrophy.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(17):9366-71.
1997: Martina C McGuinness; James M Powers; W B Bias; B J Schmeckpeper; A H Segal; V C Gowda; S L Wesselingh; J Berger; Diane E Griffin; Kirby D Smith
Human leukocyte antigens and cytokine expression in cerebral inflammatory demyelinative lesions of X-linked adrenoleukodystrophy and multiple sclerosis.
Journal of neuroimmunology 1997;75(1-2):174-82.
1997: Yen-Pei C Chang; Micheline Maier-Redelsperger; Kirby D Smith; Licinio Contu; R Ducroco; Mariane de Montalembert; Marie-Sylvaine Belloy; Jacques Elion; George J Dover; Robert Girot
The relative importance of the X-linked FCP locus and beta-globin haplotypes in determining haemoglobin F levels: a study of SS patients homozygous for beta S haplotypes.
British journal of haematology 1997;96(4):806-14.
1995: Martina C McGuinness; Diane E Griffin; Gerald V Raymond; C A Washington; Hugo W Moser; Kirby D Smith
Tumor necrosis factor-alpha and X-linked adrenoleukodystrophy.
Journal of neuroimmunology 1995;61(2):161-9.
1995: Paul A Watkins; Stephen J Gould; M A Smith; Lelita T Braiterman; H M Wei; F Kok; Ann B Moser; Hugo W Moser; Kirby D Smith
Altered expression of ALDP in X-linked adrenoleukodystrophy.
American journal of human genetics 1995;57(2):292-301.
1995: Hugo W Moser; J M Powers; Kirby D Smith
Adrenoleukodystrophy: molecular genetics, pathology, and Lorenzo's oil.
Brain pathology (Zurich, Switzerland) 1995;5(3):259-66.
1995: Yen-Pei C Chang; Kirby D Smith; Richard D Moore; G R Serjeant; George J Dover
An analysis of fetal hemoglobin variation in sickle cell disease: the relative contributions of the X-linked factor, beta-globin haplotypes, alpha-globin gene number, gender, and age.
Blood 1995;85(4):1111-7.
1994: Yen-Pei C Chang; Kirby D Smith; George J Dover
Dinucleotide repeat polymorphisms at the DXS85, DXS16 and DXS43 loci.
Human molecular genetics 1994;3(6):1029.
1994: P Y Fechner; C Rosenberg; Gail Stetten; Colyn B Cargile; P L Pearson; Kirby D Smith; Claude J Migeon; Gary D Berkovitz
Nonrandom inactivation of the Y-bearing X chromosome in a 46,XX individual: evidence for the etiology of 46,XX true hermaphroditism.
Cytogenetics and cell genetics 1994;66(1):22-6.
1993: P Y Fechner; S M Marcantonio; T Ogata; T O Rosales; Kirby D Smith; P N Goodfellow; Claude J Migeon; Gary D Berkovitz
Report of a kindred with X-linked (or autosomal dominant sex-limited) 46,XY partial gonadal dysgenesis.
The Journal of clinical endocrinology and metabolism 1993;76(5):1248-53.
1993: P Y Fechner; S M Marcantonio; V Jaswaney; Gail Stetten; P N Goodfellow; Claude J Migeon; Kirby D Smith; Gary D Berkovitz; J A Amrhein; P A Bard
The role of the sex-determining region Y gene in the etiology of 46,XX maleness.
The Journal of clinical endocrinology and metabolism 1993;76(3):690-5.
1992: JR Hawkins; A Taylor; PN Goodfellow; Claude J Migeon; Kirby D Smith; Gary D Berkovitz
Evidence for increased prevalence of SRY mutations in XY females with complete rather than partial gonadal dysgenesis.
American journal of human genetics 1992;51(5):979-84.
1992: George J Dover; Kirby D Smith; Yen-Pei C Chang; S Purvis; A Mays; Deborah A Meyers; C Sheils; G Serjeant
Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2.
Blood 1992;80(3):816-24.
1992: O Colin Stine; George J Dover; D Zhu; Kirby D Smith
The evolution of two west African populations.
Journal of molecular evolution 1992;34(4):336-44.
1992: P Y Fechner; Kirby D Smith; Ethylin Jabs; Claude J Migeon; Gary D Berkovitz
Partial gonadal dysgenesis in a patient with a marker Y chromosome.
American journal of medical genetics 1992;42(6):807-12.
1992: Gary D Berkovitz; P Y Fechner; S M Marcantonio; G Bland; Gail Stetten; P N Goodfellow; Kirby D Smith; Claude J Migeon
The role of the sex-determining region of the Y chromosome (SRY) in the etiology of 46,XX true hermaphroditism.
Human genetics 1992;88(4):411-6.
1992: Hugo W Moser; Ann B Moser; Kirby D Smith; A Bergin; J Borel; J Shankroff; O Colin Stine; C Merette; J Ott; W Krivit
Adrenoleukodystrophy: phenotypic variability and implications for therapy.
Journal of inherited metabolic disease 1992;15(4):645-64.
1990: O Colin Stine; Kirby D Smith
The estimation of selection coefficients in Afrikaners: Huntington disease, porphyria variegata, and lipoid proteinosis.
American journal of human genetics 1990;46(3):452-8.
1989: J Weissenbach; P N Goodfellow; Kirby D Smith
Report of the committee on the genetic constitution of the Y chromosome.
Cytogenetics and cell genetics 1989;51(1-4):438-49.
1988: G G Johnson; W A Kronert; Sanford I Bernstein; Verne M Chapman; Kirby D Smith
Altered turnover of allelic variants of hypoxanthine phosphoribosyltransferase is associated with N-terminal amino acid sequence variation.
The Journal of biological chemistry 1988;263(19):9079-82.
1988: J Weissenbach; P N Goodfellow; Kirby D Smith
Report of the committee on the genetic constitution of the Y chromosome.
Cytogenetics and cell genetics 1988;49(1-3):129-31.
1987: Alan F Scott; B J Schmeckpeper; M Abdelrazik; C T Comey; B O'Hara; Judith P. Rossiter; T Cooley; P Heath; Kirby D Smith; L Margolet
Origin of the human L1 elements: proposed progenitor genes deduced from a consensus DNA sequence.
Genomics 1987;1(2):113-25.
1987: Kirby D Smith; Keith E Young; C Conover Talbot; B J Schmeckpeper
Repeated DNA of the human Y chromosome.
Development (Cambridge, England) 1987;101 Suppl():77-92.
1985: B J Schmeckpeper; J Davis; H F Willard; Kirby D Smith
An anonymous single-copy X-chromosome RFLP for DXS72 from Xq13-Xq22 [HGM8 provisional no. DXS72].
Nucleic acids research 1985;13(15):5724.
1985: Robert D Burk; P Ma; Kirby D Smith
Characterization and evolution of a single-copy sequence from the human Y chromosome.
Molecular and cellular biology 1985;5(3):576-81.
1985: Robert D Burk; P Szabo; S O'Brien; W G Nash; L Yu; Kirby D Smith
Organization and chromosomal specificity of autosomal homologs of human Y chromosome repeated DNA.
Chromosoma 1985;92(3):225-33.
1984: S H Boyer; George J Dover; G R Serjeant; Kirby D Smith; S E Antonarakis; Stephen Embury; L Margolet; A N Noyes; M L Boyer; W B Bias
Production of F cells in sickle cell anemia: regulation by a genetic locus or loci separate from the beta-globin gene cluster.
Blood 1984;64(5):1053-8.
1984: B J Schmeckpeper; Alan F Scott; Kirby D Smith
Transcripts homologous to a long repeated DNA element in the human genome.
The Journal of biological chemistry 1984;259(2):1218-25.
1984: S H Boyer; Harry Ostrer; Kirby D Smith; K E Young; A N Noyes
Isolation of cDNA clones for rabbit red cell carbonic anhydrase and catalase: a pilot study directed at isolation of coordinately expressed genes.
Annals of the New York Academy of Sciences 1984;429():324-31.
1983: S Charache; George J Dover; Kirby D Smith; C Conover Talbot; M Moyer; S Boyer
Treatment of sickle cell anemia with 5-azacytidine results in increased fetal hemoglobin production and is associated with nonrandom hypomethylation of DNA around the gamma-delta-beta-globin gene complex.
Proceedings of the National Academy of Sciences of the United States of America 1983;80(15):4842-6.
1983: H F Willard; Kirby D Smith; J Sutherland
Isolation and characterization of a major tandem repeat family from the human X chromosome.
Nucleic acids research 1983;11(7):2017-33.
1983: Robert D Burk; J Stamberg; K E Young; Kirby D Smith
Use of repetitive DNA for diagnosis of chromosomal rearrangements.
Human genetics 1983;64(4):339-42.
1983: George J Dover; S H Charache; S H Boyer; C Conover Talbot; Kirby D Smith
5-Azacytidine increases fetal hemoglobin production in a patient with sickle cell disease.
Progress in clinical and biological research 1983;134():475-88.
1982: L Cavalli-Sforza; K Davies; Kirby D Smith; P Pearson; P Gerald; S Naylor; Haig Kazazian ; R White; R Elliot; L Crippa; B Young; M Skolnick; M Nei
Workshop on DNA polymorphisms.
Progress in clinical and biological research 1982;103 Pt A():79-81.
1982: Louis Kunkel; Kirby D Smith
Evolution of human Y-chromosome DNA.
Chromosoma 1982;86(2):209-28.
1981: B J Schmeckpeper; H F Willard; Kirby D Smith
Isolation and characterization of cloned human DNA fragments carrying reiterated sequences common to both autosomes and the X chromosome.
Nucleic acids research 1981;9(8):1853-72.
1981: Alan F Scott; J A Phillips; K E Young; Haig Kazazian ; Kirby D Smith; S Charache; J B Clegg
The molecular basis of hemoglobin Grady.
American journal of human genetics 1981;33(1):129-33.
1981: SUSAN PANNY; Alan F Scott; Kirby D Smith; J A Phillips; Haig Kazazian ; C Conover Talbot; Corinne D Boehm
Population heterogeneity of the Hpa I restriction site associated with the beta globin gene: implications for prenatal diagnosis.
American journal of human genetics 1981;33(1):25-35.
1980: J A Phillips; T A Vik; Alan F Scott; K E Young; Haig Kazazian ; Kirby D Smith; V F Fairbanks; H M Koenig
Unequal crossing-over: a common basis of single alpha-globin genes in Asians and American blacks with hemoglobin-H disease.
Blood 1980;55(6):1066-9.
1980: J A Phillips; SUSAN PANNY; Haig Kazazian ; Corinne D Boehm; Alan F Scott; Kirby D Smith
Prenatal diagnosis of sickle cell anemia by restriction and endonuclease analysis: HindIII polymorphisms in gamma-globin genes extend test applicability.
Proceedings of the National Academy of Sciences of the United States of America 1980;77(5):2853-6.
1979: J A Phillips; Alan F Scott; Kirby D Smith; K E Young; K L Lightbody; R M Jiji; Haig Kazazian
A molecular basis for hemoglobin-H disease in American blacks.
Blood 1979;54(6):1439-45.
1979: B J Schmeckpeper; Kirby D Smith; B P Dorman; F H Ruddle; C Conover Talbot
Partial purification and characterization of DNA from the human X chromosome.
Proceedings of the National Academy of Sciences of the United States of America 1979;76(12):6525-8.
1979: J A Phillips; Alan F Scott; Haig Kazazian ; Kirby D Smith; Gail Stetten; George H Thomas
Prenatal diagnosis of hemoglobinopathies by restriction endonuclease analysis: pregnancies at risk for sickle cell anemia and S--O Arab disease.
The Johns Hopkins medical journal 1979;145(2):57-60.
1979: Louis Kunkel; Kirby D Smith; S H Boyer
Organization and heterogeneity of sequences within a repeating unit of human Y chromosome deoxyribonucleic acid.
Biochemistry 1979;18(15):3343-53.
1979: D H Hamer; Kirby D Smith; S H Boyer; P Leder
SV40 recombinants carrying rabbit beta-globin gene coding sequences.
Cell 1979;17(3):725-35.
1978: S H Boyer; Alan F Scott; Louis Kunkel; Kirby D Smith
The proportion of all point mutations which are unacceptable: an estimate based on hemoglobin amino acid and nucleotide sequences.
Canadian journal of genetics and cytology. Journal canadien de génétique et de cytologie 1978;20(1):111-37.
1977: Louis Kunkel; Kirby D Smith; S H Boyer; D S Borgaonkar; S S Wachtel; O J Miller; W R Breg; HOWARD JONES; J M Rary
Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.
Proceedings of the National Academy of Sciences of the United States of America 1977;74(3):1245-9.
1976: Lee Bacheler; Kirby D Smith
Transcription of isolated mouse liver chromatin.
Biochemistry 1976;15(15):3281-90.
1976: Louis Kunkel; Kirby D Smith; S H Boyer
Human Y-chromosome-specific reiterated DNA.
Science (New York, N.Y.) 1976;191(4232):1189-90.
1976: Kirby D Smith; Louis Kunkel; S H Boyer
Isolation and uses of chromosome-specific reiterated DNA.
Cytogenetics and cell genetics 1976;16(1-5):401-4.
1976: Kirby D Smith; Louis Kunkel; S H Boyer
Isolation and uses of chromosome-specific reiterated DNA.
Birth defects original article series 1976;12(7):401-4.
1972: B J Schmeckpeper; Kirby D Smith
Use of formamide in nucleic acid reassociation.
Biochemistry 1972;11(7):1319-26.
1972: H Tobler; Kirby D Smith; H Ursprung
Molecular aspects of chromatin elimination in Ascaris lumbricoides.
Developmental biology 1972;27(2):190-203.
1969: Kirby D Smith; R B Church; B J McCarthy
Template specificity of isolated chromatin.
Biochemistry 1969;8(11):4271-7.
1967: Kirby D Smith; J L Armstrong; B J McCarthy
The introduction of radioisotopes into RNA by methylation in vitro.
Biochimica et biophysica acta 1967;142(2):323-30.
1967: Kirby D Smith
Genetic control of macromolecular synthesis during development of an ascidian: Ascidia nigra.
The Journal of experimental zoology 1967;164(3):393-405.