Username

Password

Forgot Password?

Preview

Sign-in free and Explore the Exciting World of BiomedExperts:

Over 1.500.000 Profiles
More than 1.800 Organizations worldwide
State of the Art Network Visualizations

Manage your own Profile
Locate Experts in your Country/Region
Locate Experts in your 1. and 2. Level Network
Connect to Experts Worldwide

NetworkView

David Barker

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Procedures

Disorders

Anatomy

Chemicals & Drugs

Concepts & Ideas

Physiology

Phenomena

Southern Blotting

Genes & Molecular Sequences

Alleles

Sign-in to see full Profile

Network (preview)

Co-Publications
Name
12
Gregory, Martin
10
Atkin, CL
7
Doll, Mark
7
Goldgar, David
7
Hein, David
6
Denison, JC
5
States, J.Christopher
4
Skolnick, Mark
4
Tryggvason, Karl
4
Econs, Michael
4
Husain, Anwar
4
Chance, Phillip
3
Zhang, Xiaoyan
3
Speer, Marcy
3
Pericak-Vance, Margaret

Sign-in to see all Coauthors

Publications

TOP 3
Barker David F; Walraven Jason M; Ristagno Elizabeth H; Doll Mark A; States J Christopher; Hein David W
Quantitative tissue and gene-specific differences and developmental changes in Nat1, Nat2, and Nat3 mRNA expression in the rat.
Martin Robert C G; Barker David F; Doll Mark A; Pine Sharon R; Mechanic Leah; Bowman Elise D; Harris Curtis C; Hein David W
Manganese superoxide dismutase gene coding region polymorphisms lack clinical incidence in general population.
Walraven Jason M; Barker David F; Doll Mark A; Hein David W
Tissue expression and genomic sequences of rat N-acetyltransferases rNat1, rNat2, rNat3, and Functional characterization of a novel rNat3*2 genetic variant.

Sign-in to see all Publications

Sign in free and see...

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the visualized research activity
of experts around the globe

Sign-in to see more

Geonetwork of David Barker (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

Sign-in to see more

All Publications

2008: Barker David F; Walraven Jason M; Ristagno Elizabeth H; Doll Mark A; States J Christopher; Hein David W
Quantitative tissue and gene-specific differences and developmental changes in Nat1, Nat2, and Nat3 mRNA expression in the rat.
Drug metabolism and disposition: the biological fate of chemicals 2008;36(12):2445-51.
2008: Martin Robert C G; Barker David F; Doll Mark A; Pine Sharon R; Mechanic Leah; Bowman Elise D; Harris Curtis C; Hein David W
Manganese superoxide dismutase gene coding region polymorphisms lack clinical incidence in general population.
DNA and cell biology 2008;27(6):321-3.
2007: Walraven Jason M; Barker David F; Doll Mark A; Hein David W
Tissue expression and genomic sequences of rat N-acetyltransferases rNat1, rNat2, rNat3, and Functional characterization of a novel rNat3*2 genetic variant.
Toxicological sciences : an official journal of the Society of Toxicology 2007;99(2):413-21.
2007: Husain Anwar; Zhang Xiaoyan; Doll Mark A; States J Christopher; Barker David F; Hein David W
Functional analysis of the human N-acetyltransferase 1 major promoter: quantitation of tissue expression and identification of critical sequence elements.
Drug metabolism and disposition: the biological fate of chemicals 2007;35(9):1649-56.
2007: Husain Anwar; Zhang Xiaoyan; Doll Mark A; States J Christopher; Barker David F; Hein David W
Identification of N-acetyltransferase 2 (NAT2) transcription start sites and quantitation of NAT2-specific mRNA in human tissues.
Drug metabolism and disposition: the biological fate of chemicals 2007;35(5):721-7.
2006: Barker David F; Husain Anwar; Neale Jason R; Martini Benjamin D; Zhang Xiaoyan; Doll Mark A; States J Christopher; Hein David W
Functional properties of an alternative, tissue-specific promoter for human arylamine N-acetyltransferase 1.
Pharmacogenetics and genomics 2006;16(7):515-25.
2004: Husain Anwar; Barker David F; States J Christopher; Doll Mark A; Hein David W
Identification of the major promoter and non-coding exons of the human arylamine N-acetyltransferase 1 gene (NAT1).
Pharmacogenetics 2004;14(7):397-406.
2003: Thielen Beth K; Barker David F; Nelson Raoul D; Zhou Jing; Kren Stefan M; Segal Yoav
Deletion mapping in Alport syndrome and Alport syndrome-diffuse leiomyomatosis reveals potential mechanisms of visceral smooth muscle overgrowth.
Human mutation 2003;22(5):419.
2001: Heath K E; Campos-Barros A; Toren A; Rozenfeld-Granot G; Carlsson L E; Savige J; Denison J C; Gregory M C; White J G; Barker D F; Greinacher A; Epstein C J; Glucksman M J; Martignetti J A
Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes.
American journal of human genetics 2001;69(5):1033-45.
2001: Barker D F; Denison J C; Atkin C L; Gregory M C
Efficient detection of Alport syndrome COL4A5 mutations with multiplex genomic PCR-SSCP.
American journal of medical genetics 2001;98(2):148-60.
2000: Barker D F
Direct genomic multiplex PCR for BRCA1 and application to mutation detection by single-strand conformation and heteroduplex analysis.
Human mutation 2000;16(4):334-44.
2000: Bennett C L; Yoshioka R; Kiyosawa H; Barker D F; Fain P R; Shigeoka A O; Chance P F
X-Linked syndrome of polyendocrinopathy, immune dysfunction, and diarrhea maps to Xp11.23-Xq13.3.
American journal of human genetics 2000;66(2):461-8.
1999: Liu X; Barker D F
Evidence for effective suppression of recombination in the chromosome 17q21 segment spanning RNU2-BRCA1.
American journal of human genetics 1999;64(5):1427-39.
1998: Sasaki S; Zhou B; Fan W W; Kim Y; Barker D F; Denison J C; Atkin C L; Gregory M C; Zhou J; Segal Y; Sado Y; Ninomiya Y; Michael A F; Kashtan C E
Expression of mRNA for type IV collagen alpha1, alpha5 and alpha6 chains by cultured dermal fibroblasts from patients with X-linked Alport syndrome.
Matrix biology : journal of the International Society for Matrix Biology 1998;17(4):279-91.
1998: Naumova A K; Leppert M; Barker D F; Morgan K; Sapienza C
Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome.
American journal of human genetics 1998;62(6):1493-9.
1997: Barker D F; Denison J C; Atkin C L; Gregory M C
Common ancestry of three Ashkenazi-American families with Alport syndrome and COL4A5 R1677Q.
Human genetics 1997;99(5):681-4.
1996: Barker D F; Liu X; Almeida E R
The BRCA1 and 1A1.3B promoters are parallel elements of a genomic duplication at 17q21.
Genomics 1996;38(2):215-22.
1996: Barker D F; Pruchno C J; Jiang X; Atkin C L; Stone E M; Denison J C; Fain P R; Gregory M C
A mutation causing Alport syndrome with tardive hearing loss is common in the western United States.
American journal of human genetics 1996;58(6):1157-65.
1996: Cambi F; Tang X M; Cordray P; Fain P R; Keppen L D; Barker D F
Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegia.
Neurology 1996;46(4):1112-7.
1996: Barker D F; Almeida E R; Casey G; Fain P R; Liao S Y; Masunaka I; Noble B; Kurosaki T; Anton-Culver H
BRCA1 R841W: a strong candidate for a common mutation with moderate phenotype.
Genetic epidemiology 1996;13(6):595-604.
1996: Barker D F; Atkin C L; Gregory M C; Fain P R
Application of linked markers for genetic diagnosis of Alport syndrome.
Contributions to nephrology 1996;117():29-45.
1996: Gregory M C; Terreros D A; Barker D F; Fain P N; Denison J C; Atkin C L
Alport syndrome--clinical phenotypes, incidence, and pathology.
Contributions to nephrology 1996;117():1-28.
1995: Pericak-Vance M A; Barker D F; Bergoffen J A; Chance P; Cochrane S; Dahl N; Exler M C; Fain P R; Fairweather N D; Fischbeck K
Consortium fine localization of X-linked Charcot-Marie-Tooth disease (CMTX1): additional support that connexin32 is the defect in CMTX1.
Human heredity 1995;45(3):121-8.
1995: Fain P R; Kort E N; Chance P F; Nguyen K; Redd D F; Econs M J; Barker D F
A 2D crossover-based map of the human X chromosome as a model for map integration.
Nature genetics 1995;9(3):261-6.
1994: Econs M J; Rowe P S; Francis F; Barker D F; Speer M C; Norman M; Fain P R; Weissenbach J; Read A; Davis K E
Fine structure mapping of the human X-linked hypophosphatemic rickets gene locus.
The Journal of clinical endocrinology and metabolism 1994;79(5):1351-4.
1994: Barker D F; Cordray P; Fain P R
The same polymorphism identified by the DXS571(B) and DXS1105 loci.
Human molecular genetics 1994;3(10):1913.
1994: Gregory M C; Atkins C L; Barker D F
Hearing loss.
The New England journal of medicine 1994;330(10):714; author reply 715.
1994: Fain P R; Barker D F; Chance P F
Refined genetic mapping of X-linked Charcot-Marie-Tooth neuropathy.
American journal of human genetics 1994;54(2):229-35.
1993: Barker D F; Fain P R
Definition and mapping of STSs at STR and RFLP loci in Xp11-Xq22.
Genomics 1993;18(3):712-6.
1993: Barker D F; Nguyen K; Fain P R
Two simple repeat polymorphisms at DXS337.
Human molecular genetics 1993;2(9):1507.
1993: Econs M J; Fain P R; Norman M; Speer M C; Pericak-Vance M A; Becker P A; Barker D F; Taylor A; Drezner M K
Flanking markers define the X-linked hypophosphatemic rickets gene locus.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 1993;8(9):1149-52.
1993: Barker D F; Nguyen K; Fain P R
A CA dinucleotide polymorphism at D17S107 (17q12-q24).
Human molecular genetics 1993;2(7):1086.
1993: Ionasescu V; Ionasescu G; Searby C; Barker D F
Is the duplication present in all family members affected with Charcot-Marie-Tooth neuropathy type 1 A?
Romanian journal of neurology and psychiatry = Revue roumaine de neurologie et psychiatrie 1993;31(3-4):179-87.
1993: Ionasescu V V; Ionasescu R; Searby C; Barker D F
Charcot-Marie-Tooth neuropathy type 1A with both duplication and non-duplication.
Human molecular genetics 1993;2(4):405-10.
1993: Zhou J; Gregory M C; Hertz J M; Barker D F; Atkin C; Spencer E S; Tryggvason K
Mutations in the codon for a conserved arginine-1563 in the COL4A5 collagen gene in Alport syndrome.
Kidney international 1993;43(3):722-9.
1993: Parolini O; Hejtmancik J F; Allen R C; Belmont J W; Lassiter G L; Henry M J; Barker D F; Conley M E
Linkage analysis and physical mapping near the gene for X-linked agammaglobulinemia at Xq22.
Genomics 1993;15(2):342-9.
1993: Barker D F
A more robust, rapid alkaline denaturation sequencing method.
BioTechniques 1993;14(2):168-9.
1992: Worley K C; Towbin J A; Zhu X M; Barker D F; Ballabio A; Chamberlain J; Biesecker L G; Blethen S L; Brosnan P; Fox J E
Identification of new markers in Xp21 between DXS28 (C7) and DMD.
Genomics 1992;13(4):957-61.
1992: Econs M J; Barker D F; Speer M C; Pericak-Vance M A; Fain P R; Drezner M K
Multilocus mapping of the X-linked hypophosphatemic rickets gene.
The Journal of clinical endocrinology and metabolism 1992;75(1):201-6.
1992: Hallam P J; Harding A E; Berciano J; Barker D F; Malcolm S
Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1).
Annals of neurology 1992;31(5):570-2.
1992: Schwartz C E; May M; Huang T; Ledbetter D; Anderson G; Barker D F; Lubs H A; Arena F; Stevenson R E
MRX8: an X-linked mental retardation condition with linkage to Xq21.
American journal of medical genetics 1992;43(1-2):467-74.
1992: Ram K T; Barker D F; Puck J M
Dinucleotide repeat polymorphism at the DXS441 locus.
Nucleic acids research 1992;20(6):1428.
1992: Stern H J; Saal H M; Lee J S; Fain P R; Goldgar D E; Rosenbaum K N; Barker D F
Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome?
Journal of medical genetics 1992;29(3):184-7.
1992: Barker D F; Cleverly J; Fain P R
Two CA-dinucleotide polymorphisms at the COL4A5 (Alport syndrome) gene in Xq22.
Nucleic acids research 1992;20(4):929.
1992: Barker D F; Nguyen K; Fain P R
A CA-dinucleotide polymorphism at the D17S113 locus, which is closely linked to D17S74.
Nucleic acids research 1992;20(4):923.
1992: Lebo R V; Lynch E D; Bird T D; Golbus M S; Barker D F; O'Connell P; Chance P F
Multicolor in situ hybridization and linkage analysis order Charcot-Marie-Tooth type I (CMTIA) gene-region markers.
American journal of human genetics 1992;50(1):42-55.
1991: Hoogendijk J E; Hensels G W; Zorn I; Valentijn L; Janssen E A; de Visser M; Barker D F; Ongerboer de Visser B W; Baas F; Bolhuis P A
The duplication in Charcot-Marie-Tooth disease type 1a spans at least 1100 kb on chromosome 17p11.2.
Human genetics 1991;88(2):215-8.
1991: Fain P R; Luty J A; Guo Z; Nguyen K; Barker D F; Litt M
Localization of the highly polymorphic microsatellite DXS456 on the genetic linkage map of the human X chromosome.
Genomics 1991;11(4):1155-7.
1991: Barker D F; Fain P R; Goldgar D E; Dietz-Band J N; Turco A E; Kashtan C E; Gregory M C; Tryggvason K; Skolnick M H; Atkin C L
High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers.
Human genetics 1991;88(2):189-94.
1991: Lafrenière R G; Brown C J; Powers V E; Carrel L; Davies K E; Barker D F; Willard H F
Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome.
Genomics 1991;11(2):352-63.
1991: Pulst S M; Pribyl T; Barker D F; Riccardi V M; Ren M; Yaari H; Korenberg J R
Molecular analysis of a patient with neurofibromatosis 1 and achondroplasia.
American journal of medical genetics 1991;40(1):84-7.
1991: Lupski J R; de Oca-Luna R M; Slaugenhaupt S; Pentao L; Guzzetta V; Trask B J; Saucedo-Cardenas O; Barker D F; Killian J M; Garcia C A; Chakravarti A; Patel P I
DNA duplication associated with Charcot-Marie-Tooth disease type 1A.
Cell 1991;66(2):219-32.
1991: Zhou J; Barker D F; Hostikka S L; Gregory M C; Atkin C L; Tryggvason K
Single base mutation in alpha 5(IV) collagen chain gene converting a conserved cysteine to serine in Alport syndrome.
Genomics 1991;9(1):10-8.
1991: Raeymaekers P; Timmerman V; Nelis E; De Jonghe P; Hoogendijk J E; Baas F; Barker D F; Martin J J; De Visser M; Bolhuis P A
Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a). The HMSN Collaborative Research Group.
Neuromuscular disorders : NMD 1991;1(2):93-7.
1990: Siewertsen M A; Barker D F; Cox D W
Two polymorphisms of the FOS oncogene.
Nucleic acids research 1990;18(20):6174.
1990: Barker D F; Hostikka S L; Zhou J; Chow L T; Oliphant A R; Gerken S C; Gregory M C; Skolnick M H; Atkin C L; Tryggvason K
Identification of mutations in the COL4A5 collagen gene in Alport syndrome.
Science (New York, N.Y.) 1990;248(4960):1224-7.
1990: Pulst S M; Graham J M; Fain P; Barker D; Pribyl T; Korenberg J R
The achondroplasia gene is not linked to the locus for neurofibromatosis 1 on chromosome 17.
Human genetics 1990;85(1):12-4.
1990: Wright E C; Goldgar D E; Fain P R; Barker D F; Skolnick M H
A genetic map of human chromosome 17p.
Genomics 1990;7(1):103-9.
1990: Jadayel D; Fain P; Upadhyaya M; Ponder M A; Huson S M; Carey J; Fryer A; Mathew C G; Barker D F; Ponder B A
Paternal origin of new mutations in von Recklinghausen neurofibromatosis.
Nature 1990;343(6258):558-9.
1990: Dietz-Band J N; Turco A E; Willard H F; Vincent A; Skolnick M H; Barker D F
Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers.
Cytogenetics and cell genetics 1990;54(3-4):137-41.
1989: Fain P R; Goldgar D E; Wallace M R; Collins F S; Wright E; Nguyen K; Barker D F
Refined physical and genetic mapping of the NF1 region on chromosome 17.
American journal of human genetics 1989;45(5):721-8.
1989: Ledbetter D H; Ledbetter S A; vanTuinen P; Summers K M; Robinson T J; Nakamura Y; Wolff R; White R; Barker D F; Wallace M R
Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome region.
Proceedings of the National Academy of Sciences of the United States of America 1989;86(13):5136-40.
1989: Baker S J; Fearon E R; Nigro J M; Hamilton S R; Preisinger A C; Jessup J M; vanTuinen P; Ledbetter D H; Barker D F; Nakamura Y; White R; Vogelstein B
Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas.
Science (New York, N.Y.) 1989;244(4901):217-21.
1989: Barker D F; Fain P R; Wright E C; Nguyen K; Tsui L C
A rare PvuII RFLP at the CRYB1 locus (17q11.2----17q12).
Nucleic acids research 1989;17(2):826.
1989: Wright E C; Fain P R; Barker D F; Chao M V
A moderately frequent HindIII polymorphism at the human NGFR locus (17q12----17q22).
Nucleic acids research 1989;17(2):825.
1989: Wright E C; Fain P R; Barker D F; Chao M V
Two polymorphic TaqI sites at the human NGFR locus (17q12----17q22).
Nucleic acids research 1989;17(2):824.
1989: Fain P R; Wright E; Willard H F; Stephens K; Barker D F
The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpoints.
American journal of human genetics 1989;44(1):68-72.
1989: Barker D F; Fain P R; Wright E C; Nguyen K; Tsui L C
MspI RFLP at CRYB1 locus (17q11.2----17q12).
Nucleic acids research 1989;17(2):827.
1989: Solomon E; Barker D F
Report of the committee on the genetic constitution of chromosome 17.
Cytogenetics and cell genetics 1989;51(1-4):319-37.
1989: Cox N J; Gogolin K J; Horvath V J; Barker D F; Wright E; Tran T; Skolnick M H; Boehm B O; Fehsel K; Bertrams J
Restriction fragment polymorphisms of the HLA-DR, HLA-DQ, and insulin gene regions in IDDM: the GAW5 data.
Genetic epidemiology 1989;6(1):21-6.
1988: Bowden D W; Müller-Kahle H; Fulton T R; Gravius T C; Barker D F; Donis-Keller H
Studies on locus expansion, library representation, and chromosome walking using an efficient method to screen cosmid libraries.
Gene 1988;71(2):391-400.
1988: Nakamura Y; Lathrop M; O'Connell P; Leppert M; Barker D; Wright E; Skolnick M; Kondoleon S; Litt M; Lalouel J M
A mapped set of DNA markers for human chromosome 17.
Genomics 1988;2(4):302-9.
1988: Schumm J W; Knowlton R G; Braman J C; Barker D F; Botstein D; Akots G; Brown V A; Gravius T C; Helms C; Hsiao K
Identification of more than 500 RFLPs by screening random genomic clones.
American journal of human genetics 1988;42(1):143-59.
1987: Fain P R; Barker D F; Goldgar D E; Wright E; Nguyen K; Carey J; Johnson J; Kivlin J; Willard H; Mathew C
Genetic analysis of NF1: identification of close flanking markers on chromosome 17.
Genomics 1987;1(4):340-5.
1987: White R; Nakamura Y; O'Connell P; Leppert M; Lalouel J M; Barker D; Goldgar D; Skolnick M; Carey J; Wallis C E
Tightly linked markers for the neurofibromatosis type 1 gene.
Genomics 1987;1(4):364-7.
1987: Barker D; Green P; Knowlton R; Schumm J; Lander E; Oliphant A; Willard H; Akots G; Brown V; Gravius T
Genetic linkage map of human chromosome 7 with 63 DNA markers.
Proceedings of the National Academy of Sciences of the United States of America 1987;84(22):8006-10.
1987: Barker D; Wright E; Nguyen K; Cannon L; Fain P; Goldgar D; Bishop D T; Carey J; Kivlin J; Willard H
A genomic search for linkage of neurofibromatosis to RFLPs.
Journal of medical genetics 1987;24(9):536-8.
1987: Barker D; Wright E; Nguyen K; Cannon L; Fain P; Goldgar D; Bishop D T; Carey J; Baty B; Kivlin J
Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17.
Science (New York, N.Y.) 1987;236(4805):1100-2.
1986: Knowlton R G; Brown V A; Braman J C; Barker D; Schumm J W; Murray C; Takvorian T; Ritz J; Donis-Keller H
Use of highly polymorphic DNA probes for genotypic analysis following bone marrow transplantation.
Blood 1986;68(2):378-85.
1986: Donis-Keller H; Barker D F; Knowlton R G; Schumm J W; Braman J C; Green P
Highly polymorphic RFLP probes as diagnostic tools.
Cold Spring Harbor symposia on quantitative biology 1986;51 Pt 1():317-24.
1985: Knowlton R G; Cohen-Haguenauer O; Van Cong N; Frézal J; Brown V A; Barker D; Braman J C; Schumm J W; Tsui L C; Buchwald M
A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7.
Nature 1985;318(6044):380-2.
1985: Tsui L C; Buchwald M; Barker D; Braman J C; Knowlton R; Schumm J W; Eiberg H; Mohr J; Kennedy D; Plavsic N
Cystic fibrosis locus defined by a genetically linked polymorphic DNA marker.
Science (New York, N.Y.) 1985;230(4729):1054-7.
1985: White R; Leppert M; Bishop D T; Barker D; Berkowitz J; Brown C; Callahan P; Holm T; Jerominski L
Construction of linkage maps with DNA markers for human chromosomes.
Nature 1985;313(5998):101-5.
1984: Barker D; Holm T; White R
A locus on chromosome 11p with multiple restriction site polymorphisms.
American journal of human genetics 1984;36(6):1159-71.
1984: Barker D; Hoff M; Oliphant A; White R
A second type II restriction endonuclease from Thermus aquaticus with an unusual sequence specificity.
Nucleic acids research 1984;12(14):5567-81.
1984: Naylor S L; Sakaguchi A Y; Barker D; White R; Shows T B
DNA polymorphic loci mapped to human chromosomes 3, 5, 9, 11, 17, 18, and 22.
Proceedings of the National Academy of Sciences of the United States of America 1984;81(8):2447-51.
1984: Barker D; Schafer M; White R
Restriction sites containing CpG show a higher frequency of polymorphism in human DNA.
Cell 1984;36(1):131-8.
1983: Barker D; McCoy M; Weinberg R; Goldfarb M; Wigler M; Burt R; Gardner E; White R
A test of the role of two oncogenes in inherited predisposition to colon cancer.
Molecular biology & medicine 1983;1(2):199-206.
1982: Page D; de Martinville B; Barker D; Wyman A; White R; Francke U; Botstein D
Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes.
Proceedings of the National Academy of Sciences of the United States of America 1982;79(17):5352-6.
1982: White R; Schäfer M; Barker D; Wyman A; Skolnick M
DNA sequence polymorphism at arbitrary loci.
Progress in clinical and biological research 1982;103 Pt A():67-77.
1981: Barker D F; Campbell A M
The birA gene of Escherichia coli encodes a biotin holoenzyme synthetase.
Journal of molecular biology 1981;146(4):451-67.
1981: Barker D F; Campbell A M
Genetic and biochemical characterization of the birA gene and its product: evidence for a direct role of biotin holoenzyme synthetase in repression of the biotin operon in Escherichia coli.
Journal of molecular biology 1981;146(4):469-92.
1981: Barker D F; Kuhn J; Campbell A M
Sequence and properties of operator mutations in the bio operon of Escherichia coli.
Gene 1981;13(1):89-102.
1980: Barker D F; Campbell A M
Use of bio-lac fusion strains to study regulation of biotin biosynthesis in Escherichia coli.
Journal of bacteriology 1980;143(2):789-800.
1978: Kleckner N; Barker D F; Ross D G; Botstein D
Properties of the translocatable tetracycline-resistance element Tn10 in Escherichia coli and bacteriophage lambda.
Genetics 1978;90(3):427-61.

Sign-in to see more