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Results: 1 to 20 of 28

1.

Construction of small-insert libraries enriched for short tandem repeat sequences by marker selection.

Pulido JC, Duyk GM.

Curr Protoc Hum Genet. 2001 May;Chapter 2:Unit 2.2. doi: 10.1002/0471142905.hg0202s14.

PMID:
18428266
[PubMed - indexed for MEDLINE]
2.

Sharper tools and simpler methods.

Duyk GM.

Nat Genet. 2002 Dec;32 Suppl:465-8.

PMID:
12454639
[PubMed - indexed for MEDLINE]
3.

A genetic screen for mutations that disrupt an auditory response in Drosophila melanogaster.

Eberl DF, Duyk GM, Perrimon N.

Proc Natl Acad Sci U S A. 1997 Dec 23;94(26):14837-42.

PMID:
9405700
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Characterization of Alu repeats that are associated with trinucleotide and tetranucleotide repeat microsatellites.

Yandava CN, Gastier JM, Pulido JC, Brody T, Sheffield V, Murray J, Buetow K, Duyk GM.

Genome Res. 1997 Jul;7(7):716-24.

PMID:
9253600
[PubMed - indexed for MEDLINE]
Free Article
5.

Novel mutations and a mutational hotspot in the MODY3 gene.

Glucksmann MA, Lehto M, Tayber O, Scotti S, Berkemeier L, Pulido JC, Wu Y, Nir WJ, Fang L, Markel P, Munnelly KD, Goranson J, Orho M, Young BM, Whitacre JL, McMenimen C, Wantman M, Tuomi T, Warram J, Forsblom CM, Carlsson M, Rosenzweig J, Kennedy G, Duyk GM, Thomas JD, et al.

Diabetes. 1997 Jun;46(6):1081-6.

PMID:
9166684
[PubMed - indexed for MEDLINE]
6.

The physical and genetic map surrounding the Lyst gene on mouse chromosome 13.

Misumi DJ, Nagle DL, McGrail SH, Dussault BJ Jr, Smutko JS, Chen H, Charlat O, Duyk GM, Ebeling C, Baldini L, Carlson GA, Moore KJ.

Genomics. 1997 Feb 15;40(1):147-50.

PMID:
9070932
[PubMed - indexed for MEDLINE]
7.

Identification and mutation analysis of the complete gene for Chediak-Higashi syndrome.

Nagle DL, Karim MA, Woolf EA, Holmgren L, Bork P, Misumi DJ, McGrail SH, Dussault BJ Jr, Perou CM, Boissy RE, Duyk GM, Spritz RA, Moore KJ.

Nat Genet. 1996 Nov;14(3):307-11.

PMID:
8896560
[PubMed - indexed for MEDLINE]
8.

A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13.

Manolis EN, Yandavi N, Nadol JB Jr, Eavey RD, McKenna M, Rosenbaum S, Khetarpal U, Halpin C, Merchant SN, Duyk GM, MacRae C, Seidman CE, Seidman JG.

Hum Mol Genet. 1996 Jul;5(7):1047-50.

PMID:
8817345
[PubMed - indexed for MEDLINE]
Free Article
9.

Identification of the murine beige gene by YAC complementation and positional cloning.

Perou CM, Moore KJ, Nagle DL, Misumi DJ, Woolf EA, McGrail SH, Holmgren L, Brody TH, Dussault BJ Jr, Monroe CA, Duyk GM, Pryor RJ, Li L, Justice MJ, Kaplan J.

Nat Genet. 1996 Jul;13(3):303-8.

PMID:
8673129
[PubMed - indexed for MEDLINE]
10.

Identification and characterization of the mouse obesity gene tubby: a member of a novel gene family.

Kleyn PW, Fan W, Kovats SG, Lee JJ, Pulido JC, Wu Y, Berkemeier LR, Misumi DJ, Holmgren L, Charlat O, Woolf EA, Tayber O, Brody T, Shu P, Hawkins F, Kennedy B, Baldini L, Ebeling C, Alperin GD, Deeds J, Lakey ND, Culpepper J, Chen H, Glücksmann-Kuis MA, Carlson GA, Duyk GM, Moore KJ.

Cell. 1996 Apr 19;85(2):281-90.

PMID:
8612280
[PubMed - indexed for MEDLINE]
Free Article
11.

Development of a screening set for new (CAG/CTG)n dynamic mutations.

Gastier JM, Brody T, Pulido JC, Businga T, Sunden S, Hu X, Maitra S, Buetow KH, Murray JC, Sheffield VC, Boguski M, Duyk GM, Hudson TJ.

Genomics. 1996 Feb 15;32(1):75-85.

PMID:
8786123
[PubMed - indexed for MEDLINE]
12.

Chromosomal assignment of 2900 tri- and tetranucleotide repeat markers using NIGMS somatic cell hybrid panel 2.

Sunden SL, Businga T, Beck J, McClain A, Gastier JM, Pulido JC, Yandava CN, Brody T, Ghazizadeh J, Weber JL, Duyk GM, Murray JC, Buetow KH, Sheffield VC.

Genomics. 1996 Feb 15;32(1):15-20.

PMID:
8786107
[PubMed - indexed for MEDLINE]
13.

Evidence that the diabetes gene encodes the leptin receptor: identification of a mutation in the leptin receptor gene in db/db mice.

Chen H, Charlat O, Tartaglia LA, Woolf EA, Weng X, Ellis SJ, Lakey ND, Culpepper J, Moore KJ, Breitbart RE, Duyk GM, Tepper RI, Morgenstern JP.

Cell. 1996 Feb 9;84(3):491-5.

PMID:
8608603
[PubMed - indexed for MEDLINE]
Free Article
14.

Periventricular heterotopia: an X-linked dominant epilepsy locus causing aberrant cerebral cortical development.

Ekşioğlu YZ, Scheffer IE, Cardenas P, Knoll J, DiMario F, Ramsby G, Berg M, Kamuro K, Berkovic SF, Duyk GM, Parisi J, Huttenlocher PR, Walsh CA.

Neuron. 1996 Jan;16(1):77-87.

PMID:
8562093
[PubMed - indexed for MEDLINE]
Free Article
15.

Survey of trinucleotide repeats in the human genome: assessment of their utility as genetic markers.

Gastier JM, Pulido JC, Sunden S, Brody T, Buetow KH, Murray JC, Weber JL, Hudson TJ, Sheffield VC, Duyk GM.

Hum Mol Genet. 1995 Oct;4(10):1829-36.

PMID:
8595403
[PubMed - indexed for MEDLINE]
16.

A small-insert bovine genomic library highly enriched for microsatellite repeat sequences.

Stone RT, Pulido JC, Duyk GM, Kappes SM, Keele JW, Beattie CW.

Mamm Genome. 1995 Oct;6(10):714-24.

PMID:
8563170
[PubMed - indexed for MEDLINE]
17.

Nonsyndromic autosomal recessive deafness is linked to the DFNB1 locus in a large inbred Bedouin family from Israel.

Scott DA, Carmi R, Elbedour K, Duyk GM, Stone EM, Sheffield VC.

Am J Hum Genet. 1995 Oct;57(4):965-8. No abstract available.

PMID:
7573061
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

cDNA cloning, tissue distribution, and chromosomal localization of Ocp2, a gene encoding a putative transcription-associated factor predominantly expressed in the auditory organs.

Chen H, Thalmann I, Adams JC, Avraham KB, Copeland NG, Jenkins NA, Beier DR, Corey DP, Thalmann R, Duyk GM.

Genomics. 1995 Jun 10;27(3):389-98.

PMID:
7558018
[PubMed - indexed for MEDLINE]
19.

Sets of short tandem repeat polymorphisms for efficient linkage screening of the human genome.

Dubovsky J, Sheffield VC, Duyk GM, Weber JL.

Hum Mol Genet. 1995 Mar;4(3):449-52.

PMID:
7795601
[PubMed - indexed for MEDLINE]
20.

MATS: a rapid and efficient method for the development of microsatellite markers from YACs.

Chen H, Pulido JC, Duyk GM.

Genomics. 1995 Jan 1;25(1):1-8.

PMID:
7774906
[PubMed - indexed for MEDLINE]

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