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Items: 1 to 20 of 126

1.

Detailed transcript map of a 810-kb region at 11p14 involving identification of 10 novel human 3' exons.

Guillemot F, Auffray C, Devignes MD.

Eur J Hum Genet. 1999 May-Jun;7(4):487-95.

2.

A 1.7-Mb YAC contig around the human BDNF gene (11p13): integration of the physical, genetic, and cytogenetic maps in relation to WAGR syndrome.

Rosier MF, Goguel AF, Martin A, Le Paslier D, Couillin P, Houlgatte R, Bernheim A, Auffray C, Devignes MD.

Genomics. 1994 Nov 1;24(1):69-77.

PMID:
7896291
3.

Human brain derived neurotrophic factor (BDNF) genes, splicing patterns, and assessments of associations with substance abuse and Parkinson's Disease.

Liu QR, Walther D, Drgon T, Polesskaya O, Lesnick TG, Strain KJ, de Andrade M, Bower JH, Maraganore DM, Uhl GR.

Am J Med Genet B Neuropsychiatr Genet. 2005 Apr 5;134B(1):93-103.

PMID:
15666411
4.

An integrated YAC clone contig for the WAGR region on human chromosome 11p13-p14.1.

Gawin B, Klamt B, König A, Thäte C, Le Paslier D, Chumakov I, Bhogal R, Zehetner G, Bruns G, Gessler M.

Genomics. 1995 Nov 1;30(1):37-45.

PMID:
8595901
5.
6.

Generation of an integrated transcription map of the BRCA2 region on chromosome 13q12-q13.

Couch FJ, Rommens JM, Neuhausen SL, Bélanger C, Dumont M, Abel K, Bell R, Berry S, Bogden R, Cannon-Albright L, Farid L, Frye C, Hattier T, Janecki T, Jiang P, Kehrer R, Leblanc JF, McArthur-Morrison J, Meney D, Miki Y, Peng Y, Samson C, Schroeder M, Snyder SC, Simard J, et al.

Genomics. 1996 Aug 15;36(1):86-99.

PMID:
8812419
7.

High-resolution mapping and transcript identification at the progressive epilepsy with mental retardation locus on chromosome 8p.

Ranta S, Lehesjoki AE, de Fatima Bonaldo M, Knowles JA, Hirvasniemi A, Ross B, de Jong PJ, Soares MB, de la Chapelle A, Gilliam TC.

Genome Res. 1997 Sep;7(9):887-96.

8.

An exon map of the AZFc male infertility region of the human Y chromosome.

Wong J, Blanco P, Affara NA.

Mamm Genome. 1999 Jan;10(1):57-61.

PMID:
9892735
9.

Localization of 16 exons to a 450-kb region involved in the autoimmune polyglandular disease type I (APECED) on human chromosome 21q22.3.

Kudoh J, Nagamine K, Asakawa S, Abe I, Kawasaki K, Maeda H, Tsujimoto S, Minoshima S, Ito F, Shimizu N.

DNA Res. 1997 Feb 28;4(1):45-52.

PMID:
9179495
10.

Construction of a transcription map surrounding the BRCA1 locus of human chromosome 17.

Brody LC, Abel KJ, Castilla LH, Couch FJ, McKinley DR, Yin G, Ho PP, Merajver S, Chandrasekharappa SC, Xu J, et al.

Genomics. 1995 Jan 1;25(1):238-47.

PMID:
7774924
11.

Localization of 102 exons to a 2.5 Mb region involved in Down syndrome.

Lucente D, Chen HM, Shea D, Samec SN, Rutter M, Chrast R, Rossier C, Buckler A, Antonarakis SE, McCormick MK.

Hum Mol Genet. 1995 Aug;4(8):1305-11.

PMID:
7581367
12.
13.
14.

Rodent BDNF genes, novel promoters, novel splice variants, and regulation by cocaine.

Liu QR, Lu L, Zhu XG, Gong JP, Shaham Y, Uhl GR.

Brain Res. 2006 Jan 5;1067(1):1-12. Epub 2005 Dec 22.

PMID:
16376315
15.

Identification of 3'-terminal exons from yeast artificial chromosomes.

Krizman DB, Hofmann TA, DeSilva U, Green ED, Meltzer PS, Trent JM.

PCR Methods Appl. 1995 Jun;4(6):322-6.

16.

A high-resolution physical and transcript map of the Cri du chat region of human chromosome 5p.

Church DM, Yang J, Bocian M, Shiang R, Wasmuth JJ.

Genome Res. 1997 Aug;7(8):787-801.

17.

Gene identification using exon amplification on human chromosome 18q21: implications for bipolar disorder.

Chen H, Huo Y, Patel S, Zhu X, Swift-Scanlan T, Reeves RH, DePaulo R Jr, Ross CA, McInnis MG.

Mol Psychiatry. 2000 Sep;5(5):502-9.

PMID:
11032383
18.

Cloning of 559 potential exons of genes of human chromosome 21 by exon trapping.

Chen H, Chrast R, Rossier C, Morris MA, Lalioti MD, Antonarakis SE.

Genome Res. 1996 Aug;6(8):747-60.

19.

Complete exon-intron organization and chromosomal location of the gene for mouse type XIII collagen (col13a1) and comparison with its human homologue.

Kvist AP, Latvanlehto A, Sund M, Horelli-Kuitunen N, Rehn M, Palotie A, Beier D, Pihlajaniemi T.

Matrix Biol. 1999 Jun;18(3):261-74.

PMID:
10429945
20.

Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21.

Kohl S, Baumann B, Broghammer M, Jägle H, Sieving P, Kellner U, Spegal R, Anastasi M, Zrenner E, Sharpe LT, Wissinger B.

Hum Mol Genet. 2000 Sep 1;9(14):2107-16.

PMID:
10958649

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