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Results: 1 to 20 of 117

1.

Divergent human and mouse orthologs of a novel gene (WBSCR15/Wbscr15) reside within the genomic interval commonly deleted in Williams syndrome.

Doyle JL, DeSilva U, Miller W, Green ED.

Cytogenet Cell Genet. 2000;90(3-4):285-90.

PMID:
11124535
[PubMed - indexed for MEDLINE]
2.

Comparative mapping of the region of human chromosome 7 deleted in williams syndrome.

DeSilva U, Massa H, Trask BJ, Green ED.

Genome Res. 1999 May;9(5):428-36.

PMID:
10330122
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

A novel human gene, WSTF, is deleted in Williams syndrome.

Lu X, Meng X, Morris CA, Keating MT.

Genomics. 1998 Dec 1;54(2):241-9.

PMID:
9828126
[PubMed - indexed for MEDLINE]
4.

Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome.

DeSilva U, Elnitski L, Idol JR, Doyle JL, Gan W, Thomas JW, Schwartz S, Dietrich NL, Beckstrom-Sternberg SM, McDowell JC, Blakesley RW, Bouffard GG, Thomas PJ, Touchman JW, Miller W, Green ED.

Genome Res. 2002 Jan;12(1):3-15.

PMID:
11779826
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes.

Meng X, Lu X, Li Z, Green ED, Massa H, Trask BJ, Morris CA, Keating MT.

Hum Genet. 1998 Nov;103(5):590-9.

PMID:
9860302
[PubMed - indexed for MEDLINE]
6.

Isolation and characterization of a novel human gene, NIF3L1, and its mouse ortholog, Nif3l1, highly conserved from bacteria to mammals.

Tascou S, Uedelhoven J, Dixkens C, Nayernia K, Engel W, Burfeind P.

Cytogenet Cell Genet. 2000;90(3-4):330-6.

PMID:
11124544
[PubMed - indexed for MEDLINE]
7.

Cloning of the novel gene TM6SF1 reveals conservation of clusters of paralogous genes between human chromosomes 15q24-->q26 and 19p13.3-->p12.

Carim-Todd L, Escarceller M, Estivill X, Sumoy L.

Cytogenet Cell Genet. 2000;90(3-4):255-60.

PMID:
11124529
[PubMed - indexed for MEDLINE]
8.

A novel human gene FKBP6 is deleted in Williams syndrome.

Meng X, Lu X, Morris CA, Keating MT.

Genomics. 1998 Sep 1;52(2):130-7.

PMID:
9782077
[PubMed - indexed for MEDLINE]
10.
11.

Mapping and characterization of the mouse and human SS18 genes, two human SS18-like genes and a mouse Ss18 pseudogene.

de Bruijn DR, Kater-Baats E, Eleveld M, Merkx G, Geurts Van Kessel A.

Cytogenet Cell Genet. 2001;92(3-4):310-9.

PMID:
11435705
[PubMed - indexed for MEDLINE]
12.

Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients.

Osborne LR, Martindale D, Scherer SW, Shi XM, Huizenga J, Heng HH, Costa T, Pober B, Lew L, Brinkman J, Rommens J, Koop B, Tsui LC.

Genomics. 1996 Sep 1;36(2):328-36.

PMID:
8812460
[PubMed - indexed for MEDLINE]
13.

Genomic structure, alternative transcripts and chromosome location of the human LIM domain binding protein 1 gene LDB1.

Drechsler M, Schumacher V, Friedrich S, Wildhardt G, Giesler S, Schroth A, Bodem J, Royer-Pokora B.

Cytogenet Cell Genet. 1999;87(1-2):119-24.

PMID:
10640831
[PubMed - indexed for MEDLINE]
14.

cDNA cloning and genomic structure of a novel gene (C11orf9) localized to chromosome 11q12-->q13.1 which encodes a highly conserved, potential membrane-associated protein.

Stöhr H, Marquardt A, White K, Weber BH.

Cytogenet Cell Genet. 2000;88(3-4):211-6.

PMID:
10828591
[PubMed - indexed for MEDLINE]
15.
16.

Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome.

Osborne LR, Campbell T, Daradich A, Scherer SW, Tsui LC.

Genomics. 1999 Apr 15;57(2):279-84.

PMID:
10198167
[PubMed - indexed for MEDLINE]
17.

WWOX, a novel WW domain-containing protein mapping to human chromosome 16q23.3-24.1, a region frequently affected in breast cancer.

Bednarek AK, Laflin KJ, Daniel RL, Liao Q, Hawkins KA, Aldaz CM.

Cancer Res. 2000 Apr 15;60(8):2140-5.

PMID:
10786676
[PubMed - indexed for MEDLINE]
Free Article
18.
19.

Cloning, characterization, and mapping of the gene encoding the human G protein gamma 2 subunit.

Modarressi MH, Taylor KE, Wolfe J.

Biochem Biophys Res Commun. 2000 Jun 7;272(2):610-5.

PMID:
10833460
[PubMed - indexed for MEDLINE]
20.

STAG3, a novel gene encoding a protein involved in meiotic chromosome pairing and location of STAG3-related genes flanking the Williams-Beuren syndrome deletion.

Pezzi N, Prieto I, Kremer L, Pérez Jurado LA, Valero C, Del Mazo J, Martínez-A C, Barbero JL.

FASEB J. 2000 Mar;14(3):581-92.

PMID:
10698974
[PubMed - indexed for MEDLINE]
Free Article

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