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Items: 1 to 20 of 29

1.

Thoughts on the etiology of clefts of the palate and lip.

FRASER FC.

Acta Genet Stat Med. 1955;5(4):358-69. No abstract available.

PMID:
13339079
2.

Fistula labii inferioris congenita and its association with cleft lip and palate.

VAN DER WOUDE A.

Am J Hum Genet. 1954 Jun;6(2):244-56. No abstract available.

3.

Signal transduction and the control of gene expression.

Brivanlou AH, Darnell JE Jr.

Science. 2002 Feb 1;295(5556):813-8. Review.

PMID:
11823631
4.

IRF family of transcription factors as regulators of host defense.

Taniguchi T, Ogasawara K, Takaoka A, Tanaka N.

Annu Rev Immunol. 2001;19:623-55. Review.

PMID:
11244049
5.

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms.

Sachidanandam R, Weissman D, Schmidt SC, Kakol JM, Stein LD, Marth G, Sherry S, Mullikin JC, Mortimore BJ, Willey DL, Hunt SE, Cole CG, Coggill PC, Rice CM, Ning Z, Rogers J, Bentley DR, Kwok PY, Mardis ER, Yeh RT, Schultz B, Cook L, Davenport R, Dante M, Fulton L, Hillier L, Waterston RH, McPherson JD, Gilman B, Schaffner S, Van Etten WJ, Reich D, Higgins J, Daly MJ, Blumenstiel B, Baldwin J, Stange-Thomann N, Zody MC, Linton L, Lander ES, Altshuler D; International SNP Map Working Group.

Nature. 2001 Feb 15;409(6822):928-33.

PMID:
11237013
6.
7.

Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63.

McGrath JA, Duijf PH, Doetsch V, Irvine AD, de Waal R, Vanmolkot KR, Wessagowit V, Kelly A, Atherton DJ, Griffiths WA, Orlow SJ, van Haeringen A, Ausems MG, Yang A, McKeon F, Bamshad MA, Brunner HG, Hamel BC, van Bokhoven H.

Hum Mol Genet. 2001 Feb 1;10(3):221-9.

PMID:
11159940
8.

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans.

van den Boogaard MJ, Dorland M, Beemer FA, van Amstel HK.

Nat Genet. 2000 Apr;24(4):342-3. No abstract available. Erratum in: Nat Genet 2000 May;25(1):125.

PMID:
10742093
9.

A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41.

Schutte BC, Bjork BC, Coppage KB, Malik MI, Gregory SG, Scott DJ, Brentzell LM, Watanabe Y, Dixon MJ, Murray JC.

Genome Res. 2000 Jan;10(1):81-94.

10.
11.

Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome.

Celli J, Duijf P, Hamel BC, Bamshad M, Kramer B, Smits AP, Newbury-Ecob R, Hennekam RC, Van Buggenhout G, van Haeringen A, Woods CG, van Essen AJ, de Waal R, Vriend G, Haber DA, Yang A, McKeon F, Brunner HG, van Bokhoven H.

Cell. 1999 Oct 15;99(2):143-53.

12.

Interferon regulatory factors: the next generation.

Mamane Y, Heylbroeck C, Génin P, Algarté M, Servant MJ, LePage C, DeLuca C, Kwon H, Lin R, Hiscott J.

Gene. 1999 Sep 3;237(1):1-14. Review.

PMID:
10524230
13.

Conserved transactivation domain shared by interferon regulatory factors and Smad morphogens.

Eroshkin A, Mushegian A.

J Mol Med (Berl). 1999 May;77(5):403-5.

PMID:
10426188
14.

Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome.

Schutte BC, Basart AM, Watanabe Y, Laffin JJ, Coppage K, Bjork BC, Daack-Hirsch S, Patil S, Dixon MJ, Murray JC.

Am J Med Genet. 1999 May 21;84(2):145-50.

PMID:
10323740
15.

Essential role of interferon regulatory factor 3 in direct activation of RANTES chemokine transcription.

Lin R, Heylbroeck C, Genin P, Pitha PM, Hiscott J.

Mol Cell Biol. 1999 Feb;19(2):959-66.

16.

Structure of IRF-1 with bound DNA reveals determinants of interferon regulation.

Escalante CR, Yie J, Thanos D, Aggarwal AK.

Nature. 1998 Jan 1;391(6662):103-6.

PMID:
9422515
17.

TGFbeta2 knockout mice have multiple developmental defects that are non-overlapping with other TGFbeta knockout phenotypes.

Sanford LP, Ormsby I, Gittenberger-de Groot AC, Sariola H, Friedman R, Boivin GP, Cardell EL, Doetschman T.

Development. 1997 Jul;124(13):2659-70.

19.

Some causes of genotypic and phenotypic discordance in monozygotic twin pairs.

Machin GA.

Am J Med Genet. 1996 Jan 22;61(3):216-28. Review.

PMID:
8741866
20.

In situ hybridization analysis of chick embryos in whole mount and tissue sections.

Nieto MA, Patel K, Wilkinson DG.

Methods Cell Biol. 1996;51:219-35. Review. No abstract available.

PMID:
8722478

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