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Results: 1 to 20 of 112

1.

A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects.

Yamagishi H, Garg V, Matsuoka R, Thomas T, Srivastava D.

Science. 1999 Feb 19;283(5405):1158-61.

PMID:
10024240
[PubMed - indexed for MEDLINE]
Free Article
2.

A gene that scrambles your heart.

Hagmann M.

Science. 1999 Feb 19;283(5405):1091,1093. No abstract available.

PMID:
10075562
[PubMed - indexed for MEDLINE]
3.

Developmental and genetic aspects of congenital heart disease.

Srivastava D.

Curr Opin Cardiol. 1999 May;14(3):263-8. Review.

PMID:
10358798
[PubMed - indexed for MEDLINE]
4.

A common cis-acting sequence in the DiGeorge critical region regulates bi-directional transcription of UFD1L and CDC45L.

Kunte A, Ivey K, Yamagishi C, Garg V, Yamagishi H, Srivastava D.

Mech Dev. 2001 Oct;108(1-2):81-92.

PMID:
11578863
[PubMed - indexed for MEDLINE]
Free Article
5.

HAND proteins: molecular mediators of cardiac development and congenital heart disease.

Srivastava D.

Trends Cardiovasc Med. 1999 Jan-Feb;9(1-2):11-8. Review.

PMID:
10189962
[PubMed - indexed for MEDLINE]
6.

A GATA-dependent right ventricular enhancer controls dHAND transcription in the developing heart.

McFadden DG, Charité J, Richardson JA, Srivastava D, Firulli AB, Olson EN.

Development. 2000 Dec;127(24):5331-41.

PMID:
11076755
[PubMed - indexed for MEDLINE]
Free Article
7.

A 22q11.2 deletion that excludes UFD1L and CDC45L in a patient with conotruncal and craniofacial defects.

Saitta SC, McGrath JM, Mensch H, Shaikh TH, Zackai EH, Emanuel BS.

Am J Hum Genet. 1999 Aug;65(2):562-6. No abstract available.

PMID:
10417299
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

A signaling cascade involving endothelin-1, dHAND and msx1 regulates development of neural-crest-derived branchial arch mesenchyme.

Thomas T, Kurihara H, Yamagishi H, Kurihara Y, Yazaki Y, Olson EN, Srivastava D.

Development. 1998 Aug;125(16):3005-14.

PMID:
9671575
[PubMed - indexed for MEDLINE]
Free Article
9.

Regulation of cardiac mesodermal and neural crest development by the bHLH transcription factor, dHAND.

Srivastava D, Thomas T, Lin Q, Kirby ML, Brown D, Olson EN.

Nat Genet. 1997 Jun;16(2):154-60. Erratum in: Nat Genet 1997 Aug;16(4):410.

PMID:
9171826
[PubMed - indexed for MEDLINE]
10.

Isolation and characterization of a human gene containing a nuclear localization signal from the critical region for velo-cardio-facial syndrome on 22q11.

Funke B, Puech A, Saint-Jore B, Pandita R, Skoultchi A, Morrow B.

Genomics. 1998 Oct 15;53(2):146-54.

PMID:
9790763
[PubMed - indexed for MEDLINE]
11.

Cardiac phenotypes in chromosome 4q- syndrome with and without a deletion of the dHAND gene.

Huang T, Lin AE, Cox GF, Golden WL, Feldman GL, Ute M, Schrander-Stumpel C, Kamisago M, Vermeulen SJ.

Genet Med. 2002 Nov-Dec;4(6):464-7.

PMID:
12509719
[PubMed - indexed for MEDLINE]
12.

An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome.

Frank DU, Fotheringham LK, Brewer JA, Muglia LJ, Tristani-Firouzi M, Capecchi MR, Moon AM.

Development. 2002 Oct;129(19):4591-603.

PMID:
12223415
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

The murine homologue of HIRA, a DiGeorge syndrome candidate gene, is expressed in embryonic structures affected in human CATCH22 patients.

Wilming LG, Snoeren CA, van Rijswijk A, Grosveld F, Meijers C.

Hum Mol Genet. 1997 Feb;6(2):247-58.

PMID:
9063745
[PubMed - indexed for MEDLINE]
Free Article
14.

Functional attenuation of UFD1l, a 22q11.2 deletion syndrome candidate gene, leads to cardiac outflow septation defects in chicken embryos.

Yamagishi C, Hierck BP, Gittenberger-De Groot AC, Yamagishi H, Srivastava D.

Pediatr Res. 2003 Apr;53(4):546-53. Epub 2003 Feb 20.

PMID:
12612215
[PubMed - indexed for MEDLINE]
15.

Molecular determinants of left and right outflow tract obstruction.

Towbin JA, Belmont J.

Am J Med Genet. 2000 Winter;97(4):297-303. Review.

PMID:
11376441
[PubMed - indexed for MEDLINE]
16.

Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients.

Carlson C, Sirotkin H, Pandita R, Goldberg R, McKie J, Wadey R, Patanjali SR, Weissman SM, Anyane-Yeboa K, Warburton D, Scambler P, Shprintzen R, Kucherlapati R, Morrow BE.

Am J Hum Genet. 1997 Sep;61(3):620-9.

PMID:
9326327
[PubMed - indexed for MEDLINE]
Free PMC Article
17.
18.

Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome.

Yamagishi H, Srivastava D.

Trends Mol Med. 2003 Sep;9(9):383-9. Review.

PMID:
13129704
[PubMed - indexed for MEDLINE]
19.

dHAND-Cre transgenic mice reveal specific potential functions of dHAND during craniofacial development.

Ruest LB, Dager M, Yanagisawa H, Charité J, Hammer RE, Olson EN, Yanagisawa M, Clouthier DE.

Dev Biol. 2003 May 15;257(2):263-77.

PMID:
12729557
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome.

Pizzuti A, Novelli G, Ratti A, Amati F, Mari A, Calabrese G, Nicolis S, Silani V, Marino B, Scarlato G, Ottolenghi S, Dallapiccola B.

Hum Mol Genet. 1997 Feb;6(2):259-65.

PMID:
9063746
[PubMed - indexed for MEDLINE]
Free Article

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