Literature DB >> 15096950

DiGeorge syndrome: an update.

Antonio Baldini1.   

Abstract

PURPOSE OF REVIEW: This article is an update on DiGeorge syndrome research focusing on the synergy of human and model systems genetics toward the understanding of conotruncal and aortic arch defects. RECENT
FINDINGS: The identification of mutations of the human T-Box1 (TBX1) gene and progress on research of Tbx1 function in mouse development demonstrate the pathogenetic role of this gene in DiGeorge syndrome and generate new hypotheses about its function in cardiovascular development.
SUMMARY: The Tbx1 genetic pathway and the cell biology of tissues contributing to pharyngeal arch arteries and cardiac outflow tract are the foundation for understanding congenital heart disease in DiGeorge syndrome.

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Year:  2004        PMID: 15096950     DOI: 10.1097/00001573-200405000-00002

Source DB:  PubMed          Journal:  Curr Opin Cardiol        ISSN: 0268-4705            Impact factor:   2.161


  18 in total

1.  A WW domain protein TAZ is a critical coactivator for TBX5, a transcription factor implicated in Holt-Oram syndrome.

Authors:  Masao Murakami; Masayo Nakagawa; Eric N Olson; Osamu Nakagawa
Journal:  Proc Natl Acad Sci U S A       Date:  2005-12-06       Impact factor: 11.205

2.  Org-1, the Drosophila ortholog of Tbx1, is a direct activator of known identity genes during muscle specification.

Authors:  Christoph Schaub; Hideyuki Nagaso; Hong Jin; Manfred Frasch
Journal:  Development       Date:  2012-03       Impact factor: 6.868

3.  2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders.

Authors:  Xudong Liu; Patrick Malenfant; Chelsea Reesor; Alana Lee; Melissa L Hudson; Chansonette Harvard; Ying Qiao; Antonio M Persico; Ira L Cohen; Albert E Chudley; Cynthia Forster-Gibson; Evica Rajcan-Separovic; M E Suzanne Lewis; Jeanette J A Holden
Journal:  Eur J Hum Genet       Date:  2011-07-13       Impact factor: 4.246

4.  The clinical spectrum of homozygous HOXA1 mutations.

Authors:  Thomas M Bosley; Ibrahim A Alorainy; Mustafa A Salih; Hesham M Aldhalaan; Khaled K Abu-Amero; Darren T Oystreck; Max A Tischfield; Elizabeth C Engle; Robert P Erickson
Journal:  Am J Med Genet A       Date:  2008-05-15       Impact factor: 2.802

5.  Neonatal Levels of T-cell Receptor Excision Circles (TREC) in Patients with 22q11.2 Deletion Syndrome and Later Disease Features.

Authors:  Kiran A Gul; Torstein Øverland; Liv Osnes; Lars O Baumbusch; Rolf D Pettersen; Kari Lima; Tore G Abrahamsen
Journal:  J Clin Immunol       Date:  2015-03-27       Impact factor: 8.317

6.  Inactivation of Bmp4 from the Tbx1 expression domain causes abnormal pharyngeal arch artery and cardiac outflow tract remodeling.

Authors:  Xuguang Nie; Christopher B Brown; Qin Wang; Kai Jiao
Journal:  Cells Tissues Organs       Date:  2010-12-01       Impact factor: 2.481

7.  Retinoic acid deficiency alters second heart field formation.

Authors:  Lucile Ryckebusch; Zengxin Wang; Nicolas Bertrand; Song-Chang Lin; Xuan Chi; Robert Schwartz; Stéphane Zaffran; Karen Niederreither
Journal:  Proc Natl Acad Sci U S A       Date:  2008-02-19       Impact factor: 11.205

8.  Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly.

Authors:  Erich Roessler; Maia V Ouspenskaia; Jayaprakash D Karkera; Jorge I Vélez; Amy Kantipong; Felicitas Lacbawan; Peter Bowers; John W Belmont; Jeffrey A Towbin; Elizabeth Goldmuntz; Benjamin Feldman; Maximilian Muenke
Journal:  Am J Hum Genet       Date:  2008-06-05       Impact factor: 11.025

9.  Fibulin-1 is required for morphogenesis of neural crest-derived structures.

Authors:  Marion A Cooley; Christine B Kern; Victor M Fresco; Andy Wessels; Robert P Thompson; Tim C McQuinn; Waleed O Twal; Corey H Mjaatvedt; Christopher J Drake; W Scott Argraves
Journal:  Dev Biol       Date:  2008-05-03       Impact factor: 3.582

10.  Disruption of Smad4 in neural crest cells leads to mid-gestation death with pharyngeal arch, craniofacial and cardiac defects.

Authors:  Xuguang Nie; Chu-xia Deng; Qin Wang; Kai Jiao
Journal:  Dev Biol       Date:  2008-02-15       Impact factor: 3.582

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