Literature DB >> 14729844

Epigenetic abnormalities of the mannose-6-phosphate/IGF2 receptor gene are uncommon in human overgrowth syndromes.

C Gicquel, J Weiss, J Amiel, V Gaston, Y Le Bouc, C D Scott.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2004        PMID： 14729844      PMCID： PMC1757252          DOI： 10.1136/jmg.2003.010488

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


× No keyword cloud information.
  3 in total

1.  Gene-specific vulnerability to imprinting variability in human embryonic stem cell lines.

Authors:  Kee-Pyo Kim; Alexandra Thurston; Christine Mummery; Dorien Ward-van Oostwaard; Helen Priddle; Cinzia Allegrucci; Chris Denning; Lorraine Young
Journal:  Genome Res       Date:  2007-11-07       Impact factor: 9.043

2.  Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci.

Authors:  Claire Louise Susan Turner; Deborah M Mackay; Jonathan L A Callaway; Louise E Docherty; Rebecca L Poole; Hilary Bullman; Margaret Lever; Bruce M Castle; Emma C Kivuva; Peter D Turnpenny; Sarju G Mehta; Sahar Mansour; Emma L Wakeling; Verghese Mathew; Jackie Madden; Justin H Davies; I Karen Temple
Journal:  Eur J Hum Genet       Date:  2010-01-27       Impact factor: 4.246

3.  The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region.

Authors:  S Rossignol; V Steunou; C Chalas; A Kerjean; M Rigolet; E Viegas-Pequignot; P Jouannet; Y Le Bouc; C Gicquel
Journal:  J Med Genet       Date:  2006-07-06       Impact factor: 6.318
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.