Double complex mutations involvingF8andFUNDC2caused by distinct break-induced replication-Reference-Cited by-同舟云学术

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Double complex mutations involvingF8andFUNDC2caused by distinct break-induced replication

Published:2007-12 Issue:12 Volume:28 Page:1198-1206
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Sheen Campbell R.,Jewell Ursula R.,Morris Christine M.,Brennan Stephen O.,Férec Claude,George Peter M.,Smith Mark P.,Chen Jian-Min

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference49 articles.

1. Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans;Aitman;Nature,2006

2. Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe hemophilia A;Bagnall;Blood,2002

3. Melanoma antigen gene protein MAGE-11 regulates androgen receptor function by modulating the interdomain interaction;Bai;Mol Cell Biol,2005

4. A first-generation X-inactivation profile of the human X chromosome;Carrel;Proc Natl Acad Sci USA,1999

5. Complex gene rearrangements caused by serial replication slippage;Chen;Hum Mutat,2005

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1. FUNDC2, a mitochondrial outer membrane protein, mediates triple-negative breast cancer progression via the AKT/GSK3β/GLI1 pathway;Acta Biochimica et Biophysica Sinica;2023-09-01

2. Molecular Characterization of Hemophilia A Patients in Duhok, Iraq;Pharmacophore;2023

3. Methylation of the HCBP6 promoter is associated with primary biliary cholangitis pathogenesis;Biochemical and Biophysical Research Communications;2022-06

4. Deletion of FUNDC2 and CMC4 on Chromosome Xq28 Is Sufficient to Cause Hypergonadotropic Hypogonadism in Men;Frontiers in Genetics;2020-09-22

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