scholarly journals RHOA (ras homolog gene family, member A)

2017 ◽  
Author(s):  
Rebeca Manso
Keyword(s):  
Gene Family ◽  
Family Member ◽  
Gene Family Member

Human fertilin β: Identification, characterization, and chromosomal mapping of an ADAM gene family member

1997 ◽  
Vol 46 (3) ◽  
pp. 363-369 ◽  
Author(s):  
Cecilia M. Vidaeus ◽  
Chris von Kap-Herr ◽  
Wendy L. Golden ◽  
Roger L. Eddy ◽  
Thomas B. Shows ◽  
...  
Keyword(s):  
Gene Family ◽  
Family Member ◽  
Chromosomal Mapping ◽  
Gene Family Member ◽  
Adam Gene

scholarly journals Identification and analysis of expression of human VACM-1, a cullin gene family member located on chromosome 11q22-23.

1997 ◽  
Vol 7 (1) ◽  
pp. 71-75 ◽  
Author(s):  
P J Byrd ◽  
T Stankovic ◽  
C M McConville ◽  
A D Smith ◽  
P R Cooper ◽  
...  
Keyword(s):  
Gene Family ◽  
Family Member ◽  
Gene Family Member

Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia

10.1038/12699 ◽  
1999 ◽  
Vol 23 (1) ◽  
pp. 94-98 ◽  
Author(s):  
Jennifer R. Hurvitz ◽  
Wafaa M. Suwairi ◽  
Wim Van Hul ◽  
Hatem El-Shanti ◽  
Andrea Superti-Furga ◽  
...  
Keyword(s):  
Gene Family ◽  
Family Member ◽  
Progressive Pseudorheumatoid Dysplasia ◽  
Gene Family Member

Transcriptional control of the human biliary glycoprotein gene, a CEA gene family member down-regulated in colorectal carcinomas

1994 ◽  
Vol 223 (2) ◽  
pp. 529-541 ◽  
Author(s):  
Wendy HAUCK ◽  
Patrick NEDELLEC ◽  
Claire TURBIDE ◽  
Clifford P. STANNERS ◽  
Thomas R. BARNETT ◽  
...  
Keyword(s):  
Gene Family ◽  
Family Member ◽  
Transcriptional Control ◽  
Colorectal Carcinomas ◽  
Glycoprotein Gene ◽  
Gene Family Member ◽  
Cea Gene

Identification of a New Human Catenin Gene Family Member (ARVCF) from the Region Deleted in Velo–Cardio–Facial Syndrome

Genomics ◽  
1997 ◽  
Vol 41 (1) ◽  
pp. 75-83 ◽  
Author(s):  
Howard Sirotkin ◽  
Hilary O'Donnell ◽  
Ruchira DasGupta ◽  
Stephanie Halford ◽  
Bruno St. Jore ◽  
...  
Keyword(s):  
Gene Family ◽  
Family Member ◽  
Gene Family Member ◽  
Velo Cardio Facial Syndrome

scholarly journals Abi3 regulates microglial ramification and dynamic tissue surveillance in vivo.

2021 ◽  
Author(s):  
Elena Simonazzi ◽  
Ruth Jones ◽  
Fangli Chen ◽  
Adam Ranson ◽  
Joshua Stevenson-Hoare ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Gene Family ◽  
Family Member ◽  
Late Onset ◽  
Gene Family Member ◽  
Surveillance Activity ◽  
Increased Risk ◽  
Microglial Morphology

A rare coding variant of Abelson-interactor gene family member 3 (Abi3) is associated with increased risk of late-onset Alzheimer's Disease (AD). Although Abi3 is recognised as a core microglial gene, its role in microglia is largely unknown. Here we demonstrate that Abi3 is crucial for normal microglial morphology, distribution, and homeostatic tissue surveillance activity in vivo.

Sign in / Sign up

Export Citation Format

Share Document