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

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

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.

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