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Fanconi Anemia Group B Protein
Known as:
FAAP95
, Protein FACB
, FANCB
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Fanconi anemia group B protein (859 aa, ~98 kDa) is encoded by the human FANCB gene. This protein may play a role in both ubiquitination and DNA…
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National Institutes of Health
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Related topics
Related topics
10 relations
BARD1 Pathway
BRCA2 Protein
BRCA2 wt Allele
Cell Cycle Control
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Mutational and Functional Analysis of FANCB as a Candidate Gene for Sporadic Head and Neck Squamous Cell Carcinomas.
M. Glaas
,
C. Wiek
,
+10 authors
K. Scheckenbach
Anticancer Research
2018
Corpus ID: 3852264
BACKGROUND/AIM Head and neck squamous cell carcinomas (HNSCCs) form a heterogeneous tumor entity located throughout the oral…
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2018
2018
X‐linked VACTERL‐H caused by deletion of exon 3 in FANCB: A case report
Norikazu Watanabe
,
S. Tsutsumi
,
Yuki Miyano
,
Hidenori Sato
,
S. Nagase
Congenital Anomalies
2018
Corpus ID: 609632
VACTERL is a congenital malformation characterized by vertebral defects (V), anal atresia (A), cardiac malformation (C…
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2016
2016
ISP-18-9 A case of X-linked VACTERL-H association with FANCB mutation(Group 18 Fetal Complication 1,International Session Poster)
Norikazu Watanabe
,
S. Tsutsumi
,
A. Sugiyama
,
Miyuki Obata
,
J. Kawagoe
,
S. Nagase
2016
Corpus ID: 78097777
2010
2010
Inactivation of the Tumor Suppressor Genes Causing the Hereditary Syndromes Predisposing to Head and Neck Cancer via Promoter Hypermethylation in Sporadic Head and Neck Cancers
I. Smith
,
S. Mithani
,
W. Mydlarz
,
Steven S. Chang
,
J. Califano
ORL
2010
Corpus ID: 35756552
Fanconi anemia (FA) and dyskeratosis congenita (DC) are rare inherited syndromes that cause head and neck squamous cell cancer…
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