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FANCI GENE
Known as:
Fanconi Anemia, Complementation Group I Gene
, FLJ10719
, FANCI
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This gene plays a role in the mediation of DNA repair.
National Institutes of Health
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Related topics
Related topics
7 relations
Cell Cycle Control
DNA Repair
DNA stability
FANCONI ANEMIA, COMPLEMENTATION GROUP I
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FANCI wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2014
Review
2014
[Function of CDK12 in Tumor initiation and progression and its clinical consequences].
D. Vrábel
,
M. Svoboda
,
J. Navrátil
,
J. Kohoutek
Klinicka onkologie
2014
Corpus ID: 11324804
Cyclin-dependent kinases (CDKs) participate in many cellular processes and play a crucial role in the regulation of cell cycle…
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2013
2013
Identification of brachyspina syndrome carriers in Chinese Holstein cattle
L. Fang
,
Yanhua Li
,
+4 authors
Shengli Zhang
Journal of Veterinary Diagnostic Investigation
2013
Corpus ID: 9088477
Brachyspina syndrome (BS) is a rare monogenic autosomal recessive hereditary disorder identified in the Holstein breed caused by…
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2013
2013
Multifunctionality of the FA pathway.
L. Hays
Blood
2013
Corpus ID: 42468055
In this issue of Blood , Kim and colleagues demonstrate that the Fanconi anemia protein FANCP/SLX4 is multifunctional by…
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2013
2013
UvA-DARE (Digital Academic Repository) A protein prioritization approach tailored for the FA/BRCA pathway
A. Haitjema
,
Bernd W. Brandt
,
+5 authors
J. Dorsman
2013
Corpus ID: 260744784
Fanconi anemia (FA) is a heterogeneous recessive disorder associated with a markedly elevated risk to develop cancer. To date…
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2012
2012
Monoubiquitination-dependent chromatin loading of FancD2 in silkworms, a species lacking the FA core complex.
R. Sugahara
,
H. Mon
,
J. M. Lee
,
T. Kusakabe
Gene
2012
Corpus ID: 9994514
2011
2011
Patient-derived C-terminal mutation of FANCI causes protein mislocalization and reveals putative EDGE motif function in DNA repair.
Luca Colnaghi
,
M. Jones
,
Xiomaris M. Cotto-Rios
,
D. Schindler
,
H. Hanenberg
,
Tony T. Huang
Blood
2011
Corpus ID: 6758869
Fanconi anemia (FA) is a rare familial genome instability syndrome caused by mutations in FA genes that results in defective DNA…
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2011
2011
Snm1B/Apollo functions in the Fanconi anemia pathway in response to DNA interstrand crosslinks.
Jennifer M O Mason
,
J. Sekiguchi
Human Molecular Genetics
2011
Corpus ID: 18229793
Fanconi anemia (FA) is an inherited chromosomal instability disorder characterized by childhood aplastic anemia, developmental…
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Review
2011
Review
2011
Fanconi Anemia/Brca Pathway and Head and Neck Squamous Cell Carcinomas
Shi-Long Lu
2011
Corpus ID: 2354934
DNA repair defect is one of the hallmarks of tumorigenesis, and is intimately linked to various human cancers, both inherited and…
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2010
2010
Material for FAN 1 Acts with FANCI-FANCD 2 to Promote DNA Interstrand Cross-Link Repair
Ting Liu
,
G. Ghosal
,
Jingsong Yuan
,
Junjie Chen
,
Jun Huang
2010
Corpus ID: 41015902
1993
1993
Ulcerostatic effect ofBacillus mucilaginosus exopolysaccharide and its possible mechanisms
M. Rasulov
,
I. G. Kuznetsov
,
L. Slutskii
,
M. V. Velikaya
,
A. G. Zabozlaev
,
M. Voronkov
Bulletin of experimental biology and medicine
1993
Corpus ID: 45574782
3. E. Branum, L. Cummius, M. Bartilson, et aL, Clin. Chem., 34, 110-113 (1988). 4. R. Clark, J. Gallin, and A. Fanci, Blood, 53…
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