- in
humans is
encoded by the
FANCB gene. The
Fanconi anemia complementation group (FANC)
currently includes FANCA,
FANCB, FANCC, FANCD1 (also
called BRCA2)...
- [citation needed]
Scientists have
identified 21 FA or FA-like genes: FANCA,
FANCB, FANCC, FANCD1 (BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI,
FANCJ (BRIP1)...
- at
frequencies of
between 13%-100% for the DNA
repair genes BRCA1, WRN,
FANCB, FANCF, MGMT, MLH1, MSH2, MSH4, ERCC1, XPF, NEIL1 and ATM.
These epigenetic...
- been
discovered include the
transcriptional regulators SOX2, MYCN, CHD7,
FANCB, and
members of FOX
transcription factor family.
Others plausible candidate...
- non-small-cell lung
cancer squamous cell carcinomas.
Promoter hypermethylation of
FANCB occurs in 46% of head and neck cancers. On the
other hand, the promoters...
-
Erythropoietic protoporphyria FECH 1:75,000-200,000
Fanconi anemia (FA) FANCA,
FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ, FANCL, FANCM...
- and hypopigmentation. To date, the
genes known to
cause FA are: FANCA,
FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ, FANCL, FANCM, FANCN,...
- The
Fanconi anemia complementation group (FANC)
currently includes FANCA,
FANCB, FANCC, FANCD1 (also
called BRCA2), FANCD2, FANCE, FANCF, FANCG, and FANCL...
-
promoter hypermethylation of DNA
repair genes LIG4, NEIL1, ATM, MLH1 or
FANCB occurs at
frequencies of
between 33% and 82% in one or more of head and...
- HGNC:54842 P0DSO1 5442 FAN1 HGNC:29170 Q9Y2M0 5443
FANCA HGNC:3582 O15360 5444
FANCB HGNC:3583 Q8NB91 5445
FANCC HGNC:3584 Q00597 5446 FANCD2 HGNC:3585 Q9BXW9...
