- The
tumor suppressor gene FLCN
encodes the
protein folliculin, also
known as Birt–Hogg–Dubé
syndrome protein,
which functions as an
inhibitor of Lactate...
- onset,
autosomal dominant genetic disorder caused by a
mutation in the
folliculin (FLCN) gene. It can
cause susceptibility to
kidney cancer,
renal and pulmonary...
- FLCN gene (located at
chromosome 17p11.2),
which encodes a
protein named folliculin. FLCN
mutations and lung
lesions have also been
identified in familial...
- or "follicular hormone";
others referred to it
variously as feminin,
folliculin, menformon, thelykinin, and emmenin. In 1926,
Parkes and
Bellerby coined...
-
different authors. PEDERSEN-BJERGAARD (1939) was able to show that 90% of the
folliculin taken up in the
blood of the vena
portae is
inactivated in the liver....
-
Folliculin-interacting
protein 1 (FNIP1)
functions as a co-chaperone
which inhibits the
ATPase activity of the
chaperone Hsp90 (heat
shock protein-90)...
- and
their corresponding Cytogenetic location on
chromosome 17: FLCN:
folliculin (17p11.2) MYO15A:
myosin XVA (17p11.2) RAI1:
retinoic acid
induced 1 (17p11...
-
different authors. PEDERSEN-BJERGAARD (1939) was able to show that 90% of the
folliculin taken up in the
blood of the vena
portae is
inactivated in the liver....
-
while Butenandt named it
progynon and
subsequently referred to it as
folliculin in his
second publication on the substance.
Butenandt was
later awarded...
-
different authors. PEDERSEN-BJERGAARD (1939) was able to show that 90% of the
folliculin taken up in the
blood of the vena
portae is
inactivated in the liver....
