-
Endothelin receptor type B, (ET-B) is a
protein that in
humans is
encoded by the
EDNRB gene.
Endothelin receptor type B is a G protein-coupled
receptor which activates...
- in humans. A
mutation in the
middle of the
endothelin receptor type B (
EDNRB) gene
causes lethal white syndrome when homozygous. Carriers,
which are...
-
copies of
EDNRB. It
leads to
death from
intestinal pseudo-obstruction due to Hirschsprung's disease. A
mutation in a
single copy of
EDNRB, however, as...
- The
syndrome is
caused by
mutation in the
endothelin B
receptor gene (
EDNRB). In the beginning,
medical officials defined ABCD
syndrome by the four...
-
neural crest cells eventually form
bundles of
nerve cells called ganglions.
EDNRB codes for
proteins that
connect these nerve cells to the
digestive tract...
- Australia.
Genes that, when mutated, can
cause leucism include c-kit, mitf and
EDNRB. The
terms leucistic and
leucism are
derived from the stem leuc- + -ism...
- RET, GDNF, GFRα, EDN3, and
EDNRB. RET, a
receptor tyrosine kinase (RTK),
forms a
complex with GDNF and GFRα. EDN3 and
EDNRB are then
implicated in the...
-
pigmentation around the body.
Studies have also
shown that
hearing loss due to
EDNRB mutation such as the ones that
cause type 4A, have a 53.3%
prevalence in...
- Li, Y.M.; Sun, J.H. (2015). "Cloning and ****ociation
analysis of KIT and
EDNRB polymorphisms with
dominant white coat
color in the
Chinese raccoon dog...
- 000 Aarskog–Scott
syndrome FGD1 X-linked
recessive 1:25,000 ABCD
syndrome EDNRB recessive 1:18,000-20,000
Absence deformity of leg-cataract
syndrome Aceruloplasminemia...
