-
humans is
encoded by the
IKBKG gene. NEMO is a
subunit of the IκB
kinase complex that
activates NF-κB. The
human gene for
IKBKG is
located on the chromosome...
-
mutation in the
IKBKG gene,
which encodes the NEMO protein,
which serves to
protect cells against TNF-alpha-induced apoptosis. A lack of
IKBKG therefore makes...
-
factors into the nucleus. The link
between IKBKG mutations and NEMO
deficiency was
identified in 1999.
IKBKG is
located on the X
chromosome and is X-linked...
-
first cause (and most
common out of the 2) is a
genetic mutation in the
IKBKG gene,
located in the X
chromosome at the q28 locus. The
protein that is...
-
between 1970 and 1986 to
oversee and
observe undersea construction work.
IKBKG or NF-Kappa-B
essential modulator (NEMO), a
protein NEMO (museum), a national...
- IKK1) (CHUK) IKK-β (also
known as IKK2) (IKBKB) IKK-γ (also
known as NEMO) (
IKBKG) The α- and β-subunits
together are
catalytically active whereas the γ-subunit...
-
microsomia SIX3, SHH, PTCH1, GLI2 AD
Holoprosencephaly types 1, 2, 3, 7, 9
IKBKG XLD
Incontinentia pigmenti PDE6D AR
Joubert syndrome 22
unknown AR Kapur–Toriello...
- 50% of
cases of AR(autosomal recessive) osteopetrosis.
Mutations in the
IKBKG gene
cause X-linked osteopetrosis.
Mutations in the CA-II gene can be an...
- instability–facial
anomalies syndrome (ICF syndrome) 20q11.2
Incontinentia pigmenti IKBKG (Xq28) P
Infantile cerebral and
cerebellar atrophy with
postnatal progressive...
-
protein kinase (EC 2.7.11.9) - IκB
kinase (EC 2.7.11.10) CHUK IKK2 TBK1
IKBKE IKBKG IKBKAP cAMP-dependent
protein kinase (EC 2.7.11.11)
Protein kinase A PRKACG...
