-
encoded by the gene DKC1.
Dyskerin is a
pseudouridine synthase enzyme which is part of the TruB
family of enzymes.
Dyskerin is an L-shaped
protein of...
- the
sequence conservation and
importance of
dyskerin within the eukaryotes. The
relevant nature of
dyskerin throughout most
species is to
catalyze the...
-
Recently an X-linked
mutation in a
third telomerase-****ociated gene,
dyskerin (DKC1), has been
described in a
family with IPF.[unreliable
medical source...
- by
mutations in DKC1, the gene
encoding for the
pseudouridine synthase dyskerin.
Pseudouridines have been
recognized as
regulators of
viral latency processes...
-
series based on the
video games Dyskeratosis congenita, a
genetic disease Dyskerin, a gene also
known as DKC1 DKC (company), a
public relations company This...
-
syndrome has been
shown to
arise from
mutations in
multiple genes,
including dyskerin,
telomerase RNA and
telomerase reverse transcriptase. Prader–Willi syndrome...
-
conserved and
essential proteins—
dyskerin (Cbf5p), GAR1, NHP2, and NOP10—which make up the core of the H/ACA box snoRNP.
Dyskerin is
likely the
catalytic component...
- on the 3’ end by a single-stranded ACA sequence. The H/ACA
domain binds Dyskerin, GAR1, NOP10, NHP2, to form an H/ACA RNP complex. The
conserved CR7 domain...
-
reverse transcriptase (TERT),
Telomerase RNA
Component (TR or TERC), and
dyskerin (DKC1). The
genes of
telomerase subunits,
which include TERT, TERC, DKC1...
- Smith–Lemli–Opitz
syndrome DTNBP1
Dysbindin Hermansky–Pudlak
syndrome type 7
Dyskerin Dyskeratosis congenita ECM1
Extracellular matrix protein-1
Lipoid proteinosis...
