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1
Nonsense mutation correction in human diseases : an approach for targeted medicine
Academic Press
Benhabiles
,
Hana
,
Jia
,
Jieshuang
,
Lejeune
,
Fabrice
nonsense
mrna
nmd
splicing
gene
protein
mutation
mutations
exon
codon
upf1
diseases
proteins
decay
readthrough
genes
mol
dystrophin
rna
correction
mediated
biol
complex
dna
patients
ejc
cftr
related
specific
binding
upf2
genet
genome
alternative
terminal
upf3x
mrnas
factors
therapy
upf3b
function
molecules
splice
approach
maquat
regulation
smg1
targeted
inhibition
containing
年:
2016
语言:
english
文件:
PDF, 12.89 MB
您的标签:
0
/
0
english, 2016
2
Advances in Genetics, Vol. 62
Academic Press
Jeffrey C. Hall (Eds.)
nmd
courtship
gene
drosophila
upf1
mrna
gal4
brain
females
behavior
specific
association
protein
studies
neurons
genes
factors
melanogaster
genome
uas
complex
cns
decay
fruitless
nonsense
termination
proteins
mediated
framingham
genet
reproductive
flies
mutations
analysis
frum
effects
villella
transcripts
yeast
involved
function
molecular
behavioral
mol
mutation
biol
neural
snps
mutant
risk
年:
2008
语言:
english
文件:
PDF, 2.89 MB
您的标签:
0
/
0
english, 2008
3
Nonsense-Mediated mRNA Decay: Pathologies and the Potential for Novel Therapeutics
MDPI
Kamila Pawlicka
,
Umesh Kalathiya
,
Javier Alfaro
nmd
crossref
nonsense
mrna
protein
mediated
decay
upf1
pathway
rna
pubmed
complex
tumour
mutations
proteins
response
transcripts
cancers
inhibition
exon
gene
genes
mol
regulation
upf2
mrnas
upf3b
stress
smg1
activity
binding
ejc
pdb
termination
biol
components
smg
factors
smg7
figure
junction
smg5
splicing
surveillance
transcript
degradation
helicase
inhibitors
interactions
smg8
年:
2020
语言:
english
文件:
PDF, 2.27 MB
您的标签:
0
/
0
english, 2020
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