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Gene Silencing and Editing Strategies for Neurodegenerative Diseases
Gene Silencing and Editing Strategies for Neurodegenerative Diseases
Autore Clévio Nóbrega
Pubbl/distr/stampa Frontiers Media SA, 2018
Descrizione fisica 1 electronic resource (115 p.)
Collana Frontiers Research Topics
Soggetto non controllato Gene silencing
Long non-coding RNAs
RNA interference
Neurodegenerative diseases
CRISPR/Cas9
Neurodegeneration
Gene editing
Antisense oligonucleotides
Neuroinflammation
iPS cells
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910346760003321
Clévio Nóbrega  
Frontiers Media SA, 2018
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Towards Mechanism-based Treatments for Fragile X Syndrome
Towards Mechanism-based Treatments for Fragile X Syndrome
Autore Kumari Daman
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2019
Descrizione fisica 1 electronic resource (250 p.)
Soggetto non controllato lymphoblast
pluripotent stem cells
FMR1
Gene editing
X chromosome
Fmr1
epigenetic gene silencing
FMR1 gene
Fragile X syndrome 1
repeat instability
characteristics that have the greatest impact
DNA instability
working memory
language development
mosaicism
CRISPR 3
clinical trials
autism spectrum disorders
Fmr1 KO mouse
automated vocal analysis
base excision repair (BER)
inhibitory control
cerebral spinal fluid
iPSC
drug development
targeted treatments
molecular biomarkers
viral vector
avoidance
biomarker
set-shifting
early identification
expansion
anxiety
planning
voice of the person
mismatch repair (MMR)
gene reactivation
double-strand break repair (DSBR)
newborn screening
intellectual disability
processing speed
voice of the patient
fragile X syndrome
adeno-associated virus
neurodevelopmental disorders
histone methylation
Non-homologous end-joining (NHEJ)
ASD
Fxr2
Fragile X-associated Tremor/Ataxia Syndrome 2
Trinucleotide Repeat 4
CGG Repeat Expansion Disease
DNA methylation
contraction
fragile X mental retardation protein
RNA:DNA hybrid
behavior
developmental disorders
cognition
females
FMRP
Fragile X Syndrome
unstable repeat diseases
protein synthesis
brain
cognitive flexibility
treatment development
fibroblast
PRC2
transcription coupled repair (TCR)
best practices
attention
Fragile X
executive function
ISBN 3-03921-506-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910367759103321
Kumari Daman  
MDPI - Multidisciplinary Digital Publishing Institute, 2019
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui