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Denis Reshetov
Denis Reshetov
slonigiraf.org
Подтвержден адрес электронной почты в домене slon-i-giraf.ru
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Год
The ctenophore genome and the evolutionary origins of neural systems
LL Moroz, KM Kocot, MR Citarella, S Dosung, TP Norekian, ...
Nature 510 (7503), 109-114, 2014
7562014
Human-specific histone methylation signatures at transcription start sites in prefrontal neurons
HP Shulha, JL Crisci, D Reshetov, JS Tushir, I Cheung, R Bharadwaj, ...
PLoS biology 10 (11), e1001427, 2012
1352012
CRISPR/Cas9-generated mouse model of Duchenne muscular dystrophy recapitulating a newly identified large 430 kb deletion in the human DMD gene
TV Egorova, ED Zotova, DA Reshetov, AV Polikarpova, SG Vassilieva, ...
Disease Models & Mechanisms 12 (4), dmm037655, 2019
422019
Analysis of clusterin gene (CLU/APOJ) polymorphism in Alzheimer’s disease patients and in normal cohorts from Russian populations
SA Golenkina, AY Goltsov, IL Kuznetsova, AP Grigorenko, TV Andreeva, ...
Molecular biology 44, 546-551, 2010
422010
Whole-genome sequencing identifies a novel ABCB7 gene mutation for X-linked congenital cerebellar ataxia in a large family of Mongolian ancestry
MS Protasova, AP Grigorenko, TV Tyazhelova, TV Andreeva, ...
European Journal of Human Genetics 24 (4), 550-555, 2016
372016
Whole exome sequencing links dental tumor to an autosomal-dominant mutation in ANO5 gene associated with gnathodiaphyseal dysplasia and muscle dystrophies
TV Andreeva, TV Tyazhelova, VN Rykalina, FE Gusev, AY Goltsov, ...
Scientific reports 6 (1), 26440, 2016
342016
Chromatin profiling of cortical neurons identifies individual epigenetic signatures in schizophrenia
FE Gusev, DA Reshetov, AC Mitchell, TV Andreeva, A Dincer, ...
Translational Psychiatry 9 (1), 256, 2019
212019
Base-calling algorithm with vocabulary (BCV) method for analyzing population sequencing chromatograms
YS Fantin, AD Neverov, AV Favorov, MV Alvarez-Figueroa, ...
PLoS One 8 (1), e54835, 2013
162013
Therapeutic potential of highly functional codon-optimized microutrophin for muscle-specific expression
AV Starikova, VV Skopenkova, AV Polikarpova, DA Reshetov, ...
Scientific Reports 12 (1), 848, 2022
152022
Epigenetic-genetic chromatin footprinting identifies novel and subject-specific genes active in prefrontal cortex neurons
FE Gusev, DA Reshetov, AC Mitchell, TV Andreeva, A Dincer, ...
The FASEB Journal 33 (7), 8161, 2019
142019
SNAD: sequence name annotation-based designer
IA Sidorov, DA Reshetov, AE Gorbalenya
Bmc Bioinformatics 10, 1-7, 2009
92009
Neurodevelopmental syndrome with intellectual disability, speech impairment, and quadrupedia is associated with glutamate receptor delta 2 gene defect
AP Grigorenko, MS Protasova, AA Lisenkova, DA Reshetov, TV Andreeva, ...
Cells 11 (3), 400, 2022
52022
DMD TREATMENT: ANIMAL MODELS: P. 203Exons 6 and 7 skipping test on new murine model of Duchenne muscular dystrophy
T Egorova, D Reshetov, A Polikarpova, S Vassilieva, D Vlodavets, ...
Neuromuscular Disorders 28, S94, 2018
32018
Modification of the method for analysis of genome editing results using CRISPR/Cas9 system on preimplantation mouse embryos
TV Dimitrieva, DA Reshetov, VE Zhernovkov, DV Vlodavets, ED Zotova, ...
Bulletin of Russian State Medical University, 15-20, 2016
32016
P. 393New advances in the neuromuscular diseases registry in Russia
D Vlodavets, A Monakhova, O Shidlovskaya, I Shulyakova, S Artemieva, ...
Neuromuscular Disorders 29, S196, 2019
22019
DMD Genetic registry in Russia.
D Vlodavets, D Reshetov, S Artemieva, I Shulyakova, O Shidlovskaya, ...
Neuromuscular Disorders 27, S128-S129, 2017
22017
Analysis of phenotype expressions of deletions in the dystrophin gene in terms of efficiency of exon skipping as a method for treatment of hereditary dystrophinopathies
ED Zotova, DA Reshetov, VE Zhernovkov, DV Vlodovets, TV Dimitrieva, ...
Bulletin of Russian State Medical University, 21-26, 2016
22016
P7-2. The evolution of alpha satellite Suprachromosomal Family 5 from orangutan to man: A story of invasion, death and rebirth
VA Shepelev, FE Gusev, DA Reshetov, AA Alexandrov, YB Yurov, ...
Molecular Phylogenetics, 136-137, 2012
22012
RNA Interference Effectors Selectively Silence the Pathogenic Variant GNAO1 c.607 G > A In Vitro
NV Klementieva, EA Lunev, AA Shmidt, EM Loseva, IM Savchenko, ...
nucleic acid therapeutics, 2024
2024
Exons 6 and 7 skipping test on new murine model of Duchenne muscular dystrophy
T Egorova, D Reshetov, A Polikarpova, S Vassilieva, D Vlodavets, ...
NEUROMUSCULAR DISORDERS 28, S94-S94, 2018
2018
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