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DNA damage and differential gene expression associated with physical stress in gilthead seabream ( Sparus aurata )

General and comparative endocrinology, 2016-09, Vol.236, p.98-104

2016

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Identification of the abiotic stress-related transcription in little Neptune grass Cymodocea nodosa with RNA-seq

Marine genomics, 2017-08, Vol.34, p.47-56

2017

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Early diagnosis of enteromyxosis in intensively reared sharpsnout seabream, Diplodus puntazzo

Aquatic living resources (Montrouge), 2014-04, Vol.27 (2), p.99-106

2014

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KIF1A-related autosomal dominant spastic paraplegias (SPG30) in Russian families

BMC neurology, 2020-08, Vol.20 (1), p.1-290, Article 290

2020

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Mitochondrial DNA maintenance disorders in 102 patients from different parts of Russia: Mutational spectrum and phenotypes

Mitochondrion, 2021-03, Vol.57, p.205-212

2021

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Alzheimer's disease pathology is attenuated in a CD38-deficient mouse model

Annals of neurology, 2015-07, Vol.78 (1), p.88-103

2015

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A New Variant of Charcot-Marie-Tooth Disease Type 2 Is Probably the Result of a Mutation in the Neurofilament-Light Gene

American journal of human genetics, 2000-07, Vol.67 (1), p.37-46

2000

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Elevated levels of mitochondrial CoQ10 induce ROS-mediated apoptosis in pancreatic cancer

Scientific reports, 2021-03, Vol.11 (1), p.5749-5749, Article 5749

2021

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Cervical stability training with and without core stability training for patients with cervical disc herniation: A randomized, single‐blind study

European journal of pain, 2017-11, Vol.21 (10), p.1678-1687

2017

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AP4-assocated hereditary spastic paraplegias

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova, 2021, Vol.121 (2), p.71

2021

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HINT1 gene pathogenic variants: the most common cause of recessive hereditary motor and sensory neuropathies in Russian patients

Molecular biology reports, 2020-02, Vol.47 (2), p.1331-1337

2020

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Clinical Genetic Characteristics of Epilepsy Due to Mutations in the PCDH19 Gene (OMIM: 300088)

Neuroscience and behavioral physiology, 2020-11, Vol.50 (9), p.1099-1104

2020

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Diversity of CACNA1A-related disorders

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova, 2021, Vol.121 (12), p.106

2021

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Clinical, Genetic and Orthopedic Characteristics of Desbuquois Dysplasia

Travmatologii͡a︡ i ortopedii͡a︡ Rossii, 2021-10, Vol.27 (3), p.71-83

2021

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Сlinical and Radiological Characteristics of Two Patients with Acromesomelic Dysplasia Maroteaux Type with New Mutation in the NRP2 Gene

Travmatologii͡a︡ i ortopedii͡a︡ Rossii, 2020-09, Vol.26 (3), p.141-149

2020

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A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21

European journal of human genetics : EJHG, 2001-08, Vol.9 (8), p.646-650

2001

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Alzheimer's disease pathology is attenuated in a CD 38‐deficient mouse model

Annals of neurology, 2015-07, Vol.78 (1), p.88-103

2015

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Molecular and Genetic Study of Limb-Girdle Muscular Dystrophy 2D in Patient Cohorts with Various Forms of Progressive Muscular Dystrophies

Russian journal of genetics, 2019-02, Vol.55 (2), p.238-245

2019

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Clinical Population Genetics of Hereditary Diseases among Children of the Karachay-Cherkess Republic

Russian journal of genetics, 2019-08, Vol.55 (8), p.1033-1040

2019

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Elevated levels of mitochondrial CoQ 10 induce ROS-mediated apoptosis in pancreatic cancer

Scientific reports, 2021-03, Vol.11 (1), p.5749

2021

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Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients

Human mutation, 2000-04, Vol.15 (4), p.340-347

2000

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Generation of Chimeric ＂ABS Nanohemostat＂ Complex and Comparing Its Histomorphological In Vivo Effects to the Traditional Ankaferd Hemostat in Controlled Experimental Partial Nephrectomy Model

International Journal of Biomaterials, 2013-01, Vol.2013, p.949460-10

2013

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Hereditary Disorders in Circassians of the Karachay-Cherkess Republic

Russian journal of genetics, 2018, Vol.54 (1), p.83-90

2018

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Clinical-genetic characteristics of limb girdle-muscular dystrophy type 2A

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova, 2010, Vol.110 (4), p.79

2010

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DNA damage and differential gene expression associated with physical stress in gilthead seabream ( Sparus aurata )

Identification of the abiotic stress-related transcription in little Neptune grass Cymodocea nodosa with RNA-seq

Early diagnosis of enteromyxosis in intensively reared sharpsnout seabream, Diplodus puntazzo

KIF1A-related autosomal dominant spastic paraplegias (SPG30) in Russian families

Mitochondrial DNA maintenance disorders in 102 patients from different parts of Russia: Mutational spectrum and phenotypes

Alzheimer's disease pathology is attenuated in a CD38-deficient mouse model

A New Variant of Charcot-Marie-Tooth Disease Type 2 Is Probably the Result of a Mutation in the Neurofilament-Light Gene

Elevated levels of mitochondrial CoQ10 induce ROS-mediated apoptosis in pancreatic cancer

Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy

Cervical stability training with and without core stability training for patients with cervical disc herniation: A randomized, single‐blind study

AP4-assocated hereditary spastic paraplegias

HINT1 gene pathogenic variants: the most common cause of recessive hereditary motor and sensory neuropathies in Russian patients

Clinical Genetic Characteristics of Epilepsy Due to Mutations in the PCDH19 Gene (OMIM: 300088)

Diversity of CACNA1A-related disorders

Clinical, Genetic and Orthopedic Characteristics of Desbuquois Dysplasia

Сlinical and Radiological Characteristics of Two Patients with Acromesomelic Dysplasia Maroteaux Type with New Mutation in the NRP2 Gene

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21

Alzheimer's disease pathology is attenuated in a CD 38‐deficient mouse model

Molecular and Genetic Study of Limb-Girdle Muscular Dystrophy 2D in Patient Cohorts with Various Forms of Progressive Muscular Dystrophies

Clinical Population Genetics of Hereditary Diseases among Children of the Karachay-Cherkess Republic

Elevated levels of mitochondrial CoQ 10 induce ROS-mediated apoptosis in pancreatic cancer

Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients

Generation of Chimeric ＂ABS Nanohemostat＂ Complex and Comparing Its Histomorphological In Vivo Effects to the Traditional Ankaferd Hemostat in Controlled Experimental Partial Nephrectomy Model

Hereditary Disorders in Circassians of the Karachay-Cherkess Republic

Clinical-genetic characteristics of limb girdle-muscular dystrophy type 2A

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