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Gene therapy to promote regeneration in Charcot-Marie-Tooth disease

Brain research, 2020-01, Vol.1727, p.146533-146533, Article 146533

2020

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AAV1.NT-3 gene therapy for X-linked Charcot–Marie–Tooth neuropathy type 1

Gene therapy, 2022-04, Vol.29 (3-4), p.127-137

2022

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AAV1.NT-3 gene therapy in the SOD1KO mouse model of accelerated sarcopenia

Journal of cachexia, sarcopenia and muscle, 2023-10, Vol.14 (5), p.2204-2215

2023

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Motor protein mutations cause a new form of hereditary spastic paraplegia

Neurology, 2014-06, Vol.82 (22), p.2007-2016

2014

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Systemic delivery of AAVrh74.tMCK.hCAPN3 rescues the phenotype in a mouse model for LGMD2A/R1

Molecular therapy. Methods & clinical development, 2021-09, Vol.22, p.401-414

2021

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Concurrent nodular lymphocytic myositis and myasthenia gravis. A case report

Neuromuscular disorders : NMD, 2024-12, Vol.45, p.105211, Article 105211

2024

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AAV1.NT-3 gene therapy prevents age-related sarcopenia

Aging (Albany, NY.), 2023-03, Vol.15 (5), p.1306-1329

2023

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AAV1.tMCK.NT-3 gene therapy improves phenotype in Sh3tc2-/- mouse model of Charcot-Marie-Tooth type 4C

Brain communications, 2024-11

2024

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SIK2 attenuates proliferation and survival of breast cancer cells with simultaneous perturbation of MAPK and PI3K/Akt pathways

Oncotarget, 2018-04, Vol.9 (31), p.21876-21892

2018

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PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia

Clinical genetics, 2017-11, Vol.92 (5), p.534-539

2017

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REMEDY: A Novel CRISPR-based Allele Specific Approach Corrects VCP Mutations (S21.006)

Neurology, 2024-04, Vol.102 (17_supplement_1)

2024

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AAV1.NT-3 gene therapy in a CMT2D model: phenotypic improvements in GarsP278KY/+ mice

Brain communications, 2021-10, Vol.3 (4), p.fcab252-fcab252

2021

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Ultrasonographic findings in hereditary neuropathy with liability to pressure palsies

Neurological research (New York), 2015-02, Vol.37 (2), p.106-111

2015

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High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher disease

Clinical genetics, 2013-01, Vol.83 (1), p.66-72

2013

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TDP-43 proteinopathies: a new player in neurodegenerative diseases with defective protein folding/TDP-43 proteinopatileri: norodejeneratif konformasyon bozuklugu hastaliklarinda yeni bir oyuncu

Türkderm, 2012-03, p.1

2012

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Clinical and genetic aspects of hereditary spastic paraplegia in patients from Turkey

Neurologia i neurochirurgia polska, 2020-01, Vol.54 (2), p.176-184

2020

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TDP-43 Proteinopathies: A New Player in Neurodegenerative Diseases with Defective Protein Folding

Türk nöroloji dergisi, 2012-03, Vol.18 (1), p.1-10

2012

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TDP-43 Proteinopathies: A New Player in Neurodegenerative Diseases with Defective Protein Folding

Türk nöroloji dergisi, 2012-03, Vol.18 (1), p.1-10

2012

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TDP-43 Proteinopatileri: Nörodejeneratif Konformasyon Bozukluğu Hastalıklarında Yeni Bir Oyuncu

Türk nöroloji dergisi, 2012-01, Vol.18 (1), p.1-10

2012

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Investigating the physiological role of S199A and S199D mutants of PHF6 protein in T-cell acute lymphoblastic leukemia

Turkish journal of medical sciences, 2023-01, Vol.53 (5), p.1234-1243

2023

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Positive regulation of TNFR1 signaling via SH3 recognition motif

Turkish journal of biology, 2021-01, Vol.45 (1), p.171-179

2021

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Investigating the physiological role of S199A and S199D mutants of PHF6 protein in T-cell acute lymphoblastic leukemia

Turkish journal of medical sciences, 2023, Vol.53 (5), p.1234

2023

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Gene therapy to promote regeneration in Charcot-Marie-Tooth disease

AAV1.NT-3 gene therapy for X-linked Charcot–Marie–Tooth neuropathy type 1

Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy

AAV1.NT-3 gene therapy in the SOD1KO mouse model of accelerated sarcopenia

Motor protein mutations cause a new form of hereditary spastic paraplegia

Systemic delivery of AAVrh74.tMCK.hCAPN3 rescues the phenotype in a mouse model for LGMD2A/R1

Unraveling the genetic landscape of autosomal recessive Charcot-Marie-Tooth neuropathies using a homozygosity mapping approach

Concurrent nodular lymphocytic myositis and myasthenia gravis. A case report

Exome sequence analysis suggests genetic burden contributes to phenotypic variability and complex neuropathy

AAV1.NT-3 gene therapy prevents age-related sarcopenia

AAV1.tMCK.NT-3 gene therapy improves phenotype in Sh3tc2-/- mouse model of Charcot-Marie-Tooth type 4C

SIK2 attenuates proliferation and survival of breast cancer cells with simultaneous perturbation of MAPK and PI3K/Akt pathways

PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia

REMEDY: A Novel CRISPR-based Allele Specific Approach Corrects VCP Mutations (S21.006)

AAV1.NT-3 gene therapy in a CMT2D model: phenotypic improvements in GarsP278KY/+ mice

Ultrasonographic findings in hereditary neuropathy with liability to pressure palsies

High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher disease

TDP-43 proteinopathies: a new player in neurodegenerative diseases with defective protein folding/TDP-43 proteinopatileri: norodejeneratif konformasyon bozuklugu hastaliklarinda yeni bir oyuncu

Clinical and genetic aspects of hereditary spastic paraplegia in patients from Turkey

TDP-43 Proteinopathies: A New Player in Neurodegenerative Diseases with Defective Protein Folding

TDP-43 Proteinopathies: A New Player in Neurodegenerative Diseases with Defective Protein Folding

TDP-43 Proteinopatileri: Nörodejeneratif Konformasyon Bozukluğu Hastalıklarında Yeni Bir Oyuncu

Investigating the physiological role of S199A and S199D mutants of PHF6 protein in T-cell acute lymphoblastic leukemia

Positive regulation of TNFR1 signaling via SH3 recognition motif

Investigating the physiological role of S199A and S199D mutants of PHF6 protein in T-cell acute lymphoblastic leukemia

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