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Muscle & Nerve
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June 15, 2010
Direct immunofluoresence in vasculitic neuropathy: specificity of vascular immune deposits
Michael P Collins, Isabel Periquet-Collins, Zarife Sahenk, et al.
Seminars in Pediatric Neurology
|
December 17, 2008
Hypotonia, weakness, and pontocerebellar hypoplasia in siblings
Chang-Yong Tsao, Jerry Mendell, Zarife Sahenk, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
August 8, 2023
AAV1.NT-3 gene therapy in the SOD1KO mouse model of accelerated sarcopenia
Lingying Tong, Burcak Ozes, Kyle Moss, et al.
Journal of the Peripheral Nervous System : JPNS
|
June 11, 2003
Evidence for impaired axonal regeneration in PMP22 duplication: studies in nerve xenografts
Zarife Sahenk, Carmen Serrano-Munuera, Lei Chen, et al.
Journal of Neuromuscular Diseases
|
October 15, 2019
A Novel De Novo Heterozygous SCN4a Mutation Causing Congenital Myopathy, Myotonia and Multiple Congenital Anomalies
Megan Waldrop, Jakkrit Amornvit, Christopher R Pierson, et al.
Aging
|
March 10, 2023
AAV1.NT-3 gene therapy prevents age-related sarcopenia
Burcak Ozes, Lingying Tong, Morgan Myers, et al.
International Journal of Molecular Sciences
|
February 27, 2026
AAVrh74.tMCK.NT-3 Surrogate Gene Therapy in a Mouse Model of CMT2A
Burcak Ozes, Lingying Tong, Kyle Moss, et al.
Gene Therapy
|
March 11, 2018
AAV1.NT-3 gene therapy increases muscle fiber diameter through activation of mTOR pathway and metabolic remodeling in a CMT mouse model
Mehmet E Yalvac, Jakkrit Amornvit, Lei Chen, et al.
Brain Communications
|
November 10, 2021
AAV1.NT-3 gene therapy in a CMT2D model: phenotypic improvements in <i>Gars</i> mice
Burcak Ozes, Kyle Moss, Morgan Myers, et al.
Brain Communications
|
November 15, 2024
AAV1.tMCK.NT-3 gene therapy improves phenotype in <i>Sh3tc2</i> mouse model of Charcot-Marie-Tooth Type 4C
Burcak Ozes, Lingying Tong, Kyle Moss, et al.
Page
of 8
Search research articles
Search
Showing results (11-20 of 75) with videos related to
Sort By:
Page
of 8
Muscle & Nerve
|
June 15, 2010
Direct immunofluoresence in vasculitic neuropathy: specificity of vascular immune deposits
Michael P Collins, Isabel Periquet-Collins, Zarife Sahenk, et al.
Seminars in Pediatric Neurology
|
December 17, 2008
Hypotonia, weakness, and pontocerebellar hypoplasia in siblings
Chang-Yong Tsao, Jerry Mendell, Zarife Sahenk, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
August 8, 2023
AAV1.NT-3 gene therapy in the SOD1KO mouse model of accelerated sarcopenia
Lingying Tong, Burcak Ozes, Kyle Moss, et al.
Journal of the Peripheral Nervous System : JPNS
|
June 11, 2003
Evidence for impaired axonal regeneration in PMP22 duplication: studies in nerve xenografts
Zarife Sahenk, Carmen Serrano-Munuera, Lei Chen, et al.
Journal of Neuromuscular Diseases
|
October 15, 2019
A Novel De Novo Heterozygous SCN4a Mutation Causing Congenital Myopathy, Myotonia and Multiple Congenital Anomalies
Megan Waldrop, Jakkrit Amornvit, Christopher R Pierson, et al.
Aging
|
March 10, 2023
AAV1.NT-3 gene therapy prevents age-related sarcopenia
Burcak Ozes, Lingying Tong, Morgan Myers, et al.
International Journal of Molecular Sciences
|
February 27, 2026
AAVrh74.tMCK.NT-3 Surrogate Gene Therapy in a Mouse Model of CMT2A
Burcak Ozes, Lingying Tong, Kyle Moss, et al.
Gene Therapy
|
March 11, 2018
AAV1.NT-3 gene therapy increases muscle fiber diameter through activation of mTOR pathway and metabolic remodeling in a CMT mouse model
Mehmet E Yalvac, Jakkrit Amornvit, Lei Chen, et al.
Brain Communications
|
November 10, 2021
AAV1.NT-3 gene therapy in a CMT2D model: phenotypic improvements in <i>Gars</i> mice
Burcak Ozes, Kyle Moss, Morgan Myers, et al.
Brain Communications
|
November 15, 2024
AAV1.tMCK.NT-3 gene therapy improves phenotype in <i>Sh3tc2</i> mouse model of Charcot-Marie-Tooth Type 4C
Burcak Ozes, Lingying Tong, Kyle Moss, et al.
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of 8