Sen Zeng

Changsha, 410013, China

Last Updated: 09/26/2026

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Found 16 publications

Generation of induced pluripotent stem cells from peripheral blood mononuclear cells of a patient with autosomal recessive Charcot-Marie-Tooth disease type 2S caused by IGHMBP2 mutations

Generation of induced pluripotent stem cells from peripheral blood mononuclear cells of a patient with autosomal recessive Charcot-Marie-Tooth disease type 2S caused by IGHMBP2 mutations

Journal: Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences

Published: April 25, 2026

Corrigendum to "Impaired PARP1-dependent DNA repair in MORC2 mutations drives axonal degeneration in Charcot-Marie-Tooth disease subtype 2Z and spinal muscular atrophy-like neuromotor disorders" [Pharmacol. Res. 224 (2026) 108103].

Corrigendum to "Impaired PARP1-dependent DNA repair in MORC2 mutations drives axonal degeneration in Charcot-Marie-Tooth disease subtype 2Z and spinal muscular atrophy-like neuromotor disorders" [Pharmacol. Res. 224 (2026) 108103].

Journal: Pharmacological research

Published: February 13, 2026

Novel VRK1 Variants and a Founder Effect in Axonal Polyneuropathy.

Novel VRK1 Variants and a Founder Effect in Axonal Polyneuropathy.

Journal: Neurology. Genetics

Published: September 20, 2025

Impaired PARP1-dependent DNA repair in MORC2 mutations drives axonal degeneration in Charcot-Marie-Tooth disease subtype 2Z and spinal muscular atrophy-like neuromotor disorders.

Impaired PARP1-dependent DNA repair in MORC2 mutations drives axonal degeneration in Charcot-Marie-Tooth disease subtype 2Z and spinal muscular atrophy-like neuromotor disorders.

Journal: Pharmacological research

Published: August 23, 2025

Genetic and Clinical Features of 10 Families With Hereditary Sensory Neuropathies.

Genetic and Clinical Features of 10 Families With Hereditary Sensory Neuropathies.

Journal: Journal of the peripheral nervous system : JPNS

Published: February 25, 2025

Genotype-phenotype characteristics of Chinese Charcot-Marie-Tooth disease type 2A and related MRI features.

Genotype-phenotype characteristics of Chinese Charcot-Marie-Tooth disease type 2A and related MRI features.

Journal: Chinese medical journal

Published: October 04, 2024

Genotype-phenotype correlations of AR-CMT2S in a cohort of axonal Charcot-Marie-Tooth patients from Central South China.

Genotype-phenotype correlations of AR-CMT2S in a cohort of axonal Charcot-Marie-Tooth patients from Central South China.

Journal: Journal of the peripheral nervous system : JPNS

Published: April 03, 2024

Genetic and clinical profile of 15 Chinese families with GDAP1-related Charcot-Marie-Tooth disease and identification of H256R as a frequent mutation.

Genetic and clinical profile of 15 Chinese families with GDAP1-related Charcot-Marie-Tooth disease and identification of H256R as a frequent mutation.

Journal: Journal of the peripheral nervous system : JPNS

Published: January 19, 2024

Diagnostic value of nerve conduction study in NOTCH2NLC-related neuronal intranuclear inclusion disease.

Diagnostic value of nerve conduction study in NOTCH2NLC-related neuronal intranuclear inclusion disease.

Journal: Journal of the peripheral nervous system : JPNS

Published: August 17, 2023

The MORC2 p.S87L mutation reduces proliferation of pluripotent stem cells derived from a patient with the spinal muscular atrophy-like phenotype by inhibiting proliferation-related signaling pathways.

The MORC2 p.S87L mutation reduces proliferation of pluripotent stem cells derived from a patient with the spinal muscular atrophy-like phenotype by inhibiting proliferation-related signaling pathways.

Journal: Neural regeneration research

Published: July 25, 2023

Phenotype-driven reanalysis reveals five novel pathogenic variants in 40 exome-negative families with Charcot-Marie-Tooth Disease.

Phenotype-driven reanalysis reveals five novel pathogenic variants in 40 exome-negative families with Charcot-Marie-Tooth Disease.

Journal: Journal of neurology

Published: June 11, 2023

Expanding the genetic and clinical spectrum of SORD-related peripheral neuropathy by reporting a novel variant c.210T>G and evidence of subclinical muscle involvement.

Expanding the genetic and clinical spectrum of SORD-related peripheral neuropathy by reporting a novel variant c.210T>G and evidence of subclinical muscle involvement.

Journal: Journal of the peripheral nervous system : JPNS

Published: May 06, 2023

Showing 1-12 of 16

Last Updated: 09/26/2026