X. Zi

发表

Mutant presenilin2 promotes apoptosis through the p53/miR-34a axis in neuronal cells

Liu-Hong Li, Q. Tu, X. Deng, 2017, Brain Research.

A SIGMAR1 splice-site mutation causes distal hereditary motor neuropathy

K. Xia, Zhengmao Hu, B. Tang, 2015, Neurology.

Phenotypes and cellular effects of GJB1 mutations causing CMT1X in a cohort of 226 Chinese CMT families

K. Xia, B. Tang, B. Tang, 2017, Clinical genetics.

Epigenetic modulation of Cdk5 contributes to memory deficiency induced by amyloid fibrils

Q. Tu, X. Zi, K. Guo, 2014, Experimental Brain Research.

Three novel mutations of the spastin gene in Chinese patients with hereditary spastic paraplegia.

K. Xia, Q. Pan, H. Dai, 2004, Archives of neurology.

A novel transgenic mouse model of Chinese Charcot-Marie-Tooth disease type 2L

K. Xia, Q. Pan, B. Tang, 2014, Neural regeneration research.

Krüppel-like factor 4 regulates amyloid-β (Aβ)-induced neuroinflammation in Alzheimer’s disease

Q. Tu, X. Zi, Liuhong Li, 2017, Neuroscience Letters.

A novel hemizygous SACS mutation identified by whole exome sequencing and SNP array analysis in a Chinese ARSACS patient

H. Li, D. Yu, K. Xia, 2016, Journal of the Neurological Sciences.

Screening for SH3TC2, PMP2, and BSCL2 Variants in a Cohort of Chinese Patients with Charcot-Marie-Tooth

K. Xia, B. Tang, Zhengmao Hu, 2018, Chinese medical journal.

Mutation Detection in Candidate Genes for Benign Familial Infantile Seizures on a Novel Locus

K. Xia, Q. Pan, Zhengmao Hu, 2010, The International journal of neuroscience.

MFN2‐related genetic and clinical features in a cohort of Chinese CMT2 patients

K. Xia, Zhengmao Hu, B. Tang, 2016, Journal of the peripheral nervous system : JPNS.

PMP22‐Related neuropathies and other clinical manifestations in Chinese han patients with charcot‐marie‐tooth disease type 1

K. Xia, Zhengmao Hu, B. Tang, 2015, Muscle & nerve.

MORC2 mutations in a cohort of Chinese patients with Charcot-Marie-Tooth disease type 2.

K. Xia, Zhengmao Hu, B. Tang, 2016, Brain : a journal of neurology.

LncRNA SNHG1 alleviates OGD induced injury in BMEC via miR-338/HIF-1α axis

X. Zi, Xia Yang, 2019, Brain Research.

Rapid genetic screening of Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies patients★

K. Xia, Zhengmao Hu, B. Tang, 2012, Neural regeneration research.

[Mutation analysis of LITAF, RAB7, LMNA and MTMR2 genes in Chinese Charcot-Marie-Tooth disease.].

K. Xia, B. Tang, Zhengmao Hu, 2010, Yi chuan = Hereditas.

The electrophysiological characteristics of the four most common genotypes of Charcot-Marie-Tooth disease

B. Tang, X. Zi, Huadong Zhao, 2019 .

[Mutation analysis of MFN2 gene in Chinese patients with Charcot-Marie-Tooth disease].

K. Xia, Q. Pan, B. Tang, 2009, Zhonghua yi xue za zhi.

IGHMBP2-related clinical and genetic features in a cohort of Chinese Charcot–Marie–Tooth disease type 2 patients

K. Xia, Zhengmao Hu, B. Tang, 2017, Neuromuscular Disorders.

Epigenetic modulation of Cdk5 contributes to memory deficiency induced by amyloid fibrils

Q. Tu, X. Zi, K. Guo, 2014, Experimental Brain Research.

Two novel MPZ mutations in Chinese CMT patients

K. Xia, B. Tang, Ji-feng Guo, 2013, Journal of the peripheral nervous system : JPNS.

Bag5 Protects Neuronal Cells from Amyloid β-induced Cell Death

X. Zi, K. Guo, Liuhong Li, 2015, Journal of Molecular Neuroscience.

A novel genetic locus for benign familial infantile seizures maps to chromosome 1p36.12‐p35.1

K. Xia, Q. Pan, B. Tang, 2008, Clinical genetics.

Effect of selective serotonin reuptake inhibitors on expression of 5-HT1AR and neurotransmitters in rats with vascular dementia.

X. Zi, H. Zhu, Ke Guo, 2016, Genetics and molecular research : GMR.