Yucai Chen

发表

Functional Characterization and Neuronal Modeling of the Effects of Childhood Absence Epilepsy Variants of CACNA1H, a T-Type Calcium Channel

E. Perez-Reyes, Iuliia Vitko, Yucai Chen, 2005, The Journal of Neuroscience.

Clinical Study of 8 Cases of CHD2 Gene Mutation–Related Neurological Diseases and Their Mechanisms

Xiaoping Lan, F. Zeng, Jingbin Yan, 2022, Frontiers in Cell and Developmental Biology.

Role of receptor complexes in the extranuclear actions of estrogen receptor alpha in breast cancer.

R. Santen, W. Yue, P. Fan, 2006, Endocrine-related cancer.

Role of receptor complexes in the f estrogen receptor a in breast cancer

R. Santen, W. Yue, P. Fan, 2007 .

[T-type calcium channel gene-CACNA1H is a susceptibility gene to childhood absence epilepsy].

Yan Shen, Yuehua Zhang, Yucai Chen, 2005, Zhonghua er ke za zhi = Chinese journal of pediatrics.

MED12-Related Disease in a Chinese Girl: Clinical Characteristics and Underlying Mechanism

Xiaoping Lan, Shengnan Wu, Yucai Chen, 2020, Frontiers in Genetics.

Correlation Between Tic Disorders and Serum 25-Hydroxyvitamin D Levels in Chinese Children

Yucai Chen, Xiaona Luo, Yilin Wang, 2022, Frontiers in Pediatrics.

Case-control study and transmission/disequilibrium tests of the genes encoding GABRA5 and GABRB3 in a Chinese population affected by childhood absence epilepsy.

Yan Shen, Yuehua Zhang, X. Bao, 2004, Chinese medical journal.

Novel Mutations of the ALMS1 Gene in Patients with Alström Syndrome

Xiaoping Lan, Shengnan Wu, F. Zeng, 2021, Internal medicine.

Mechanisms of Congenital Myasthenia Caused by Three Mutations in the COLQ Gene

Xiaoping Lan, Shengnan Wu, F. Zeng, 2021, Frontiers in Pediatrics.

Clinical characteristics and prognosis of pediatric myelin oligodendrocyte glycoprotein antibody-associated diseases in China

Yucai Chen, Xiaona Luo, Xiaoang Sun, 2022, BMC Pediatrics.

Clinical characteristics and genetics of ten Chinese children with PRRT2-associated neurological diseases

Xiaoping Lan, Yucai Chen, Xiaona Luo, 2022, Frontiers in Pediatrics.

Two heterozygous mutations in the calcium/calmodulin‐dependent serine protein kinase gene (CASK) in cases with developmental disorders

Xiaoping Lan, Yucai Chen, Yilin Wang, 2022, Molecular genetics & genomic medicine.

CaV3.2 calcium channels control NMDA receptor-mediated transmission: a new mechanism for absence epilepsy

K. Deisseroth, A. Erisir, J. Zhu, 2015, Genes & development.

Association between genetic variation of CACNA1H and childhood absence epilepsy

Zhijian Yao, Yan Shen, P. Chan, 2003, Annals of neurology.

The Role of T-Type Calcium Channel Genes in Absence Seizures

W. Parker, Yucai Chen, Keling Wang, 2014, Front. Neurol..

A multicenter retrospective cohort study of ketogenic diet therapy in 481 children with infantile spasms

Yuwu Jiang, Guo Zheng, Like Gao, 2022, Acta Epileptologica.

Compound heterozygous mutations of two eIF2B genes in early childhood onset form of vanishing white matter disease

Xiaoping Lan, Shengnan Wu, Yucai Chen, 2020 .

Link between absence seizures and t-type calcium channels

W. Parker, Yucai Chen, 2015 .

Novel homozygous mutation in the FBXL4 gene is associated with mitochondria DNA depletion syndrome-13

Xiaoping Lan, Shengnan Wu, Changsheng Liu, 2020, Journal of the Neurological Sciences.

Segawa syndrome caused by TH gene mutation and its mechanism

Zhiping Liu, F. Zeng, Yucai Chen, 2022, Frontiers in Genetics.

Dopa-Responsive Dystonia in Han Chinese Patients: One Novel Heterozygous Mutation in GTP Cyclohydrolase 1 (GCH1) and Three Known Mutations in TH

Xiaoping Lan, Yucai Chen, Jianjun Huang, 2018, Medical science monitor : international medical journal of experimental and clinical research.

Mutation screen of the gene encoding GABRB3 in Chinese patients with childhood absence epilepsy

Yan Shen, Yuehua Zhang, X. Bao, 2003, American journal of medical genetics. Part A.

Estrogen signaling via a linear pathway involving insulin-like growth factor I receptor, matrix metalloproteinases, and epidermal growth factor receptor to activate mitogen-activated protein kinase in MCF-7 breast cancer cells.

R. Santen, Yucai Chen, R. Song, 2007, Endocrinology.

GENETIC VARIANTS IN ABSENCE EPILEPSY :AC ONTEXTUAL CONSIDERATION OF CALCIUM CURRENT KINETICS

E. Perez-Reyes, Iuliia Vitko, Yucai Chen, 2006 .

CHRNE compound heterozygous mutations in congenital myasthenic syndrome

Yucai Chen, Simei Wang, Yuanfeng Zhang, 2018, Medicine.

The Study on the Clinical Phenotype and Function of HPRT1 Gene

Yucai Chen, Yilin Wang, Longlong Lin, 2021, Child neurology open.

DWT-Net: Seizure Detection System with Structured EEG Montage and Multiple Feature Extractor in Convolution Neural Network

Zhe Zhang, Nabil Sabor, Guoxing Wang, 2020, J. Sensors.

A novel compound heterozygous mutation of the L2HGDH gene in a Chinese boy with L-2-hydroxyglutaric aciduria: case report and literature review

Yucai Chen, G. Tian, Simei Wang, 2018, Neurological Sciences.

Mutation screen of the GABAA receptor gamma 2 subunit gene in Chinese patients with childhood absence epilepsy

Yan Shen, Yuehua Zhang, X. Bao, 2002, Neuroscience Letters.

Generation and characterization of the induced pluripotent stem cell line SHCDNi004-A from a ten-year-old Chinese boy with X-linked mental retardation in IL1RAPL1 deficiency.

F. Zeng, Yucai Chen, Xiaona Luo, 2021, Stem cell research.

Mitochondrial DNA Rearrangement Spectrum in Brain Tissue of Alzheimer’s Disease: Analysis of 13 Cases

T. Beach, G. Serrano, W. Parker, 2016, PloS one.

FBXL4 mutations cause excessive mitophagy via BNIP3/BNIP3L accumulation leading to mitochondrial DNA depletion syndrome.

H. Saiyin, Yucai Chen, Xiaona Luo, 2023, Cell death and differentiation.

[Association analysis of childhood absence epilepsy by microsatellite DNA].

Yan Shen, Yuehua Zhang, Yucai Chen, 2002, Zhonghua yi xue za zhi.

[Case-control study and transmission/disequilibrium test of childhood absence epilepsy].

Yan Shen, Yuehua Zhang, Yuwu Jiang, 2002, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Clinical features and underlying mechanisms of KAT6B disease in a Chinese boy

Xiaoping Lan, Yucai Chen, Xiaona Luo, 2023, Molecular genetics & genomic medicine.

Aberrant mitochondrial RNA in the role of aging and aging associated diseases.

W. Parker, Yucai Chen, Hongyi Chen, 2015, Medical hypotheses.

T-type calcium channel gene alpha (1G) is not associated with childhood absence epilepsy in the Chinese Han population

Yan Shen, Yuehua Zhang, X. Bao, 2003, Neuroscience Letters.