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Altered hydroxymethylome in the substantia nigra of Parkinson's disease.
Min, Shishi; Xu, Qian; Qin, Lixia; Li, Yujing; Li, Ziyi; Chen, Chao; Wu, Hao; Han, Junhai; Zhu, Xiongwei; Jin, Peng; Tang, Beisha.
Afiliação
  • Min S; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
  • Xu Q; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
  • Qin L; Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, Hunan 410008, China.
  • Li Y; National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan 410078, China.
  • Li Z; Department of Neurology, the Second Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
  • Chen C; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA.
  • Wu H; Department of Biostatistics and Bioinformatics, Emory University School of Public Health, Atlanta, GA 30322, USA.
  • Han J; Center for Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, and Department of Psychiatry, The Second Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
  • Zhu X; Department of Biostatistics and Bioinformatics, Emory University School of Public Health, Atlanta, GA 30322, USA.
  • Jin P; School of Life Science and Technology, Key Laboratory of Developmental Genes and Human Disease, Southeast University, Nanjing, Jiangsu 210096, China.
  • Tang B; Department of Pathology, Case Western Reserve University, Cleveland, OH 44106, USA.
Hum Mol Genet ; 31(20): 3494-3503, 2022 10 10.
Article em En | MEDLINE | ID: mdl-35661211
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Fosfolipase D Limite: Humans Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Fosfolipase D Limite: Humans Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China