Resultados da busca - Han‐Xiang Deng
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Genetics of amyotrophic lateral sclerosis por Teepu Siddique, Han‐Xiang Deng
Publicado em 1996Revisão -
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Hyperactive Intracellular Calcium Signaling Associated with Localized Mitochondrial Defects in Skeletal Muscle of an Animal Model of Amyotrophic Lateral Sclerosis por Jingsong Zhou, Jianxun Yi, Ronggen Fu, Erdong Liu, Teepu Siddique, Eduardo Rı́os, Han‐Xiang Deng
Publicado em 2009Artigo -
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Intense Superoxide Dismutase-1 Immunoreactivity in Intracytoplasmic Hyaline Inclusions of Familial Amyotrophic Lateral Sclerosis with Posterior Column Involvement por Noriyuki Shibata, Asao Hirano, Makio Kobayashi, Teepu Siddique, Han‐Xiang Deng, Wu-Yen Hung, Takeo Kato, Kohtaro Asayama
Publicado em 1996Artigo -
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Molecular dissection of ALS-associated toxicity of SOD1 in transgenic mice using an exon-fusion approach por Han-Xiang, Deng, Hujun, Jiang, Ronggen, Fu, Hong, Zhai, Yong, Shi, Erdong, Liu, Makito, Hirano, Mauro, C. Dal Canto, Teepu, Siddique
Publicado em 2008Texto -
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Marked accumulation of 27-hydroxycholesterol in SPG5 patients with hereditary spastic paresis por Rebecca Schüle, Teepu Siddique, Han‐Xiang Deng, Yi Yang, Sandra Donkervoort, Magnus Hansson, R. E. Madrid, Nailah Siddique, Lüdger Schöls, Ingemar Björkhem
Publicado em 2009Artigo -
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Nuclear export of misfolded SOD1 mediated by a normally buried NES-like sequence reduces proteotoxicity in the nucleus por Yongwang Zhong, Jiou Wang, Mark J. Henderson, Peixin Yang, Brian M. Hagen, Teepu Siddique, Bruce E. Vogel, Han‐Xiang Deng, Shengyun Fang
Publicado em 2017Artigo -
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TDP-43 pathology in primary progressive aphasia and frontotemporal dementia with pathologic Alzheimer disease por Eileen H. Bigio, Manjari Mishra, Kimmo J. Hatanpaa, Charles L. White, Nancy Johnson, Alfred Rademaker, Bing Bing Weitner, Han‐Xiang Deng, Steven Dubner, Sandra Weıntraub, Marsel Mesulam
Publicado em 2010Artigo -
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Inclusions in frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), but not FTLD with FUS proteinopathy (FTLD-FUS), have p... por Eileen H. Bigio, Jane Y. Wu, Han‐Xiang Deng, Esther N. Bit‐Ivan, Qinwen Mao, Rakhee Ganti, Melanie Peterson, Nailah Siddique, Changiz Geula, Teepu Siddique, Marsel Mesulam
Publicado em 2013Carta -
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Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy por Senda Ajroud‐Driss, Faisal Fecto, Kaouther Ajroud, Irfan Lalani, Sarah E. Calvo, Vamsi K. Mootha, Han‐Xiang Deng, Nailah Siddique, Albert J. Tahmoush, Terry Heiman‐Patterson, Teepu Siddique
Publicado em 2014Artigo -
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FUS‐immunoreactive inclusions are a common feature in sporadic and non‐SOD1 familial amyotrophic lateral sclerosis por Han‐Xiang Deng, Hong Zhai, Eileen H. Bigio, Jianhua Yan, Faisal Fecto, Kaouther Ajroud, Manjari Mishra, Senda Ajroud‐Driss, Scott Heller, Robert Sufit, Nailah Siddique, Enrico Mugnaini, Teepu Siddique
Publicado em 2010Artigo
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Assuntos relacionados
Biology
Gene
Medicine
Genetics
Disease
Pathology
Amyotrophic lateral sclerosis
Mutation
SOD1
Biochemistry
Cell biology
Internal medicine
Dementia
Frontotemporal dementia
Mutant
Chemistry
Neuroscience
Transgene
Frontotemporal lobar degeneration
Genetically modified mouse
Mitochondrion
Molecular biology
Oxidative stress
C9orf72
Endocrinology
Phenotype
Neurodegeneration
Protein aggregation
Superoxide dismutase
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