Risultati della ricerca - Han‐Xiang Deng
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Genetics of amyotrophic lateral sclerosis di Teepu Siddique, Han‐Xiang Deng
Pubblicazione 1996Revisão -
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PvuII RFLPs in the DMD gene detected by a subclone (cDMD1a) of the cDNA di Han-Xiang, Deng, Niikawa, Norio
Pubblicazione 1990testo -
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Wild-type SOD1 overexpression accelerates disease onset of a G85R SOD1 mouse di Lijun Wang, Han‐Xiang Deng, Gabriella Grisotti, Hong Zhai, Teepu Siddique, Raymond P. Roos
Pubblicazione 2009Artigo -
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Sirt3 protects dopaminergic neurons from mitochondrial oxidative stress di Han Shi, Han‐Xiang Deng, David Gius, Paul T. Schumacker, D. James Surmeier, Yongchao Ma
Pubblicazione 2017Artigo -
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A novel ALS-associated variant in UBQLN4 regulates motor axon morphogenesis di Brittany M. Edens, Jianhua Yan, Nimrod Miller, Han‐Xiang Deng, Teepu Siddique, Yongchao Ma
Pubblicazione 2017Artigo -
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Hyperactive Intracellular Calcium Signaling Associated with Localized Mitochondrial Defects in Skeletal Muscle of an Animal Model of Amyotrophic Lateral Sclerosis di Jingsong Zhou, Jianxun Yi, Ronggen Fu, Erdong Liu, Teepu Siddique, Eduardo Rı́os, Han‐Xiang Deng
Pubblicazione 2009Artigo -
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Intense Superoxide Dismutase-1 Immunoreactivity in Intracytoplasmic Hyaline Inclusions of Familial Amyotrophic Lateral Sclerosis with Posterior Column Involvement di Noriyuki Shibata, Asao Hirano, Makio Kobayashi, Teepu Siddique, Han‐Xiang Deng, Wu-Yen Hung, Takeo Kato, Kohtaro Asayama
Pubblicazione 1996Artigo -
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Age and founder effect of <i>SOD1</i> A4V mutation causing ALS di Mohammad Saeed, Yan Yang, Han‐Xiang Deng, W-Y. Hung, N. Siddique, Lisa Dellefave, Cinzia Gellera, P. M. Andersen, Teepu Siddique
Pubblicazione 2009Artigo -
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TDP-43 pathology in primary progressive aphasia and frontotemporal dementia with pathologic Alzheimer disease di 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
Pubblicazione 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... di 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
Pubblicazione 2013Carta -
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Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy di 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
Pubblicazione 2014Artigo -
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FUS‐immunoreactive inclusions are a common feature in sporadic and non‐SOD1 familial amyotrophic lateral sclerosis di 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
Pubblicazione 2010Artigo
Strumenti per la ricerca:
Soggetti correlati
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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