Torthaí cuardaigh - Han‐Xiang Deng
- 1 - 20 toradh as 33 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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1
Genetics of amyotrophic lateral sclerosis de réir Teepu Siddique, Han‐Xiang Deng
Foilsithe / Cruthaithe 1996Revisão -
2
PvuII RFLPs in the DMD gene detected by a subclone (cDMD1a) of the cDNA de réir Han-Xiang, Deng, Niikawa, Norio
Foilsithe / Cruthaithe 1990Téacs -
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Mutant TRPV4-mediated Toxicity Is Linked to Increased Constitutive Function in Axonal Neuropathies de réir Faisal Fecto, Yong Shi, Rafiq Huda, Marco Martina, Teepu Siddique, Han‐Xiang Deng
Foilsithe / Cruthaithe 2011Artigo -
5
Disulfide cross-linked protein represents a significant fraction of ALS-associated Cu, Zn-superoxide dismutase aggregates in spinal cords of model mice de réir Yoshiaki Furukawa, Ronggen Fu, Han‐Xiang Deng, Teepu Siddique, Thomas V. O’Halloran
Foilsithe / Cruthaithe 2006Artigo -
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Wild-type SOD1 overexpression accelerates disease onset of a G85R SOD1 mouse de réir Lijun Wang, Han‐Xiang Deng, Gabriella Grisotti, Hong Zhai, Teepu Siddique, Raymond P. Roos
Foilsithe / Cruthaithe 2009Artigo -
8
Sirt3 protects dopaminergic neurons from mitochondrial oxidative stress de réir Han Shi, Han‐Xiang Deng, David Gius, Paul T. Schumacker, D. James Surmeier, Yongchao Ma
Foilsithe / Cruthaithe 2017Artigo -
9
A novel ALS-associated variant in UBQLN4 regulates motor axon morphogenesis de réir Brittany M. Edens, Jianhua Yan, Nimrod Miller, Han‐Xiang Deng, Teepu Siddique, Yongchao Ma
Foilsithe / Cruthaithe 2017Artigo -
10
Hyperactive Intracellular Calcium Signaling Associated with Localized Mitochondrial Defects in Skeletal Muscle of an Animal Model of Amyotrophic Lateral Sclerosis de réir Jingsong Zhou, Jianxun Yi, Ronggen Fu, Erdong Liu, Teepu Siddique, Eduardo Rı́os, Han‐Xiang Deng
Foilsithe / Cruthaithe 2009Artigo -
11
Intense Superoxide Dismutase-1 Immunoreactivity in Intracytoplasmic Hyaline Inclusions of Familial Amyotrophic Lateral Sclerosis with Posterior Column Involvement de réir Noriyuki Shibata, Asao Hirano, Makio Kobayashi, Teepu Siddique, Han‐Xiang Deng, Wu-Yen Hung, Takeo Kato, Kohtaro Asayama
Foilsithe / Cruthaithe 1996Artigo -
12
miR-1228 promotes the proliferation and metastasis of hepatoma cells through a p53 forward feedback loop de réir Y. Zhang, Junren Dai, Han‐Xiang Deng, Haisu Wan, M. Liu, Jialin Wang, Shiyong Li, Xiaoyu Li, Hua Tang
Foilsithe / Cruthaithe 2014Artigo -
13
Age and founder effect of <i>SOD1</i> A4V mutation causing ALS de réir Mohammad Saeed, Yan Yang, Han‐Xiang Deng, W-Y. Hung, N. Siddique, Lisa Dellefave, Cinzia Gellera, P. M. Andersen, Teepu Siddique
Foilsithe / Cruthaithe 2009Artigo -
14
Molecular dissection of ALS-associated toxicity of SOD1 in transgenic mice using an exon-fusion approach de réir Han-Xiang, Deng, Hujun, Jiang, Ronggen, Fu, Hong, Zhai, Yong, Shi, Erdong, Liu, Makito, Hirano, Mauro, C. Dal Canto, Teepu, Siddique
Foilsithe / Cruthaithe 2008Téacs -
15
Marked accumulation of 27-hydroxycholesterol in SPG5 patients with hereditary spastic paresis de réir Rebecca Schüle, Teepu Siddique, Han‐Xiang Deng, Yi Yang, Sandra Donkervoort, Magnus Hansson, R. E. Madrid, Nailah Siddique, Lüdger Schöls, Ingemar Björkhem
Foilsithe / Cruthaithe 2009Artigo -
16
Nuclear export of misfolded SOD1 mediated by a normally buried NES-like sequence reduces proteotoxicity in the nucleus de réir Yongwang Zhong, Jiou Wang, Mark J. Henderson, Peixin Yang, Brian M. Hagen, Teepu Siddique, Bruce E. Vogel, Han‐Xiang Deng, Shengyun Fang
Foilsithe / Cruthaithe 2017Artigo -
17
TDP-43 pathology in primary progressive aphasia and frontotemporal dementia with pathologic Alzheimer disease de réir 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
Foilsithe / Cruthaithe 2010Artigo -
18
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... de réir 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
Foilsithe / Cruthaithe 2013Carta -
19
Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy de réir 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
Foilsithe / Cruthaithe 2014Artigo -
20
FUS‐immunoreactive inclusions are a common feature in sporadic and non‐SOD1 familial amyotrophic lateral sclerosis de réir 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
Foilsithe / Cruthaithe 2010Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
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
Allele