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Teepu Siddique

Showing results (41-50 of 86) with videos related to

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Neuromolecular Medicine|August 31, 2019
Incidence and Clinical Features of TRPV4-Linked Axonal Neuropathies in a USA Cohort of Charcot-Marie-Tooth Disease Type 2Sheng Deng, Shawna M E Feely, Yong Shi, et al.
Archives of Neurology|July 23, 2003
Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in TunisiaGhada El Euch-Fayache, Irfan Lalani, Rim Amouri, et al.
Cell & Bioscience|February 20, 2025
Whole-genome bisulfite sequencing of cell-free DNA unveils age-dependent and ALS-associated methylation alterationsYulin Jin, Karen N Conneely, Wenjing Ma, et al.
Elife|May 3, 2017
Nuclear export of misfolded SOD1 mediated by a normally buried NES-like sequence reduces proteotoxicity in the nucleusYongwang Zhong, Jiou Wang, Mark J Henderson, et al.
Journal of Lipid Research|October 9, 2009
Marked accumulation of 27-hydroxycholesterol in SPG5 patients with hereditary spastic paresisRebecca Schüle, Teepu Siddique, Han-Xiang Deng, et al.
Human Molecular Genetics|September 15, 2007
Distal axonopathy in an alsin-deficient mouse modelHan-Xiang Deng, Hong Zhai, Ronggen Fu, et al.
Journal of Neuropathology and Experimental Neurology|August 28, 2004
Neuronal ubiquitinated intranuclear inclusions in familial and non-familial frontotemporal dementia of the motor neuron disease type associated with amyotrophic lateral sclerosisEileen H Bigio, Nancy A Johnson, Alfred W Rademaker, et al.
Journal of Neurophysiology|October 3, 2003
Hyperexcitability of cultured spinal motoneurons from presymptomatic ALS miceJason J Kuo, Martijn Schonewille, Teepu Siddique, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|September 14, 2007
Riluzole metabolism and CYP1A1/2 polymorphisms in patients with ALSSenda Ajroud-Driss, Mohammad Saeed, Humaira Khan, et al.
Neuroepidemiology|June 7, 2003
A4T mutation in the SOD1 gene causing familial amyotrophic lateral sclerosisHatice Aksoy, Geoffrey Dean, Marta Elian, et al.
Pageof 9

Showing results (41-50 of 86) with videos related to

Sort By:
Pageof 9
Neuromolecular Medicine|August 31, 2019
Incidence and Clinical Features of TRPV4-Linked Axonal Neuropathies in a USA Cohort of Charcot-Marie-Tooth Disease Type 2Sheng Deng, Shawna M E Feely, Yong Shi, et al.
Archives of Neurology|July 23, 2003
Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in TunisiaGhada El Euch-Fayache, Irfan Lalani, Rim Amouri, et al.
Cell & Bioscience|February 20, 2025
Whole-genome bisulfite sequencing of cell-free DNA unveils age-dependent and ALS-associated methylation alterationsYulin Jin, Karen N Conneely, Wenjing Ma, et al.
Elife|May 3, 2017
Nuclear export of misfolded SOD1 mediated by a normally buried NES-like sequence reduces proteotoxicity in the nucleusYongwang Zhong, Jiou Wang, Mark J Henderson, et al.
Journal of Lipid Research|October 9, 2009
Marked accumulation of 27-hydroxycholesterol in SPG5 patients with hereditary spastic paresisRebecca Schüle, Teepu Siddique, Han-Xiang Deng, et al.
Human Molecular Genetics|September 15, 2007
Distal axonopathy in an alsin-deficient mouse modelHan-Xiang Deng, Hong Zhai, Ronggen Fu, et al.
Journal of Neuropathology and Experimental Neurology|August 28, 2004
Neuronal ubiquitinated intranuclear inclusions in familial and non-familial frontotemporal dementia of the motor neuron disease type associated with amyotrophic lateral sclerosisEileen H Bigio, Nancy A Johnson, Alfred W Rademaker, et al.
Journal of Neurophysiology|October 3, 2003
Hyperexcitability of cultured spinal motoneurons from presymptomatic ALS miceJason J Kuo, Martijn Schonewille, Teepu Siddique, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|September 14, 2007
Riluzole metabolism and CYP1A1/2 polymorphisms in patients with ALSSenda Ajroud-Driss, Mohammad Saeed, Humaira Khan, et al.
Neuroepidemiology|June 7, 2003
A4T mutation in the SOD1 gene causing familial amyotrophic lateral sclerosisHatice Aksoy, Geoffrey Dean, Marta Elian, et al.
Pageof 9