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H X Deng

Showing results (41-50 of 61) with videos related to

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Neurogenetics|May 1, 1997
Exon 5 encoded domain is not required for the toxic function of mutant SOD1 but essential for the dismutase activity: identification and characterization of two new SOD1 mutations associated with familial amyotrophic lateral sclerosisJ S Zu, H X Deng, T P Lo, et al.
Human Molecular Genetics|September 1, 1996
Linkage of scapuloperoneal spinal muscular atrophy to chromosome 12q24.1-q24.31K Isozumi, R DeLong, J Kaplan, et al.
Neuroepidemiology|June 7, 2003
A4T mutation in the SOD1 gene causing familial amyotrophic lateral sclerosisHatice Aksoy, Geoffrey Dean, Marta Elian, et al.
Science (New York, N.Y.)|June 17, 1994
Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutationM E Gurney, H Pu, A Y Chiu, et al.
Yi Chuan Xue Bao = Acta Genetica Sinica|July 2, 1998
[Localization of the gene for 4 hereditary multiple exostoses families]Y Tang, J H Xia, J N Zhou, et al.
Neurology|August 9, 2006
Lack of association of VEGF promoter polymorphisms with sporadic ALSW Chen, M Saeed, H Mao, et al.
Neurology|July 30, 2010
Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementiaJ Yan, H-X Deng, N Siddique, et al.
Neurology|February 4, 2011
TRPV4 mutations and cytotoxic hypercalcemia in axonal Charcot-Marie-Tooth neuropathiesC J Klein, Y Shi, F Fecto, et al.
The British Journal of Dermatology|October 9, 2002
A novel locus (DSAP2) for disseminated superficial actinic porokeratosis maps to chromosome 15q25.1-26.1K Xia, H Deng, J H Xia, et al.
Journal of Human Genetics|June 4, 1998
The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32M Fujimoto, P N Kantaputra, S Ikegawa, et al.
Pageof 7

Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
Neurogenetics|May 1, 1997
Exon 5 encoded domain is not required for the toxic function of mutant SOD1 but essential for the dismutase activity: identification and characterization of two new SOD1 mutations associated with familial amyotrophic lateral sclerosisJ S Zu, H X Deng, T P Lo, et al.
Human Molecular Genetics|September 1, 1996
Linkage of scapuloperoneal spinal muscular atrophy to chromosome 12q24.1-q24.31K Isozumi, R DeLong, J Kaplan, et al.
Neuroepidemiology|June 7, 2003
A4T mutation in the SOD1 gene causing familial amyotrophic lateral sclerosisHatice Aksoy, Geoffrey Dean, Marta Elian, et al.
Science (New York, N.Y.)|June 17, 1994
Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutationM E Gurney, H Pu, A Y Chiu, et al.
Yi Chuan Xue Bao = Acta Genetica Sinica|July 2, 1998
[Localization of the gene for 4 hereditary multiple exostoses families]Y Tang, J H Xia, J N Zhou, et al.
Neurology|August 9, 2006
Lack of association of VEGF promoter polymorphisms with sporadic ALSW Chen, M Saeed, H Mao, et al.
Neurology|July 30, 2010
Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementiaJ Yan, H-X Deng, N Siddique, et al.
Neurology|February 4, 2011
TRPV4 mutations and cytotoxic hypercalcemia in axonal Charcot-Marie-Tooth neuropathiesC J Klein, Y Shi, F Fecto, et al.
The British Journal of Dermatology|October 9, 2002
A novel locus (DSAP2) for disseminated superficial actinic porokeratosis maps to chromosome 15q25.1-26.1K Xia, H Deng, J H Xia, et al.
Journal of Human Genetics|June 4, 1998
The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32M Fujimoto, P N Kantaputra, S Ikegawa, et al.
Pageof 7