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A Hentati

Showing results (11-20 of 21) with videos related to

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Nature|March 4, 1993
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosisD R Rosen, T Siddique, D Patterson, et al.
Science (New York, N.Y.)|August 20, 1993
Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutaseH X Deng, A Hentati, J A Tainer, 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.
International Journal of Neurology|January 1, 1991
A molecular genetic approach to amyotrophic lateral sclerosisT Siddique, P Hu, A Hentati, et al.
Human Molecular Genetics|October 1, 1994
Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markersA Hentati, M A Pericak-Vance, F Lennon, et al.
Nature Genetics|July 1, 1994
Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35A Hentati, K Bejaoui, M A Pericak-Vance, 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.
Neurogenetics|May 18, 1999
Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markersA Hentati, K Ouahchi, M A Pericak-Vance, et al.
Neurology|June 1, 1996
Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working groupJ K Fink, T Heiman-Patterson, T Bird, et al.
Nature Genetics|October 5, 2001
The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosisY Yang, A Hentati, H X Deng, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Nature|March 4, 1993
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosisD R Rosen, T Siddique, D Patterson, et al.
Science (New York, N.Y.)|August 20, 1993
Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutaseH X Deng, A Hentati, J A Tainer, 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.
International Journal of Neurology|January 1, 1991
A molecular genetic approach to amyotrophic lateral sclerosisT Siddique, P Hu, A Hentati, et al.
Human Molecular Genetics|October 1, 1994
Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markersA Hentati, M A Pericak-Vance, F Lennon, et al.
Nature Genetics|July 1, 1994
Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35A Hentati, K Bejaoui, M A Pericak-Vance, 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.
Neurogenetics|May 18, 1999
Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markersA Hentati, K Ouahchi, M A Pericak-Vance, et al.
Neurology|June 1, 1996
Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working groupJ K Fink, T Heiman-Patterson, T Bird, et al.
Nature Genetics|October 5, 2001
The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosisY Yang, A Hentati, H X Deng, et al.
Pageof 3