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P Poorkaj

Showing results (21-30 of 32) with videos related to

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Genomics|February 28, 1998
An expression map from human chromosome 14q24.3V Sharma, P Poorkaj, F Hisama, et al.
Human Molecular Genetics|May 1, 1996
Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb developmentM A Crackower, S W Scherer, J M Rommens, et al.
Neurology|September 17, 1999
A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degenerationM Yasuda, T Kawamata, O Komure, et al.
Archives of Neurology|March 20, 2001
Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementiaP Poorkaj, M Grossman, E Steinbart, et al.
Neuroreport|April 20, 1999
A distinct familial presenile dementia with a novel missense mutation in the tau geneM Iijima, T Tabira, P Poorkaj, et al.
Annals of Neurology|August 1, 1996
Amyloid beta protein (Abeta) deposition in chromosome 14-linked Alzheimer's disease: predominance of Abeta42(43)D M Mann, T Iwatsubo, N J Cairns, et al.
Archives of Neurology|November 16, 2001
TAU as a susceptibility gene for amyotropic lateral sclerosis-parkinsonism dementia complex of GuamP Poorkaj, D Tsuang, E Wijsman, et al.
Annals of Neurology|April 13, 2000
A novel mutation at position +12 in the intron following exon 10 of the tau gene in familial frontotemporal dementia (FTD-Kumamoto)M Yasuda, J Takamatsu, I D'Souza, et al.
Annals of Neurology|December 1, 1996
The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patientsM Ikeda, V Sharma, S M Sumi, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 1998
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17L N Clark, P Poorkaj, Z Wszolek, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Genomics|February 28, 1998
An expression map from human chromosome 14q24.3V Sharma, P Poorkaj, F Hisama, et al.
Human Molecular Genetics|May 1, 1996
Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb developmentM A Crackower, S W Scherer, J M Rommens, et al.
Neurology|September 17, 1999
A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degenerationM Yasuda, T Kawamata, O Komure, et al.
Archives of Neurology|March 20, 2001
Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementiaP Poorkaj, M Grossman, E Steinbart, et al.
Neuroreport|April 20, 1999
A distinct familial presenile dementia with a novel missense mutation in the tau geneM Iijima, T Tabira, P Poorkaj, et al.
Annals of Neurology|August 1, 1996
Amyloid beta protein (Abeta) deposition in chromosome 14-linked Alzheimer's disease: predominance of Abeta42(43)D M Mann, T Iwatsubo, N J Cairns, et al.
Archives of Neurology|November 16, 2001
TAU as a susceptibility gene for amyotropic lateral sclerosis-parkinsonism dementia complex of GuamP Poorkaj, D Tsuang, E Wijsman, et al.
Annals of Neurology|April 13, 2000
A novel mutation at position +12 in the intron following exon 10 of the tau gene in familial frontotemporal dementia (FTD-Kumamoto)M Yasuda, J Takamatsu, I D'Souza, et al.
Annals of Neurology|December 1, 1996
The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patientsM Ikeda, V Sharma, S M Sumi, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 1998
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17L N Clark, P Poorkaj, Z Wszolek, et al.
Pageof 4