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A C Warren

Showing results (31-40 of 42) with videos related to

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American Journal of Medical Genetics|June 22, 2000
Are hereditary hemochromatosis mutations involved in Alzheimer disease?S Moalem, M E Percy, D F Andrews, et al.
Human Genetics|November 1, 1990
Assignment of the Nance-Horan syndrome to the distal short arm of the X chromosomeD Zhu, D M Alcorn, S E Antonarakis, et al.
Genomics|March 1, 1993
A contiguous physical map of the pericentromeric region of chromosome 21q between D21Z1 and D21S13EW Van Hul, G Van Camp, L Stuyver, et al.
Genomics|October 1, 1990
Linkage mapping of the highly informative DNA marker D21S156 to human chromosome 21 using a polymorphic GT dinucleotide repeatJ G Lewis, J L Weber, M B Petersen, et al.
International Journal of Neurology|January 1, 1991
A molecular genetic approach to amyotrophic lateral sclerosisT Siddique, P Hu, A Hentati, et al.
American Journal of Human Genetics|September 1, 1992
Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndromeM B Peterson, M Frantzen, S E Antonarakis, et al.
Genomics|May 1, 1993
The CEPH consortium linkage map of human chromosome 13A M Bowcock, S C Gerken, R I Barnes, et al.
Genomics|December 1, 1987
beta-Amyloid gene is not present in three copies in autopsy-validated Alzheimer's diseaseA C Warren, N K Robakis, N Ramakrishna, et al.
Annals of the New York Academy of Sciences|January 1, 1985
Linkage map on chromosome 21q and the association of a DNA haplotype with a propensity to nondisjunction and trisomy 21S E Antonarakis, S D Kittur, C Metaxotou, et al.
Endothelium : Journal of Endothelial Cell Research|January 27, 2004
Interferon (IFN)-beta 1a and IFN-beta 1b block IFN-gamma-induced disintegration of endothelial junction integrity and barrierA Minagar, A Long, T Ma, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|June 22, 2000
Are hereditary hemochromatosis mutations involved in Alzheimer disease?S Moalem, M E Percy, D F Andrews, et al.
Human Genetics|November 1, 1990
Assignment of the Nance-Horan syndrome to the distal short arm of the X chromosomeD Zhu, D M Alcorn, S E Antonarakis, et al.
Genomics|March 1, 1993
A contiguous physical map of the pericentromeric region of chromosome 21q between D21Z1 and D21S13EW Van Hul, G Van Camp, L Stuyver, et al.
Genomics|October 1, 1990
Linkage mapping of the highly informative DNA marker D21S156 to human chromosome 21 using a polymorphic GT dinucleotide repeatJ G Lewis, J L Weber, M B Petersen, et al.
International Journal of Neurology|January 1, 1991
A molecular genetic approach to amyotrophic lateral sclerosisT Siddique, P Hu, A Hentati, et al.
American Journal of Human Genetics|September 1, 1992
Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndromeM B Peterson, M Frantzen, S E Antonarakis, et al.
Genomics|May 1, 1993
The CEPH consortium linkage map of human chromosome 13A M Bowcock, S C Gerken, R I Barnes, et al.
Genomics|December 1, 1987
beta-Amyloid gene is not present in three copies in autopsy-validated Alzheimer's diseaseA C Warren, N K Robakis, N Ramakrishna, et al.
Annals of the New York Academy of Sciences|January 1, 1985
Linkage map on chromosome 21q and the association of a DNA haplotype with a propensity to nondisjunction and trisomy 21S E Antonarakis, S D Kittur, C Metaxotou, et al.
Endothelium : Journal of Endothelial Cell Research|January 27, 2004
Interferon (IFN)-beta 1a and IFN-beta 1b block IFN-gamma-induced disintegration of endothelial junction integrity and barrierA Minagar, A Long, T Ma, et al.
Pageof 5