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S Minoshima

Showing results (161-170 of 265) with videos related to

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Neurology|April 1, 1998
Absence of normal activation of the left anterior fusiform gyrus during naming in left temporal lobe epilepsyT R Henry, H A Buchtel, R A Koeppe, et al.
Journal of Neurochemistry|June 20, 2001
Developmental changes in the expression of parkin and UbcR7, a parkin-interacting and ubiquitin-conjugating enzyme, in rat brainM Wang, T Suzuki, T Kitada, et al.
Journal of Neural Transmission. Supplementum|December 29, 2000
PARKIN as a pathogenic gene for autosomal recessive juvenile parkinsonismN Shimizu, S Asakawa, S Minoshima, et al.
Clinical Nephrology|November 1, 1993
Serum myeloperoxidase and serum cytokines in anti-myeloperoxidase antibody-associated glomerulonephritisY Arimura, S Minoshima, Y Kamiya, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|July 1, 1997
Quantitative assessment of cerebral blood flow in patients with Alzheimer's disease by SPECTP Bartenstein, S Minoshima, C Hirsch, et al.
Dementia and Geriatric Cognitive Disorders|March 1, 1997
Reduction of regional cerebral blood flow and cognitive impairment in patients with Alzheimer's disease: evaluation of an observer-independent analytic approachC Hirsch, P Bartenstein, S Minoshima, et al.
Annals of the New York Academy of Sciences|October 31, 1996
Structure, 5'-upstream sequence and chromosomal assignment of the human 14.3.3 eta chain gene in relation to the effects of methamphetamineT Muratake, S Hayashi, T Ichikawa, et al.
Nature|April 29, 1998
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonismT Kitada, S Asakawa, N Hattori, et al.
Journal of Cellular Biochemistry|June 19, 1998
Novel nuclear localization signal between the two DNA-binding zinc fingers in the human vitamin D receptorJ C Hsieh, Y Shimizu, S Minoshima, et al.
Genomics|September 1, 1993
Structure and chromosomal localization of the gene encoding the human myelin protein zero (MPZ)K Hayasaka, M Himoro, Y Wang, et al.
Pageof 27

Showing results (161-170 of 265) with videos related to

Sort By:
Pageof 27
Neurology|April 1, 1998
Absence of normal activation of the left anterior fusiform gyrus during naming in left temporal lobe epilepsyT R Henry, H A Buchtel, R A Koeppe, et al.
Journal of Neurochemistry|June 20, 2001
Developmental changes in the expression of parkin and UbcR7, a parkin-interacting and ubiquitin-conjugating enzyme, in rat brainM Wang, T Suzuki, T Kitada, et al.
Journal of Neural Transmission. Supplementum|December 29, 2000
PARKIN as a pathogenic gene for autosomal recessive juvenile parkinsonismN Shimizu, S Asakawa, S Minoshima, et al.
Clinical Nephrology|November 1, 1993
Serum myeloperoxidase and serum cytokines in anti-myeloperoxidase antibody-associated glomerulonephritisY Arimura, S Minoshima, Y Kamiya, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|July 1, 1997
Quantitative assessment of cerebral blood flow in patients with Alzheimer's disease by SPECTP Bartenstein, S Minoshima, C Hirsch, et al.
Dementia and Geriatric Cognitive Disorders|March 1, 1997
Reduction of regional cerebral blood flow and cognitive impairment in patients with Alzheimer's disease: evaluation of an observer-independent analytic approachC Hirsch, P Bartenstein, S Minoshima, et al.
Annals of the New York Academy of Sciences|October 31, 1996
Structure, 5'-upstream sequence and chromosomal assignment of the human 14.3.3 eta chain gene in relation to the effects of methamphetamineT Muratake, S Hayashi, T Ichikawa, et al.
Nature|April 29, 1998
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonismT Kitada, S Asakawa, N Hattori, et al.
Journal of Cellular Biochemistry|June 19, 1998
Novel nuclear localization signal between the two DNA-binding zinc fingers in the human vitamin D receptorJ C Hsieh, Y Shimizu, S Minoshima, et al.
Genomics|September 1, 1993
Structure and chromosomal localization of the gene encoding the human myelin protein zero (MPZ)K Hayasaka, M Himoro, Y Wang, et al.
Pageof 27