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M Shimadzu

Showing results (11-20 of 24) with videos related to

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Cancer|December 26, 2001
Detection of HER-2/neu (c-erb B-2) DNA amplification in primary breast carcinoma. Interobserver reproducibility and correlation with immunohistochemical HER-2 overexpressionH Tsuda, F Akiyama, H Terasaki, et al.
American Journal of Medical Genetics|March 17, 1997
Familial lethal inheritance of a mutated paternal gene in females causing X-linked ornithine transcarbamylase (OTC) deficiencyS Komaki, T Matsuura, K Oyanagi, et al.
Human Genetics|December 18, 1998
The polymorphic 43Thr bcl-2 protein confers relative resistance to autoimmunity: an analytical evaluationS Komaki, M Kohno, N Matsuura, et al.
International Journal of Hematology|March 24, 2000
Mutations of the WASP gene in 10 Japanese patients with Wiskott-Aldrich syndrome and X-linked thrombocytopeniaS Itoh, S Nonoyama, T Morio, et al.
Human Genetics|May 1, 1997
Mutations of the CD40 ligand gene in 13 Japanese patients with X-linked hyper-IgM syndromeS Nonoyama, M Shimadzu, H Toru, et al.
Human Genetics|March 10, 1999
A new assay for the analysis of X-chromosome inactivation based on methylation-specific PCRT Kubota, S Nonoyama, H Tonoki, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|October 1, 1995
[Neutropenia in patient with X-linked hyper-IgM syndrome]M Iwata, H Nunoi, S Nonoyama, et al.
American Journal of Respiratory and Critical Care Medicine|May 12, 2000
Familial pulmonary Mycobacterium avium complex diseaseE Tanaka, T Kimoto, H Matsumoto, et al.
Journal of Medical Genetics|August 1, 1996
Phenotypic variability in male patients carrying the mutant ornithine transcarbamylase (OTC) allele, Arg40His, ranging from a child with an unfavourable prognosis to an asymptomatic older adultI Matsuda, T Matsuura, A Nishiyori, et al.
Annals of Neurology|July 17, 1998
Dystonia with motor delay in compound heterozygotes for GTP-cyclohydrolase I gene mutationsY Furukawa, S J Kish, E M Bebin, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Cancer|December 26, 2001
Detection of HER-2/neu (c-erb B-2) DNA amplification in primary breast carcinoma. Interobserver reproducibility and correlation with immunohistochemical HER-2 overexpressionH Tsuda, F Akiyama, H Terasaki, et al.
American Journal of Medical Genetics|March 17, 1997
Familial lethal inheritance of a mutated paternal gene in females causing X-linked ornithine transcarbamylase (OTC) deficiencyS Komaki, T Matsuura, K Oyanagi, et al.
Human Genetics|December 18, 1998
The polymorphic 43Thr bcl-2 protein confers relative resistance to autoimmunity: an analytical evaluationS Komaki, M Kohno, N Matsuura, et al.
International Journal of Hematology|March 24, 2000
Mutations of the WASP gene in 10 Japanese patients with Wiskott-Aldrich syndrome and X-linked thrombocytopeniaS Itoh, S Nonoyama, T Morio, et al.
Human Genetics|May 1, 1997
Mutations of the CD40 ligand gene in 13 Japanese patients with X-linked hyper-IgM syndromeS Nonoyama, M Shimadzu, H Toru, et al.
Human Genetics|March 10, 1999
A new assay for the analysis of X-chromosome inactivation based on methylation-specific PCRT Kubota, S Nonoyama, H Tonoki, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|October 1, 1995
[Neutropenia in patient with X-linked hyper-IgM syndrome]M Iwata, H Nunoi, S Nonoyama, et al.
American Journal of Respiratory and Critical Care Medicine|May 12, 2000
Familial pulmonary Mycobacterium avium complex diseaseE Tanaka, T Kimoto, H Matsumoto, et al.
Journal of Medical Genetics|August 1, 1996
Phenotypic variability in male patients carrying the mutant ornithine transcarbamylase (OTC) allele, Arg40His, ranging from a child with an unfavourable prognosis to an asymptomatic older adultI Matsuda, T Matsuura, A Nishiyori, et al.
Annals of Neurology|July 17, 1998
Dystonia with motor delay in compound heterozygotes for GTP-cyclohydrolase I gene mutationsY Furukawa, S J Kish, E M Bebin, et al.
Pageof 3