Showing results (51-60 of 86) with videos related to
Sort By:
Pageof 9
Clinical Genetics|June 8, 2011
Exome sequencing of two patients in a family with atypical X-linked leukodystrophyY Tsurusaki, N Okamoto, Y Suzuki, et al.Biochimica Et Biophysica Acta|July 31, 2001
Identification of xanthine dehydrogenase/xanthine oxidase as a rat Paneth cell zinc-binding proteinY Morita, M Sawada, H Seno, et al.Clinical Nephrology|March 9, 1999
Hypoalbuminemia accelerates erythrocyte membrane lipid peroxidation in chronic hemodialysis patientsA Soejima, N Matsuzawa, N Miyake, et al.DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|April 28, 1997
Characterization of the promoter region, first ten exons and nine intron-exon boundaries of the DNA-dependent protein kinase catalytic subunit gene, DNA-PKcs (XRCC7)M Fujimoto, N Matsumoto, T Tsujita, et al.[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|March 1, 1990
[A case of autoimmune hemolytic anemia and bullous pemphigoid-like skin lesion combined with idiopathic thrombocytopenic purpura]Y Aoki, N Miyake, M Yamasowa, et al.The Journal of Biological Chemistry|November 5, 1992
Insulin treatment stimulates the tyrosine phosphorylation of the alpha-type 85-kDa subunit of phosphatidylinositol 3-kinase in vivoH Hayashi, S Kamohara, Y Nishioka, et al.Clinical Genetics|May 29, 2008
Alu-related 5q35 microdeletions in Sotos syndromeJ Mochizuki, H Saitsu, T Mizuguchi, et al.Cancer Research|November 1, 1988
Generation of two murine monoclonal antibodies that can discriminate N-glycolyl and N-acetyl neuraminic acid residues of GM2 gangliosidesM Miyake, M Ito, S Hitomi, et al.Gan No Rinsho. Japan Journal of Cancer Clinics|November 1, 1987
[An immunohistochemical study using a double staining method for regional lymph nodes in gastric cancer]S Chohno, T Horimi, T Okabayashi, et al.Clinical Genetics|May 3, 2012
Exome sequencing in a family with an X-linked lethal malformation syndrome: clinical consequences of hemizygous truncating OFD1 mutations in male patientsY Tsurusaki, T Kosho, K Hatasaki, et al.Pageof 9