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Neuroscience Research|February 9, 1999
Cloning and chromosomal mapping of the human gene of neuroglycan C (NGC), a neural transmembrane chondroitin sulfate proteoglycan with an EGF moduleY Yasuda, Y Tokita, S Aono, et al.Biochemical and Biophysical Research Communications|May 9, 2000
Mouse myosin X: molecular architecture and tissue expression as revealed by northern blot and in situ hybridization analysesS Yonezawa, A Kimura, S Koshiba, et al.Cytogenetics and Cell Genetics|August 31, 2000
Comparative mapping of seven genes in mouse, rat and Chinese hamster chromosomes by fluorescence in situ hybridizationT Ono, S Hirano, S Yonezawa, et al.Haematology and Blood Transfusion|January 1, 1977
Establishment and characterization of leukemic T-cell lines, B-cell lines, and null-cell line: a progress report on surface antigen study of fresh lymphatic leukemias in manJ Minowada, T Tsubota, S Nakazawa, et al.Nature Genetics|March 30, 2001
Mutations in SIP1, encoding Smad interacting protein-1, cause a form of Hirschsprung diseaseN Wakamatsu, Y Yamada, K Yamada, et al.American Journal of Human Genetics|October 10, 2001
Nonsense and frameshift mutations in ZFHX1B, encoding Smad-interacting protein 1, cause a complex developmental disorder with a great variety of clinical featuresK Yamada, Y Yamada, N Nomura, et al.Journal of Human Genetics|June 4, 1998
The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32M Fujimoto, P N Kantaputra, S Ikegawa, et al.Pageof 4