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Results: 1-13 |
Results: 13
Mapping of 262 DNA markers into 24 intervals on human chromosome 11.
Authors: Tanigami, Akira Tokino, Takashi Takiguchi, Shuya Mori, Masaki Glaser, Tom Park, J. W. Jones, Carol Nakamura, Yusuke
Citation: Tanigami, Akira et al., Mapping of 262 DNA markers into 24 intervals on human chromosome 11., American journal of human genetics , 50-I(1), 1992, pp. 56-64
Isolation and mapping of 68 RFLP markers on human chromosome 6.
Authors: Saito, Susumo Okui, Keiko Tokino, Takashi Oshimura, Mitsuo Nakamura, Yusuke
Citation: Saito, Susumo et al., Isolation and mapping of 68 RFLP markers on human chromosome 6., American journal of human genetics , 50-I(1), 1992, pp. 65-70
Identification of CRYM as a Candidate Responsible for Nonsyndromic Deafness, through cDNA Microarray Analysis of Human Cochlear and Vestibular Tissues
Authors: Abe, Satoko Katagiri, Toyomasa Saito-Hisaminato, Akihiko Usami, Shin-ichi Inoue, Yasuhiro Tsunoda, Tatsuhiko Nakamura, Yusuke
Citation: Abe, Satoko et al., Identification of CRYM as a Candidate Responsible for Nonsyndromic Deafness, through cDNA Microarray Analysis of Human Cochlear and Vestibular Tissues, American journal of human genetics , 72(1), 2003, pp. 73-82
Large-Scale Single-Nucleotide Polymorphism (SNP) and Haplotype Analyses, Using Dense SNP Maps, of 199 Drug-Related Genes in 752 Subjects: the Analysis of the Association between Uncommon SNPs within Haplotype Blocks and the Haplotypes Constructed with Haplotype-Tagging SNPs
Authors: Kamatani, Naoyuki Sekine, Akihiro Kitamoto, Takuya Iida, Aritoshi Saito, Susumu Kogame, Akifumi Inoue, Eisuke Kawamoto, Manabu Harigai, Masayoshi Nakamura, Yusuke
Citation: Kamatani, Naoyuki et al., Large-Scale Single-Nucleotide Polymorphism (SNP) and Haplotype Analyses, Using Dense SNP Maps, of 199 Drug-Related Genes in 752 Subjects: the Analysis of the Association between Uncommon SNPs within Haplotype Blocks and the Haplotypes Constructed with Haplotype-Tagging SNPs, American journal of human genetics , 75(2), 2004, pp. 190-203
Isolation and mapping of 62 new RFLP markers on human chromosome 11.
Authors: Tokino, Takashi Takahashi, Ei-ichi Mori, Masaki Tanigami, Akira Glaser, Tom Park, J.W. Jones, Carol Hori, Tada-aki Nakamura, Yusuke
Citation: Tokino, Takashi et al., Isolation and mapping of 62 new RFLP markers on human chromosome 11., American journal of human genetics , 48-I(2), 1991, pp. 258-268
Fine-scale mapping of the gene responsible for multiple endocrine neoplasia type 1 (MEN 1).
Authors: Fujimori, Minoru Wells, SamuelA. Nakamura, Yusuke
Citation: Fujimori, Minoru et al., Fine-scale mapping of the gene responsible for multiple endocrine neoplasia type 1 (MEN 1)., American journal of human genetics , 50-I(2), 1992, pp. 399-403
Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5
Authors: Nakamura, Yusuke Lathrop, Mark Leppert, Mark Dobbs, Marc Wasmuth, John Wolff, Erica Carlson, Mary Fujimoto, Esther Krapcho, Karen Sears, Tena Woodward, Scott Hughes, J. Burt, Randy Gardner, Eldon Lalouel, Jean-Marc White, Ray
Citation: Nakamura, Yusuke et al., Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5, American journal of human genetics , 43-II(5), 1988, pp. 638-644
Localization of the genetic defect in multiple endocrine neoplasia type i within a small region of chromosome Il
Authors: Nakamura, Yusuke Larson, Catharina Julier, Cecile Byström, Camilla Skogseid, Britt Wells, Samuel Öberg, Kjell Carlson, Mary Taggart, Thomas O'Connell, Peter Leppert, Mark Lalouel, Jean-Marc Nordenskjöld, Magnus White, Ray
Citation: Nakamura, Yusuke et al., Localization of the genetic defect in multiple endocrine neoplasia type i within a small region of chromosome Il, American journal of human genetics , 44(5), 1989, pp. 751-755
Genetic mapping of autosomal dominant charcot-marie-tooth disease in a large french-acadian kindred; identification of new linked markers on chromosome 17
Authors: Patel, Pragna I. Franco, Brunella Garcia, Carlos Slaugenhaupt, Susan A. Nakamura, Yusuke Ledbetter, David H. Chakravarti, Aravinda Lupski, James R.
Citation: I. Patel, Pragna et al., Genetic mapping of autosomal dominant charcot-marie-tooth disease in a large french-acadian kindred; identification of new linked markers on chromosome 17, American journal of human genetics , 46-II(4), 1990, pp. 801-809
Association of the Gene Encoding Wingless-Type Mammary Tumor Virus Integration-Site Family Member 5B (WNT5B) with Type 2 Diabetes
Authors: Kanazawa, Akio Tsukada, Syuuichi Sekine, Akihiro Tsunoda, Tatsuhiko Takahashi, Atsushi Kashiwagi, Atsunori Tanaka, Yasushi Babazono, Tetsuya Matsuda, Masafumi Kaku, Kohei Iwamoto, Yasuhiko Kawamori, Ryuzo Kikkawa, Ryuichi Nakamura, Yusuke Maeda, Shiro
Citation: Kanazawa, Akio et al., Association of the Gene Encoding Wingless-Type Mammary Tumor Virus Integration-Site Family Member 5B (WNT5B) with Type 2 Diabetes, American journal of human genetics , 75(5), 2004, pp. 832-843
New approach for isolation of VNTR markers
Authors: Nakamura, Yusuke Carlson, Mary Krapcho, Karen Kanamori, Masao White, Ray
Citation: Nakamura, Yusuke et al., New approach for isolation of VNTR markers, American journal of human genetics , 43-II(6), 1988, pp. 854-859
A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates
Authors: Buetow, Kenneth H. Shiang, Rita Yang, Ping Nakamura, Yusuke Lathrop, G.Mark White, Raymond Wasmuth, John J. Wood, Stephen Berdahl, Laura D. Leysens, Nancy J. Ritty, Timothy M. Wise, Molly E. Murray, Jeffrey C.
Citation: H. Buetow, Kenneth et al., A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates, American journal of human genetics , 48-II(5), 1991, pp. 911-925
Etiological heterogeneity in X-linked spastic paraplegia
Authors: Keppen, Laura D. Leppert, Mark F. O'Connell, Peter Nakamura, Yusuke Stauffer, Dora Lathrop, Mark Lalouel, Jean-Marc White, Ray
Citation: D. Keppen, Laura et al., Etiological heterogeneity in X-linked spastic paraplegia, American journal of human genetics , 41-II(5), 1987, pp. 933-943
Risultati: 1-13 |