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Connection

Richard Yanagihara to Mutation

This is a "connection" page, showing publications Richard Yanagihara has written about Mutation.
Connection Strength

0.079
  1. Lu Y, Nerurkar VR, Dashwood WM, Woodward CL, Ablan S, Shikuma CM, Grandinetti A, Chang H, Nguyen HT, Wu Z, Yamamura Y, Boto WO, Merriwether A, Kurata T, Detels R, Yanagihara R. Genotype and allele frequency of a 32-base pair deletion mutation in the CCR5 gene in various ethnic groups: absence of mutation among Asians and Pacific Islanders. Int J Infect Dis. 1999; 3(4):186-91.
    View in: PubMed
    Score: 0.031
  2. Yanagihara R, Saitou N, Nerurkar VR, Song KJ, Bastian I, Franchini G, Gajdusek DC. Molecular phylogeny and dissemination of human T-cell lymphotropic virus type I viewed within the context of primate evolution and human migration. Cell Mol Biol (Noisy-le-grand). 1995; 41 Suppl 1:S145-61.
    View in: PubMed
    Score: 0.023
  3. Goldfarb LG, Brown P, Goldgaber D, Garruto RM, Yanagihara R, Asher DM, Gajdusek DC. Identical mutation in unrelated patients with Creutzfeldt-Jakob disease. Lancet. 1990 Jul 21; 336(8708):174-5.
    View in: PubMed
    Score: 0.017
  4. Ryschkewitsch CF, Friedlaender JS, Mgone CS, Jobes DV, Agostini HT, Chima SC, Alpers MP, Koki G, Yanagihara R, Stoner GL. Human polyomavirus JC variants in Papua New Guinea and Guam reflect ancient population settlement and viral evolution. Microbes Infect. 2000 Jul; 2(9):987-96.
    View in: PubMed
    Score: 0.009
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
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