Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Kusuki Nishoka"'
Autor:
Mary Whittaker, P.R. Rao, Bernardo Erdtmann, C. Rahuel, Rosa Maria Corbo, Yoshiro Wada, R. Palmarino, R.J. Mitchell, Gérard Lucotte, E. Calzolari, K.B. Gopalam, M. Frain, S. Lavareda de Souza, Cécile Rahuel, D.G. Woodfield, Renato Scacchi, José M. Sala-Trepat, F. Martuzzi Veronesi, Luc Noel, G. Marogna, Ives José Sbalqueiro, Judith J. Britten, K. Sampat Narasimha Char, Kusuki Nishoka, G. Mulas, Rick Johnson, G. Cossu, C.R. Srikumari, Hisashi Yamanaka, A. Stangoni, G. Laconi, Davide Pettener, Paola Lucarelli, Néria A. Maia, J. Rajanikumari, S.A. Fabb, Iglenir J. Cavalli, G.B. Cuccuru, Tsutomu Ohtani, C.J. Lyne, Naoyuki Kamatani, P.L. Clark, M.A. Lyne, Michio Kobayashi, Margarete S. Mattevi, T. Venkateswara Rao, Kiyonobu Mikanagi
Publikováno v:
Human Heredity. 35:I-VI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e91b05adc0e3a4006a7ebe67828d5d8a
https://doi.org/10.1159/000153577
https://doi.org/10.1159/000153577
Autor:
Yoshiro Wada, Kiyonobu Mikanagi, Kusuki Nishoka, Tsutomu Ohtani, Naoyuki Kamatani, Hisashi Yamanaka, Michio Kobayashi
Publikováno v:
Human heredity. 35(6)
Peripheral T cells from 3 Lesch-Nyhan patients, 3 normal subjects, and 3 brothers with hypoxanthine-guanine phosphoribosyltransferase (HGPRT) deficiency but without Lesch-Nyhan syndrome (so-called partial deficiency) have been analyzed. Although thes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::561e3ab8b94f5e254c9865207bbac8bb
https://pubmed.ncbi.nlm.nih.gov/3876977
https://pubmed.ncbi.nlm.nih.gov/3876977
Autor:
Mary Whittaker, Margarete S. Mattevi, C.R. Srikumari, Cécile Rahuel, G. Laconi, Rick Johnson, C. Rahuel, Luc Noel, Judith J. Britten, R.J. Mitchell, Tsutomu Ohtani, C.J. Lyne, G. Marogna, Renato Scacchi, E. Calzolari, Paola Lucarelli, Bernardo Erdtmann, G.B. Cuccuru, Ives José Sbalqueiro, Gérard Lucotte, Kiyonobu Mikanagi, S. Lavareda de Souza, M. Frain, R. Palmarino, Néria A. Maia, Iglenir J. Cavalli, D.G. Woodfield, G. Cossu, Yoshiro Wada, G. Mulas, K. Sampat Narasimha Char, Naoyuki Kamatani, Davide Pettener, P.L. Clark, Hisashi Yamanaka, Rosa Maria Corbo, Kusuki Nishoka, J. Rajanikumari, T. Venkateswara Rao, M.A. Lyne, F. Martuzzi Veronesi, José M. Sala-Trepat, A. Stangoni, Michio Kobayashi, S.A. Fabb, P.R. Rao, K.B. Gopalam
Publikováno v:
Human Heredity. 35:408-409
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::514f31f37873a9d859842468470538b6
https://doi.org/10.1159/000153590
https://doi.org/10.1159/000153590