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Bidirectional Electron Transfer in the Reaction Centre of Photosystem I
Santabarbara, Stefano, Galuppini, Luca, Casazza, Anna Paola
Published in Journal of integrative plant biology (01.08.2010)
Published in Journal of integrative plant biology (01.08.2010)
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Association between Tourette Syndrome and the Dopamine D3 Receptor Gene Rs6280
He, Fan, Zheng, Yi, Huang, Huan-Huan, Cheng, Yu-Hang, Wang, Chuan-Yue
Published in Chinese medical journal (05.03.2015)
Published in Chinese medical journal (05.03.2015)
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聴覚障害のリハビリテーションと聴力検査の現状
日本聴覚医学会, 難聴対策委員会, 柿木, 章伸, 鈴木, 光也, 曾根, 三千彦, 川瀬, 哲明, 坂田, 俊文, 坂田, 英明, 工, 穣, 内藤, 泰, 藤岡, 正人, 米本, 清
Published in AUDIOLOGY JAPAN (30.06.2023)
Published in AUDIOLOGY JAPAN (30.06.2023)
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Altered insulin secretory responses to glucose in diabetic and nondiabetic subjects with mutations in the diabetes susceptibility gene MODY3 on chromosome 12
Byrne, M. M., Sturis, J., Menzel, S., Yamagata, K., Fajans, S. S., Dronsfield, M. J., Bain, S. C., Hattersley, A. T., Velho, G., Froguel, P., Bell, G. I., Polonsky, K. S.
Published in Diabetes (New York, N.Y.) (01.11.1996)
Published in Diabetes (New York, N.Y.) (01.11.1996)
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Insulin secretion and insulin sensitivity in diabetic and non-diabetic subjects with hepatic nuclear factor-1alpha (maturity-onset diabetes of the young-3) mutations
Vaxillaire, M, Pueyo, ME, Clement, K, Fiet, J, Timsit, J, Philippe, J, Robert, JJ, Tappy, L, Froguel, P, Velho, G
Published in European journal of endocrinology (01.12.1999)
Published in European journal of endocrinology (01.12.1999)
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Overwhelming genetic heterogeneity and exhausting molecular diagnostic process in chronic and progressive ataxias: facing it up with an algorithm, a gene, a panel at a time
Perez Maturo, J., Zavala, L., Vega, P., González-Morón, D., Medina, N., Salinas, V., Rosales, J., Córdoba, M., Arakaki, T., Garretto, N., Rodríguez-Quiroga, S., Kauffman, M. A.
Published in Journal of human genetics (01.10.2020)
Published in Journal of human genetics (01.10.2020)
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Tryptophan hydroxylase polymorphism and suicidality in unipolar and bipolar affective disorders: a multicenter association study
Souery, Daniel, Van Gestel, Sophie, Massat, Isabelle, Blairy, Sylvie, Adolfsson, Rolf, Blackwood, Douglas, Del-Favero, Jurgen, Dikeos, Dimitris, Jakovljevic, Miro, Kaneva, Radka, Lattuada, Enrico, Lerer, Bernard, Lilli, Roberta, Milanova, Vihbra, Muir, Walter, Nöthen, Markus, Oruc, Lilijana, Papadimitriou, George, Propping, Peter, Schulze, Thomas, Serretti, Alessandro, Shapira, Baruch, Smeraldi, Enrico, Stefanis, Costas, Thomson, Marian, Van Broeckhoven, Christine, Mendlewicz, Julien
Published in Biological psychiatry (1969) (01.03.2001)
Published in Biological psychiatry (1969) (01.03.2001)
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Association Between Bipolar Disorder and Monoamine Oxidase A Gene Polymorphisms: Results of a Multicenter Study
Preisig, Martin, Bellivier, Frank, Fenton, Brenda T., Baud, Patrick, Berney, Alexandre, Courtet, Philippe, Hardy, Patrick, Golaz, Jean, Leboyer, Marion, Mallet, Jacques, Matthey, Marie-Louise, Mouthon, Dominique, Neidhart, Elisabeth, Nosten-Bertrand, Marika, Stadelmann-Dubuis, Emmanuelle, Guimon, Jose, Ferrero, Fran殩s, Buresi, Catherine, Malafosse, Alain
Published in The American journal of psychiatry (01.06.2000)
Published in The American journal of psychiatry (01.06.2000)
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The cardiac β-myosin heavy chain gene is not the predominant gene for hypertrophic cardiomyopathy in the Finnish population
Jääskeläinen, Pertti, Soranta, Marja, Miettinen, Raija, Saarinen, Laura, Pihlajamäki, Jussi, Silvennoinen, Karoliina, Tikanoja, Tero, Laakso, Markku, Kuusisto, Johanna
Published in Journal of the American College of Cardiology (15.11.1998)
Published in Journal of the American College of Cardiology (15.11.1998)
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Maturity-onset diabetes of the young due to a mutation in the hepatocyte nuclear factor-4 alpha binding site in the promoter of the hepatocyte nuclear factor-1 alpha gene
Gragnoli, C., Lindner, T., Cockburn, B. N., Kaisaki, P. J., Gragnoli, F., Marozzi, G., Bell, G. I.
Published in Diabetes (New York, N.Y.) (01.10.1997)
Published in Diabetes (New York, N.Y.) (01.10.1997)
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A case of megalencephalic leukoencephalopathy with subcortical cysts (van der Knaap disease): molecular genetic study
Saijo, Harumi, Nakayama, Harumi, Ezoe, Takanori, Araki, Katsuhito, Sone, Sui, Hamaguchi, Hiroshi, Suzuki, Hisaharu, Shiroma, Naohide, Kanazawa, Naomi, Tsujino, Seiichi, Hirayama, Yoshito, Arima, Masataka
Published in Brain & development (01.08.2003)
Published in Brain & development (01.08.2003)
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A prevalent amino acid polymorphism at codon 98 in the hepatocyte nuclear factor-1alpha gene is associated with reduced serum C-peptide and insulin responses to an oral glucose challenge
Urhammer, S. A., Fridberg, M., Hansen, T., Rasmussen, S. K., Moller, A. M., Clausen, J. O., Pedersen, O.
Published in Diabetes (New York, N.Y.) (01.05.1997)
Published in Diabetes (New York, N.Y.) (01.05.1997)
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