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Distribution of Malassezia species in pityriasis versicolor and seborrhoeic dermatitis in Greece. Typing of the major pityriasis versicolor isolate M. globosa
Gaitanis, G., Velegraki, A., Alexopoulos, E.C., Chasapi, V., Tsigonia, A., Katsambas, A.
Published in British journal of dermatology (1951) (01.05.2006)
Published in British journal of dermatology (1951) (01.05.2006)
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A genotype-phenotype correlation for GJB2 (connexin 26) deafness
Cryns, K, Orzan, E, Murgia, A, Huygen, P L M, Moreno, F, del Castillo, I, Parker Chamberlin, G, Azaiez, H, Prasad, S, Cucci, R A, Leonardi, E, Snoeckx, R L, Govaerts, P J, Van de Heyning, P H, Van de Heyning, C M, Smith, R J H, Van Camp, G
Published in Journal of medical genetics (01.03.2004)
Published in Journal of medical genetics (01.03.2004)
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Evidence of an association between genetic variation of the coactivator PGC-1β and obesity
Andersen, G, Wegner, L, Yanagisawa, K, Rose, C S, Lin, J, Glümer, C, Drivsholm, T, Borch-Johnsen, K, Jørgensen, T, Hansen, T, Spiegelman, B M, Pedersen, O
Published in Journal of medical genetics (01.05.2005)
Published in Journal of medical genetics (01.05.2005)
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Novel amyloid precursor protein gene missense mutation (D678N) in probable familial Alzheimer’s disease
Wakutani, Y, Watanabe, K, Adachi, Y, Wada-Isoe, K, Urakami, K, Ninomiya, H, Saido, T C, Hashimoto, T, Iwatsubo, T, Nakashima, K
Published in Journal of neurology, neurosurgery and psychiatry (01.07.2004)
Published in Journal of neurology, neurosurgery and psychiatry (01.07.2004)
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An insight into the genetic pathway of adenocarcinoma of the small intestine
Wheeler, J M D, Warren, B F, Mortensen, N J McC, Kim, H C, Biddolph, S C, Elia, G, Beck, N E, Williams, G T, Shepherd, N A, Bateman, A C, Bodmer, W F
Published in Gut (01.02.2002)
Published in Gut (01.02.2002)
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Screening for mutations of the androgen receptor gene in patients with isolated cryptorchidism
Suzuki, Yasuhiro, Sasagawa, Isoji, Ashida, Junko, Nakada, Teruhiro, Muroya, Koji, Ogata, Tsutomu
Published in Fertility and sterility (01.10.2001)
Published in Fertility and sterility (01.10.2001)
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Search for genetic variants in the p66Shc longevity gene by PCR-single strand conformational polymorphism in patients with early-onset cardiovascular disease
Sentinelli, Federica, Romeo, Stefano, Barbetti, Fabrizio, Berni, Andrea, Filippi, Emanuela, Fanelli, Marzia, Fallarino, Mara, Baroni, Marco G
Published in BMC genetics (06.03.2006)
Published in BMC genetics (06.03.2006)
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Search for genetic variants in the p66 super(Shc )longevity gene by PCR-single strand conformational polymorphism in patients with early-onset cardiovascular disease
Sentinelli, Federica, Romeo, Stefano, Barbetti, Fabrizio, Berni, Andrea, Filippi, Emanuela, Fanelli, Marzia, Fallarino, Mara, Baroni, Marco G
Published in BMC genetics (01.01.2006)
Published in BMC genetics (01.01.2006)
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Search for genetic variants in the p66 super(Shc )ulongevity gene by PCR-single strand conformational polymorphism in patients with early-onset cardiovascular disease
Sentinelli, Federica, Romeo, Stefano, Barbetti, Fabrizio, Berni, Andrea, Filippi, Emanuela, Fanelli, Marzia, Fallarino, Mara, Baroni, Marco G
Published in BMC genetics (01.01.2006)
Published in BMC genetics (01.01.2006)
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Amino acid substitutions in human erythroid protein band 3 account for the low-incidence antigens NFLD and BOW
McManus, K., Pongoski, J., Coghlan, G., Zelinski, T.
Published in Transfusion (Philadelphia, Pa.) (01.03.2000)
Published in Transfusion (Philadelphia, Pa.) (01.03.2000)
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Genetic polymorphisms of human melatonin 1b receptor gene in circadian rhythm sleep disorders and controls
Ebisawa, Takashi, Uchiyama, Makoto, Kajimura, Naofumi, Kamei, Yuichi, Shibui, Kayo, Kim, Keiko, Kudo, Yoshinao, Iwase, Toshio, Sugishita, Mariko, Jodoi, Takako, Ikeda, Masaaki, Ozeki, Yuji, Watanabe, Tsuyoshi, Sekimoto, Masanori, Katoh, Masaaki, Yamada, Naoto, Toyoshima, Ryoichi, Okawa, Masako, Takahashi, Kiyohisa, Yamauchi, Toshio
Published in Neuroscience letters (11.02.2000)
Published in Neuroscience letters (11.02.2000)
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Two novel single nucleotide polymorphisms in the promoter of the Cellular Retinoic Acid Binding Protein II gene ( CRABP-II)
Salazar, Juliana, Ferré, Raimon, Vallvé, Joan-Carles, Pocovı́, Miguel, Cabezas, Manuel Castro, Masana, Lluı́s, Ribalta, Josep
Published in Molecular and cellular probes (01.02.2003)
Published in Molecular and cellular probes (01.02.2003)
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The beta cell glucokinase promoter variant is an unlikely risk factor for diabetes mellitus
Lotfi, K., Sund, G., Lowe, R., Graham, J., Landin-Olsson, M., Kockum, I., Deeb, S., Lernmark, Å.
Published in Diabetologia (1997)
Published in Diabetologia (1997)
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The p.Arg86Gln change in GARP2 (glutamic acid-rich protein-2) is a common West African-related polymorphism
Gibriel, Abdullah A.Y., Tate, Rothwelle J., Yu, Yongbin, Rawson-Lax, Emma, Hammer, Harold M., Tettey, Justice N.A., Pyne, Nigel J., Converse, Carolyn A.
Published in Gene (15.02.2013)
Published in Gene (15.02.2013)
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Evaluation of optineurin sequence variations in 1,048 patients with open-angle glaucoma
Alward, Wallace L.M, Kwon, Young H, Kawase, Kazuhide, Craig, Jamie E, Hayreh, Sohan S, Johnson, A.Tim, Khanna, Cheryl L, Yamamoto, Tetsuya, Mackey, David A, Roos, Benjamin R, Affatigato, Louisa M, Sheffield, Val C, Stone, Edwin M
Published in American journal of ophthalmology (01.11.2003)
Published in American journal of ophthalmology (01.11.2003)
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