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PubMed Central (PMC3 - NLM DTD) (2,081,148 recursos)
Archive of life sciences journal literature at the U.S. National Institutes of Health (NIH), developed and managed by NIH's National Center for Biotechnology Information (NCBI) in the National Library of Medicine (NLM).

Mostrando recursos 61 - 80 de 900

61. No major association between TGFBR1*6A and prostate cancer - Kaklamani, Virginia; Baddi, Lisa; Rosman, Diana; Liu, Junjian; Ellis, Nathan; Oddoux, Carole; Ostrer, Harry; Chen, Yu; Ahsan, Habibul; Offit, Kenneth; Pasche, Boris
Prostate cancer is the most commonly diagnosed cancer in men and one of the leading causes of cancer deaths. There is strong genetic evidence indicating that a large proportion of prostate cancers are caused by heritable factors but the search for prostate cancer susceptibility genes has thus far remained elusive. TGFBR1*6A, a common hypomorphic variant of the type I Transforming Growth Factor Beta receptor, is emerging as a tumor susceptibility allele that predisposes to the development of breast, colon and ovarian cancer. The association with prostate cancer has not yet been explored. A total of 907 cases and controls from...

62. Diagnostic polymorphisms in the mitochondrial cytochrome b gene allow discrimination between cattle, sheep, goat, roe buck and deer by PCR-RFLP - Pfeiffer, Ina; Burger, Joachim; Brenig, Bertram

63. On modeling locus heterogeneity using mixture distributions - Lin, Shili; Biswas, Swati

64. Density-independent population projection trajectories of chromosome-substituted lines resistant and susceptible to organophosphate insecticides in Drosophila melanogaster - Miyo, Takahiro; Charlesworth, Brian

65. Method for determination of (-102C>T) single nucleotide polymorphism in the human manganese superoxide dismutase promoter - Martin, Robert CG; Hughes, Kalista; Doll, Mark A; Lan, Qing; Martini, Benjamin D; Lissowska, Jolanta; Rothman, Nathaniel; Hein, David W

66. The exceptionally high rate of spontaneous mutations in the polymerase delta proofreading exonuclease-deficient Saccharomyces cerevisiae strain starved for adenine - Achilli, Alessandro; Matmati, Nabil; Casalone, Enrico; Morpurgo, Giorgio; Lucaccioni, Angela; Pavlov, Youri I; Babudri, Nora

67. The Prader-Willi syndrome murine imprinting center is not involved in the spatio-temporal transcriptional regulation of the Necdin gene - Watrin, Françoise; Le Meur, Elodie; Roeckel, Nathalie; Ripoche, Marie-Anne; Dandolo, Luisa; Muscatelli, Françoise

68. Screening large-scale association study data: exploiting interactions using random forests - Lunetta, Kathryn L; Hayward, L Brooke; Segal, Jonathan; Van Eerdewegh, Paul

69. Variants in the vitamin D receptor gene and asthma - Wjst, Matthias

70. Influence of language and ancestry on genetic structure of contiguous populations: A microsatellite based study on populations of Orissa - Sahoo, Sanghamitra; Kashyap, VK

71. Transient expression analysis of allelic variants of a VNTR in the dopamine transporter gene (DAT1) - Mill, Jonathan; Asherson, Philip; Craig, Ian; D'Souza, Ursula M

72. An automated system for measuring parameters of nematode sinusoidal movement - Cronin, Christopher J; Mendel, Jane E; Mukhtar, Saleem; Kim, Young-Mee; Stirbl, Robert C; Bruck, Jehoshua; Sternberg, Paul W

73. Genetic variation analysis of the Bali street dog using microsatellites - Irion, Dawn N; Schaffer, Alison L; Grant, Sherry; Wilton, Alan N; Pedersen, Niels C

74. Comparative linkage analysis and visualization of high-density oligonucleotide SNP array data - Leykin, Igor; Hao, Ke; Cheng, Junsheng; Meyer, Nicole; Pollak, Martin R; Smith, Richard JH; Wong, Wing Hung; Rosenow, Carsten; Li, Cheng

75. Construction and analysis of tag single nucleotide polymorphism maps for six human-mouse orthologous candidate genes in type 1 diabetes - Maier, Lisa M; Smyth, Deborah J; Vella, Adrian; Payne, Felicity; Cooper, Jason D; Pask, Rebecca; Lowe, Christopher; Hulme, John; Smink, Luc J; Fraser, Heather; Moule, Carolyn; Hunter, Kara M; Chamberlain, Giselle; Walker, Neil; Nutland, Sarah; Undlien, Dag E; Rønningen, Kjersti S; Guja, Cristian; Ionescu-Tîrgovi?te, Constantin; Savage, David A; Strachan, David P; Peterson, Laurence B; Todd, John A; Wicker, Linda S; Twells, Rebecca C

76. A novel replication-independent histone H2a gene in mouse - Nishida, Hiromi; Suzuki, Takahiro; Tomaru, Yasuhiro; Hayashizaki, Yoshihide

77. An interactional network of genes involved in chitin synthesis in Saccharomyces cerevisiae - Lesage, Guillaume; Shapiro, Jesse; Specht, Charles A; Sdicu, Anne-Marie; Ménard, Patrice; Hussein, Shamiza; Tong, Amy Hin Yan; Boone, Charles; Bussey, Howard

78. Genetic linkage analysis supports the presence of two susceptibility loci for alcoholism and heavy drinking on chromosome 1p22.1-11.2 and 1q21.3-24.2 - Guerrini, Irene; Cook, Christopher CH; Kest, Wendy; Devitgh, Audrey; McQuillin, Andrew; Curtis, David; Gurling, Hugh MD

79. Two new plumage mutations in the Japanese quail: "curly" feather and "rusty" plumage - Minvielle, Francis; Gourichon, David; Moussu, Chantal

80. Searching QTL by gene expression: analysis of diabesity - Brown, Aaron C; Olver, William I; Donnelly, Charles J; May, Marjorie E; Naggert, Jürgen K; Shaffer, Daniel J; Roopenian, Derry C

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