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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 81 - 100 de 900

81. ISSR markers show differentiation among Italian populations of Asparagus acutifolius L - Sica, Maria; Gamba, Graziella; Montieri, Stefania; Gaudio, Luciano; Aceto, Serena

82. Isolation by distance, web service - Jensen, Jeffrey L; Bohonak, Andrew J; Kelley, Scott T

83. Rim 2/Hipa CACTA transposon display ; A new genetic marker technique in Oryza species - Kwon, Soon-Jae; Park, Kyong-Chul; Kim, Jin-Hong; Lee, Ju Kyong; Kim, Nam-Soo

84. X- and Y-chromosome specific variants of the amelogenin gene allow sex determination in sheep (Ovis aries) and European red deer (Cervus elaphus) - Pfeiffer, I; Brenig, B

85. Differential selection and mutation between dsDNA and ssDNA phages shape the evolution of their genomic AT percentage - Xia, Xuhua; Yuen, Kwok Yung

86. Analysis of sequence variability in the CART gene in relation to obesity in a Caucasian population - Guérardel, Audrey; Barat-Houari, Mouna; Vasseur, Francis; Dina, Christian; Vatin, Vincent; Clément, Karine; Eberlé, Delphine; Vasseur-Delannoy, Valérie; Bell, Christopher G; Galan, Pilar; Hercberg, Serge; Helbecque, Nicole; Potoczna, Natascha; Horber, Fritz F; Boutin, Philippe; Froguel, Philippe

87. Characterisation of the genomic architecture of human chromosome 17q and evaluation of different methods for haplotype block definition - Zeggini, Eleftheria; Barton, Anne; Eyre, Stephen; Ward, Daniel; Ollier, William; Worthington, Jane; John, Sally

88. Power and sample size calculations in the presence of phenotype errors for case/control genetic association studies - Edwards, Brian J; Haynes, Chad; Levenstien, Mark A; Finch, Stephen J; Gordon, Derek

89. Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humans - Petry, Clive J; Ong, Ken K; Barratt, Bryan J; Wingate, Diane; Cordell, Heather J; Ring, Susan M; Pembrey, Marcus E; ; Reik, Wolf; Todd, John A; Dunger, David B

90. Naturally occurring antisense RNA of histone H2a in mouse cultured cell lines - Nishida, Hiromi; Tomaru, Yasuhiro; Oho, Yuko; Hayashizaki, Yoshihide

91. Estimating haplotype frequencies in pooled DNA samples when there is genotyping error - Quade, Shannon RE; Elston, Robert C; Goddard, Katrina AB

92. PAX6 mutations: genotype-phenotype correlations - Tzoulaki, Ioanna; White, Ian MS; Hanson, Isabel M

93. Use of SNPs to determine the breakpoints of complex deficiencies, facilitating gene mapping in Caenorhabditis elegans - Kadandale, Pavan; Geldziler, Brian; Hoffmann, Melissa; Singson, Andrew

94. Development of novel heminested PCR assays based on mitochondrial 16s rRNA gene for identification of seven pecora species - Guha, Saurav; Kashyap, VK

95. A screen for proteins that interact with PAX6: C-terminal mutations disrupt interaction with HOMER3, DNCL1 and TRIM11 - Cooper, Simon T; Hanson, Isabel M

96. Tests for the replication of an association between Egfr and natural variation in Drosophila melanogaster wing morphology - Palsson, Arnar; Dodgson, James; Dworkin, Ian; Gibson, Greg

97. G2D: a tool for mining genes associated with disease - Perez-Iratxeta, Carolina; Wjst, Matthias; Bork, Peer; Andrade, Miguel A

98. MAOA haplotypes associated with thrombocyte-MAO activity - Jansson, Mårten; McCarthy, Shane; Sullivan, Patrick F; Dickman, Paul; Andersson, Björn; Oreland, Lars; Schalling, Martin; Pedersen, Nancy L

99. Epigenetic predisposition to expression of TIMP1 from the human inactive X chromosome - Anderson, Catherine L; Brown, Carolyn J

100. Reconstructing recent human phylogenies with forensic STR loci: A statistical approach - Agrawal, Suraksha; Khan, Faisal

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