Occurrence and consequences of coding sequence insertions and deletions in Mammalian genomes. حسب Taylor, MS, Ponting, C, Copley, R

The radiological perspective of juvenile nasopharyngeal angiofibroma: A case report حسب Kaleb Taylor, MS, Marco DiBlasi, BA, Erik Pedersen, MD, Nastaran Shahsavari, MD

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Evidence of a large-scale functional organization of mammalian chromosomes: Authors' reply حسب Shifman, S, Bell, J, Copley, R, Taylor, MS, Williams, R, Mott, R, Flint, J

A high-resolution single nucleotide polymorphism genetic map of the mouse genome. حسب Shifman, S, Bell, J, Copley, R, Taylor, MS, Williams, R, Mott, R, Flint, J

A high-resolution single nucleotide polymorphism genetic map of the mouse genome. حسب Shifman, S, Bell, J, Copley, R, Taylor, MS, Williams, R, Mott, R, Flint, J

High resolution mapping of expression QTLs in heterogeneous stock mice in multiple tissues. حسب Huang, G, Shifman, S, Valdar, W, Johannesson, M, Yalcin, B, Taylor, MS, Taylor, J, Mott, R, Flint, J

Pervasive haplotypic variation in the spliceo-transcriptome of the human major histocompatibility complex. حسب Vandiedonck, C, Taylor, MS, Lockstone, H, Plant, K, Taylor, J, Durrant, C, Broxholme, J, Fairfax, B, Knight, J

Genome-wide genetic association of complex traits in heterogeneous stock mice. حسب Valdar, W, Solberg, L, Gauguier, D, Burnett, S, Klenerman, P, Cookson, W, Taylor, MS, Rawlins, J, Mott, R, Flint, J

Dynamic and physical clustering of gene expression during epidermal barrier formation in differentiating keratinocytes. حسب Taylor, J, Street, T, Hao, L, Copley, R, Taylor, MS, Hayden, P, Stolper, G, Mott, R, Hein, J, Moffatt, M, Cookson, W

Genetic analysis of pathways regulated by the von Hippel-Lindau tumor suppressor in Caenorhabditis elegans حسب Bishop, T, Lau, K, Epstein, A, Kim, S, Jiang, M, O'Rourke, D, Pugh, C, Gleadle, J, Taylor, MS, Hodgkin, J, Ratcliffe, P

Identification of common genetic variation that modulates alternative splicing. حسب Hull, J, Campino, S, Rowlands, K, Chan, MS, Copley, R, Taylor, MS, Rockett, K, Elvidge, G, Keating, B, Knight, J, Kwiatkowski, D

Identification of common genetic variation that modulates alternative splicing حسب Hull, J, Campino, S, Rowlands, K, Chan, MS, Copley, R, Taylor, MS, Rockett, K, Elvidge, G, Keating, B, Knight, J, Kwiatkowski, D

Manipulation of dipeptidylpeptidase 10 in mouse and human in vivo and in vitro models indicates a protective role in asthma حسب Zhang, Y, Poobalasingam, T, Yates, LL, Walker, SA, Taylor, MS, Chessum, L, Harrison, J, Tsaprouni, L, Adcock, IM, Lloyd, CM, Cookson, WO, Moffatt, MF, Dean, CH

Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects. حسب Williamson, K, Rainger, J, Floyd, J, Ansari, M, Meynert, A, Aldridge, K, Rainger, J, Anderson, C, Moore, A, Hurles, M, Clarke, A, van Heyningen, V, Verloes, A, Taylor, MS, Wilkie, A, Fitzpatrick, DR