Suchergebnisse

Tumor induction by human adenovirus type 12 in hamsters: loss of the viral genome from adenovirus type 12-induced tumor cells is compatible with tumor formation. von Ingrid Kuhlmann, Sabine Achten, Ross Rudolph, Walter Doerfler

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Genomic risk prediction of complex human disease and its clinical application von Gad Abraham, Michael Inouye

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Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals von Masao Nagasaki, Jun Yasuda, Fumiki Katsuoka, Naoki Nariai, Kaname Kojima, Yosuke Kawai, Yumi Yamaguchi‐Kabata, Junji Yokozawa, Inaho Danjoh, Sakae Saito, Yukuto Sato, Takahiro Mimori, Kaoru Tsuda, Rumiko Saito, Xiaoqing Pan, Satoshi Nishikawa, Shin Ito, Yoko Kuroki, Osamu Tanabe, Nobuo Fuse, Shinichi Kuriyama, Hideyasu Kiyomoto, Atsushi Hozawa, Naoko Minegishi, James Douglas Engel, Kengo Kinoshita, Shigeo Kure, Nobuo Yaegashi, Akito Tsuboi, Fuji Nagami, Hiroshi Kawame, Hiroaki Tomita, Ichiro Tsuji, Jun Nakaya, Junichi Sugawara, Kichiya Suzuki, Masahiro Kikuya, Michiaki Abe, Naoki Nakaya, Noriko Osumi, Riu Yamashita, Soichi Ogishima, Takako Takai, Teiji Tominaga, Yasuyuki Taki, Yoichi Suzuki, Masayuki Yamamoto

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Hypobetalipoproteinemia Due to an Apolipoprotein B Gene Exon 21 Deletion Derived by Alu-Alu Recombination von Lei Huang, M E Ripps, Stanley H. Korman, Richard J. Deckelbaum, Jan L. Breslow

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Human uniqueness: genome interactions with environment, behaviour and culture von Ajit Varki, Daniel H. Geschwind, Evan E. Eichler

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Gene Targeting in Mice: A Review von Hicham Bouabe, Klaus Okkenhaug

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A comparison of cataloged variation between International HapMap Consortium and 1000 Genomes Project data von Carrie C Buchanan, Eric S. Torstenson, William S. Bush, Marylyn D. Ritchie

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Genetic testing in asymptomatic minors: recommendations of the European Society of Human Genetics von Pascal Borry

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Precise Gene Deletion and Replacement Using the CRISPR/Cas9 System in Human Cells von Qiupeng Zheng, Xiaohong Cai, Meng How Tan, Steven Schaffert, Christopher P. Arnold, Xue Gong, Changzheng Chen, Shenglin Huang

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Involvement of Alu sequences in the cell-specific regulation of transcription of the gamma chain of Fc and T cell receptors. von A.T. Brini, G.M. Lee, Jean‐Pierre Kinet

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ISIS, the intron information system, reveals the high frequency of alternative splicing in the human genome von Larry Croft, Soeren Schandorff, Francis Clark, Kevin Burrage, Peter Arctander, John S. Mattick

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Comparison of GENCODE and RefSeq gene annotation and the impact of reference geneset on variant effect prediction von Adam Frankish, Barbara Uszczyńska, Graham R. S. Ritchie, José M. González, Dmitri D. Pervouchine, Robert Petryszak, Jonathan M. Mudge, Nuno A. Fonseca, Alvis Brāzma, Roderic Guigó, Jennifer Harrow

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MicroRNAs: critical mediators of differentiation, development and disease von Jan M. Friedman, P. A. Jones

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Alternative mapping of probes to genes for Affymetrix chips von Laurent Gautier, Morten Hylander Møller, Lennart Friis‐Hansen, Steen Knudsen

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Atherosclerosis von David T. Miller, Paul M. Ridker, Peter Libby, David J. Kwiatkowski

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MECP2, a gene associated with Rett syndrome in humans, shows conserved coding regions, independent Alu insertions, and a novel transcript across primate evolution von Maria Carolina Viana, Albert N. Menezes, Miguel Ângelo Martins Moreira, Alcides Pissinatti, Héctor N. Seuánez

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The gene wars: science, politics, and the human genome von Robert Cook‐Deegan

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Disease-associated variants in different categories of disease located in distinct regulatory elements von Meng Ma, Ru Ying, Ling-Shiang Chuang, Nai-Yun Hsu, Lisong Shi, Jörg Hakenberg, Wei‐Yi Cheng, Andrew Uzilov, Wei Ding, Benjamin S. Glicksberg, Rong Chen

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Chromosome-scale shotgun assembly using an in vitro method for long-range linkage von Nicholas H. Putnam, Brendan L. O’Connell, Jonathan C. Stites, Brandon Rice, Marco Blanchette, Robert Calef, Christopher J. Troll, Andrew J. Fields, Paul D. Hartley, Charles W. Sugnet, David Haussler, Daniel S. Rokhsar, Richard E. Green

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Complete nucleotide sequence of the chromosomal gene for human IL-4 and its expression. von Naoko Arai, D Nomura, Douglas B. Villaret, R DeWaal Malefijt, Motoharu Seiki, M. Yoshida, Satoshi Minoshima, R. Fukuyama, Masato Maekawa, Jun Kudoh

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