Arama Sonuçları

Genetics of congenital heart disease: the contribution of the noncoding regulatory genome Yazar: Alex V. Postma, Connie R. Bezzina, Vincent M. Christoffels

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A Genomic Score Prognostic of Outcome in Trauma Patients Yazar: H. Shaw Warren, Constance M. Elson, Ivor S. Douglas, David Schoenfeld, J. Perren Cobb, Ronald V. Maier, Lyle L. Moldawer, Ernest E. Moore, Brian G. Harbrecht, Kimberly Pelak, Joseph Cuschieri, David N. Herndon, Marc G. Jeschke, Celeste C. Finnerty, Bernard H. Brownstein, Laura Hennessy, Philip H. Mason, Ronald G. Tompkins

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Massively parallel high-order combinatorial genetics in human cells Yazar: Alan S.L. Wong, Gigi C.G. Choi, Allen A. Cheng, Oliver Purcell, Timothy K. Lu

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Parents’ Experience with Pediatric Microarray: Transferrable Lessons in the Era of Genomic Counseling Yazar: Robin Z. Hayeems, Riyana Babul‐Hirji, Ny Hoang, Rosanna Weksberg, Cheryl Shuman

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Pervasive pleiotropy between psychiatric disorders and immune disorders revealed by integrative analysis of multiple GWAS Yazar: Qian Wang, Can Yang, Joel Gelernter, Hongyu Zhao

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Activation of the platelet-derived growth factor receptor by the bovine papillomavirus E5 transforming protein. Yazar: Lisa M. Petti, Laura A. Nilson, Daniel DiMaio

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Identification of Genes Potentially Involved in the Increased Risk of Malignancy in NF1-Microdeleted Patients Yazar: Éric Pasmant, Julien Masliah‐Planchon, Pascale Lévy, Ingrid Laurendeau, Nicolás Ortonne, Béatrice Parfait, L. Valeyrie‐Allanore, Karen Leroy, P. Wolkenstein, Michel Vidaud, Dominique Vidaud, Ivan Bièche

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

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Genomic Organization and Sequence of the Human NRAMP Gene: Identification and Mapping of a Promoter Region Polymorphism Yazar: Jenefer M. Blackwell, Chris Barton, Jacqueline K. White, Susan Searle, Anne-Marie Baker, Hazel Williams, Marie‐Anne Shaw

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A Novel Protease Homolog Differentially Expressed in Breast and Ovarian Cancer Yazar: Anthony Anisowicz, Georgia Sotiropoulou, Göran Stenman, Samuel C. Mok, Ruth Sager

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Systematic RNAi in C. elegans Yazar: Rachel B. Brem

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Design and implementation of microarray gene expression markup language (MAGE-ML) Yazar: Paul T. Spellman, Michael Miller, Jason Stewart, Charles Troup, Uğis Sarkans, Steve Chervitz, Derek Bernhart, Gavin Sherlock, Catherine A. Ball, Marc Lepage, Marcin Świątek, W.L. Marks, Jason Gonçalves, Scott Markel, Daniel Iordan, Mohammadreza Shojatalab, Angel Pizarro, Joe White, Robert Hubley, Eric W. Deutsch, Martin Senger, Bruce J. Aronow, Alan J. Robinson, Doug Bassett, Christian J. Stoeckert, Alvis Brāzma

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Disease-associated variants in different categories of disease located in distinct regulatory elements Yazar: 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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Association of Severe Noncerebral Plasmodium falciparum Malaria in Brazil With Expressed PfEMP1 DBL1α Sequences Lacking Cysteine Residues Yazar: Karin Kirchgatter, Hernando A. del Portillo

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Genetics of cleft lip and cleft palate Yazar: Elizabeth J. Leslie, Mary L. Marazita

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Assessment of copy number variations in the brain genome of schizophrenia patients Yazar: Miwako Sakai, Yuichiro Watanabe, Toshiyuki Someya, Kazuaki Araki, Masako Shibuya, Kazuhiro Niizato, Kenichi Oshima, Yasuto Kunii, Hirooki Yabe, Junya Matsumoto, Akira Wada, Mizuki Hino, Takeshi Hashimoto, Akitoyo Hishimoto, Noboru Kitamura, Shuji Iritani, Osamu Shirakawa, Kiyoshi Maeda, Akinori Miyashita, Shin‐ichi Niwa, Hitoshi Takahashi, Akiyoshi Kakita, Ryozo Kuwano, Hiroyuki Nawa

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Molecular and clinical analyses of 84 patients with tuberous sclerosis complex Yazar: Chia‐Cheng Hung, Yi‐Ning Su, Shu‐Chin Chien, Horng‐Huei Liou, Chih‐Cheng Chen, Pau‐Chung Chen, Chia‐Jung Hsieh, Chih‐Ping Chen, Wang‐Tso Lee, Win-Li Lin, Chien‐Nan Lee

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Gestational tissue transcriptomics in term and preterm human pregnancies: a systematic review and meta-analysis Yazar: Haley Eidem, William E. Ackerman, Kriston L. McGary, Patrick Abbot, Antonis Rokas

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Mutations in human IFT140 cause non-syndromic retinal degeneration Yazar: Mingchu Xu, Lizhu Yang, Feng Wang, Huajin Li, Xia Wang, Weichen Wang, Zhongqi Ge, Keqing Wang, Li Zhao, Hui Li, Yumei Li, Ruifang Sui, Rui Chen

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XACT, a long non-coding transcript coating the active X chromosome in human pluripotent cells Yazar: Céline Vallot, Christophe Huret, Yann Lesecque, Alissa Resch, Noufϊssa Oudrhiri, Annelise Bennaceur‐Griscelli, Laurent Duret, Claire Rougeulle

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