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There are 8717 results for: content related to: Anorectal atresia and Variants at Predicted Regulatory Sites in Candidate Genes

  1. Joint Analysis of SNPs and Proteins Identifies Regulatory IL18 Gene Variations Decreasing the Chance of Spastic Cerebral Palsy

    Human Mutation

    Volume 34, Issue 1, January 2013, Pages: 143–148, Mads Vilhelm Hollegaard, Kristin Skogstrand, Poul Thorsen, Bent Nørgaard-Pedersen, David Michael Hougaard and Jakob Grove

    Version of Record online : 4 SEP 2012, DOI: 10.1002/humu.22173

  2. Sensory organ generation in the chicken inner ear: Contributions of Bone morphogenetic protein 4, Serrate1, and Lunatic fringe

    Journal of Comparative Neurology

    Volume 424, Issue 3, 28 August 2000, Pages: 509–520, Laura K. Cole, Isabelle Le Roux, Fabio Nunes, Edward Laufer, Julian Lewis and Doris K. Wu

    Version of Record online : 18 JUL 2000, DOI: 10.1002/1096-9861(20000828)424:3<509::AID-CNE8>3.0.CO;2-Q

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    Variants in ABCB1, TGFB1, and XRCC1 genes and susceptibility to viral hepatitis A infection in Mexican Americans

    Hepatology

    Volume 55, Issue 4, April 2012, Pages: 1008–1018, Lyna Zhang, Ajay Yesupriya, Dale J. Hu, Man-huei Chang, Nicole F. Dowling, Renée M. Ned, Venkatachalam Udhayakumar, Mary Lou Lindegren and Yury Khudyakov

    Version of Record online : 27 MAR 2012, DOI: 10.1002/hep.25513

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    Disease variants in genomes of 44 centenarians

    Molecular Genetics & Genomic Medicine

    Volume 2, Issue 5, September 2014, Pages: 438–450, Yun Freudenberg-Hua, Jan Freudenberg, Vladimir Vacic, Avinash Abhyankar, Anne-Katrin Emde, Danny Ben-Avraham, Nir Barzilai, Dayna Oschwald, Erika Christen, Jeremy Koppel, Blaine Greenwald, Robert B. Darnell, Soren Germer, Gil Atzmon and Peter Davies

    Version of Record online : 15 JUN 2014, DOI: 10.1002/mgg3.86

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    Renal Agenesis in Kallmann Syndrome: A Network Approach

    Annals of Human Genetics

    Volume 78, Issue 6, November 2014, Pages: 424–433, Nili Tickotsky and Moti Moskovitz

    Version of Record online : 17 SEP 2014, DOI: 10.1111/ahg.12079

  6. Uniparental disomy causes deficiencies of vitamin K-dependent proteins

    Journal of Thrombosis and Haemostasis

    Volume 14, Issue 12, December 2016, Pages: 2410–2418, M. A. Dasi, R. Gonzalez-Conejero, S. Izquierdo, J. Padilla, J. L. Garcia, N. Garcia-Barberá, B. Argilés, M. E. de la Morena-Barrio, J. M. Hernández-Sánchez, J. M. Hernández-Rivas, V. Vicente and J. Corral

    Version of Record online : 19 NOV 2016, DOI: 10.1111/jth.13517

  7. Elucidating the molecular basis of MSH2-deficient tumors by combined germline and somatic analysis

    International Journal of Cancer

    Volume 141, Issue 7, 1 October 2017, Pages: 1365–1380, Gardenia M. Vargas-Parra, Maribel González-Acosta, Bryony A. Thompson, Carolina Gómez, Anna Fernández, Estela Dámaso, Tirso Pons, Monika Morak, Jesús del Valle, Silvia Iglesias, Àngela Velasco, Ares Solanes, Xavier Sanjuan, Natàlia Padilla, Xavier de la Cruz, Alfonso Valencia, Elke Holinski-Feder, Joan Brunet, Lídia Feliubadaló, Conxi Lázaro, Matilde Navarro, Marta Pineda and Gabriel Capellá

    Version of Record online : 3 JUL 2017, DOI: 10.1002/ijc.30820

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    Canonical Wnt signaling modulates Tbx1, Eya1, and Six1 expression, restricting neurogenesis in the otic vesicle

    Developmental Dynamics

    Volume 239, Issue 6, June 2010, Pages: 1708–1722, Laina Freyer and Bernice E. Morrow

    Version of Record online : 12 MAY 2010, DOI: 10.1002/dvdy.22308

  9. Prioritizing Variants in Complete Hereditary Breast and Ovarian Cancer Genes in Patients Lacking Known BRCA Mutations

    Human Mutation

    Volume 37, Issue 7, July 2016, Pages: 640–652, Natasha G. Caminsky, Eliseos J. Mucaki, Ami M. Perri, Ruipeng Lu, Joan H. M. Knoll and Peter K. Rogan

    Version of Record online : 18 MAR 2016, DOI: 10.1002/humu.22972

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    Malleal processus brevis is dispensable for normal hearing in mice

    Developmental Dynamics

    Volume 227, Issue 1, May 2003, Pages: 69–77, Zunyi Zhang, Xiaoyun Zhang, Wilma A. Avniel, Yiqiang Song, Sherri M. Jones, Timothy A. Jones, Cesar Fermin and Yiping Chen

    Version of Record online : 20 MAR 2003, DOI: 10.1002/dvdy.10288

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    BMP4 modulates fibroblast growth factor–mediated induction of proximal and distal lung differentiation in mouse embryonic tracheal epithelium in mesenchyme-free culture

    Developmental Dynamics

    Volume 225, Issue 2, October 2002, Pages: 153–165, Brian A. Hyatt, Xiaofei Shangguan and John M. Shannon

    Version of Record online : 5 SEP 2002, DOI: 10.1002/dvdy.10145

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    Dynamics and Cellular Localization of Bmp2, Bmp4, and Noggin Transcription in the Postnatal Mouse Skeleton

    Journal of Bone and Mineral Research

    Volume 30, Issue 1, January 2015, Pages: 64–70, Steven K Pregizer and Douglas P Mortlock

    Version of Record online : 26 DEC 2014, DOI: 10.1002/jbmr.2313

  13. Genetic enhancement of limb defects in a mouse model of Cornelia de Lange syndrome

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 172, Issue 2, June 2016, Pages: 146–154, Martha E. Lopez-Burks, Rosaysela Santos, Shimako Kawauchi, Anne L. Calof and Arthur D. Lander

    Version of Record online : 27 APR 2016, DOI: 10.1002/ajmg.c.31491

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    Prenatal and newborn screening for hemoglobinopathies

    International Journal of Laboratory Hematology

    Volume 35, Issue 3, June 2013, Pages: 297–305, C. C. Hoppe

    Version of Record online : 17 APR 2013, DOI: 10.1111/ijlh.12076

  15. Conservation and divergence of BMP2/4 genes in the lamprey: expression and phylogenetic analysis suggest a single ancestral vertebrate gene

    Evolution & Development

    Volume 6, Issue 6, November 2004, Pages: 411–422, David W. McCauley and Marianne Bronner-Fraser

    Version of Record online : 27 OCT 2004, DOI: 10.1111/j.1525-142X.2004.04054.x

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    Levels of Gli3 repressor correlate with Bmp4 expression and apoptosis during limb development

    Developmental Dynamics

    Volume 231, Issue 1, September 2004, Pages: 148–160, Maria Félix Bastida, M. Dolores Delgado, Baolin Wang, John F. Fallon, Marian Fernandez-Teran and Maria A. Ros

    Version of Record online : 29 JUN 2004, DOI: 10.1002/dvdy.20121

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    A Clinical and Molecular Analysis of Branchio-Oculo-Facial Syndrome Patients in Russia Revealed New Mutations in TFAP2A

    Annals of Human Genetics

    Volume 79, Issue 2, March 2015, Pages: 148–152, Tatiana I. Meshcheryakova, Rena A. Zinchenko, Tatiana A. Vasilyeva, Andrey V. Marakhonov, Svetlana S. Zhylina, Nika V. Petrova, Tatiana V. Kozhanova, Maxim S. Belenikin, Alexander N. Petrin and Gennady R. Mutovin

    Version of Record online : 15 JAN 2015, DOI: 10.1111/ahg.12098

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    Induction of bud formation of embryonic mouse tracheal epithelium by fibroblast growth factor plus transferrin in mesenchyme-free culture

    Developmental Dynamics

    Volume 222, Issue 2, October 2001, Pages: 263–272, Norie Ohtsuka, Koko Urase, Takashi Momoi and Hiroyuki Nogawa

    Version of Record online : 29 AUG 2001, DOI: 10.1002/dvdy.1206

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    Regulation of Sox9 by Sonic Hedgehog (Shh) is essential for patterning and formation of tracheal cartilage

    Developmental Dynamics

    Volume 239, Issue 2, February 2010, Pages: 514–526, Jinhyung Park, Jennifer J.R. Zhang, Anne Moro, Michelle Kushida, Michael Wegner and Peter C.W. Kim

    Version of Record online : 23 DEC 2009, DOI: 10.1002/dvdy.22192

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    Reduced BMP4 abundance in Gata2 hypomorphic mutant mice result in uropathies resembling human CAKUT

    Genes to Cells

    Volume 13, Issue 2, February 2008, Pages: 159–170, Tomofumi Hoshino, Ritsuko Shimizu, Shinya Ohmori, Masumi Nagano, Xiaoqing Pan, Osamu Ohneda, Melin Khandekar, Masayuki Yamamoto, Kim-Chew Lim and James Douglas Engel

    Version of Record online : 30 JAN 2008, DOI: 10.1111/j.1365-2443.2007.01158.x