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There are 2739 results for: content related to: Physiological functions of imprinted genes

  1. Mechanisms of imprinting of the Prader–Willi/Angelman region

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 16, 15 August 2008, Pages: 2041–2052, Bernhard Horsthemke and Joseph Wagstaff

    Version of Record online : 14 JUL 2008, DOI: 10.1002/ajmg.a.32364

  2. You have full text access to this Open Access content
    Yolk sac tumor but not seminoma or teratoma is associated with abnormal epigenetic reprogramming pathway and shows frequent hypermethylation of various tumor suppressor genes

    Cancer Science

    Volume 100, Issue 4, April 2009, Pages: 698–708, Shinsuke Furukawa, Masayuki Haruta, Yasuhito Arai, Shohei Honda, Junjiro Ohshima, Waka Sugawara, Yukio Kageyama, Yotsuo Higashi, Kazunori Nishida, Yukiko Tsunematsu, Hisaya Nakadate, Masahiro Ishii and Yasuhiko Kaneko

    Version of Record online : 24 FEB 2009, DOI: 10.1111/j.1349-7006.2009.01102.x

  3. You have free access to this content
    The mouse Snrpn minimal promoter and its human orthologue: activity and imprinting

    Genes to Cells

    Volume 6, Issue 11, November 2001, Pages: 967–975, Alon Y. Hershko, Yael Finberg, Boris Kantor, Ruth Shemer and Aharon Razin

    Version of Record online : 12 JAN 2002, DOI: 10.1046/j.1365-2443.2001.00474.x

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    Imprinting centers, chromatin structure, and disease

    Journal of Cellular Biochemistry

    Volume 95, Issue 2, 15 May 2005, Pages: 226–233, Hidenobu Soejima and Joseph Wagstaff

    Version of Record online : 18 MAR 2005, DOI: 10.1002/jcb.20443

  5. Imprinting in Prader–Willi and Angelman syndromes

    Standard Article

    Encyclopedia of Genetics, Genomics, Proteomics and Bioinformatics

    Bernhard Horsthemke and Karin Buiting

    Published Online : 15 NOV 2005, DOI: 10.1002/047001153X.g103214

  6. RNAs of the human chromosome 15q11-q13 imprinted region

    Wiley Interdisciplinary Reviews: RNA

    Volume 4, Issue 2, March/April 2013, Pages: 155–166, Stormy J. Chamberlain

    Version of Record online : 3 DEC 2012, DOI: 10.1002/wrna.1150

  7. Identification of CpG methylation of the SNRPN gene by methylation-specific multiplex PCR

    ELECTROPHORESIS

    Volume 30, Issue 2, January 2009, Pages: 410–416, Chia-Cheng Hung, Shin-Yu Lin, Shuan-Pei Lin, Dou-Ming Niu, Ni-Chung Lee, Wen-Fang Cheng, Chih-Ping Chen, Win-Li Lin, Chien-Nan Lee and Yi-Ning Su

    Version of Record online : 9 JAN 2009, DOI: 10.1002/elps.200800225

  8. SNRPN methylation patterns in germ cell tumors as a reflection of primordial germ cell development

    Genes, Chromosomes and Cancer

    Volume 32, Issue 4, December 2001, Pages: 342–352, Kimberly J. Bussey, Helen J. Lawce, Eleanor Himoe, Xiao Ou Shu, Nyla A. Heerema, Elizabeth J. Perlman, Susan B. Olson and R. Ellen Magenis

    Version of Record online : 10 OCT 2001, DOI: 10.1002/gcc.1199

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    Aberrant Genomic Imprinting in Rhesus Monkey Embryonic Stem Cells

    STEM CELLS

    Volume 24, Issue 3, March 2006, Pages: 595–603, Akihisa Fujimoto, Shoukhrat M. Mitalipov, Hung-Chih Kuo and Don P. Wolf

    Version of Record online : 3 NOV 2005, DOI: 10.1634/stemcells.2005-0301

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    Oocyte growth-dependent progression of maternal imprinting in mice

    Genes to Cells

    Volume 11, Issue 4, April 2006, Pages: 353–361, Hitoshi Hiura, Yayoi Obata, Junichi Komiyama, Motomu Shirai and Tomohiro Kono

    Version of Record online : 7 FEB 2006, DOI: 10.1111/j.1365-2443.2006.00943.x

  11. You have free access to this content
    DNA methylation in genomic imprinting, development, and disease

    The Journal of Pathology

    Volume 195, Issue 1, September 2001, Pages: 97–110, Martina Paulsen and Anne C. Ferguson-Smith

    Version of Record online : 17 MAY 2001, DOI: 10.1002/path.890

  12. Imprinting centre deletions in two PWS families: implications for diagnostic testing and genetic counselling

    Clinical Genetics

    Volume 58, Issue 4, October 2000, Pages: 284–290, K Buiting, C Färber, P Kroisel, K Wagner, L Brueton, ME Robertson, C Lich and B Horsthemke

    Version of Record online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.2000.580406.x

  13. Prader–Willi syndrome and Angelman syndrome

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

    Volume 154C, Issue 3, 15 August 2010, Pages: 365–376, Karin Buiting

    Version of Record online : 20 AUG 2010, DOI: 10.1002/ajmg.c.30273

  14. Angelman syndrome: Current and emerging therapies in 2016

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

    Volume 172, Issue 4, December 2016, Pages: 384–401, Wen-Hann Tan and Lynne M. Bird

    Version of Record online : 8 NOV 2016, DOI: 10.1002/ajmg.c.31536

  15. Mosaicism of proximal 15q duplication/deletion resulting in Prader–Willi syndrome with normal methylation

    American Journal of Medical Genetics Part A

    Volume 138A, Issue 2, 1 October 2005, Pages: 181–184, Luke Boyd, Michael G. Brown, Stephen Kelson, Helen Lawce, Sarah Shuttleworth, Nancy Unsworth and R. Ellen Magenis

    Version of Record online : 12 AUG 2005, DOI: 10.1002/ajmg.a.30819

  16. DNA demethylation reactivation of imprinted genes in cell lines from patients with Prader-Willi syndrome and a mouse model

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 12, 15 June 2007, Pages: 1386–1390, Kyoko Takano, Maki Okajima and Shinji Saitoh

    Version of Record online : 15 MAY 2007, DOI: 10.1002/ajmg.a.31765

  17. Neuronal chromatin dynamics of imprinting in development and disease

    Journal of Cellular Biochemistry

    Volume 112, Issue 2, February 2011, Pages: 365–373, Karen N. Leung, Stormy J. Chamberlain, Marc Lalande and Janine M. LaSalle

    Version of Record online : 25 JAN 2011, DOI: 10.1002/jcb.22958

  18. Small mosaic deletion encompassing the snoRNAs and SNURF-SNRPN results in an atypical Prader–Willi syndrome phenotype

    American Journal of Medical Genetics Part A

    Volume 164, Issue 2, February 2014, Pages: 425–431, Britt-Marie Anderlid, Johanna Lundin, Helena Malmgren, Mikael Lehtihet and Ann Nordgren

    Version of Record online : 5 DEC 2013, DOI: 10.1002/ajmg.a.36307

  19. Maternally and paternally silenced imprinted genes differ in their intron content

    Comparative and Functional Genomics

    Volume 5, Issue 8, December 2004, Pages: 572–583, Marie E Fahey, Walter Mills, Desmond G Higgins and Tom Moore

    Version of Record online : 28 FEB 2005, DOI: 10.1002/cfg.437

  20. Polymorphisms in the SNRPN gene are associated with obesity susceptibility in a Spanish population

    The Journal of Gene Medicine

    Volume 19, Issue 5, May 2017, David Albuquerque, Licínio Manco, Luz M. González, Guillermo Gervasini, Goitzane Marcaida Benito, Juan R. González and Raquel Rodríguez-López

    Version of Record online : 23 MAY 2017, DOI: 10.1002/jgm.2956