Search Results

There are 2040758 results for: content related to: Heterogeneous growth patterns in carriers of chromosome 7p12.2 imbalances affecting GRB10

  1. Isolated hypermethylation of GRB10 (7p12.2) in a Silver–Russell syndrome patient carrying a 20p13 microdeletion

    Clinical Genetics

    Volume 85, Issue 4, April 2014, Pages: 399–400, T. Eggermann, B. Schneider-Rätzke, M. Begemann and S. Spengler

    Version of Record online : 9 JUN 2013, DOI: 10.1111/cge.12186

  2. Maternally inherited duplication of chromosome 7, dup(7)(p11.2p12), associated with mild cognitive deficit without features of Silver–Russell syndrome

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 13, 1 July 2007, Pages: 1489–1493, Natalia T. Leach, Ilse Chudoba, Tasheena V. Stewart, Lewis B. Holmes and Stanislawa Weremowicz

    Version of Record online : 5 JUN 2007, DOI: 10.1002/ajmg.a.31794

  3. Uniparental disomy (UPD) other than 15: Phenotypes and bibliography updated

    American Journal of Medical Genetics Part A

    Volume 136A, Issue 3, 30 July 2005, Pages: 287–305, Dieter Kotzot and Gerd Utermann

    Version of Record online : 14 JUN 2005, DOI: 10.1002/ajmg.a.30483

  4. Genetics of Silver–Russell Syndrome

    Standard Article


    Thomas Eggermann

    Published Online : 15 FEB 2012, DOI: 10.1002/9780470015902.a0023847

  5. You have free access to this content
    Regulation of insulin and type 1 insulin-like growth factor signaling and action by the Grb10/14 and SH2B1/B2 adaptor proteins

    The FEBS Journal

    Volume 280, Issue 3, February 2013, Pages: 794–816, Bernard Desbuquois, Nadège Carré and Anne-Françoise Burnol

    Version of Record online : 2 JAN 2013, DOI: 10.1111/febs.12080

  6. Lmx1a is an activator of Rgs4 and Grb10 and is responsible for the correct specification of rostral and medial mdDA neurons

    European Journal of Neuroscience

    Volume 37, Issue 1, January 2013, Pages: 23–32, Elisa J. Hoekstra, Lars von Oerthel, Annemarie J. A. van der Linden, Raymond D. Schellevis, Gerard Scheppink, Frank C. P. Holstege, Marian J. Groot-Koerkamp, Lars P. van der Heide and Marten P. Smidt

    Version of Record online : 29 OCT 2012, DOI: 10.1111/ejn.12022

  7. You have free access to this content
    A functional analysis of KlSRB10: implications in Kluyveromyces lactis transcriptional regulation


    Volume 24, Issue 12, December 2007, Pages: 1061–1073, Laura Núñez, Isabel González-Siso, Esther Rodríguez-Belmonte, Pilar Soengas, Mónica Lamas-Maceiras and Maria Esperanza Cerdán

    Version of Record online : 17 SEP 2007, DOI: 10.1002/yea.1540

  8. Detection of maternal uniparental disomy at the two imprinted genes on chromosome 7, GRB10 and PEG1/MEST, in a Silver–Russell syndrome patient using methylation-specific PCR assays

    Clinical Genetics

    Volume 67, Issue 3, March 2005, Pages: 267–269,

    Version of Record online : 24 NOV 2004, DOI: 10.1111/j.1399-0004.2004.00387.x

  9. You have free access to this content
    A transcriptional autoregulatory loop for KIN28CCL1 and SRB10SRB11, each encoding RNA polymerase II CTD kinase–cyclin pair, stimulates the meiotic development of S. cerevisiae


    Volume 16, Issue 9, 30 June 2000, Pages: 829–846, Kentaro Ohkuni and Ichiro Yamashita

    Version of Record online : 7 JUN 2000, DOI: 10.1002/1097-0061(20000630)16:9<829::AID-YEA581>3.0.CO;2-6

  10. Congenital glaucoma and Silver-Russell phenotype associated with partial trisomy 7q and monosomy 15q

    American Journal of Medical Genetics

    Volume 104, Issue 4, 15 December 2001, Pages: 319–322, Rumiko Kato, Jun Kishibayashi, Osamu Shimokawa, Naoki Harada, Norio Niikawa and Naomichi Matsumoto

    Version of Record online : 27 NOV 2001, DOI: 10.1002/1096-8628(20011215)104:4<319::AID-AJMG10090>3.0.CO;2-1

  11. No evidence of submicroscopic deletion or segmental uniparental disomy within the candidate regions 7p11.2-p13 and 7q31-qter in a series of non-uniparental disomy Silver–Russell syndrome cases

    Clinical Genetics

    Volume 64, Issue 3, September 2003, Pages: 252–254, M. Riegel, A. Baumer and A. Schinzel

    Version of Record online : 12 AUG 2003, DOI: 10.1034/j.1399-0004.2003.00135.x

  12. You have free access to this content
    Essential role of the VirB machinery in the maturation of the Brucella abortus-containing vacuole

    Cellular Microbiology

    Volume 3, Issue 3, March 2001, Pages: 159–168, Diego J. Comerci, Maria José Martínez-Lorenzo, Rodrigo Sieira, Jean-Pierre Gorvel and Rodolfo A. Ugalde

    Version of Record online : 20 DEC 2001, DOI: 10.1046/j.1462-5822.2001.00102.x

  13. You have free access to this content
    A mono-allelic bivalent chromatin domain controls tissue-specific imprinting at Grb10

    The EMBO Journal

    Volume 27, Issue 19, October 8, 2008, Pages: 2523–2532, Lionel A Sanz, Stormy Chamberlain, Jean-Charles Sabourin, Amandine Henckel, Terry Magnuson, Jean-Philippe Hugnot, Robert Feil and Philippe Arnaud

    Version of Record online : 24 JUL 2008, DOI: 10.1038/emboj.2008.142

  14. No evidence of dup(7)(p11.2p13) in Silver-Russell syndrome

    American Journal of Medical Genetics

    Volume 99, Issue 4, 1 April 2001, Pages: 335–337, Maria-Jose Martinez, Franz Binkert, Albert Schinzel and Dieter Kotzot

    Version of Record online : 26 FEB 2001, DOI: 10.1002/1096-8628(2001)9999:9999<::AID-AJMG1177>3.0.CO;2-Q

  15. Segmental maternal uniparental disomy 7q associated with DLK1/GTL2 (14q32) hypomethylation

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 2, February 2012, Pages: 423–428, Matthias Begemann, Sabrina Spengler, Ulrike Kordaß, Carmen Schröder and Thomas Eggermann

    Version of Record online : 13 JAN 2012, DOI: 10.1002/ajmg.a.34412

  16. Is there a genomically imprinted social brain?


    Volume 33, Issue 9, September 2011, Pages: 662–668, James P. Curley

    Version of Record online : 1 AUG 2011, DOI: 10.1002/bies.201100060

  17. Review and hypothesis: Syndromes with severe intrauterine growth restriction and very short stature—Are they related to the epigenetic mechanism(s) of fetal survival involved in the developmental origins of adult health and disease?

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 2, February 2010, Pages: 512–527, Judith G. Hall

    Version of Record online : 25 JAN 2010, DOI: 10.1002/ajmg.a.33251

  18. Chromosome 7

    Standard Article


    Stephen W Scherer

    Published Online : 27 JAN 2006, DOI: 10.1038/npg.els.0005816

  19. You have free access to this content
    The KlSRB10 gene from Kluyveromyces lactis


    Volume 21, Issue 6, 30 April 2004, Pages: 511–518, Laura Núñez, Cristina Fernández-Otero, Esther Rodríguez-Belmonte and M. Esperanza Cerdán

    Version of Record online : 14 APR 2004, DOI: 10.1002/yea.1117

  20. Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver–Russell syndrome

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 10, October 2010, Pages: 2521–2528, Shin-Yu Lin, Chien-Nan Lee, Chia-Cheng Hung, Wen-Yu Tsai, Shuan-Pei Lin, Ni-Chung Li, Wu-Shiun Hsieh, Yi-Ching Tung, Dau-Ming Niu, Wen-Ming Hsu, Lang-Yao Chen, Mei-Ya Fang, Mei-Pin Tu, Pei-Wen Kuo, Chiou-Ya Lin, Yi-Ning Su and Hong-Nerng Ho

    Version of Record online : 9 SEP 2010, DOI: 10.1002/ajmg.a.33629