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There are 12595 results for: content related to: Increased incidence of aberrant DNA methylation within diverse imprinted gene loci outside of IGF2 / H19 in Silver–Russell syndrome

  1. You have free access to this content
    Loss of imprinting and marked gene elevation are 2 forms of aberrant IGF2 expression in colorectal cancer

    International Journal of Cancer

    Volume 127, Issue 3, 1 August 2010, Pages: 568–577, Yu-Wei Cheng, Kamran Idrees, Richard Shattock, Sajid A. Khan, Zhaoshi Zeng, Cameron W. Brennan, Philip Paty and Francis Barany

    Version of Record online : 2 DEC 2009, DOI: 10.1002/ijc.25086

  2. Complex Tissue-Specific Epigenotypes in Russell–Silver Syndrome Associated with 11p15 ICR1 Hypomethylation

    Human Mutation

    Volume 35, Issue 10, October 2014, Pages: 1211–1220, Salah Azzi, Annick Blaise, Virginie Steunou, Madeleine D. Harbison, Jennifer Salem, Frédéric Brioude, Sylvie Rossignol, Walid Abi Habib, Nathalie Thibaud, Cristina Das Neves, Marilyne Le Jule, Cécile Brachet, Claudine Heinrichs, Yves Le Bouc and Irène Netchine

    Version of Record online : 22 AUG 2014, DOI: 10.1002/humu.22623

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    Correction of aberrant imprinting of IGF2 in human tumors by nuclear transfer-induced epigenetic reprogramming

    The EMBO Journal

    Volume 25, Issue 22, November 15, 2006, Pages: 5329–5338, Hui Ling Chen, Tao Li, Xin Wen Qiu, Jie Wu, Jian Qun Ling, Zhi Hong Sun, Weibo Wang, Wei Chen, Aiju Hou, Thanh H Vu, Andrew R Hoffman and Ji-Fan Hu

    Version of Record online : 2 NOV 2006, DOI: 10.1038/sj.emboj.7601399

  4. Epigenetic regulation of Igf2/H19 imprinting at CTCF insulator binding sites

    Journal of Cellular Biochemistry

    Volume 90, Issue 5, 1 December 2003, Pages: 1038–1055, Youwen Yang, Ji-Fan Hu, Gary A. Ulaner, Tao Li, Xiaoming Yao, Thanh H. Vu and Andrew R. Hoffman

    Version of Record online : 30 OCT 2003, DOI: 10.1002/jcb.10684

  5. Hepatocellular carcinomas of the albumin SV40 T-antigen transgenic rat display fetal-like re-expression of Igf2 and deregulation of H19

    Molecular Carcinogenesis

    Volume 46, Issue 9, September 2007, Pages: 747–757, Matthew J. Czarny, Karlee Babcock, Rebecca M. Baus, Herbert Manoharan and Henry C. Pitot

    Version of Record online : 28 MAR 2007, DOI: 10.1002/mc.20286

  6. Beckwith–Wiedemann and Silver–Russell syndromes: opposite developmental imbalances in imprinted regulators of placental function and embryonic growth

    Clinical Genetics

    Volume 84, Issue 4, October 2013, Pages: 326–334, KJ Jacob, WP Robinson and L Lefebvre

    Version of Record online : 9 APR 2013, DOI: 10.1111/cge.12143

  7. You have full text access to this OnlineOpen article
    Igf2 pathway dependency of the Trp53 developmental and tumour phenotypes

    EMBO Molecular Medicine

    Volume 4, Issue 8, August 2012, Pages: 705–718, Victoria L. Haley, David J. Barnes, Ionel Sandovici, Miguel Constancia, Christopher F. Graham, Francesco Pezzella, Claudia Bühnemann, Emma J. Carter and A. Bassim Hassan

    Version of Record online : 6 JUN 2012, DOI: 10.1002/emmm.201101105

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    H19 sense and antisense transgenes modify insulin-like growth factor-II mRNA levels

    European Journal of Biochemistry

    Volume 267, Issue 13, July 2000, Pages: 4020–4027, Françoise Wilkin, Jean Paquette, Elisabeth Ledru, Catherine Mamelin, Michael Pollak and Cheri L. Deal

    Version of Record online : 25 DEC 2001, DOI: 10.1046/j.1432-1327.2000.01438.x

  9. Insulin-like growth factor-2 (IGF2) loss of imprinting marks a field defect within human prostates containing cancer

    The Prostate

    Volume 71, Issue 15, November 2011, Pages: 1621–1630, Sachin Bhusari, Bing Yang, Jessica Kueck, Wei Huang and David F. Jarrard

    Version of Record online : 22 MAR 2011, DOI: 10.1002/pros.21379

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    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

  11. Genome-wide analysis of allelic imbalances reveals 4q deletions as a poor prognostic factor and MDM4 amplification at 1q32.1 in hepatoblastoma

    Genes, Chromosomes and Cancer

    Volume 49, Issue 7, July 2010, Pages: 596–609, Yasuhito Arai, Shohei Honda, Masayuki Haruta, Fumio Kasai, Yuiko Fujiwara, Junjiro Ohshima, Fumiaki Sasaki, Akira Nakagawara, Hiroshi Horie, Hiroyuki Yamaoka, Eiso Hiyama and Yasuhiko Kaneko

    Version of Record online : 13 APR 2010, DOI: 10.1002/gcc.20770

  12. Pancreatic impairment and Igf2 hypermethylation induced by developmental exposure to bisphenol A can be counteracted by maternal folate supplementation

    Journal of Applied Toxicology

    Volume 37, Issue 7, July 2017, Pages: 825–835, Zhenxing Mao, Wei Xia, Wenqian Huo, Tongzhang Zheng, Bryan A. Bassig, Huailong Chang, Tian Chen, Feie Li, Yunxin Pan, Yang Peng, Yuanyuan Li and Shunqing Xu

    Version of Record online : 6 FEB 2017, DOI: 10.1002/jat.3430

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    Lipid A and O-chain modifications cause Rhizobium lipopolysaccharides to become hydrophobic during bacteroid development

    Molecular Microbiology

    Volume 39, Issue 2, January 2001, Pages: 379–392, Elmar L. Kannenberg and Russell W. Carlson

    Version of Record online : 21 DEC 2001, DOI: 10.1046/j.1365-2958.2001.02225.x

  14. De novo IGF2 mutation on the paternal allele in a patient with Silver–Russell syndrome and ectrodactyly

    Human Mutation

    Volume 38, Issue 8, August 2017, Pages: 953–958, Kaori Yamoto, Hirotomo Saitsu, Norio Nakagawa, Hisakazu Nakajima, Tatsuji Hasegawa, Yasuko Fujisawa, Masayo Kagami, Maki Fukami and Tsutomu Ogata

    Version of Record online : 29 MAY 2017, DOI: 10.1002/humu.23253

  15. Blood as a surrogate marker for tissue-specific DNA methylation and changes due to folate depletion in post-partum female mice

    Molecular Nutrition & Food Research

    Volume 55, Issue 7, July 2011, Pages: 1026–1035, Jill A. McKay, Long Xie, Sarah Harris, Yi K. Wong, Dianne Ford and John C. Mathers

    Version of Record online : 24 MAR 2011, DOI: 10.1002/mnfr.201100008

  16. Duplication of paternal IGF2 or loss of maternal IGF2 imprinting occurs in half of Wilms tumors with various structural WT1 abnormalities

    Genes, Chromosomes and Cancer

    Volume 47, Issue 8, August 2008, Pages: 712–727, Masayuki Haruta, Yasuhito Arai, Waka Sugawara, Naoki Watanabe, Shohei Honda, Junjiro Ohshima, Hidenobu Soejima, Hisaya Nakadate, Hajime Okita, Jun-ichi Hata, Masahiro Fukuzawa and Yasuhiko Kaneko

    Version of Record online : 7 MAY 2008, DOI: 10.1002/gcc.20572

  17. Molecular dissection of structure and function in the lipopolysaccharide of Rhizobium leguminosarum strain 3841 using monoclonal antibodies and genetic analysis

    Molecular Microbiology

    Volume 6, Issue 17, September 1992, Pages: 2477–2487, E. L. Kannenberg, E. A. Rathbun and N. J. Brewin

    Version of Record online : 27 OCT 2006, DOI: 10.1111/j.1365-2958.1992.tb01424.x

  18. DNA methylation patterns at the IGF2-H19 locus in sperm of Swiss Landrace and Swiss Large White boars

    Journal of Animal Breeding and Genetics

    Volume 126, Issue 6, December 2009, Pages: 475–479, Petra Giannini and Martin Braunschweig

    Version of Record online : 30 JUN 2009, DOI: 10.1111/j.1439-0388.2009.00802.x

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    High frequency of inactivation of the imprinted H19 gene in “sporadic” hepatoblastoma

    International Journal of Cancer

    Volume 82, Issue 4, 12 August 1999, Pages: 490–497, Ryuji Fukuzawa, Akihiro Umezawa, Kensuke Ochi, Fumihiko Urano, Hitoshi Ikeda and Jun-ichi Hata

    Version of Record online : 10 NOV 1999, DOI: 10.1002/(SICI)1097-0215(19990812)82:4<490::AID-IJC4>3.0.CO;2-I

  20. Expression of delta-like 1 homologue and insulin-like growth factor 2 through epigenetic regulation of the genes during development of mouse molar

    European Journal of Oral Sciences

    Volume 120, Issue 4, August 2012, Pages: 292–302, Qalb-E-Saleem Khan, Amer Sehic, Natalie Skalleberg, Maria A. Landin, Cuong Khuu, Steinar Risnes and Harald Osmundsen

    Version of Record online : 19 JUL 2012, DOI: 10.1111/j.1600-0722.2012.00976.x