Literature DB >> 10995782

The two-domain hypothesis in Beckwith-Wiedemann syndrome.

A P Feinberg.   

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Year:  2000        PMID： 10995782      PMCID： PMC381397          DOI： 10.1172/JCI10911

Source DB:  PubMed          Journal:  J Clin Invest        ISSN： 0021-9738            Impact factor:   14.808


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  6 in total

1.  LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids.

Authors:  K Mitsuya; M Meguro; M P Lee; M Katoh; T C Schulz; H Kugoh; M A Yoshida; N Niikawa; A P Feinberg; M Oshimura
Journal:  Hum Mol Genet       Date:  1999-07       Impact factor: 6.150

Review 2.  Beckwith-Wiedemann syndrome: imprinting in clusters revisited.

Authors:  E R Maher; W Reik
Journal:  J Clin Invest       Date:  2000-02       Impact factor: 14.808

3.  Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting.

Authors:  M P Lee; M R DeBaun; K Mitsuya; H L Galonek; S Brandenburg; M Oshimura; A P Feinberg
Journal:  Proc Natl Acad Sci U S A       Date:  1999-04-27       Impact factor: 11.205

4.  Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation.

Authors:  W W Lam; I Hatada; S Ohishi; T Mukai; J A Joyce; T R Cole; D Donnai; W Reik; P N Schofield; E R Maher
Journal:  J Med Genet       Date:  1999-07       Impact factor: 6.318

5.  Relaxation of imprinted genes in human cancer.

Authors:  S Rainier; L A Johnson; C J Dobry; A J Ping; P E Grundy; A P Feinberg
Journal:  Nature       Date:  1993-04-22       Impact factor: 49.962

6.  Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5.

Authors:  M P Lee; C Reeves; A Schmitt; K Su; T D Connors; R J Hu; S Brandenburg; M J Lee; G Miller; A P Feinberg
Journal:  Cancer Res       Date:  1998-09-15       Impact factor: 12.701
  6 in total
  9 in total

1.  Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control region.

Authors:  Hitomi Yatsuki; Keiichiro Joh; Ken Higashimoto; Hidenobu Soejima; Yuji Arai; Youdong Wang; Izuho Hatada; Yayoi Obata; Hiroko Morisaki; Zhongming Zhang; Tetsuji Nakagawachi; Yuji Satoh; Tsunehiro Mukai
Journal:  Genome Res       Date:  2002-12       Impact factor: 9.043

2.  Autonomous silencing of the imprinted Cdkn1c gene in stem cells.

Authors:  Michelle D Wood; Hitoshi Hiura; Simon J Tunster; Takahiro Arima; Jong-Yeon Shin; Michael J Higgins; Rosalind M John
Journal:  Epigenetics       Date:  2010-04-01       Impact factor: 4.528

3.  Addition of H19 'loss of methylation testing' for Beckwith-Wiedemann syndrome (BWS) increases the diagnostic yield.

Authors:  Jochen K Lennerz; Robert J Timmerman; Dorothy K Grange; Michael R DeBaun; Andrew P Feinberg; Barbara A Zehnbauer
Journal:  J Mol Diagn       Date:  2010-07-08       Impact factor: 5.568

4.  Biallelic expression of HRAS and MUCDHL in human and mouse.

Authors:  Michael Goldberg; Michelle Wei; Luwa Yuan; Vundavalli V Murty; Benjamin Tycko
Journal:  Hum Genet       Date:  2003-02-14       Impact factor: 4.132

5.  E Proteins and Id2 converge on p57Kip2 to regulate cell cycle in neural cells.

Authors:  Gerson Rothschild; Xudong Zhao; Antonio Iavarone; Anna Lasorella
Journal:  Mol Cell Biol       Date:  2006-06       Impact factor: 4.272

6.  Induction of p57(KIP2) expression by p73beta.

Authors:  Eva Balint; Andrew C Phillips; Serguei Kozlov; Colin L Stewart; Karen H Vousden
Journal:  Proc Natl Acad Sci U S A       Date:  2002-03-12       Impact factor: 11.205

7.  Fetal overgrowth in the Cdkn1c mouse model of Beckwith-Wiedemann syndrome.

Authors:  Simon J Tunster; Mathew Van de Pette; Rosalind M John
Journal:  Dis Model Mech       Date:  2011-07-04       Impact factor: 5.758

8.  Genetic and epigenetic alterations on the short arm of chromosome 11 are involved in a majority of sporadic Wilms' tumours.

Authors:  Y Satoh; H Nakadate; T Nakagawachi; K Higashimoto; K Joh; Z Masaki; J Uozumi; Y Kaneko; T Mukai; H Soejima
Journal:  Br J Cancer       Date:  2006-08-08       Impact factor: 7.640

9.  Cdkn1c (p57Kip2) is the major regulator of embryonic growth within its imprinted domain on mouse distal chromosome 7.

Authors:  Stuart C Andrews; Michelle D Wood; Simon J Tunster; Sheila C Barton; M Azim Surani; Rosalind M John
Journal:  BMC Dev Biol       Date:  2007-05-21       Impact factor: 1.978
  9 in total

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