Literature DB >> 21614087

SOX2 and CHD7 cooperatively regulate human disease genes.

Janusz Puc, Michael G Rosenfeld.   

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Year:  2011        PMID： 21614087     DOI： 10.1038/ng.843

Source DB:  PubMed          Journal:  Nat Genet        ISSN： 1061-4036            Impact factor:   38.330


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  12 in total

1.  Mutations in a new member of the chromodomain gene family cause CHARGE syndrome.

Authors:  Lisenka E L M Vissers; Conny M A van Ravenswaaij; Ronald Admiraal; Jane A Hurst; Bert B A de Vries; Irene M Janssen; Walter A van der Vliet; Erik H L P G Huys; Pieter J de Jong; Ben C J Hamel; Eric F P M Schoenmakers; Han G Brunner; Joris A Veltman; Ad Geurts van Kessel
Journal:  Nat Genet       Date:  2004-08-08       Impact factor: 38.330

2.  SOX9 induces and maintains neural stem cells.

Authors:  Charlotte E Scott; Sarah L Wynn; Abdul Sesay; Catarina Cruz; Martin Cheung; Maria-Victoria Gomez Gaviro; Sarah Booth; Bo Gao; Kathryn S E Cheah; Robin Lovell-Badge; James Briscoe
Journal:  Nat Neurosci       Date:  2010-10       Impact factor: 24.884

3.  Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns.

Authors:  Michael P Schnetz; Cynthia F Bartels; Kuntal Shastri; Dheepa Balasubramanian; Gabriel E Zentner; Ravishankar Balaji; Xiaodong Zhang; Lingyun Song; Zhenghe Wang; Thomas Laframboise; Gregory E Crawford; Peter C Scacheri
Journal:  Genome Res       Date:  2009-02-27       Impact factor: 9.043

4.  SOX2 mutation causes anophthalmia, hearing loss, and brain anomalies.

Authors:  Stephanie A Hagstrom; Gayle J T Pauer; Janet Reid; Ellen Simpson; Sue Crowe; Irene H Maumenee; Elias I Traboulsi
Journal:  Am J Med Genet A       Date:  2005-10-01       Impact factor: 2.802

5.  CHD7 cooperates with PBAF to control multipotent neural crest formation.

Authors:  Ruchi Bajpai; Denise A Chen; Alvaro Rada-Iglesias; Junmei Zhang; Yiqin Xiong; Jill Helms; Ching-Pin Chang; Yingming Zhao; Tomek Swigut; Joanna Wysocka
Journal:  Nature       Date:  2010-02-03       Impact factor: 49.962

6.  CHD7 targets active gene enhancer elements to modulate ES cell-specific gene expression.

Authors:  Michael P Schnetz; Lusy Handoko; Batool Akhtar-Zaidi; Cynthia F Bartels; C Filipe Pereira; Amanda G Fisher; David J Adams; Paul Flicek; Gregory E Crawford; Thomas Laframboise; Paul Tesar; Chia-Lin Wei; Peter C Scacheri
Journal:  PLoS Genet       Date:  2010-07-15       Impact factor: 5.917

7.  Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes.

Authors:  Erik Engelen; Umut Akinci; Jan Christian Bryne; Jun Hou; Cristina Gontan; Maaike Moen; Dorota Szumska; Christel Kockx; Wilfred van Ijcken; Dick H W Dekkers; Jeroen Demmers; Erik-Jan Rijkers; Shoumo Bhattacharya; Sjaak Philipsen; Larysa H Pevny; Frank G Grosveld; Robbert J Rottier; Boris Lenhard; Raymond A Poot
Journal:  Nat Genet       Date:  2011-05-01       Impact factor: 38.330

8.  Mutations in SOX2 cause anophthalmia-esophageal-genital (AEG) syndrome.

Authors:  Kathleen A Williamson; Ann M Hever; Joe Rainger; R Curtis Rogers; Alex Magee; Zdenek Fiedler; Wee Teik Keng; Freddie H Sharkey; Niolette McGill; Clare J Hill; Adele Schneider; Mario Messina; Peter D Turnpenny; Judy A Fantes; Veronica van Heyningen; David R FitzPatrick
Journal:  Hum Mol Genet       Date:  2006-03-16       Impact factor: 6.150

9.  A gene mapping to the sex-determining region of the mouse Y chromosome is a member of a novel family of embryonically expressed genes.

Authors:  J Gubbay; J Collignon; P Koopman; B Capel; A Economou; A Münsterberg; N Vivian; P Goodfellow; R Lovell-Badge
Journal:  Nature       Date:  1990-07-19       Impact factor: 49.962

10.  Multipotent cell lineages in early mouse development depend on SOX2 function.

Authors:  Ariel A Avilion; Silvia K Nicolis; Larysa H Pevny; Lidia Perez; Nigel Vivian; Robin Lovell-Badge
Journal:  Genes Dev       Date:  2003-01-01       Impact factor: 11.361
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  7 in total

1.  New Genetic Insights into Congenital Heart Disease.

Authors:  Stephanie M Ware; John Lynn Jefferies
Journal:  J Clin Exp Cardiolog       Date:  2012-06-15

Review 2.  The multiple roles for Sox2 in stem cell maintenance and tumorigenesis.

Authors:  Kuancan Liu; Baoshun Lin; Meng Zhao; Xiangyue Yang; Min Chen; Anding Gao; Fei Liu; Jianwen Que; Xiaopeng Lan
Journal:  Cell Signal       Date:  2013-02-15       Impact factor: 4.315

Review 3.  Reproductive endocrine phenotypes relating to CHD7 mutations in humans.

Authors:  Ravikumar Balasubramanian; William F Crowley
Journal:  Am J Med Genet C Semin Med Genet       Date:  2017-11-20       Impact factor: 3.908

4.  Transcriptomic analysis of pluripotent stem cells: insights into health and disease.

Authors:  Jia-Chi Yeo; Huck-Hui Ng
Journal:  Genome Med       Date:  2011-10-27       Impact factor: 11.117

5.  CHD7 deficiency in "Looper", a new mouse model of CHARGE syndrome, results in ossicle malformation, otosclerosis and hearing impairment.

Authors:  Jacqueline M Ogier; Marina R Carpinelli; Benedicta D Arhatari; R C Andrew Symons; Benjamin T Kile; Rachel A Burt
Journal:  PLoS One       Date:  2014-05-19       Impact factor: 3.240

6.  Genotranscriptomic meta-analysis of the CHD family chromatin remodelers in human cancers - initial evidence of an oncogenic role for CHD7.

Authors:  Xiaofang Chu; Xuhui Guo; Yuanyuan Jiang; Huimei Yu; Lanxin Liu; Wenqi Shan; Zeng-Quan Yang
Journal:  Mol Oncol       Date:  2017-07-21       Impact factor: 6.603

7.  Sox2 acts as a rheostat of epithelial to mesenchymal transition during neural crest development.

Authors:  Nikolaos Mandalos; Muriel Rhinn; Zoraide Granchi; Ioannis Karampelas; Thimios Mitsiadis; Aris N Economides; Pascal Dollé; Eumorphia Remboutsika
Journal:  Front Physiol       Date:  2014-09-12       Impact factor: 4.566
  7 in total

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