Literature DB >> 22644616

RUNX1T1, a chromatin repression protein, is a candidate gene for autosomal dominant intellectual disability.

Minh Tuan Huynh1, Mylène Béri-Dexheimer, Céline Bonnet, Myriam Bronner, Asma Ali Khan, Lila Allou, Christophe Philippe, Jacqueline Vigneron, Philippe Jonveaux.   

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Year:  2012        PMID： 22644616     DOI： 10.1002/ajmg.a.35386

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  3 in total

1.  A familial chromosomal complex rearrangement confirms RUNX1T1 as a causative gene for intellectual disability and suggests that 1p22.1p21.3 duplication is likely benign.

Authors:  Fabrizia Restaldi; Viola Alesi; Angela Aquilani; Silvia Genovese; Serena Russo; Valentina Coletti; Daniele Pompili; Roberto Falasca; Bruno Dallapiccola; Rossella Capolino; Matteo Luciani; Antonio Novelli
Journal:  Mol Cytogenet       Date:  2019-06-14       Impact factor: 2.009

Review 2.  RUNX1T1 function in cell fate.

Authors:  Nan Hu; Linqing Zou; Cheng Wang; Guoqi Song
Journal:  Stem Cell Res Ther       Date:  2022-07-28       Impact factor: 8.079

3.  MTG8 interacts with LHX6 to specify cortical interneuron subtype identity.

Authors:  Zeinab Asgarian; Marcio Guiomar Oliveira; Agata Stryjewska; Ioannis Maragkos; Anna Noren Rubin; Lorenza Magno; Vassilis Pachnis; Mohammadmersad Ghorbani; Scott Wayne Hiebert; Myrto Denaxa; Nicoletta Kessaris
Journal:  Nat Commun       Date:  2022-09-05       Impact factor: 17.694
  3 in total

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