Literature DB >> 27383655

A commentary on de novo MEIS2 mutation causes syndromic developmental delay with persistent gastro-esophageal reflux.

Rie Takai1, Tohru Ohta1.   

Abstract

Entities:  

Mesh:

Substances:

Year:  2016        PMID: 27383655     DOI: 10.1038/jhg.2016.81

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


× No keyword cloud information.
  12 in total

1.  Further evidence for the possible role of MEIS2 in the development of cleft palate and cardiac septum.

Authors:  Moira A Crowley; Laura K Conlin; Elaine H Zackai; Matthew A Deardorff; Brian D Thiel; Nancy B Spinner
Journal:  Am J Med Genet A       Date:  2010-05       Impact factor: 2.802

2.  Spatiotemporal distribution of PAX6 and MEIS2 expression and total cell numbers in the ganglionic eminence in the early developing human forebrain.

Authors:  Karen B Larsen; Melissa C Lutterodt; Henning Laursen; Niels Graem; Bente Pakkenberg; Kjeld Møllgård; Morten Møller
Journal:  Dev Neurosci       Date:  2010-06-03       Impact factor: 2.984

3.  Haploinsufficiency of MEIS2 is associated with orofacial clefting and learning disability.

Authors:  Stefan Johansson; Siren Berland; Gyri Aasland Gradek; Ernie Bongers; Nicole de Leeuw; Rolph Pfundt; Madeleine Fannemel; Olaug Rødningen; Atle Brendehaug; Bjørn Ivar Haukanes; Randi Hovland; Gunnar Helland; Gunnar Houge
Journal:  Am J Med Genet A       Date:  2014-03-26       Impact factor: 2.802

4.  MEIS2 involvement in cardiac development, cleft palate, and intellectual disability.

Authors:  Jacoba J Louw; Anniek Corveleyn; Yaojuan Jia; Greet Hens; Marc Gewillig; Koenraad Devriendt
Journal:  Am J Med Genet A       Date:  2015-02-25       Impact factor: 2.802

5.  Identification of a new family of Pbx-related homeobox genes.

Authors:  T Nakamura; N A Jenkins; N G Copeland
Journal:  Oncogene       Date:  1996-11-21       Impact factor: 9.867

Review 6.  To Be Specific or Not: The Critical Relationship Between Hox And TALE Proteins.

Authors:  Samir Merabet; Richard S Mann
Journal:  Trends Genet       Date:  2016-04-08       Impact factor: 11.639

Review 7.  De novo MEIS2 mutation causes syndromic developmental delay with persistent gastro-esophageal reflux.

Authors:  Atsushi Fujita; Bertrand Isidor; Hugues Piloquet; Pierre Corre; Nobuhiko Okamoto; Mitsuko Nakashima; Yoshinori Tsurusaki; Hirotomo Saitsu; Noriko Miyake; Naomichi Matsumoto
Journal:  J Hum Genet       Date:  2016-05-26       Impact factor: 3.172

8.  Classification and nomenclature of all human homeobox genes.

Authors:  Peter W H Holland; H Anne F Booth; Elspeth A Bruford
Journal:  BMC Biol       Date:  2007-10-26       Impact factor: 7.431

Review 9.  Role of central vagal 5-HT3 receptors in gastrointestinal physiology and pathophysiology.

Authors:  Kirsteen N Browning
Journal:  Front Neurosci       Date:  2015-10-29       Impact factor: 4.677

10.  Meis2 is essential for cranial and cardiac neural crest development.

Authors:  Ondrej Machon; Jan Masek; Olga Machonova; Stefan Krauss; Zbynek Kozmik
Journal:  BMC Dev Biol       Date:  2015-11-06       Impact factor: 1.978

View more
  1 in total

1.  Identification of novel candidate disease genes from de novo exonic copy number variants.

Authors:  Tomasz Gambin; Bo Yuan; Weimin Bi; Pengfei Liu; Jill A Rosenfeld; Zeynep Coban-Akdemir; Amber N Pursley; Sandesh C S Nagamani; Ronit Marom; Sailaja Golla; Lauren Dengle; Heather G Petrie; Reuben Matalon; Lisa Emrick; Monica B Proud; Diane Treadwell-Deering; Hsiao-Tuan Chao; Hannele Koillinen; Chester Brown; Nora Urraca; Roya Mostafavi; Saunder Bernes; Elizabeth R Roeder; Kimberly M Nugent; Patricia I Bader; Gary Bellus; Michael Cummings; Hope Northrup; Myla Ashfaq; Rachel Westman; Robert Wildin; Anita E Beck; LaDonna Immken; Lindsay Elton; Shaun Varghese; Edward Buchanan; Laurence Faivre; Mathilde Lefebvre; Christian P Schaaf; Magdalena Walkiewicz; Yaping Yang; Sung-Hae L Kang; Seema R Lalani; Carlos A Bacino; Arthur L Beaudet; Amy M Breman; Janice L Smith; Sau Wai Cheung; James R Lupski; Ankita Patel; Chad A Shaw; Paweł Stankiewicz
Journal:  Genome Med       Date:  2017-09-21       Impact factor: 11.117

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.