Literature DB >> 11598956

Midline and laterality defects: left and right meet in the middle.

E Roessler1, M Muenke.   

Abstract

The aim of this review is to summarize some of the recent advances in molecular embryology that help to explain the pathogenesis of holoprosencephaly (HPE), or its related malformation in model organisms, cyclopia, and laterality defects in humans, derived from detailed analysis of similar malformations in animal models. Recently, defects in several developmental pathways including those operated by the Sonic hedgehog and Nodal signaling factors have been implicated as causes of HPE or laterality defects in humans. Here we summarize the findings in animal models that indicate that both defects can be explained by mechanisms that relate to the proper development of the axial midline in vertebrates. Published 2001 John Wiley & Sons, Inc.

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Year:  2001        PMID: 11598956     DOI: 10.1002/bies.1130

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  13 in total

1.  BMP antagonism protects Nodal signaling in the gastrula to promote the tissue interactions underlying mammalian forebrain and craniofacial patterning.

Authors:  Yu-Ping Yang; Ryan M Anderson; John Klingensmith
Journal:  Hum Mol Genet       Date:  2010-05-27       Impact factor: 6.150

2.  Six3 represses nodal activity to establish early brain asymmetry in zebrafish.

Authors:  Adi Inbal; Seok-Hyung Kim; Jimann Shin; Lilianna Solnica-Krezel
Journal:  Neuron       Date:  2007-08-02       Impact factor: 17.173

Review 3.  From cytoskeletal dynamics to organ asymmetry: a nonlinear, regulative pathway underlies left-right patterning.

Authors:  Gary McDowell; Suvithan Rajadurai; Michael Levin
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2016-12-19       Impact factor: 6.237

4.  Cerberus-Nodal-Lefty-Pitx signaling cascade controls left-right asymmetry in amphioxus.

Authors:  Guang Li; Xian Liu; Chaofan Xing; Huayang Zhang; Sebastian M Shimeld; Yiquan Wang
Journal:  Proc Natl Acad Sci U S A       Date:  2017-03-20       Impact factor: 11.205

5.  Embryonic fibroblasts from mice lacking Tgif were defective in cell cycling.

Authors:  Lynn Mar; Pamela A Hoodless
Journal:  Mol Cell Biol       Date:  2006-06       Impact factor: 4.272

6.  The full spectrum of holoprosencephaly-associated mutations within the ZIC2 gene in humans predicts loss-of-function as the predominant disease mechanism.

Authors:  Erich Roessler; Felicitas Lacbawan; Christèle Dubourg; Aimee Paulussen; Jos Herbergs; Ute Hehr; Claude Bendavid; Nan Zhou; Maia Ouspenskaia; Sherri Bale; Sylvie Odent; Vèronique David; Maximilian Muenke
Journal:  Hum Mutat       Date:  2009-04       Impact factor: 4.878

7.  The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis.

Authors:  Erich Roessler; Kenia B El-Jaick; Christèle Dubourg; Jorge I Vélez; Benjamin D Solomon; Daniel E Pineda-Alvarez; Felicitas Lacbawan; Nan Zhou; Maia Ouspenskaia; Aimée Paulussen; Hubert J Smeets; Ute Hehr; Claude Bendavid; Sherri Bale; Sylvie Odent; Véronique David; Maximilian Muenke
Journal:  Hum Mutat       Date:  2009-10       Impact factor: 4.878

8.  Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly.

Authors:  Erich Roessler; Maia V Ouspenskaia; Jayaprakash D Karkera; Jorge I Vélez; Amy Kantipong; Felicitas Lacbawan; Peter Bowers; John W Belmont; Jeffrey A Towbin; Elizabeth Goldmuntz; Benjamin Feldman; Maximilian Muenke
Journal:  Am J Hum Genet       Date:  2008-06-05       Impact factor: 11.025

9.  A protein disulfide isomerase expressed in the embryonic midline is required for left/right asymmetries.

Authors:  Kazuyuki Hoshijima; James E Metherall; David Jonah Grunwald
Journal:  Genes Dev       Date:  2002-10-01       Impact factor: 11.361

10.  Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.

Authors:  Erich Roessler; Yang-Zhu Du; Jose L Mullor; Esther Casas; William P Allen; Gabriele Gillessen-Kaesbach; Elizabeth R Roeder; Jeffrey E Ming; Ariel Ruiz i Altaba; Maximilian Muenke
Journal:  Proc Natl Acad Sci U S A       Date:  2003-10-27       Impact factor: 11.205

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