Literature DB >> 10603005

The molecular genetics of holoprosencephaly: a model of brain development for the next century.

E Roessler1, M Muenke.   

Abstract

The recent identification of some of the human holoprosencephaly genes is beginning to elucidate the intricate developmental programs that pattern normal and abnormal brain development. Here we present some of these advances in the context of our present understanding and conclude with some speculations regarding the direction for future investigations. We are living in a tremendously exciting time in medicine with the rapid application of molecular genetic approaches to the understanding of human disease. It is the purpose of this review to stress the underlying principals of our approach at a level that can be readily appreciated by colleagues who themselves are experts in brain anatomy but not necessarily the molecular genetics of brain development.

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Year:  1999        PMID: 10603005     DOI: 10.1007/s003810050453

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  3 in total

1.  Midline "brain in brain": an unusual variant of holoprosencephaly with anterior prosomeric cortical dysplasia.

Authors:  E Widjaja; L Massimi; S Blaser; C Di Rocco; C Raybaud
Journal:  Childs Nerv Syst       Date:  2006-11-11       Impact factor: 1.475

2.  Temporal perturbations in sonic hedgehog signaling elicit the spectrum of holoprosencephaly phenotypes.

Authors:  Dwight Cordero; Ralph Marcucio; Diane Hu; William Gaffield; Minal Tapadia; Jill A Helms
Journal:  J Clin Invest       Date:  2004-08       Impact factor: 14.808

Review 3.  Facial Morphogenesis: Physical and Molecular Interactions Between the Brain and the Face.

Authors:  Ralph Marcucio; Benedikt Hallgrimsson; Nathan M Young
Journal:  Curr Top Dev Biol       Date:  2015-10-19       Impact factor: 4.897

  3 in total

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