Literature DB >> 19778712

Model organisms inform the search for the genes and developmental pathology underlying malformations of the human hindbrain.

Kimberly A Aldinger1, Gina E Elsen, Victoria E Prince, Kathleen J Millen.   

Abstract

Congenital malformations of the human hindbrain, including the cerebellum, are poorly understood largely because their recognition is a relatively recent advance for imaging diagnostics. Cerebellar malformations are the most obvious and best characterized hindbrain malformations due to their relative ease of viewing by magnetic resonance imaging and the recent identification of several causative genes (Millen et al. Curr Opin Neurobiol 18:12-19, 2008). Malformations of the pons and medulla have also been described both in isolation and in association with cerebellar malformations (Barkovich et al. Ann Neurol 62:625-639, 2007). Although little is understood regarding the specific developmental pathologies underlying hindbrain malformations in humans, much is known regarding the mechanisms and genes driving hindbrain development in vertebrate model organisms. Thus, studies in vertebrate models provide a developmental framework in which to categorize human hindbrain malformations and serve to provide information regarding disrupted developmental processes and candidate genes. Here, we survey the basic principles of vertebrate hindbrain development and integrate our current knowledge of human hindbrain malformations into this framework.

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Year:  2009        PMID: 19778712      PMCID: PMC2778478          DOI: 10.1016/j.spen.2009.06.003

Source DB:  PubMed          Journal:  Semin Pediatr Neurol        ISSN: 1071-9091            Impact factor:   1.636


  84 in total

1.  Eph receptors and ephrins restrict cell intermingling and communication.

Authors:  G Mellitzer; Q Xu; D G Wilkinson
Journal:  Nature       Date:  1999-07-01       Impact factor: 49.962

Review 2.  Congenital disorders of glycosylation (CDG): a rapidly expanding group of neurometabolic disorders.

Authors:  S Grünewald; G Matthijs
Journal:  Neuropediatrics       Date:  2000-04       Impact factor: 1.947

Review 3.  From hindbrain segmentation to breathing after birth: developmental patterning in rhombomeres 3 and 4.

Authors:  Fabrice Chatonnet; Eduardo Domínguez del Toro; Muriel Thoby-Brisson; Jean Champagnat; Gilles Fortin; Filippo M Rijli; Christelle Thaëron-Antôno
Journal:  Mol Neurobiol       Date:  2003-12       Impact factor: 5.590

Review 4.  Molecular mechanisms of axon guidance in the developing corticospinal tract.

Authors:  A J Canty; M Murphy
Journal:  Prog Neurobiol       Date:  2008-02-15       Impact factor: 11.685

5.  Organization of hindbrain segments in the zebrafish embryo.

Authors:  B Trevarrow; D L Marks; C B Kimmel
Journal:  Neuron       Date:  1990-05       Impact factor: 17.173

6.  The mouse Dreher gene Lmx1a controls formation of the roof plate in the vertebrate CNS.

Authors:  J H Millonig; K J Millen; M E Hatten
Journal:  Nature       Date:  2000-02-17       Impact factor: 49.962

7.  Analysis and classification of cerebellar malformations.

Authors:  Sandeep Patel; A James Barkovich
Journal:  AJNR Am J Neuroradiol       Date:  2002-08       Impact factor: 3.825

8.  NSCL-1 and -2 control the formation of precerebellar nuclei by orchestrating the migration of neuronal precursor cells.

Authors:  Thomas Schmid; Marcus Krüger; Thomas Braun
Journal:  J Neurochem       Date:  2007-06-15       Impact factor: 5.372

9.  Roles of retinoic acid receptors in early embryonic morphogenesis and hindbrain patterning.

Authors:  O Wendling; N B Ghyselinck; P Chambon; M Mark
Journal:  Development       Date:  2001-06       Impact factor: 6.868

10.  Large recurrent microdeletions associated with schizophrenia.

Authors:  Hreinn Stefansson; Dan Rujescu; Sven Cichon; Olli P H Pietiläinen; Andres Ingason; Stacy Steinberg; Ragnheidur Fossdal; Engilbert Sigurdsson; Thordur Sigmundsson; Jacobine E Buizer-Voskamp; Thomas Hansen; Klaus D Jakobsen; Pierandrea Muglia; Clyde Francks; Paul M Matthews; Arnaldur Gylfason; Bjarni V Halldorsson; Daniel Gudbjartsson; Thorgeir E Thorgeirsson; Asgeir Sigurdsson; Adalbjorg Jonasdottir; Aslaug Jonasdottir; Asgeir Bjornsson; Sigurborg Mattiasdottir; Thorarinn Blondal; Magnus Haraldsson; Brynja B Magnusdottir; Ina Giegling; Hans-Jürgen Möller; Annette Hartmann; Kevin V Shianna; Dongliang Ge; Anna C Need; Caroline Crombie; Gillian Fraser; Nicholas Walker; Jouko Lonnqvist; Jaana Suvisaari; Annamarie Tuulio-Henriksson; Tiina Paunio; Timi Toulopoulou; Elvira Bramon; Marta Di Forti; Robin Murray; Mirella Ruggeri; Evangelos Vassos; Sarah Tosato; Muriel Walshe; Tao Li; Catalina Vasilescu; Thomas W Mühleisen; August G Wang; Henrik Ullum; Srdjan Djurovic; Ingrid Melle; Jes Olesen; Lambertus A Kiemeney; Barbara Franke; Chiara Sabatti; Nelson B Freimer; Jeffrey R Gulcher; Unnur Thorsteinsdottir; Augustine Kong; Ole A Andreassen; Roel A Ophoff; Alexander Georgi; Marcella Rietschel; Thomas Werge; Hannes Petursson; David B Goldstein; Markus M Nöthen; Leena Peltonen; David A Collier; David St Clair; Kari Stefansson
Journal:  Nature       Date:  2008-09-11       Impact factor: 49.962

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  4 in total

Review 1.  Novel approaches to studying the genetic basis of cerebellar development.

Authors:  Samin A Sajan; Kathryn E Waimey; Kathleen J Millen
Journal:  Cerebellum       Date:  2010-09       Impact factor: 3.847

2.  The cerebellum in children with spina bifida and Chiari II malformation: Quantitative volumetrics by region.

Authors:  Jenifer Juranek; Maureen Dennis; Paul T Cirino; Lyla El-Messidi; Jack M Fletcher
Journal:  Cerebellum       Date:  2010-06       Impact factor: 3.847

Review 3.  Anomalous development of brain structure and function in spina bifida myelomeningocele.

Authors:  Jenifer Juranek; Michael S Salman
Journal:  Dev Disabil Res Rev       Date:  2010

4.  A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hair.

Authors:  Karen W Gripp; Kimberly A Aldinger; James T Bennett; Laura Baker; Jessica Tusi; Nina Powell-Hamilton; Deborah Stabley; Katia Sol-Church; Andrew E Timms; William B Dobyns
Journal:  Am J Med Genet A       Date:  2016-06-05       Impact factor: 2.802

  4 in total

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