Literature DB >> 16928355

Genetic defects of human brain development.

Jenny Carmichael1, Christopher Woods.   

Abstract

This review focuses on malformations of the central nervous system that have a genetic etiology. One can view each malformation as giving us unique details on a map entitled "how to make a human brain." The gene(s) that cause each malformation are being identified, allowing discovery of their specific role in neurodevelopment, and defining a "road" on the map. The malformation is then the developmental consequence of "taking a wrong turn." Assimilation of complementary data from other species with human malformation phenotype and genotype is revealing just how wonderful and complex the neurodevelopment map is. Here we highlight recent research on brain malformations and how this is illuminating the map of normal human brain formation.

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Mesh:

Year:  2006        PMID: 16928355     DOI: 10.1007/s11910-996-0026-7

Source DB:  PubMed          Journal:  Curr Neurol Neurosci Rep        ISSN: 1528-4042            Impact factor:   5.081


  50 in total

Review 1.  Vertebrate aristaless-related genes.

Authors:  F Meijlink; A Beverdam; A Brouwer; T C Oosterveen; D T Berge
Journal:  Int J Dev Biol       Date:  1999       Impact factor: 2.203

Review 2.  Modes of neuronal migration in the developing cerebral cortex.

Authors:  Bagirathy Nadarajah; John G Parnavelas
Journal:  Nat Rev Neurosci       Date:  2002-06       Impact factor: 34.870

3.  Filamin A-interacting protein (FILIP) regulates cortical cell migration out of the ventricular zone.

Authors:  Takashi Nagano; Takunari Yoneda; Yumiko Hatanaka; Chikara Kubota; Fujio Murakami; Makoto Sato
Journal:  Nat Cell Biol       Date:  2002-07       Impact factor: 28.824

4.  Ongoing adaptive evolution of ASPM, a brain size determinant in Homo sapiens.

Authors:  Nitzan Mekel-Bobrov; Sandra L Gilbert; Patrick D Evans; Eric J Vallender; Jeffrey R Anderson; Richard R Hudson; Sarah A Tishkoff; Bruce T Lahn
Journal:  Science       Date:  2005-09-09       Impact factor: 47.728

5.  Dual origin of the mammalian neocortex and evolution of the cortical plate.

Authors:  M Marin-Padilla
Journal:  Anat Embryol (Berl)       Date:  1978-02-20

6.  Mutations in Col4a1 cause perinatal cerebral hemorrhage and porencephaly.

Authors:  Douglas B Gould; F Campbell Phalan; Guido J Breedveld; Saskia E van Mil; Richard S Smith; John C Schimenti; Umberto Aguglia; Marjo S van der Knaap; Peter Heutink; Simon W M John
Journal:  Science       Date:  2005-05-20       Impact factor: 47.728

7.  Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.

Authors:  S E Hong; Y Y Shugart; D T Huang; S A Shahwan; P E Grant; J O Hourihane; N D Martin; C A Walsh
Journal:  Nat Genet       Date:  2000-09       Impact factor: 38.330

8.  Distinguishing the four genetic causes of Jouberts syndrome-related disorders.

Authors:  Enza Maria Valente; Sarah E Marsh; Marco Castori; Tracy Dixon-Salazar; Enrico Bertini; Lihadh Al-Gazali; Jean Messer; Clara Barbot; C Geoffrey Woods; Eugen Boltshauser; Asma A Al-Tawari; Carmelo D Salpietro; Hulya Kayserili; László Sztriha; Moez Gribaa; Michel Koenig; Bruno Dallapiccola; Joseph G Gleeson
Journal:  Ann Neurol       Date:  2005-04       Impact factor: 10.422

9.  Expression of a novel Ski-like gene in Xenopus development.

Authors:  Daniel W Seufert; Rashmi S Hegde; Srivamsi Nekkalapudi; Lisa E Kelly; Heithem M El-Hodiri
Journal:  Gene Expr Patterns       Date:  2005-10-05       Impact factor: 1.224

10.  AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders.

Authors:  Enza Maria Valente; Francesco Brancati; Jennifer L Silhavy; Marco Castori; Sarah E Marsh; Giuseppe Barrano; Enrico Bertini; Eugen Boltshauser; Maha S Zaki; Alice Abdel-Aleem; Ghada M H Abdel-Salam; Emanuele Bellacchio; Roberta Battini; Robert P Cruse; William B Dobyns; Kalpathy S Krishnamoorthy; Clotilde Lagier-Tourenne; Alex Magee; Ignacio Pascual-Castroviejo; Carmelo D Salpietro; Dean Sarco; Bruno Dallapiccola; Joseph G Gleeson
Journal:  Ann Neurol       Date:  2006-03       Impact factor: 10.422

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