Literature DB >> 19471300

Diversifying microtubules in brain development.

Andrew P Jackson.   

Abstract

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Year:  2009        PMID： 19471300     DOI： 10.1038/ng0609-638

Source DB:  PubMed          Journal:  Nat Genet        ISSN： 1061-4036            Impact factor:   38.330


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  14 in total

1.  SRPX2 mutations in disorders of language cortex and cognition.

Authors:  Patrice Roll; Gabrielle Rudolf; Sandrine Pereira; Barbara Royer; Ingrid E Scheffer; Annick Massacrier; Maria-Paola Valenti; Nathalie Roeckel-Trevisiol; Sarah Jamali; Christophe Beclin; Caroline Seegmuller; Marie-Noëlle Metz-Lutz; Arnaud Lemainque; Marc Delepine; Christophe Caloustian; Anne de Saint Martin; Nadine Bruneau; Danièle Depétris; Marie-Geneviève Mattéi; Elisabeth Flori; Andrée Robaglia-Schlupp; Nicolas Lévy; Bernd A Neubauer; Rivka Ravid; Christian Marescaux; Samuel F Berkovic; Edouard Hirsch; Mark Lathrop; Pierre Cau; Pierre Szepetowski
Journal:  Hum Mol Genet       Date:  2006-02-23       Impact factor: 6.150

Review 2.  Tubulin modifications and their cellular functions.

Authors:  Jennetta W Hammond; Dawen Cai; Kristen J Verhey
Journal:  Curr Opin Cell Biol       Date:  2008-01-15       Impact factor: 8.382

Review 3.  Evolution of the cytoskeleton.

Authors:  Harold P Erickson
Journal:  Bioessays       Date:  2007-07       Impact factor: 4.345

4.  A lineage-restricted and divergent beta-tubulin isoform is essential for the biogenesis, structure and function of blood platelets.

Authors:  H D Schwer; P Lecine; S Tiwari; J E Italiano; J H Hartwig; R A Shivdasani
Journal:  Curr Biol       Date:  2001-04-17       Impact factor: 10.834

Review 5.  Genetic mechanisms underlying abnormal neuronal migration in classical lissencephaly.

Authors:  Geraldine Kerjan; Joseph G Gleeson
Journal:  Trends Genet       Date:  2007-11-08       Impact factor: 11.639

Review 6.  Tubulin proteomics: towards breaking the code.

Authors:  Pascal Verdier-Pinard; Eddy Pasquier; Hui Xiao; Berta Burd; Claude Villard; Daniel Lafitte; Leah M Miller; Ruth H Angeletti; Susan Band Horwitz; Diane Braguer
Journal:  Anal Biochem       Date:  2008-09-18       Impact factor: 3.365

7.  Mutation in beta1-tubulin correlates with macrothrombocytopenia in Cavalier King Charles Spaniels.

Authors:  B Davis; M Toivio-Kinnucan; S Schuller; M K Boudreaux
Journal:  J Vet Intern Med       Date:  2008-05-02       Impact factor: 3.333

8.  Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria.

Authors:  Xavier Hubert Jaglin; Karine Poirier; Yoann Saillour; Emmanuelle Buhler; Guoling Tian; Nadia Bahi-Buisson; Catherine Fallet-Bianco; Françoise Phan-Dinh-Tuy; Xiang Peng Kong; Pascale Bomont; Laëtitia Castelnau-Ptakhine; Sylvie Odent; Philippe Loget; Manoelle Kossorotoff; Irina Snoeck; Ghislaine Plessis; Philippe Parent; Cherif Beldjord; Carlos Cardoso; Alfonso Represa; Jonathan Flint; David Anthony Keays; Nicholas Justin Cowan; Jamel Chelly
Journal:  Nat Genet       Date:  2009-05-24       Impact factor: 38.330

9.  G protein-coupled receptor-dependent development of human frontal cortex.

Authors:  Xianhua Piao; R Sean Hill; Adria Bodell; Bernard S Chang; Lina Basel-Vanagaite; Rachel Straussberg; William B Dobyns; Bassam Qasrawi; Robin M Winter; A Micheil Innes; Thomas Voit; M Elizabeth Ross; Jacques L Michaud; Jean-Claude Déscarie; A James Barkovich; Christopher A Walsh
Journal:  Science       Date:  2004-03-26       Impact factor: 47.728

10.  Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans.

Authors:  David A Keays; Guoling Tian; Karine Poirier; Guo-Jen Huang; Christian Siebold; James Cleak; Peter L Oliver; Martin Fray; Robert J Harvey; Zoltán Molnár; Maria C Piñon; Neil Dear; William Valdar; Steve D M Brown; Kay E Davies; J Nicholas P Rawlins; Nicholas J Cowan; Patrick Nolan; Jamel Chelly; Jonathan Flint
Journal:  Cell       Date:  2007-01-12       Impact factor: 41.582
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  3 in total

1.  Expanding the spectrum of TUBA1A-related cortical dysgenesis to Polymicrogyria.

Authors:  Karine Poirier; Yoann Saillour; Franck Fourniol; Fiona Francis; Isabelle Souville; Stéphanie Valence; Isabelle Desguerre; Jean Marie Lepage; Nathalie Boddaert; Marine Line Jacquemont; Cherif Beldjord; Jamel Chelly; Nadia Bahi-Buisson
Journal:  Eur J Hum Genet       Date:  2012-09-05       Impact factor: 4.246

2.  Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly.

Authors:  Catherine Fallet-Bianco; Annie Laquerrière; Karine Poirier; Ferechte Razavi; Fabien Guimiot; Patricia Dias; Laurence Loeuillet; Karine Lascelles; Cherif Beldjord; Nathalie Carion; Aurélie Toussaint; Nicole Revencu; Marie-Claude Addor; Benoit Lhermitte; Marie Gonzales; Jelena Martinovich; Bettina Bessieres; Maryse Marcy-Bonnière; Frédérique Jossic; Pascale Marcorelles; Philippe Loget; Jamel Chelly; Nadia Bahi-Buisson
Journal:  Acta Neuropathol Commun       Date:  2014-07-25       Impact factor: 7.801

3.  TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis.

Authors:  Setsuri Yokoi; Naoko Ishihara; Fuyuki Miya; Makiko Tsutsumi; Itaru Yanagihara; Naoko Fujita; Hiroyuki Yamamoto; Mitsuhiro Kato; Nobuhiko Okamoto; Tatsuhiko Tsunoda; Mami Yamasaki; Yonehiro Kanemura; Kenjiro Kosaki; Seiji Kojima; Shinji Saitoh; Hiroki Kurahashi; Jun Natsume
Journal:  Sci Rep       Date:  2015-10-23       Impact factor: 4.379
  3 in total

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