Literature DB >> 25678890

Cortical Compass: EML1 Helps Point the Way in Neuronal Migration.

Kyle A Lyman, Dane M Chetkovich.   

Abstract

Entities:  

Year:  2015        PMID： 25678890      PMCID： PMC4320960          DOI： 10.5698/1535-7597-15.1.43

Source DB:  PubMed          Journal:  Epilepsy Curr        ISSN： 1535-7511            Impact factor:   7.500


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  6 in total

1.  Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human.

Authors:  Michel Kielar; Françoise Phan Dinh Tuy; Sara Bizzotto; Cécile Lebrand; Camino de Juan Romero; Karine Poirier; Renske Oegema; Grazia Maria Mancini; Nadia Bahi-Buisson; Robert Olaso; Anne-Gaëlle Le Moing; Katia Boutourlinsky; Dominique Boucher; Wassila Carpentier; Patrick Berquin; Jean-François Deleuze; Richard Belvindrah; Victor Borrell; Egbert Welker; Jamel Chelly; Alexandre Croquelois; Fiona Francis
Journal:  Nat Neurosci       Date:  2014-05-25       Impact factor: 24.884

Review 2.  Diffuse malformations of cortical development.

Authors:  Nadia Bahi-Buisson; Renzo Guerrini
Journal:  Handb Clin Neurol       Date:  2013

Review 3.  Molecular genetics of neuronal migration disorders.

Authors:  Judy S Liu
Journal:  Curr Neurol Neurosci Rep       Date:  2011-04       Impact factor: 5.081

4.  Characterization of the HeCo mutant mouse: a new model of subcortical band heterotopia associated with seizures and behavioral deficits.

Authors:  Alexandre Croquelois; Fabienne Giuliani; Christine Savary; Michel Kielar; Clotilde Amiot; Françoise Schenk; Egbert Welker
Journal:  Cereb Cortex       Date:  2008-06-18       Impact factor: 5.357

5.  Neuroepithelial progenitors undergo LGN-dependent planar divisions to maintain self-renewability during mammalian neurogenesis.

Authors:  Daijiro Konno; Go Shioi; Atsunori Shitamukai; Asako Mori; Hiroshi Kiyonari; Takaki Miyata; Fumio Matsuzaki
Journal:  Nat Cell Biol       Date:  2007-12-16       Impact factor: 28.824

6.  Somatic mutations in cerebral cortical malformations.

Authors:  Saumya S Jamuar; Anh-Thu N Lam; Martin Kircher; Alissa M D'Gama; Jian Wang; Brenda J Barry; Xiaochang Zhang; Robert Sean Hill; Jennifer N Partlow; Aldo Rozzo; Sarah Servattalab; Bhaven K Mehta; Meral Topcu; Dina Amrom; Eva Andermann; Bernard Dan; Elena Parrini; Renzo Guerrini; Ingrid E Scheffer; Samuel F Berkovic; Richard J Leventer; Yiping Shen; Bai Lin Wu; A James Barkovich; Mustafa Sahin; Bernard S Chang; Michael Bamshad; Deborah A Nickerson; Jay Shendure; Annapurna Poduri; Timothy W Yu; Christopher A Walsh
Journal:  N Engl J Med       Date:  2014-08-21       Impact factor: 91.245
  6 in total
  3 in total

1.  Genetic variants of EML1 and HIST1H4E in myeloid cell-related pathway genes independently predict cutaneous melanoma-specific survival.

Authors:  Yuanmin He; Hongliang Liu; Sheng Luo; Christopher I Amos; Jeffrey E Lee; Keming Yang; Abrar A Qureshi; Jiali Han; Qingyi Wei
Journal:  Am J Cancer Res       Date:  2021-06-15       Impact factor: 6.166

2.  A Forward Genetic Screen and Whole Genome Sequencing Identify Deflagellation Defective Mutants in Chlamydomonas, Including Assignment of ADF1 as a TRP Channel.

Authors:  Laura K Hilton; Fabian Meili; Paul D Buckoll; Julie C Rodriguez-Pike; Courtney P Choutka; Jaime A Kirschner; Freda Warner; Mette Lethan; Fabian A Garces; Jingnan Qi; Lynne M Quarmby
Journal:  G3 (Bethesda)       Date:  2016-10-13       Impact factor: 3.154

3.  A novel missense variant in the EML1 gene associated with bilateral ribbon-like subcortical heterotopia leads to ciliary defects.

Authors:  Fenja Markus; Annika Kannengießer; Patricia Näder; Paul Atigbire; Alexander Scholten; Christine Vössing; Eva Bültmann; G Christoph Korenke; Marta Owczarek-Lipska; John Neidhardt
Journal:  J Hum Genet       Date:  2021-07-01       Impact factor: 3.172
  3 in total

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