Literature DB >> 28772118

Wiring the Human Brain: A User's Handbook.

Raphael M Bendriem1, M Elizabeth Ross2.   

Abstract

Brain function requires connecting neuronal networks to empower movement, sensation, behavior, and cognition. Studies published early this year provide evidence that in humans, Netrin receptor, Deleted in Colorectal Cancer (DCC), is a master regulator of axonal crossing throughout the neuraxis.
Copyright © 2017 Elsevier Inc. All rights reserved.

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Year:  2017        PMID： 28772118      PMCID： PMC8274317          DOI： 10.1016/j.neuron.2017.07.008

Source DB:  PubMed          Journal:  Neuron        ISSN： 0896-6273            Impact factor:   17.173


  9 in total

1.  Binding of DCC by netrin-1 to mediate axon guidance independent of adenosine A2B receptor activation.

Authors:  E Stein; Y Zou; M Poo ; M Tessier-Lavigne
Journal:  Science       Date:  2001-03-09       Impact factor: 47.728

2.  Robo3: the road taken.

Authors:  Ian V Beamish; Timothy E Kennedy
Journal:  Dev Cell       Date:  2015-01-12       Impact factor: 12.270

3.  Mutations in DCC cause congenital mirror movements.

Authors:  Myriam Srour; Jean-Baptiste Rivière; Jessica M T Pham; Marie-Pierre Dubé; Simon Girard; Steves Morin; Patrick A Dion; Géraldine Asselin; Daniel Rochefort; Pascale Hince; Sabrina Diab; Naser Sharafaddinzadeh; Sylvain Chouinard; Hugo Théoret; Frédéric Charron; Guy A Rouleau
Journal:  Science       Date:  2010-04-30       Impact factor: 47.728

Review 4.  Human disorders of axon guidance.

Authors:  Alicia A Nugent; Adrianne L Kolpak; Elizabeth C Engle
Journal:  Curr Opin Neurobiol       Date:  2012-03-05       Impact factor: 6.627

5.  Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance.

Authors:  Ashley P L Marsh; Delphine Heron; Timothy J Edwards; Angélique Quartier; Charles Galea; Caroline Nava; Agnès Rastetter; Marie-Laure Moutard; Vicki Anderson; Pierre Bitoun; Jens Bunt; Anne Faudet; Catherine Garel; Greta Gillies; Ilan Gobius; Justine Guegan; Solveig Heide; Boris Keren; Fabien Lesne; Vesna Lukic; Simone A Mandelstam; George McGillivray; Alissandra McIlroy; Aurélie Méneret; Cyril Mignot; Laura R Morcom; Sylvie Odent; Annalisa Paolino; Kate Pope; Florence Riant; Gail A Robinson; Megan Spencer-Smith; Myriam Srour; Sarah E M Stephenson; Rick Tankard; Oriane Trouillard; Quentin Welniarz; Amanda Wood; Alexis Brice; Guy Rouleau; Tania Attié-Bitach; Martin B Delatycki; Jean-Louis Mandel; David J Amor; Emmanuel Roze; Amélie Piton; Melanie Bahlo; Thierry Billette de Villemeur; Elliott H Sherr; Richard J Leventer; Linda J Richards; Paul J Lockhart; Christel Depienne
Journal:  Nat Genet       Date:  2017-02-27       Impact factor: 38.330

6.  Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis.

Authors:  Joanna C Jen; Wai-Man Chan; Thomas M Bosley; Jijun Wan; Janai R Carr; Udo Rüb; David Shattuck; Georges Salamon; Lili C Kudo; Jing Ou; Doris D M Lin; Mustafa A M Salih; Tülay Kansu; Hesham Al Dhalaan; Zayed Al Zayed; David B MacDonald; Bent Stigsby; Andreas Plaitakis; Emmanuel K Dretakis; Irene Gottlob; Christina Pieh; Elias I Traboulsi; Qing Wang; Lejin Wang; Caroline Andrews; Koki Yamada; Joseph L Demer; Shaheen Karim; Jeffry R Alger; Daniel H Geschwind; Thomas Deller; Nancy L Sicotte; Stanley F Nelson; Robert W Baloh; Elizabeth C Engle
Journal:  Science       Date:  2004-04-22       Impact factor: 47.728

7.  Clinical and developmental findings in children with giant interhemispheric cysts and dysgenesis of the corpus callosum.

Authors:  M L Griebel; J P Williams; S S Russell; G T Spence; C M Glasier
Journal:  Pediatr Neurol       Date:  1995-09       Impact factor: 3.372

8.  Horizontal gaze palsy with progressive scoliosis can result from compound heterozygous mutations in ROBO3.

Authors:  W-M Chan; E I Traboulsi; B Arthur; N Friedman; C Andrews; E C Engle
Journal:  J Med Genet       Date:  2006-03       Impact factor: 6.318

9.  Biallelic mutations in human DCC cause developmental split-brain syndrome.

Authors:  Saumya S Jamuar; Klaus Schmitz-Abe; Alissa M D'Gama; Marie Drottar; Wai-Man Chan; Maya Peeva; Sarah Servattalab; Anh-Thu N Lam; Mauricio R Delgado; Nancy J Clegg; Zayed Al Zayed; Mohammad Asif Dogar; Ibrahim A Alorainy; Abdullah Abu Jamea; Khaled Abu-Amero; May Griebel; Wendy Ward; Ed S Lein; Kyriacos Markianos; A James Barkovich; Caroline D Robson; P Ellen Grant; Thomas M Bosley; Elizabeth C Engle; Christopher A Walsh; Timothy W Yu
Journal:  Nat Genet       Date:  2017-02-27       Impact factor: 38.330
  9 in total
  2 in total

1.  Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders.

Authors: 
Journal:  Cell       Date:  2019-12-12       Impact factor: 41.582

Review 2.  Shared genetic architecture across psychiatric disorders.

Authors:  Andrew D Grotzinger
Journal:  Psychol Med       Date:  2021-03-17       Impact factor: 10.592
  2 in total

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