DCCmutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome

Author:

Marsh Ashley P. L.12ORCID,Edwards Timothy J.34,Galea Charles5,Cooper Helen M.3,Engle Elizabeth C.678910,Jamuar Saumya S.6781112,Méneret Aurélie1314,Moutard Marie-Laure151617,Nava Caroline1318,Rastetter Agnès13,Robinson Gail19,Rouleau Guy2021,Roze Emmanuel1314,Spencer-Smith Megan2223,Trouillard Oriane13,Billette de Villemeur Thierry15162425,Walsh Christopher A.678926,Yu Timothy W.62711,Heron Delphine1618,Sherr Elliott H.28,Richards Linda J.329,Depienne Christel13183031,Leventer Richard J.23233,Lockhart Paul J.12,

Affiliation:

1. Bruce Lefroy Centre for Genetic Health Research, Murdoch Children's Research Institute; Royal Children's Hospital; Parkville Victoria Australia

2. Department of Paediatrics; University of Melbourne; Parkville Victoria Australia

3. Queensland Brain Institute; The University of Queensland; St Lucia Brisbane Australia

4. Faculty of Medicine; The University of Queensland; Herston Brisbane Australia

5. Drug Delivery; Disposition and Dynamics (D4); Monash Institute of Pharmaceutical Sciences; Monash University; Parkville Victoria Australia

6. Division of Genetics and Genomics; Boston Children's Hospital; Boston Massachusetts

7. Manton Center for Orphan Disease Research; Boston Children's Hospital; Boston Massachusetts

8. Howard Hughes Medical Institute; Boston Children's Hospital; Boston Massachusetts

9. Department of Neurology; Boston Children's Hospital and Harvard Medical School; Boston Massachusetts

10. Department of Ophthalmology; Boston Children's Hospital and Harvard Medical School; Boston Massachusetts. Program in Medical and Population Genetics; Broad Institute of Massachusetts Institute of Technology (MIT) and Harvard; Cambridge Massachusetts

11. Department of Pediatrics; Harvard Medical School; Boston Massachusetts

12. Department of Paediatrics; KK Women's and Children's Hospital; Paediatric Academic Clinical Programme; Duke-NUS Medical School; Singapore Singapore

13. INSERM; U 1127; CNRS UMR 7225; Sorbonne Universités; UPMC Univ Paris 06 UMR S 1127; Institut du Cerveau et de la Moelle épinière; ICM; Paris France

14. Département de Neurologie; AP-HP; Hôpital de la Pitié-Salpêtrière; Paris France

15. Service de Neuropédiatrie; AP-HP; Hôpital Trousseau; Paris France

16. UPMC; GRC ConCer-LD; Sorbonne Université; Paris France

17. Centre de référence “Neurogénétique”; Paris France

18. Département de Génétique; AP-HP; Hôpital de la Pitié-Salpêtrière; Paris France

19. Neuropsychology Research Unit; School of Psychology; The University of Queensland; Brisbane Queensland Australia

20. Department of Neurology and Neurosurgery; McGill University Health Center; Montreal Quebec Canada

21. Montreal Neurological Institute and Hospital; McGill University; Montréal Quebec Canada

22. Clinical Sciences; Murdoch Children's Research Institute; Parkville Victoria Australia

23. School of Psychological Sciences and Monash Institute of Cognitive and Clinical Neurosciences; Monash University; Clayton Campus Clayton Victoria Australia

24. Centre de Référence “déficiences intellectuelles de causes rares”; Paris France

25. INSERM U1141; Paris France

26. Program in Medical and Population Genetics; Broad Institute of Massachusetts Institute of Technology (MIT) and Harvard; Cambridge Massachusetts. Department of Pediatrics; Harvard Medical School; Boston Massachusetts

27. Program in Medical and Population Genetics; Broad Institute of Massachusetts Institute of Technology (MIT) and Harvard; Cambridge Massachusetts

28. Department of Neurology; UCSF Benioff Children's Hospital; San Francisco California

29. The University of Queensland; School of Biomedical Sciences; St Lucia Brisbane Australia

30. Département de Médicine translationnelle et Neurogénétique; IGBMC; CNRS UMR 7104 INSERM U964, Université de Strasbourg Illkirch France

31. Laboratoires de génétique, Institut de génétique médicale d'Alsace; Hôpitaux Universitaires de Strasbourg; Strasbourg France

32. Neuroscience Research Group; Murdoch Children's Research Institute; Parkville Victoria Australia

33. Department of Neurology, University of Melbourne; Royal Children's Hospital; Parkville Victoria Australia

Funder

National Health and Medical Research Council

Campbell Edwards Trust

Boston Children's Hospital

Intellectual and Developmental Disabilities Research Center

Australian Postgraduate Award

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference121 articles.

1. The role of the anterior commissure in callosal agenesis;Barr;Neuropsychology,2002

2. Deleted in colorectal carcinoma (DCC) binds heparin via its fifth fibronectin type III domain;Bennett;Journal of Biological Chemistry,1997

3. Complete loss of netrin-1 results in embryonic lethality and severe axon guidance defects without increased neural cell death;Bin;Cell Reports,2015

4. Neuronal cell bodies remotely regulate axonal growth response to localized netrin-1 treatment via second messenger and DCC dynamics;Blasiak;Frontiers in Cellular Neuroscience,2017

5. Variability of forebrain commissures in callosal agenesis: A prenatal MR imaging study;Cesaretti;American Journal of Neuroradiology,2016

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