Functional divergence of the two Elongator subcomplexes during neurodevelopment-Reference-Cited by-同舟云学术

Functional divergence of the two Elongator subcomplexes during neurodevelopment

Published:2022-06-13 Issue:7 Volume:14 Page:
ISSN:1757-4676
Container-title:EMBO Molecular Medicine
language:en
Short-container-title:EMBO Mol Med

Author:

Gaik Monika¹^ORCID,Kojic Marija²^ORCID,Stegeman Megan R²,Öncü‐Öner Tülay³^ORCID,Kościelniak Anna¹,Jones Alun⁴^ORCID,Mohamed Ahmed⁵⁶⁷,Chau Pak Yan Stefanie⁸,Sharmin Sazia⁸,Chramiec‐Głąbik Andrzej¹^ORCID,Indyka Paulina¹⁹,Rawski Michał¹,Biela Anna¹,Dobosz Dominika¹,Millar Amanda²,Chau Vann¹⁰,Ünalp Aycan¹¹^ORCID,Piper Michael⁸^ORCID,Bellingham Mark C⁸,Eichler Evan E¹²¹³,Nickerson Deborah A¹²,Güleryüz Handan¹⁴,Abbassi Nour El Hana¹¹⁵^ORCID,Jazgar Konrad¹^ORCID,Davis Melissa J²⁵⁷¹⁶,Mercimek‐Andrews Saadet¹⁷¹⁸^ORCID,Cingöz Sultan³¹²^ORCID,Wainwright Brandon J²,Glatt Sebastian¹^ORCID

Affiliation:

1. Malopolska Centre of Biotechnology Jagiellonian University Krakow Poland

2. The University of Queensland Diamantina Institute Faculty of Medicine The University of Queensland Woolloongabba QLD Australia

3. Department of Medical Biology and Genetics Faculty of Medicine Dokuz Eylül University İzmir Turkey

4. Institute for Molecular Bioscience The University of Queensland Brisbane QLD Australia

5. Bioinformatics Division The Walter and Eliza Hall Institute of Medical Research Parkville VIC Australia

6. Colonial Foundation Healthy Ageing Centre The Walter and Eliza Hall Institute of Medical Research Parkville VIC Australia

7. The Department of Medical Biology Faculty of Medicine Dentistry and Health Science The University of Melbourne Parkville VIC Australia

8. School of Biomedical Sciences The University of Queensland Brisbane QLD Australia

9. National Synchrotron Radiation Centre SOLARIS Jagiellonian University Krakow Poland

10. Department of Paediatrics (Neurology) The Hospital for Sick Children and University of Toronto Toronto ON Canada

11. Department of Pediatric Neurology Dr. Behçet Uz Children's Hospital İzmir Turkey

12. Department of Genome Sciences University of Washington School of Medicine Seattle WA USA

13. Howard Hughes Medical Institute University of Washington Seattle WA USA

14. Department of Pediatric Radiology School of Medicine Dokuz Eylül University İzmir Turkey

15. Postgraduate School of Molecular Medicine Medical University of Warsaw Warsaw Poland

16. The Department of Clinical Pathology Faculty of Medicine, Dentistry and Health Science The University of Melbourne Parkville VIC Australia

17. The Hospital for Sick Children Toronto ON Canada

18. Department of Medical Genetics Faculty of Medicine and Dentistry The University of Alberta Edmonton AB Canada

Funder

Fundacja na rzecz Nauki Polskiej

H2020 European Research Council

National Institutes of Health

National Heart, Lung, and Blood Institute

Dokuz Eylül Üniversitesi

Publisher

EMBO

Subject

Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/emmm.202115608

Reference69 articles.

1. Microdeletions ofELP4Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation

2. Whole exome sequencing reveals a mutation in ELP2 gene in Iranian family suffering from autosomal recessive mental retardation;Alizadeh N;J Mol Genet Med,2018

3. Hippocampus in health and disease: An overview

4. Familial Dysautonomia Is Caused by Mutations of the IKAP Gene

5. Elongator subunit 3 (ELP3) modifies ALS through tRNA modification

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