Motor protein binding and mitochondrial transport are altered by pathogenic TUBB4A variants

Author:

Vulinovic Franca1ORCID,Krajka Victor1,Hausrat Torben J.2,Seibler Philip1,Alvarez-Fischer Daniel1,Madoev Harutyun1,Park Jin-Sung3,Kumar Kishore R.34,Sue Carolyn M.3,Lohmann Katja1,Kneussel Matthias2,Klein Christine1,Rakovic Aleksandar1

Affiliation:

1. Institute of Neurogenetics; University of Lübeck; Lübeck Germany

2. Institute of Molecular Neurogenetics; Center for Molecular Neurobiology; ZMNH; University Medical Center Hamburg-Eppendorf; Hamburg Germany

3. Department of Neurogenetics; Kolling Institute; Royal North Shore Hospital and the University of Sydney; St. Leonards New South Wales Australia

4. Kinghorn Centre for Clinical Genomics; Garvan Institute of Medical Research; Darlinghurst Australia

Funder

Deutsche Forschungsgemeinschaft

Fritz Thyssen Stiftung

Universität zu Lübeck

National Health and Medical Research Council of Australia (NHMRC) Early Career Fellowship

Royal North Shore Hospital Scholarship Program

The Royal Australasian College of Physicians Foundation

UCB Australia Pty Ltd.

Novartis Pharmaceuticals

American Academy of Neurology

Brain Foundation Grant

NHMRC Practitioner Fellowship

German Ministry of Education and Research

Hermann and Lilly Schilling Foundation

Bundesministerium für Bildung und Forschung

Erzincan Üniversitesi

Possehl Foundation

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Cited by 20 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. 21-jährige Patientin mit progredienter Paraspastik bei infantiler Zerebralparese;DGNeurologie;2024-08-13

2. Genetics and Pathogenesis of Dystonia;Annual Review of Pathology: Mechanisms of Disease;2024-01-24

3. Inherited Dystonias;Reference Module in Neuroscience and Biobehavioral Psychology;2024

4. Developmental regression with early feeding difficulties and characteristic neuroimaging features of H‐ABC in an infant from a TUBB4A genetic variant;Journal of Paediatrics and Child Health;2023-09-12

5. Molecular Pathogenic Mechanisms of Hypomyelinating Leukodystrophies (HLDs);Neurology International;2023-09-11

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3