Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

Cited by (1,000)

Items 901–1,000 of 1,000

1. Uncovering the important role of mitochondrial dynamics in oogenesis: impact on fertility and metabolic disorder transmission
   Marcos Roberto Chiaratti · 2021 · Biophysical Reviews
2. The integrated stress response promotes neural stem cell survival under conditions of mitochondrial dysfunction in neurodegeneration
   Mohamed Ariff Iqbal, Maria Bilen, Yubing Liu, Vanessa Jabre, Bensun C. Fong, Imane Chakroun, Smitha Paul, Jingwei Chen, Steven Wade, Michel Kanaan et al. · 2024 · Aging Cell
3. Ethambutol toxicity exacerbating the phenotype of CMT2A2
   Ekokobe Fonkem, Monica A. Skordilis, Elaine M. Binkley, David S. Raymer, Avrom D. Epstein, William David Arnold, John T. Kissel, Victoria H. Lawson · 2013 · Muscle & Nerve
4. MFN2 deletion of exons 7 and 8: founder mutation in the UK population
   Aisling S. Carr, James M. Polke, Jacob Wilson, Ana L. Pelayo‐Negro, Matilde Laurá, Tina Nanji, James K. L. Holt, Jennifer Vaughan, Julia Rankin, Mary G. Sweeney et al. · 2015 · Journal of the Peripheral Nervous System
5. Complex patterns of mitochondrial dynamics in human pancreatic cells revealed by fluorescent confocal imaging
   Andrey V. Kuznetsov, Martin Hermann, Jakob Troppmair, Raimund Margreiter, Paul Hengster · 2009 · Journal of Cellular and Molecular Medicine
6. Prevalence of Symptomatic Charcot-Marie-Tooth Disease in Iceland: A Study of a Well-Defined Population
   Bjarni Guðmundsson, Elías Ólafsson, Finnbogi Jakobsson, Pétur Lúðvígsson · 2009 · Neuroepidemiology
7. Pla2g6 Deficiency in Zebrafish Leads to Dopaminergic Cell Death, Axonal Degeneration, Increased β-Synuclein Expression, and Defects in Brain Functions and Pathways
   Elena Sánchez, Luis J. Azcona, Coro Paisán‐Ruiz · 2018 · Molecular Neurobiology
8. Mitofusin-2 Triggers Cervical Carcinoma Cell Hela Apoptosis via Mitochondrial Pathway in Mouse Model
   Weiqiong Wang, Xiaowen Liu, Xiaomei Guo, Huanhuan Quan · 2018 · Cellular Physiology and Biochemistry
9. Mitochondrial fusion and Bid-mediated mitochondrial apoptosis are perturbed by alcohol with distinct dependence on its metabolism
   Shamim Naghdi, William S. Slovinsky, Muniswamy Madesh, Emanuel Rubin, György Hajnóczky · 2018 · Cell Death and Disease
10. Fetal Cerebral Artery Mitochondrion as Target of Prenatal Alcohol Exposure
    Anna N. Bukiya · 2019 · International Journal of Environmental Research and Public Health
11. Mitochondrial dynamics and interorganellar communication in the development and dysmorphism of mammalian oocytes
    Osamu Udagawa, Naotada Ishihara · 2019 · The Journal of Biochemistry
12. S1P/S1P Receptor Signaling in Neuromuscolar Disorders
    Elisabetta Meacci, Mercedes Garcia‐Gil · 2019 · International Journal of Molecular Sciences
13. Mitochondrial Dynamics in Retinal Ganglion Cell Axon Regeneration and Growth Cone Guidance
    Kira L. Lathrop, Michael B. Steketee · 2013 · Journal of Ocular Biology
14. Mitochondrial complementation preventing respiratory dysfunction caused by mutant mtDNA
    Akitsugu Sato, Kazuto Nakada, Jun‐Ichi Hayashi · 2009 · BioFactors
15. Co-occurrence of amyotrophic lateral sclerosis and Charcot-Marie-Tooth disease type 2A in a patient with a novel mutation in the mitofusin-2 gene
    Chiara Marchesi, Claudia Ciano, Ettore Salsano, Lorenzo Nanetti, Micaela Milani, Cinzia Gellera, Franco Taroni, Gian Maria Fabrizi, Antonino Uncini, Davide Pareyson · 2010 · Neuromuscular Disorders
16. Analysis of mitochondrial structure and function in the Drosophila larval musculature
    Zong-Heng Wang, Cheryl P. Clark, Erika R. Geisbrecht · 2015 · Mitochondrion
17. The challenges of axon survival: Introduction to the special issue on axonal degeneration
    Michael P. Coleman · 2013 · Experimental Neurology
18. Altered mitochondrial fusion drives defensive glutathione synthesis in cells able to switch to glycolytic ATP production
    David A. Patten, Shawn McGuirk, Ujval Anilkumar, Ghadi Antoun, Karan Gandhi, Gaganvir Parmar, Mohamed Ariff Iqbal, Jacob Wong, Richard B. Richardson, Julie St‐Pierre et al. · 2020 · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
19. Mitochondrial fission is a critical modulator of mutant APP-induced neural toxicity
    Lauren Y. Shields, Huihui Li, Kevin Nguyen, Hwajin Kim, Zak Doric, Joseph H. Garcia, T. Michael Gill, Dominik Haddad, Keith A. Vossel, Meredith Calvert et al. · 2021 · Journal of Biological Chemistry
20. Mitofusin 2 Deficiency Causes Pro-Inflammatory Effects in Human Primary Macrophages
    Vera Khodzhaeva, Yannick Schreiber, Gerd Geißlinger, Ralf Peter Brandes, Bernhard Brüne, Dmitry Namgaladze · 2021 · Frontiers in Immunology
21. Peripheral neuropathy in mitochondrial disease
    Rita Horváth, Jessica M. Medina, Mary M. Reilly, Michael E. Shy, Stephan L. Zuchner · 2023 · Handbook of clinical neurology
22. Mitochondrial hyperfusion induces metabolic remodeling in lung endothelial cells by modifying the activities of electron transport chain complexes I and III
    Manivannan Yegambaram, Xutong Sun, Qing Lü, Yan Jin, Wojciech Ornatowski, Jamie E. Soto, Saurabh Aggarwal, Ting Wang, Kim Tieu, Haiwei Gu et al. · 2023 · Free Radical Biology and Medicine
23. MFN2‐related genetic and clinical features in a cohort of Chinese CMT2 patients
    Yongzhi Xie, Xiaobo Li, Lei Liu, Zhengmao Hu, Shunxiang Huang, Yajin Zhan, Xiaohong Zi, Kun Xia, Beisha Tang, Ruxu Zhang · 2016 · Journal of the Peripheral Nervous System
24. Drosophila Charcot-Marie-Tooth Disease Models
    Masamitsu Yamaguchi, Hiroshi Takashima · 2018 · Advances in experimental medicine and biology
25. Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutation
    Liesbet Deprez, Lieve R. F. Claes, Kristl G. Claeys, Dominique Audenaert, Tine Van Dyck, Dirk Goossens, Wim Van Paesschen, Jurgen Del‐Favero, Christine Van Broeckhoven, Peter De Jonghe · 2005 · Human Genetics
26. Positively charged residues within the MYO19 MyMOMA domain are essential for proper localization of MYO19 to the mitochondrial outer membrane
    Jenci L. Hawthorne, Prachi R. Mehta, Pali P. Singh, Nathan Q. Wong, Omar A. Quintero · 2016 · Cytoskeleton
27. Mechanisms of Modulation of Mitochondrial Architecture
    Juan Pablo Muñoz, Fernanda Luisa Basei, Maria Laura Rojas, David Galvis, Antonio Zorzano A · 2023 · Biomolecules
28. MFN2 coordinates mitochondria motility with α-tubulin acetylation and this regulation is disrupted in CMT2A
    Atul Kumar, Delfina Larrea, Maria Elena Pero, Paola Infante, Marilisa Conenna, Grace Ji-eun Shin, Vincent Van Elias, Wesley B. Grueber, Lucia Di Marcotullio, Estela Área-Gómez et al. · 2024 · iScience
29. Hearing loss in inherited peripheral neuropathies: Molecular diagnosis by NGS in a French series
    Justine Lerat, Corinne Magdelaine, Anne‐Françoise Roux, Léa Darnaud, Hélène Beauvais‐Dzugan, Steven Naud, Laurence Richard, Paco Derouault, Karima Ghorab, Laurent Magy et al. · 2019 · Molecular Genetics & Genomic Medicine
30. Repeated exposure of cocaine alters mitochondrial dynamics in mouse neuroblastoma Neuro2a.
    T. Funakoshi, M. Furukawa, Toshihiko Aki, Koichi Uemura · 2019 · Neurotoxicology
31. Mitochondrial Miro GTPases coordinate mitochondrial and peroxisomal dynamics
    Konrad E. Zinsmaier · 2020 · Small GTPases
32. Held Up in Traffic—Defects in the Trafficking Machinery in Charcot-Marie-Tooth Disease
    Ronja Markworth, Mathias Bähr, Katja Burk · 2021 · Frontiers in Molecular Neuroscience
33. Modeling neuromuscular diseases in zebrafish
    Jaskaran Singh, Shunmoogum A. Patten · 2022 · Frontiers in Molecular Neuroscience
34. Combined RNA interference and gene replacement therapy targeting MFN2 as proof of principle for the treatment of Charcot–Marie–Tooth type 2A
    Federica Rizzo, Silvia Bono, Marc‐David Ruepp, Sabrina Salani, Linda Ottoboni, Elena Abati, Valentina Melzi, Chiara Cordiglieri, Serena Pagliarani, Roberta De Gioia et al. · 2023 · Cellular and Molecular Life Sciences
35. Mitochondrial fission and fusion in Dictyostelium discoideum: a search for proteins involved in membrane dynamics
    Brixey G Schimmel, Gregory W. Berbusse, Kari Naylor · 2012 · BMC Research Notes
36. D. melanogaster, mitochondria and neurodegeneration: small model organism, big discoveries
    Valentina Debattisti, Luca Scorrano · 2012 · Molecular and Cellular Neuroscience
37. Control of mitochondrial integrity in Parkinson’s disease
    Cristòfol Vives-Bauzá, Maja Aleksandra Tocilescu, Rosa L.A. deVries, Dana M. Alessi Wolken, Vernice R. Jackson-Lewis, Serge Przedborski · 2010 · Progress in brain research
38. Regulation of dynamin family proteins by post-translational modifications
    Usha Pallabi Kar, Himani Dey, Abdur Rahaman · 2017 · Journal of Biosciences
39. A yeast-based screening assay identifies repurposed drugs that suppress mitochondrial fusion and mtDNA maintenance defects
    Thomas Delerue, Déborah Tribouillard‐Tanvier, Marlène Daloyau, Farnoosh Khosrobakhsh, Laurent Jean Emorine, Gaëlle Friocourt, Pascale Belenguer, Marc Blondel, Laetitia Pelloquin · 2019 · Disease Models & Mechanisms
40. Acute optic neuropathy associated with a novel MFN2 mutation
    Luca Leonardi, Christian Marcotulli, Eugenia Storti, Alessandra Tessa, Mariano Serrao, Vincenzo Parisi, Filippo Maria Santorelli, Francesco Pierelli, Carlo Casali · 2015 · Journal of Neurology
41. Identification and Characterization of Unique Proline-rich Peptides Binding to the Mitochondrial Fission Protein hFis1
    Madhavika N. Serasinghe, A.M.P.B. Seneviratne, Alan V. Smrcka, Yisang Yoon · 2009 · Journal of Biological Chemistry
42. Deficiency of the zinc finger protein ZFP106 causes motor and sensory neurodegeneration
    Peter I. Joyce, Pietro Fratta, Allison S. Landman, Philip McGoldrick, Henning Wackerhage, Michael Groves, Bharani Shiva Busam, Jorge Galino, Silvia Corrochano, Olga A. Beskina et al. · 2015 · Human Molecular Genetics
43. A network biology approach to unraveling inherited axonopathies
    Dana M. Bis‐Brewer, Matt C. Danzi, Stefan Wuchty, Stephan L. Zuchner · 2019 · Scientific Reports
44. Animal Models as a Tool to Design Therapeutical Strategies for CMT-like Hereditary Neuropathies
    Luca Bosco, Yuri Falzone, Stefano Carlo Previtali · 2021 · Brain Sciences
45. Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies
    Aymane Bouzidi, Hicham Charoute, Majida Charif, Ghita Amalou, Mostafa Kandil, Abdelhamid Barakat, Guy Lenaers · 2022 · Orphanet Journal of Rare Diseases
46. A mitofusin 2/HIF1α axis sets a maturation checkpoint in regenerating skeletal muscle
    Xun Wang, Yuemeng Jia, Jiawei Zhao, Nicholas P. Lesner, Cameron J. Menezes, Spencer D. Shelton, Siva Sai Krishna Venigalla, Jian Xu, Chunyu Cai, Prashant Mishra · 2022 · Journal of Clinical Investigation
47. MIRO‐1 interacts with VDAC‐1 to regulate mitochondrial membrane potential in Caenorhabditis elegans
    Xuecong Ren, Hengda Zhou, Yujie Sun, Hongying Fu, Yu Ran, Bing Yang, Fan Yang, Mikael Björklund, Suhong Xu · 2023 · EMBO Reports
48. Ascorbic Acid and Sodium-Dependent Vitamin C Transporters in the Peripheral Nervous System: From Basic Science to Clinical Trials
    Burkhard Gess, Dominik Röhr, Peter Young · 2013 · Antioxidants and Redox Signaling
49. Two Spanish families with Charcot–Marie–Tooth type 2A: Clinical, electrophysiological and molecular findings
    Isabel Banchs, Carlos Casasnovas, J. Montero, Juan Antonio Martínez‐Matos, V. Volpini · 2008 · Neuromuscular Disorders
50. Loss of laforin or malin results in increased Drp1 level and concomitant mitochondrial fragmentation in Lafora disease mouse models
    Mamta Upadhyay, Saloni Agarwal, Pratibha Bhadauriya, Subramaniam Ganesh · 2017 · Neurobiology of Disease
51. Molecular pathogenesis of peripheral neuropathies: insights from Drosophila models
    Julia Bussmann, Erik Storkebaum · 2017 · Current Opinion in Genetics & Development
52. The Shape of Mitochondrial Dysfunction in Down Syndrome
    Emiliano Zamponi, Pablo R. Helguera · 2019 · Developmental Neurobiology
53. Human Induced Pluripotent Stem Cell Models of Neurodegenerative Disorders for Studying the Biomedical Implications of Autophagy
    Elena Seranova, Adina Maria Palhegyi, Surbhi Verma, Simona Dimova, Rachel Lasry, Moriyah Naama, Congxin Sun, Timothy Geoffrey Barrett, Tatiana Rosado Rosenstock, Dhiraj Kumar et al. · 2020 · Journal of Molecular Biology
54. Aberrant Mitochondrial Dynamics and Exacerbated Response to Neuroinflammation in a Novel Mouse Model of CMT2A
    Filippos Stavropoulos, Irene Sargiannidou, Louiza Potamiti, Alexia Kagiava, Mihalis I. Panayiotidis, Ji Hyun Bae, Su Cheong Yeom, Jae Young Lee, Kleopas A. Kleopa · 2021 · International Journal of Molecular Sciences
55. Mitochondrial disorders and the eye
    Ian Andrew Trounce, Van Bergen, Chakrabarti, Jonathan Guy Crowston, Evelyn C. O’Neill · 2011 · Eye and Brain
56. Ultrastructural mitochondrial modifications characteristic of mitofusin 2 mutations (CMT2A)
    Guilhem Solé, Xavier Ferrer, Claude Vital, Marie‐Laure Martin‐Négrier, Anne Vital, Philippe Latour · 2009 · Journal of the Peripheral Nervous System
57. Mechanism of Activation-Induced Downregulation of Mitofusin 2 in Human Peripheral Blood T Cells
    Asish Dasgupta, Kuang‐Hueih Chen, Rachel B. Munk, Carl Y. Sasaki, Jessica Curtis, Dan L. Longo, Paritosh Ghosh · 2015 · The Journal of Immunology
58. Mitofusin-2 Expression Is Implicated in Cervical Cancer Pathogenesis
    Sung Yong Ahn, Chengri Li, Xianglan Zhang, Young‐Min Hyun · 2018 · Anticancer Research
59. Current Studies of Mitochondrial Quality Control in the Preeclampsia
    Xiaoqing Peng, Ruirui Hou, Yuanyuan Yang, Zhigang Luo, Yunxia Cao · 2022 · Frontiers in Cardiovascular Medicine
60. Mitochondrial Phenotypes in Genetically Diverse Neurodegenerative Diseases and Their Response to Mitofusin Activation
    Xiawei Dang, Emily K. Walton, Barbara Zabłocka, Robert H. Baloh, Michael E. Shy, Gerald W. Dorn · 2022 · Cells
61. Hepatitis B virus X protein inhibits p53-mediated upregulation of mitofusin-2 in hepatocellular carcinoma cells
    Weilin Wang, Dongkai Zhou, Jianfeng Wei, Zehui Wu, Xiaofei Cheng, Qiang Sun, Haiyang Xie, Lin Zhou, Shusen Zheng · 2012 · Biochemical and Biophysical Research Communications
62. Exercise and Mitochondrial Remodeling in Skeletal Muscle in Type 2 Diabetes
    Hojun Lee, Wook Jae Song · 2018 · Journal of Obesity & Metabolic Syndrome
63. Relationship between mitofusin 2 and cancer
    Alessandro Allegra, Vanessa Innao, Andrea Gaetano Allegra, Caterina Musolino · 2018 · Advances in protein chemistry and structural biology
64. Open and cut: allosteric motion and membrane fission by dynamin superfamily proteins
    Raghav Kalia, Adam S. Frost · 2019 · Molecular Biology of the Cell
65. Mitochondrial Metabolism in Cancer Cachexia: Novel Drug Target
    Dhwani T. Dave, Bhoomika M. Patel · 2019 · Current Drug Metabolism
66. The ubiquitous role of mitochondria in Parkinson and other neurodegenerative diseases
    Georgia Theocharopoulou · 2020 · AIMS neuroscience
67. Defects of the Respiratory Chain
    Arnold Münnich, Agnès Rötig, Marlène Rio · 2011 · Springer eBooks
68. Contribution of mitochondria to pain in diabetic neuropathy
    Natalia Hernández-Beltrán, Carlos B. Moreno, Ángela María Gutiérrez‐Álvarez · 2013 · Endocrinología y Nutrición (English Edition)
69. Pathogenic mechanisms underlying X-linked Charcot-Marie-Tooth neuropathy (CMTX6) in patients with a pyruvate dehydrogenase kinase 3 mutation
    Gonzalo Pérez‐Siles, Carolyn Ly, Adrienne J. Grant, Alexander P. Drew, Eppie Mildred Yiu, Monique M. Ryan, David Chuang, Shih-Chia Tso, Garth A. Nicholson, Marina L. Kennerson · 2016 · Neurobiology of Disease
70. The abundance of the ARL2 GTPase and its GAP, ELMOD2, at mitochondria are modulated by the fusogenic activity of mitofusins and stressors
    Laura E. Newman, Cara R. Schiavon, Chengjing Zhou, Richard Kahn · 2017 · PLoS ONE
71. Dynamic properties of mitochondria during human corticogenesis
    Tierney Baum, Vivian Gama · 2021 · Development
72. Fueling Synapses
    Erin Margaret Schuman, David C. Chan · 2004 · Cell
73. Molecular diagnosis of inheritable neuromuscular disorders. Part II: Application of genetic testing in neuromuscular disease
    Steven A. Greenberg, Ronan J. Walsh · 2005 · Muscle & Nerve
74. A quantitative assay for mitochondrial fusion using Renilla luciferase complementation
    Huiyan Huang, Seok‐Yong Choi, Michael A. Frohman · 2010 · Mitochondrion
75. What Role Does Mitochondrial Stress Play in Neurodegenerative Diseases?
    Alicia M. Pickrell, Carlos Torres Moraes · 2010 · Methods in molecular biology
76. A catalytic domain variant of mitofusin requiring a wildtype paralog for function uncouples mitochondrial outer-membrane tethering and fusion
    E.A. Engelhart, Suzanne C. Hoppins · 2019 · Journal of Biological Chemistry
77. Marf-mediated mitochondrial fusion is imperative for the development and functioning of indirect flight muscles (IFMs) in drosophila
    Prasanna Katti, Mamta Rai, Shubhi Srivastava, Patrick D’Silva, Upendra Nongthomba · 2021 · Experimental Cell Research
78. Molecular Mechanisms behind Inherited Neurodegeneration of the Optic Nerve
    Alessandra Maresca, Valério Carelli · 2021 · Biomolecules
79. Mitofusin-mediated contacts between mitochondria and peroxisomes regulate mitochondrial fusion
    Cynthia Alsayyah, Manish Kumar Singh, María Ángeles Morcillo-Parra, Laetitia Cavellini, Nadav Shai, Christine Schmitt, Maya Schuldiner, Einat Zalckvar, Adeline Mallet, Naïma Belgareh‐Touzé et al. · 2024 · PLoS Biology
80. Neuronal protein trafficking: Emerging consequences of endoplasmic reticulum dynamics
    José Ignacio Valenzuela, Matías Jaureguiberry-Bravo, Andrés Couve · 2011 · Molecular and Cellular Neuroscience
81. Clinical and allelic heterogeneity in a pediatric cohort of 11 patients carrying MFN2 mutation
    Chloé Di Meglio, Nathalie Bonello‐Palot, C. Boulay, Mathieu Milh, Caroline Ovaert, Nicolas Lévy, B. Chabrol · 2015 · Brain and Development
82. Neurophysiological profile of peripheral neuropathy associated with childhood mitochondrial disease
    Manoj P. Menezes, Shamima Rahman, Kaustuv Bhattacharya, Damian R. Clark, John Christodoulou, Carolyn Ellaway, Michelle Anne Farrar, Matthew C. Pitt, Hugo A. Sampaio, Tyson L. Ware et al. · 2016 · Mitochondrion
83. The Effect of a Novel c.820C>T (Arg274Trp) Mutation in the Mitofusin 2 Gene on Fibroblast Metabolism and Clinical Manifestation in a Patient
    M Beresewicz, Anna Boratyńska-Jasińska, Łukasz Charzewski, Maria Kawalec, Dagmara Kabzińska, Andrzej Kochański, Krystiana A. Krzyśko, Barbara Zabłocka · 2017 · PLoS ONE
84. Molecular modelling of mitofusin 2 for a prediction for Charcot-Marie-Tooth 2A clinical severity
    M Beresewicz, Łukasz Charzewski, Krystiana A. Krzyśko, Andrzej Kochański, Barbara Zabłocka · 2018 · Scientific Reports
85. A zebrafish model to study small-fiber neuropathy reveals a potential role for GDAP1
    Ivo Eijkenboom, Jo M. Vanoevelen, Janneke G. J. Hoeijmakers, Iris G. M. Wijnen, Mike Gerards, Catharina Gerritdina Faber, Hubert J.M. Smeets · 2019 · Mitochondrion
86. Mitofusin-2 is a novel anti-angiogenic factor in pancreatic cancer
    Zhichuan Lin, Xiaoyi Lin, Jinhong Chen, Guoqiang Huang, Tangen Chen, Liling Zheng · 2021 · Journal of Gastrointestinal Oncology
87. Predicting Mitochondrial Dynamic Behavior in Genetically Defined Neurodegenerative Diseases
    Gerald W. Dorn, Xiawei Dang · 2022 · Cells
88. Role of Mitochondria in Drug-Induced Cholestatic Injury
    George E.N. Kass, Shirley C. Price · 2008 · Clinics in Liver Disease
89. Nagarse treatment of cardiac subsarcolemmal and interfibrillar mitochondria leads to artefacts in mitochondrial protein quantification
    Gábor Koncsos, Zoltán V. Varga, Tamás Baranyai, Péter Ferdinándy, Rainer Schulz, Zoltán Giricz, Kerstin Boengler · 2018 · Journal of Pharmacological and Toxicological Methods
90. Heterogeneity in motoneuron disease
    Diether Lambrechts, Wim Robberecht, Peter Carmeliet · 2007 · Trends in Neurosciences
91. The multifaceted mitochondrion: An attractive candidate for therapeutic strategies
    Flavie Strappazzon, Francesco Cecconi · 2015 · Pharmacological Research
92. Maintenance mechanisms of circuit-integrated axons
    Vittoria Mariano, Nuria Domıńguez-Iturza, Lukas Jakob Neukomm, Claudia Bagni · 2018 · Current Opinion in Neurobiology
93. MFN2 interacts with nuage-associated proteins and is essential for male germ cell development by controlling mRNA fate during spermatogenesis
    Xiaoli Wang, Yujiao Wen, Jin Zhang, Grace Swanson, Shuangshuang Guo, Congcong Cao, Stephen A. Krawetz, Zhibing Zhang, Shuiqiao Yuan · 2021 · Development
94. Formin 3 directs dendritic architecture via microtubule regulation and is required for somatosensory nociceptive behavior
    Ravi Das, Shatabdi Bhattacharjee, Jamin M. Letcher, Jenna M Harris, Sumit Nanda, István Földi, Erin N. Lottes, Hansley M. Bobo, Benjamin D. Grantier, József Mihály et al. · 2021 · Development
95. Genetic and phenotypic variability of optic neuropathies
    T. Neuhann, B. Rautenstrauss · 2013 · Expert Review of Neurotherapeutics
96. Defective Mitochondrial Function and Motility Due to Mitofusin 1 Overexpression in Insulin Secreting Cells
    Kyu‐Sang Park, Andreas Wiederkehr, Claes B. Wollheim · 2012 · Korean Journal of Physiology and Pharmacology
97. Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience
    Marco Luigetti, Gian Maria Fabrizi, Giulia Bisogni, Ângela Romano, Federica Taioli, Moreno Ferrarini, Daniela Bernardo, Paolo Maria Rossini, Mario Sabatelli · 2016 · Clinical Neurology and Neurosurgery
98. Angiotensin II stimulation promotes mitochondrial fusion as a novel mechanism involved in protein kinase compartmentalization and cholesterol transport in human adrenocortical cells
    Katia E. Helfenberger, Ana Fernanda Castillo, Pablo G. Mele, Ana Fiore, Lucía M. Herrera, Paola Vanesa Finocchietto, Ernesto Jorge Podesta, Cecilia Poderoso · 2019 · The Journal of Steroid Biochemistry and Molecular Biology
99. Non-convulsive status epilepticus causing focal neurological deficits in CADASIL
    Philipp O. Valko, Massimiliano M. Siccoli, Andreas U. Schiller, Heinz Gregor Wieser, Hae Hyuk Jung · 2007 · Journal of Neurology Neurosurgery & Psychiatry
100. Mitochondrial Function and Neurodegenerative Diseases
     Wilkins, Heather M., Weidling, Ian, Koppel, Scott, Wang, Xiaowan, von Schulze, Alex, Swerdlow, Russell H. · 2018 · The Molecular and Cellular Basis of Neurodegenerative Diseases