A Family with Vocal Cord Paralysis Associated with GDAP1 Mutation in Giresun, Turkey by Nilgün Erten, Esra Battaloğlu, Alperen Erdoğan, Erdal Seren

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GDAP1 Involvement in Mitochondrial Function and Oxidative Stress, Investigated in a Charcot-Marie-Tooth Model of hiPSCs-Derived Motor Neurons by Federica Miressi, Nesrine Benslimane, Frédéric Favreau, Marion Rassat, Laurence Richard, Sylvie Bourthoumieu, Cécile Laroche, Laurent Magy, Corinne Magdelaine, Franck Sturtz, Anne-Sophie Lia, Pierre-Antoine Faye

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Epigenetic regulation of the human GDAP1 gene by Kaja Karaś, Joanna Pastwińska, Anna Sałkowska, Iwona Karwaciak, Marcin Ratajewski

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Differential effects of Mendelian GDAP1 clinical variants on mitochondria-lysosome membrane contacts sites by Lara Cantarero, Gisela García-Vargas, Janet Hoenicka, Francesc Palau

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A case of hereditary motor and sensory neuropathy type IVA with unusual genealogy by S. A. Kurbatov, T. B. Milovidova, V. P. Fedotov, A. F. Murtazina, G. E. Rudenskaya, O. A. Shchagina, A. V. Polyakov

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Autosomal dominant GDAP1 mutation with severe phenotype and respiratory involvement: A case report by Adrian Rodriguez-Hernandez, Meagan Mayo, Lilibeth Jauregui, Pooja Patel, Pooja Patel

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Structural insights into Charcot–Marie–Tooth disease‐linked mutations in human GDAP1 by Aleksi Sutinen, Giang Thi Tuyet Nguyen, Arne Raasakka, Gopinath Muruganandam, Remy Loris, Emil Ylikallio, Henna Tyynismaa, Luca Bartesaghi, Salla Ruskamo, Petri Kursula

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Mitochondria and calcium defects correlate with axonal dysfunction in GDAP1-related Charcot-Marie-Tooth mouse model by Azahara Civera-Tregón, Laura Domínguez, Paula Martínez-Valero, Clàudia Serrano, Alex Vallmitjana, Raúl Benítez, Janet Hoenicka, Jorgina Satrústegui, Francesc Palau

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The Pathological Features of Common Hereditary Mitochondrial Dynamics Neuropathy by Rui Wu, Rui Wu, He Lv, Hui Wang, Zhaoxia Wang, Yun Yuan

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Case report: exome sequencing achieved a definite diagnosis in a Chinese family with muscle atrophy by Hui Jiang, Chunmiao Guo, Jie Xie, Jingxin Pan, Ying Huang, Miaoxin Li, Yibin Guo

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Amlexanox: Readthrough Induction and Nonsense-Mediated mRNA Decay Inhibition in a Charcot–Marie–Tooth Model of hiPSCs-Derived Neuronal Cells Harboring a Nonsense Mutation in <i>GDA... by Nesrine Benslimane, Federica Miressi, Camille Loret, Laurence Richard, Angélique Nizou, Ioanna Pyromali, Pierre-Antoine Faye, Frédéric Favreau, Fabrice Lejeune, Anne-Sophie Lia

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Silencing of the Charcot–Marie–Tooth disease-associated gene GDAP1 induces abnormal mitochondrial distribution and affects Ca2+ homeostasis by reducing store-operated Ca2+ entry... by David Pla-Martín, Carlos B. Rueda, Anna Estela, Maribel Sánchez-Piris, Paloma González-Sánchez, Javier Traba, Sergio de la Fuente, Luca Scorrano, Jaime Renau-Piqueras, Javier Alvarez, Jorgina Satrústegui, Francesc Palau

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2,4-Dimethoxy-6-Methylbenzene-1,3-diol, a Benzenoid From Antrodia cinnamomea, Mitigates Psoriasiform Inflammation by Suppressing MAPK/NF-κB Phosphorylation and GDAP1L1/Drp1 Translo... by Shih-Yi Chuang, Chi-Yuan Chen, Chi-Yuan Chen, Chi-Yuan Chen, Shih-Chun Yang, Ahmed Alalaiwe, Chih-Hung Lin, Jia-You Fang, Jia-You Fang, Jia-You Fang

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A locus-specific database for mutations in <it>GDAP1 </it>allows analysis of genotype-phenotype correlations in Charcot-Marie-Tooth diseases type 4A and 2K by Cassereau Julien, Chevrollier Arnaud, Bonneau Dominique, Verny Christophe, Procaccio Vincent, Reynier Pascal, Ferré Marc

Subjects: “…ganglioside-induced differentiation-associated protein 1 (GDAP1)…”
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