The Popeye domain–containing 1 (
Roland F.R. Schindler, Chiara Scotton, Jianguo Zhang, Chiara Passarelli, Beatriz Ortiz-Bonnin, Subreena Simrick, Thorsten Schwerte, Kar-Lai Poon, Mingyan Fang, Susanne Rinné, Alexander Froese, Viacheslav O. Nikolaev, Christiane Grunert, Thomas Müller, Giorgio Tasca, Padmini Sarathchandra, Fabrizio Drago, Bruno Dallapiccola, Claudio Rapezzi, Eloisa Arbustini, Francesca Romana Di Raimo, Marcella Neri, Rita Selvatici, Francesca Gualandi, Fabiana Fattori, Antonello Pietrangelo, Wenyan Li, Hui Jiang, Xun Xu, Enrico Bertini, Niels Decher, Jun Wang, Thomas Brand, Alessandra Ferlini
Title and authors | Publication | Year |
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Loss of popdc3 Impairs Mitochondrial Function and Causes Skeletal Muscle Atrophy and Reduced Swimming Ability in Zebrafish
Sun C, Chen Z, Yang D, Xiao J, Chen X, Peng X, Wu X, Tang C |
Journal of Cachexia, Sarcopenia and Muscle | 2025 |
POPDC1 Variants Cause Atrioventricular Node Dysfunction and Arrhythmogenic Changes in Cardiac Electrophysiology and Intracellular Calcium Handling in Zebrafish
Stoyek MR, Doane SE, Dallaire SE, Long ZD, Ramia JM, Cassidy-Nolan DL, Poon KL, Brand T, Quinn TA |
Genes & development | 2024 |
Popeye domain containing proteins modulate the voltage-gated cardiac sodium channel Nav1.5
Rinné S, Kiper AK, Jacob R, Ortiz-Bonnin B, Schindler RF, Fischer S, Komadowski M, De Martino E, Schäfer MK, Cornelius T, Fabritz L, Helker CS, Brand T, Decher N |
iScience | 2024 |
Pathogenesis and Clinical Characteristics of Hereditary Arrhythmia Diseases
Guo S, Zha L |
Genes | 2024 |
Differential effects of mutations of POPDC proteins on heteromeric interaction and membrane trafficking
Alexander Swan, Roland Schindler, Marco Savarese, Isabelle Mayer, Susanne Rinné, Felix Bleser, Anne Schaenzer, Andreas Hahn, Mario Sabatelli, Francesco Perna, Kathryn Chapman, Mark Pfuhl, Alan C Spivey, Niels Decher, Bjarne Udd, Giorgio Tasca, Thomas Brand |
Acta Neuropathologica Communications | 2023 |
Defective BVES-mediated feedback control of cAMP in muscular dystrophy.
Li H, Wang P, Zhang C, Zuo Y, Zhou Y, Han R |
Nature Communications | 2023 |
Modeling Human Muscular Dystrophies in Zebrafish: Mutant Lines, Transgenic Fluorescent Biosensors, and Phenotyping Assays.
Tesoriero C, Greco F, Cannone E, Ghirotto F, Facchinello N, Schiavone M, Vettori A |
International journal of molecular sciences | 2023 |
Genetics of sinoatrial node function and heart rate disorders
van der Maarel LE, Postma AV, Christoffels VM |
Disease models & mechanisms | 2023 |
Establishing a genomic radiation-age association for space exploration supplements lung disease differentiation
Ruprecht NA, Singhal S, Schaefer K, Gill JS, Bansal B, Sens D, Singhal SK |
Frontiers in public health | 2023 |
Human-specific epigenomic states in spermatogenesis
Liao C, Walters BW, DiStasio M, Lesch BJ |
Computational and Structural Biotechnology Journal | 2023 |
Mice Lacking the cAMP Effector Protein POPDC1 Show Enhanced Hippocampal Synaptic Plasticity.
Shetty MS, Ris L, Schindler RFR, Mizuno K, Fedele L, Giese KP, Brand T, Abel T |
Cerebral Cortex | 2022 |
Engineering a precise adenine base editor with minimal bystander editing.
Chen L, Zhang S, Xue N, Hong M, Zhang X, Zhang D, Yang J, Bai S, Huang Y, Meng H, Wu H, Luan C, Zhu B, Ru G, Gao H, Zhong L, Liu M, Liu M, Cheng Y, Yi C, Wang L, Zhao Y, Song G, Li D |
Nature Chemical Biology | 2022 |
POPDC1 scaffolds a complex of adenylyl cyclase 9 and the potassium channel TREK‐1 in heart
Baldwin TA, Li Y, Marsden AN, Rinné S, Garza\u2010Carbajal A, Schindler RF, Zhang M, Garcia MA, Venna VR, Decher N, Brand T, Dessauer CW |
EMBO reports | 2022 |
The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family (ARMC3).
Rehman AU, Hamid M, Khan SA, Eisa M, Ullah W, Rehman ZU, Khan MA, Basit S, Muhammad N, Khan S, Wasif N |
Genes & development | 2022 |
European Neuromuscular Centre consensus statement on anaesthesia in patients with neuromuscular disorders
van den Bersselaar LR, Heytens L, Silva HC, Reimann J, Tasca G, Díaz\u2010Cambronero Ó, Løkken N, Hellblom A, Hopkins PM, Rueffert H, Bastian B, Vilchez JJ, Gillies R, Johannsen S, Veyckemans F, Muenster T, Klein A, Litman R, Jungbluth H, Riazi S, Voermans NC, Snoeck MM |
European Journal of Neurology | 2022 |
Systemic AAV9.BVES delivery ameliorates muscular dystrophy in a mouse model of LGMDR25
Li H, Wang P, Hsu E, Pinckard KM, Stanford KI, Han R |
Molecular Therapy | 2022 |
Cardiac cAMP-PKA Signaling Compartmentalization in Myocardial Infarction
AS Colombe, G Pidoux |
Cells | 2021 |
Negative Influence by the Force: Mechanically Induced Hyperpolarization via K2P Background Potassium Channels
M Lengyel, P Enyedi, G Czirják |
International journal of molecular sciences | 2021 |
Two-Pore-Domain Potassium (K2P-) Channels: Cardiac Expression Patterns and Disease-Specific Remodelling Processes
F Wiedmann, N Frey, C Schmidt |
Cells | 2021 |
A Journey with LGMD: From Protein Abnormalities to Patient Impact
DG Georganopoulou, VG Moisiadis, FA Malik, A Mohajer, TM Dashevsky, ST Wuu, CK Hu |
The Protein Journal | 2021 |
The Role of POPDC Proteins in Cardiac Pacemaking and Conduction
L Gruscheski, T Brand |
Journal of Cardiovascular Development and Disease | 2021 |
BVES is a novel interactor of ANO5 and regulates myoblast differentiation
H Li, L Xu, Y Gao, Y Zuo, Z Yang, L Zhao, Z Chen, S Guo, R Han |
Cell & Bioscience | 2021 |
Physiological Roles of Mammalian Transmembrane Adenylyl Cyclase Isoforms
K Ostrom, J LaVigne, T Brust, R Seifert, C Dessauer, V Watts, R Ostrom |
Physiological reviews | 2021 |
The Intrinsic Cardiac Nervous System and Its Role in Cardiac Pacemaking and Conduction
L Fedele, T Brand |
Journal of Cardiovascular Development and Disease | 2020 |
An interaction of heart disease-associated proteins POPDC1/2 with XIRP1 in transverse tubules and intercalated discs
I Holt, HR Fuller, RF Schindler, SL Shirran, T Brand, GE Morris |
2020 | |
BVES downregulation in non-syndromic tetralogy of fallot is associated with ventricular outflow tract stenosis
Y Shi, Y Li, Y Wang, P Zhu, Y Chen, H Wang, S Yue, X Xia, J Chen, Z Jiang, C Zhou, W Cai, H Yuan, Y Wu, Y Wan, X Li, X Zhu, Z Zhou, G Dai, F Li, X Mo, X Ye, X Fan, J Zhuang, X Wu, W Yuan |
Scientific Reports | 2020 |
Zebrafish models of sarcopenia
A Daya, R Donaka, D Karasik |
Disease models & mechanisms | 2020 |
The ties that bind: functional clusters in limb-girdle muscular dystrophy
ER Barton, CA Pacak, WL Stoppel, PB Kang |
Skeletal Muscle | 2020 |
Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness
A Töpf, K Johnson, A Bates, L Phillips, KR Chao, EM England, KM Laricchia, T Mullen, E Valkanas, L Xu, M Bertoli, A Blain, AB Casasús, J Duff, M Mroczek, S Specht, M Lek, M Ensini, DG MacArthur, E Akay, J Alonso-Pérez, J Baets, N Barisic, A Bastian, S Borell, T Chamova, K Claeys, J Colomer, S Coppens, N Deconinck, W de Ridder, J Díaz-Manera, C Domínguez-González, A Duncan, H Durmus, NA Fahmy, ME Farrugia, R Fernández-Torrón, L Gonzalez-Quereda, J Haberlova, M von der Hagen, A Hahn, A Jakovčević, IJ Pascual, S Kapetanovic, V Kenina, J Kirschner, A Klein, H Kölbel, A Kostera-Pruszczyk, R Kulshrestha, J Lähdetie, M Layegh, C Longman, AL de Munain, W Loscher, A Lusakowska, P Maddison, A Magot, A Majumdar, P Martí, AM Arroyo, R Mazanec, S Mercier, T Mongini, N Muelas, A Nascimento, S Nafissi, S Omidi, C Ortez, S Paquay, Y Pereon, S Perić, V Ponzalino, VR Stojanović, G Remiche, AR Sainz, S Rudnik, IS Albisua, M Santos, U Schara, A Shatillo, J Sertić, U Stephani, S Strang-Karlsson, Y Sznajer, A Tanev, I Tournev, PV den Bergh, VV Parijs, J Vílchez, K Vill, J Vissing, C Wallgren-Pettersson, J Wanschitz, T Willis, N Witting, M Zulaica, V Straub |
Genetics in Medicine | 2020 |
Improving diagnosis for rare diseases: the experience of the Italian undiagnosed Rare diseases network
M Salvatore, A Polizzi, MC Stefano, G Floridia, S Baldovino, D Roccatello, S Sciascia, E Menegatti, G Remuzzi, E Daina, P Iatropoulos, B Bembi, RM Riol, A Ferlini, M Neri, G Novelli, F Sangiuolo, F Brancati, D Taruscio |
Italian Journal of Pediatrics | 2020 |
Ten years of research on the role of BVES/POPDC1 in human disease: a review P Han, Y Lei, D Li, J Liu, W Yan, D Tian |
OncoTargets and therapy | 2019 |
The Popeye domain containing gene family encoding a family of cAMP-effector proteins with important functions in striated muscle and beyond
AH Swan, L Gruscheski, LA Boland, T Brand |
Journal of Muscle Research and Cell Motility | 2019 |
The Role of the Popeye Domain Containing Gene Family in Organ Homeostasis
JN Amunjela, AH Swan, T Brand |
Cells | 2019 |
Muscular dystrophy with arrhythmia caused by loss-of-function mutations in BVES
WD Ridder, I Nelson, B Asselbergh, BD Paepe, M Beuvin, RB Yaou, C Masson, A Boland, JF Deleuze, T Maisonobe, B Eymard, S Symoens, R Schindler, T Brand, K Johnson, A Töpf, V Straub, PD Jonghe, JL Bleecker, G Bonne, J Baets |
Neurology Genetics | 2019 |
The Functional Polymorphism R129W in the BVES Gene Is Associated with Sporadic Tetralogy of Fallot in the Han Chinese Population
Y Shi, Y Li, Y Wang, J Zhuang, H Wang, M Hu, X Mo, S Yue, Y Chen, X Fan, J Chen, W Cai, X Zhu, Y Wan, Y Zhong, X Ye, F Li, Z Zhou, G Dai, R Luo, K Ocorr, Z Jiang, X Li, P Zhu, X Wu, W Yuan |
Genetic Testing and Molecular Biomarkers | 2019 |
Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family
S Bigoni, M Neri, C Scotton, R Farina, P Sabatelli, C Jiang, J Zhang, MS Falzarano, R Rossi, D Ognibene, R Selvatici, F Gualandi, D Bosshardt, P Perri, C Campa, F Brancati, M Salvatore, MC Stefano, D Taruscio, L Trombelli, M Fang, A Ferlini |
Frontiers in Genetics | 2019 |
Genomic Divergence in Swedish Warmblood Horses Selected for Equestrian Disciplines
M Ablondi, S Eriksson, S Tetu, A Sabbioni, Å Viklund, S Mikko |
Genes & development | 2019 |
Blood Vessel Epicardial Substance (BVES) in junctional signaling and cancer
B Parang, JJ Thompson, CS Williams |
Tissue Barriers | 2018 |
NGS Technologies as a Turning Point in Rare Disease Research , Diagnosis and Treatment
A Fernandez-Marmiesse, S Gouveia, ML Couce |
Current medicinal chemistry | 2018 |
The Popeye Domain Containing Genes and Their Function as cAMP Effector Proteins in Striated Muscle
T Brand |
Journal of Cardiovascular Development and Disease | 2018 |
The Molecular Basis for Specificity at the Level of the Protein Kinase a Catalytic Subunit
K Søberg, BS Skålhegg |
Frontiers in Endocrinology | 2018 |
Antagonistic Effect of a Cytoplasmic Domain on the Basal Activity of Polymodal Potassium Channels
IB Soussia, FS Choveau, S Blin, EJ Kim, S Feliciangeli, FC Chatelain, D Kang, D Bichet, F Lesage |
Frontiers in molecular neuroscience | 2018 |
New kids on the block: The Popeye domain containing (POPDC) protein family acting as a novel class of cAMP effector proteins in striated muscle
T Brand, R Schindler |
Cellular Signalling | 2017 |
Development of the cardiac pacemaker
X Liang, SM Evans, Y Sun |
Cellular and Molecular Life Sciences | 2016 |
The Popeye Domain Containing Genes and Their Function in Striated Muscle
R Schindler, C Scotton, V French, A Ferlini, T Brand |
Journal of Cardiovascular Development and Disease | 2016 |
The Popeye domain containing protein family – A novel class of cAMP effectors with important functions in multiple tissues
RF Schindler, T Brand |
Progress in Biophysics and Molecular Biology | 2016 |
Limb-girdle muscular dystrophies — international collaborations for translational research
R Thompson, V Straub |
Nature Reviews Neurology | 2016 |
"Muscling" Throughout Life: Integrating Studies of Muscle Development, Homeostasis, and Disease in Zebrafish.
Goody MF, Carter EV, Kilroy EA, Maves L, Henry CA |
Current topics in developmental biology | 2016 |