Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Marie Louise Bang"'
Publikováno v:
Neural Plasticity, Vol 2015 (2015)
Neurexins (NXs) and neuroligins (NLs) are cell adhesion molecules that are localized at opposite sites of synaptic membranes. They interact with each other to promote the assembly, maintenance, and function of synapses in the central nervous system.
Externí odkaz:
https://doaj.org/article/5c452cb0ac5141979161249e89356dee
Autor:
Michelle Mendiola Pla, Silvia Berrettoni, Franklin H. Lee, Giacomo Rozzi, Federica Marrano, Ryan T. Gross, Amy Evans, David C. Wendell, Paul Lezberg, Margherita Burattini, Francesco Paolo lo Muzio, Lorenzo Fassina, Carmelo A. Milano, Marie-Louise Bang, Dawn E. Bowles, Michele Miragoli
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
BackgroundReliable biomarkers for assessing the viability of the donor hearts undergoing ex vivo perfusion remain elusive. A unique feature of normothermic ex vivo perfusion on the TransMedics® Organ Care System (OCS™) is that the donor heart is m
Externí odkaz:
https://doaj.org/article/a0e21047825d4ff7b2b72737bb167bf0
Autor:
Giuseppina Mastrototaro, Pierluigi Carullo, Jianlin Zhang, Beatrice Scellini, Nicoletta Piroddi, Simona Nemska, Maria Carmela Filomena, Simone Serio, Carol A Otey, Chiara Tesi, Fabian Emrich, Wolfgang A Linke, Corrado Poggesi, Simona Boncompagni, Marie-Louise Bang
Publikováno v:
eLife, Vol 12 (2023)
Palladin (PALLD) belongs to the PALLD/myopalladin (MYPN)/myotilin family of actin-associated immunoglobulin-containing proteins in the sarcomeric Z-line. PALLD is ubiquitously expressed in several isoforms, and its longest 200 kDa isoform, predominan
Externí odkaz:
https://doaj.org/article/48822b874b00423185ecb43b08a61552
Autor:
Simona Nemska, Simone Serio, Veronica Larcher, Giulia Beltrame, Nicola Marcello Portinaro, Marie-Louise Bang
Publikováno v:
Biomedicines, Vol 11, Iss 11, p 2918 (2023)
Cerebral palsy (CP) is the most common movement disorder in children, with a prevalence ranging from 1.5 to 4 per 1000 live births. CP is caused by a non-progressive lesion of the developing brain, leading to progressive alterations of the musculoske
Externí odkaz:
https://doaj.org/article/3f0e134bca6a438ead6375bc43a6a27a
Autor:
Maria Carmela Filomena, Daniel L Yamamoto, Pierluigi Carullo, Roman Medvedev, Andrea Ghisleni, Nicoletta Piroddi, Beatrice Scellini, Roberta Crispino, Francesca D'Autilia, Jianlin Zhang, Arianna Felicetta, Simona Nemska, Simone Serio, Chiara Tesi, Daniele Catalucci, Wolfgang A Linke, Roman Polishchuk, Corrado Poggesi, Mathias Gautel, Marie-Louise Bang
Publikováno v:
eLife, Vol 10 (2021)
Myopalladin (MYPN) is a striated muscle-specific immunoglobulin domain-containing protein located in the sarcomeric Z-line and I-band. MYPN gene mutations are causative for dilated (DCM), hypertrophic, and restrictive cardiomyopathy. In a yeast two-h
Externí odkaz:
https://doaj.org/article/1cdf953f8be642ebad6c7360bd93e8d7
Autor:
Vittoria Di Mauro, Paola Ceriotti, Francesco Lodola, Nicolò Salvarani, Jessica Modica, Marie-Louise Bang, Andrea Mazzanti, Carlo Napolitano, Silvia G. Priori, Daniele Catalucci
Publikováno v:
Frontiers in Physiology, Vol 11 (2021)
Brugada syndrome (BrS) is an inherited arrhythmogenic disease that may lead to sudden cardiac death in young adults with structurally normal hearts. No pharmacological therapy is available for BrS patients. This situation highlights the urgent need t
Externí odkaz:
https://doaj.org/article/185089ae836f4f82a40fa10a9c2cfed3
Publikováno v:
Am J Physiol Heart Circ Physiol
Inherited cardiomyopathies are a major cause of mortality and morbidity worldwide and can be caused by mutations in a wide range of proteins located in different cellular compartments. The present review is based on Dr. Ju Chen’s 2021 Robert M. Ber
Autor:
Giuseppina Mastrototaro, Pierluigi Carullo, Jianlin Zhang, Beatrice Scellini, Nicoletta Piroddi, Simona Nemska, Maria Carmela Filomena, Simone Serio, Carol A Otey, Chiara Tesi, Fabian Emrich, Wolfgang A Linke, Corrado Poggesi, Simona Boncompagni, Marie-Louise Bang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f70767f05fda83932e263fc193f693cd
https://doi.org/10.7554/elife.78629.sa2
https://doi.org/10.7554/elife.78629.sa2
Autor:
Marie Louise Bang, Daniel L. Yamamoto, Giuseppina Mastrototaro, Simone Serio, Marco Caremani, Richard L. Lieber, Ralph Knöll, Anupama Vydyanath, Marco Linari, Arcamaria Garofalo, Vinay Kumar Kadarla, Vincenzo Nigro, Irene Pertici, Maria Carmela Filomena, Margherita Mutarelli, Moriah R. Beck, Pradeep K. Luther
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle, Vol 11, Iss 1, Pp 169-194 (2020)
Journal of Cachexia, Sarcopenia and Muscle
Journal of Cachexia, Sarcopenia and Muscle
Background Myopalladin (MYPN) is a striated muscle‐specific, immunoglobulin‐containing protein located in the Z‐line and I‐band of the sarcomere as well as the nucleus. Heterozygous MYPN gene mutations are associated with hypertrophic, dilate
Left-ventricular hypertrophy, characterized by cardiomyocyte hypertrophy, interstitial cell proliferation, and immune cell infiltration, is a high risk factor for heart failure and death. Chemokines interacting with G protein-coupled chemokine recept
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35756e659c1ce649d7372cff6e0ba085
https://www.zora.uzh.ch/id/eprint/213443/
https://www.zora.uzh.ch/id/eprint/213443/