Commentary: Long-Term Exercise Reduces Formation of Tubular Aggregates and Promotes Maintenance of Ca2+ Entry Units in Aged Muscle

Autor: Alexandra Salvi, André Maues De Paula, Nicolas Lévy, Shahram Attarian, Marc Bartoli

Publikováno v: Frontiers in Physiology, Vol 12 (2021)

Externí odkaz: https://doaj.org/article/c14a995b479046868d2975b78fcc1256

Identification of novel BDNF-specific corticostriatal circuitries

Autor: Yann Ehinger, Drishti Soneja, Khanhky Phamluong, Alexandra Salvi, Dorit Ron

BDNF is released from axon terminals originating in the cerebral cortex onto striatal neurons. Here, we characterized BDNF in the corticostriatal circuitry. First, we utilized Bdnf-Cre and Ribotag transgenic mouse lines to label BDNF-positive cells i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a985a5b139dcb3d255503ff2052818b6
https://doi.org/10.1101/2021.08.26.457842

A novel bi-allelic loss-of-function mutation in STIM1 expands the phenotype of STIM1-related diseases

Autor: Alexandra Salvi, Nathalie Da Silva, Nicolas Lévy, Jon Andoni Urtizberea, Marc Bartoli, Catherine Robert, André Mégarbané, Moiz Bakhiet, Valérie Delague, Cristina Skrypnyk

Publikováno v: Clinical Genetics
Clinical Genetics, Wiley, In press
HAL

International audience; STIM1, the stromal interaction molecule 1, is the key protein for maintaining calciumconcentration in the endoplasmic reticulum by triggering the Store Operated CalciumEntry (SOCE). Bi-allelic mutations in STIM1 gene are respo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77455758ec4205d194d0c7302b6a8a40
https://hal-amu.archives-ouvertes.fr/hal-03184458v2/document

Novel CAPN3 variant associated with an autosomal dominant calpainopathy

Autor: Pascal Cintas, Emmanuelle Campana-Salort, Alexandra Salvi, A. Maues de Paula, Jérémie Mortreux, T. Stojkovic, Céline Tard, Marc Bartoli, F. Leturcq, S. Attarian, Jean Pouget, Svetlana Gorokhova, Nathalie Bonello-Palot, Mathieu Cerino, Nicolas Lévy, Mireille Cossée, Martin Krahn, R. Juntas Morales, Dimitri Renard

Publikováno v: Neuropathology and Applied Neurobiology
Neuropathology and Applied Neurobiology, Wiley, 2020, ⟨10.1111/nan.12624⟩
Neuropathology and Applied Neurobiology, 2020, ⟨10.1111/nan.12624⟩

International audience; AimsThe most common autosomal recessive limb girdle muscular dystrophy is associated with the CAPN3 gene. The exclusively recessive inheritance of this disorder has been recently challenged by the description of the recurrent

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cdf736e275ca2034f875f0970d190dd
https://pubmed.ncbi.nlm.nih.gov/32342993

Identification of Novel BDNF-Specific Corticostriatal Circuitries.

Autor: Ehinger, Yann, Soneja, Drishti, Phamluong, Khanhky, Salvi, Alexandra, Ron, Dorit

Publikováno v: eNeuro; May2023, Vol. 10 Issue 5, p1-13, 13p