Alexandra Salvi

University of California, San Francisco — United States

Medicine · Health Sciences

5h-index85citations22works1.32yr avg
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Research Topics

Asthma and respiratory diseases(3), Neurotransmitter Receptor Influence on Behavior(3), Neuroscience and Neuropharmacology Research(3), Nerve injury and regeneration(2), Ion channel regulation and function(2)

Publications22 total

Author response: Prosapip1 (encoded by the Lzts3 gene) in the dorsal hippocampus mediates synaptic protein composition, long-term potentiation, and spatial memory
2025Open Access
Paradoxical mTORC1-Dependent microRNA-mediated Translation Repression in the Nucleus Accumbens of Male Mice Consuming Alcohol Attenuates Glycolysis
Nature Communications·2025· 1 citedOpen Access
The Small G-Protein Rac1 in the Dorsomedial Striatum Promotes Alcohol-Dependent Structural Plasticity and Goal-Directed Learning in Mice
Journal of Neuroscience·2024· 3 citedOpen Access
Paradoxical mTORC1-Dependent microRNA-mediated Translation Repression in the Nucleus Accumbens of Mice Consuming Alcohol Attenuates Glycolysis
2023Open Access
The small G-protein Rac1 in the dorsomedial striatum promotes alcohol-dependent structural plasticity and goal-directed learning in mice
2023Open Access
Alcohol Inhibits Glycolysis in the Nucleus Accumbens of Mice Through mTORC1-Dependent Repression of Translation
Alcohol·2023Open Access
The Small G-Protein Rac1 Promotes Neuroadaptations that Underlie Alcohol Use Disorder
Alcohol·2023Open Access
Identification of Novel BDNF-Specific Corticostriatal Circuitries
eNeuro·2023· 8 citedOpen Access
Identification of novel BDNF-specific corticostriatal circuitries
2021· 1 citedOpen Access
Commentary: Long-Term Exercise Reduces Formation of Tubular Aggregates and Promotes Maintenance of Ca2+ Entry Units in Aged Muscle
Frontiers in Physiology·2021Open Access
A novel bi‐allelic loss‐of‐function mutation in <scp> <i>STIM1</i> </scp> expands the phenotype of <scp>STIM1</scp> ‐related diseases
Clinical Genetics·2021· 7 cited
Author response for "A novel bi‐allelic loss‐of‐function mutation in STIM1 expands the phenotype of STIM1 ‐related diseases"
2021
Author response for "A novel bi‐allelic loss‐of‐function mutation in STIM1 expands the phenotype of STIM1 ‐related diseases"
2021Open Access
Author response for "A novel bi‐allelic loss‐of‐function mutation in STIM1 expands the phenotype of STIM1 ‐related diseases"
2021Open Access
Novel phenotype in STIM1-related disorders including bones abnormalities and absence of immune defect
HAL (Le Centre pour la Communication Scientifique Directe)·2021Open Access
A novel bi-allelic loss-of-function mutation in STIM1 expands the phenotype of STIM1-related diseases
HAL (Le Centre pour la Communication Scientifique Directe)·2021· 1 citedOpen Access
Autosomal dominant segregation of <i>CAPN3</i> c.598_612del15 associated with a mild form of calpainopathy
Annals of Clinical and Translational Neurology·2020· 12 citedOpen Access
MUSCLE FUNCTION &amp; HOMEOSTASIS / MOLECULAR THERAPEUTIC APPROACHES
Neuromuscular Disorders·2020
Splicing impact of deep exonic missense variants in <i>CAPN3</i> explored systematically by minigene functional assay
Human Mutation·2020· 19 citedOpen Access
Novel <i>CAPN3</i> variant associated with an autosomal dominant calpainopathy
Neuropathology and Applied Neurobiology·2020· 31 citedOpen Access
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Frequent Co-authors

Marc Bartoli(12), Nicolas Lévy(10), Yann Ehinger(9), Khanhky Phamluong(9), Dorit Ron(9), Nathalie Da Silva(8), Cristina Skrypnyk(6), André Mégarbané(6), Valérie Delague(6), Zachary W. Hoisington(6), Jon Andoni Urtizberea(5), Sophie Laguesse(5), Martin Krahn(4), Drishti Soneja(4), Moiz Bakhiet(4), Catherine Robert(4), Svetlana Gorokhova(3), Chhavi Shukla(3), Yoshitaka Sei(3), Ken Nakamura(3)