Silvia Moleri
Milan, Italy
Last Updated: 09/26/2026
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Found 9 publications
Global downstream BMP15 pathway analysis in human ovarian granulosa cells reveals novel genetic variations associated with primary ovarian insufficiency.
Journal: Maturitas
Published: December 19, 2025
A TAp63alpha truncating variant associated with primary ovarian insufficiency lowers the cellular apoptotic rate.
Journal: Journal of ovarian research
Published: May 05, 2025
Primary ovarian insufficiency: update on clinical and genetic findings.
Journal: Frontiers in endocrinology
Published: July 15, 2024
Lymphatic Defects in Zebrafish sox18 Mutants Are Exacerbated by Perturbed VEGFC Signaling, While Masked by Elevated sox7 Expression.
Journal: Cells
Published: June 23, 2023
Targeted Next-Generation Sequencing Indicates a Frequent Oligogenic Involvement in Primary Ovarian Insufficiency Onset.
Journal: Frontiers in endocrinology
Published: February 05, 2021
Fundamental role of BMP15 in human ovarian folliculogenesis revealed by null and missense mutations associated with primary ovarian insufficiency.
Journal: Human mutation
Published: April 10, 2019
A light-gated potassium channel for sustained neuronal inhibition.
Journal: Nature methods
Published: January 23, 2018
Characterization and expression analysis of mcoln1.1 and mcoln1.2, the putative zebrafish co-orthologs of the gene responsible for human mucolipidosis type IV.
Journal: The International journal of developmental biology
Published: April 16, 2013
Sox18 genetically interacts with VegfC to regulate lymphangiogenesis in zebrafish.
Journal: Arteriosclerosis, thrombosis, and vascular biology
Published: March 23, 2013
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Last Updated: 09/26/2026