Showing results (31-40 of 70) with videos related to

Sort By:
Pageof 7
Human Mutation|May 18, 2022
MiRLog and dbmiR: Prioritization and functional annotation tools to study human microRNA sequence variantsAgnese Giovannetti, Salvatore Daniele Bianco, Alice Traversa, et al.
Molecular and Cellular Biology|July 4, 2007
ROCK2 and its alternatively spliced isoform ROCK2m positively control the maturation of the myogenic programMichele Pelosi, Francesco Marampon, Bianca M Zani, et al.
Genes|December 23, 2022
Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center StudyCarolina Putotto, Federica Pulvirenti, Flaminia Pugnaloni, et al.
Bone|December 17, 2020
GDF5 mutation case report and a systematic review of molecular and clinical spectrum: Expanding current knowledge on genotype-phenotype correlationsMaria Luce Genovesi, Daniele Guadagnolo, Enrica Marchionni, et al.
Journal of Dental Sciences|September 30, 2024
Small RNAs and tooth development: The role of microRNAs in tooth agenesis and impactionAgnese Giovannetti, Rosanna Guarnieri, Francesco Petrizzelli, et al.
Gene|December 15, 2015
Molecular analysis of sarcomeric and non-sarcomeric genes in patients with hypertrophic cardiomyopathyIrene Bottillo, Daniela D'Angelantonio, Viviana Caputo, et al.
Journal of Pediatric Genetics|December 1, 2021
Correlating Neuroimaging and CNVs Data: 7 Years of Cytogenomic Microarray Analysis on Patients Affected by Neurodevelopmental DisordersRoberta Milone, Claudia Cesario, Marina Goldoni, et al.
Translational Psychiatry|June 11, 2020
Genomic and physiological resilience in extreme environments are associated with a secure attachment styleViviana Caputo, Maria Giuseppina Pacilli, Ivan Arisi, et al.
Archives of Oral Biology|April 30, 2018
Whole exome sequencing in an Italian family with isolated maxillary canine agenesis and canine eruption anomaliesErsilia Barbato, Alice Traversa, Rosanna Guarnieri, et al.
Molecular Genetics & Genomic Medicine|November 23, 2019
Prenatal whole exome sequencing detects a new homozygous fukutin (FKTN) mutation in a fetus with an ultrasound suspicion of familial Dandy-Walker malformationAlice Traversa, Silvia Bernardo, Alessandro Paiardini, et al.
Pageof 7