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Clinical and Translational Gastroenterology|October 23, 2020
Targeted Sequencing of Sorted Esophageal Adenocarcinoma Cells Unveils Known and Novel Mutations in the Separated SubpopulationsFederica Isidori, Isotta Bozzarelli, Luca Mastracci, et al.
American Journal of Human Genetics|May 7, 2005
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficitsKay D MacDermot, Elena Bonora, Nuala Sykes, et al.
International Journal of Molecular Sciences|June 2, 2021
Detecting Variants in the NBN Gene While Testing for Hereditary Breast Cancer: What to Do Next?Roberta Zuntini, Elena Bonora, Laura Maria Pradella, et al.
Advances in Experimental Medicine and Biology|December 31, 2022
Clinical and Pathological Features of Severe Gut DysmotilityFrancesca Bianco, Elena Bonora, Giulia Lattanzio, et al.
Human Molecular Genetics|March 6, 2015
HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brainLachlan A Jolly, Lam Son Nguyen, Deepti Domingo, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|February 20, 2016
Prucalopride exerts neuroprotection in human enteric neuronsFrancesca Bianco, Elena Bonora, Dipa Natarajan, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|September 24, 2019
Enteric neuron density correlates with clinical features of severe gut dysmotilityElisa Boschetti, Carolina Malagelada, Anna Accarino, et al.
Cancers|February 10, 2024
miRNA-221 and miRNA-483-3p Dysregulation in Esophageal AdenocarcinomaIsotta Bozzarelli, Arianna Orsini, Federica Isidori, et al.
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