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Giulia Babbi

Showing results (21-30 of 44) with videos related to

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Frontiers in Molecular Biosciences|May 26, 2023
Resources and tools for rare disease variant interpretationLuana Licata, Allegra Via, Paola Turina, et al.
International Journal of Cancer|April 20, 2018
Mutant MYO1F alters the mitochondrial network and induces tumor proliferation in thyroid cancerChiara Diquigiovanni, Christian Bergamini, Cecilia Evangelisti, et al.
Human Genetics|February 11, 2025
Evaluating predictors of kinase activity of STK11 variants identified in primary human non-small cell lung cancersYile Chen, Kyoungyeul Lee, Junwoo Woo, et al.
Research Square|July 16, 2024
Evaluating predictors of kinase activity of STK11 variants identified in primary human non-small cell lung cancersYile Chen, Kyoungyeul Lee, Junwoo Woo, et al.
Human Mutation|June 19, 2019
Evaluating the predictions of the protein stability change upon single amino acid substitutions for the FXN CAGI5 challengeCastrense Savojardo, Maria Petrosino, Giulia Babbi, et al.
Human Mutation|July 2, 2019
Performance of computational methods for the evaluation of pericentriolar material 1 missense variants in CAGI-5Alexander Miguel Monzon, Marco Carraro, Luigi Chiricosta, et al.
Msphere|January 15, 2026
<i>Acinetobacter</i> enrichment shapes composition and function of the bacterial microbiota of field-grown tomato plantsSenga Robertson, Alexandros Mosca, Saira Ashraf, et al.
Research Square|August 14, 2023
CAGI6 ID-Challenge: Assessment of phenotype and variant predictions in 415 children with Neurodevelopmental Disorders (NDDs)Maria Cristina Aspromonte, Alessio Del Conte, Shaowen Zhu, et al.
Human Mutation|June 27, 2019
Assessing the performance of in silico methods for predicting the pathogenicity of variants in the gene CHEK2, among Hispanic females with breast cancerAlin Voskanian, Panagiotis Katsonis, Olivier Lichtarge, et al.
Human Genetics|January 9, 2025
CAGI6 ID panel challenge: assessment of phenotype and variant predictions in 415 children with neurodevelopmental disorders (NDDs)Maria Cristina Aspromonte, Alessio Del Conte, Shaowen Zhu, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
Frontiers in Molecular Biosciences|May 26, 2023
Resources and tools for rare disease variant interpretationLuana Licata, Allegra Via, Paola Turina, et al.
International Journal of Cancer|April 20, 2018
Mutant MYO1F alters the mitochondrial network and induces tumor proliferation in thyroid cancerChiara Diquigiovanni, Christian Bergamini, Cecilia Evangelisti, et al.
Human Genetics|February 11, 2025
Evaluating predictors of kinase activity of STK11 variants identified in primary human non-small cell lung cancersYile Chen, Kyoungyeul Lee, Junwoo Woo, et al.
Research Square|July 16, 2024
Evaluating predictors of kinase activity of STK11 variants identified in primary human non-small cell lung cancersYile Chen, Kyoungyeul Lee, Junwoo Woo, et al.
Human Mutation|June 19, 2019
Evaluating the predictions of the protein stability change upon single amino acid substitutions for the FXN CAGI5 challengeCastrense Savojardo, Maria Petrosino, Giulia Babbi, et al.
Human Mutation|July 2, 2019
Performance of computational methods for the evaluation of pericentriolar material 1 missense variants in CAGI-5Alexander Miguel Monzon, Marco Carraro, Luigi Chiricosta, et al.
Msphere|January 15, 2026
<i>Acinetobacter</i> enrichment shapes composition and function of the bacterial microbiota of field-grown tomato plantsSenga Robertson, Alexandros Mosca, Saira Ashraf, et al.
Research Square|August 14, 2023
CAGI6 ID-Challenge: Assessment of phenotype and variant predictions in 415 children with Neurodevelopmental Disorders (NDDs)Maria Cristina Aspromonte, Alessio Del Conte, Shaowen Zhu, et al.
Human Mutation|June 27, 2019
Assessing the performance of in silico methods for predicting the pathogenicity of variants in the gene CHEK2, among Hispanic females with breast cancerAlin Voskanian, Panagiotis Katsonis, Olivier Lichtarge, et al.
Human Genetics|January 9, 2025
CAGI6 ID panel challenge: assessment of phenotype and variant predictions in 415 children with neurodevelopmental disorders (NDDs)Maria Cristina Aspromonte, Alessio Del Conte, Shaowen Zhu, et al.
Pageof 5