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Circulation. Genomic and Precision Medicine
|
October 26, 2018
Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy
Marzia De Bortoli, Alex V Postma, Giulia Poloni, et al.
Science Advances
|
January 6, 2023
Antagonistic effect of cyclin-dependent kinases and a calcium-dependent phosphatase on polyglutamine-expanded androgen receptor toxic gain of function
Diana Piol, Laura Tosatto, Emanuela Zuccaro, et al.
JACC. Clinical Electrophysiology
|
December 18, 2025
Desmoplakin Cardiomyopathy: Gene Dose-Dependent Myocardial Remodeling, Arrhythmias, and Premature Death
Anna Guazzo, Induja Perumal Vanaja, Anna Di Bona, et al.
Acta Neuropathologica Communications
|
April 16, 2022
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study
Aurora Fusto, Denise Cassandrini, Chiara Fiorillo, et al.
Human Mutation
|
April 26, 2017
Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI
Marco Carraro, Giovanni Minervini, Manuel Giollo, et al.
Nucleic Acids Research
|
December 1, 2016
DisProt 7.0: a major update of the database of disordered proteins
Damiano Piovesan, Francesco Tabaro, Ivan Mičetić, et al.
Nucleic Acids Research
|
December 15, 2016
Corrigendum: DisProt 7.0: a major update of the database of disordered proteins
Damiano Piovesan, Francesco Tabaro, Ivan Mičetić, et al.
Nucleic Acids Research
|
December 11, 2020
PED in 2021: a major update of the protein ensemble database for intrinsically disordered proteins
Tamas Lazar, Elizabeth Martínez-Pérez, Federica Quaglia, et al.
Nucleic Acids Research
|
December 1, 2021
DisProt in 2022: improved quality and accessibility of protein intrinsic disorder annotation
Federica Quaglia, Bálint Mészáros, Edoardo Salladini, et al.
Nucleic Acids Research
|
November 13, 2019
DisProt: intrinsic protein disorder annotation in 2020
András Hatos, Borbála Hajdu-Soltész, Alexander M Monzon, et al.
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Showing results (71-80 of 80) with videos related to
Sort By:
Page
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This site can display upto 80 results.
Circulation. Genomic and Precision Medicine
|
October 26, 2018
Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy
Marzia De Bortoli, Alex V Postma, Giulia Poloni, et al.
Science Advances
|
January 6, 2023
Antagonistic effect of cyclin-dependent kinases and a calcium-dependent phosphatase on polyglutamine-expanded androgen receptor toxic gain of function
Diana Piol, Laura Tosatto, Emanuela Zuccaro, et al.
JACC. Clinical Electrophysiology
|
December 18, 2025
Desmoplakin Cardiomyopathy: Gene Dose-Dependent Myocardial Remodeling, Arrhythmias, and Premature Death
Anna Guazzo, Induja Perumal Vanaja, Anna Di Bona, et al.
Acta Neuropathologica Communications
|
April 16, 2022
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study
Aurora Fusto, Denise Cassandrini, Chiara Fiorillo, et al.
Human Mutation
|
April 26, 2017
Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI
Marco Carraro, Giovanni Minervini, Manuel Giollo, et al.
Nucleic Acids Research
|
December 1, 2016
DisProt 7.0: a major update of the database of disordered proteins
Damiano Piovesan, Francesco Tabaro, Ivan Mičetić, et al.
Nucleic Acids Research
|
December 15, 2016
Corrigendum: DisProt 7.0: a major update of the database of disordered proteins
Damiano Piovesan, Francesco Tabaro, Ivan Mičetić, et al.
Nucleic Acids Research
|
December 11, 2020
PED in 2021: a major update of the protein ensemble database for intrinsically disordered proteins
Tamas Lazar, Elizabeth Martínez-Pérez, Federica Quaglia, et al.
Nucleic Acids Research
|
December 1, 2021
DisProt in 2022: improved quality and accessibility of protein intrinsic disorder annotation
Federica Quaglia, Bálint Mészáros, Edoardo Salladini, et al.
Nucleic Acids Research
|
November 13, 2019
DisProt: intrinsic protein disorder annotation in 2020
András Hatos, Borbála Hajdu-Soltész, Alexander M Monzon, et al.
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of 8