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Oncotarget
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September 9, 2017
TGFbeta and miRNA regulation in familial and sporadic breast cancer
Katia Danza, Simona De Summa, Rosamaria Pinto, et al.
Genes
|
November 29, 2019
Novel <i>TNXB</i> Variants in Two Italian Patients with Classical-Like Ehlers-Danlos Syndrome
Lucia Micale, Vito Guarnieri, Bartolomeo Augello, et al.
Molecular Syndromology
|
November 22, 2016
<i>PARK2</i> Microduplication: Clinical and Molecular Characterization of a Further Case and Review of the Literature
Orazio Palumbo, Pietro Palumbo, Maria P Leone, et al.
Plos One
|
August 20, 2015
Identification and Clinical Characterization of Adult Patients with Multigenerational Diabetes Mellitus
Ornella Ludovico, Massimo Carella, Luigi Bisceglia, et al.
Computational and Structural Biotechnology Journal
|
August 18, 2020
Mechanisms of pathogenesis of missense mutations on the KDM6A-H3 interaction in type 2 Kabuki Syndrome
Francesco Petrizzelli, Tommaso Biagini, Alessandro Barbieri, et al.
Evolutionary Bioinformatics Online
|
June 18, 2019
Are Gaming-Enabled Graphic Processing Unit Cards Convenient for Molecular Dynamics Simulation?
Tommaso Biagini, Francesco Petrizzelli, Mauro Truglio, et al.
International Journal of Molecular Sciences
|
August 7, 2021
A Novel Genetic Variant in the WFS1 Gene in a Patient with Partial Uniparental Mero-Isodisomy of Chromosome 4
Maurizio Delvecchio, Federica Ortolani, Orazio Palumbo, et al.
Oncotarget
|
December 30, 2017
A primary tumor gene expression signature identifies a crucial role played by tumor stroma myofibroblasts in lymph node involvement in oral squamous cell carcinoma
Gianluigi Mazzoccoli, Stefano Castellana, Massimo Carella, et al.
Pediatrics
|
June 22, 2017
Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome
Alessandro Mussa, Cristina Molinatto, Flavia Cerrato, et al.
European Journal of Human Genetics : EJHG
|
February 22, 2019
A novel dominant-negative FGFR1 variant causes Hartsfield syndrome by deregulating RAS/ERK1/2 pathway
Pietro Palumbo, Antonio Petracca, Roberto Maggi, et al.
Page
of 21
Search research articles
Search
Showing results (61-70 of 207) with videos related to
Sort By:
Page
of 21
Oncotarget
|
September 9, 2017
TGFbeta and miRNA regulation in familial and sporadic breast cancer
Katia Danza, Simona De Summa, Rosamaria Pinto, et al.
Genes
|
November 29, 2019
Novel <i>TNXB</i> Variants in Two Italian Patients with Classical-Like Ehlers-Danlos Syndrome
Lucia Micale, Vito Guarnieri, Bartolomeo Augello, et al.
Molecular Syndromology
|
November 22, 2016
<i>PARK2</i> Microduplication: Clinical and Molecular Characterization of a Further Case and Review of the Literature
Orazio Palumbo, Pietro Palumbo, Maria P Leone, et al.
Plos One
|
August 20, 2015
Identification and Clinical Characterization of Adult Patients with Multigenerational Diabetes Mellitus
Ornella Ludovico, Massimo Carella, Luigi Bisceglia, et al.
Computational and Structural Biotechnology Journal
|
August 18, 2020
Mechanisms of pathogenesis of missense mutations on the KDM6A-H3 interaction in type 2 Kabuki Syndrome
Francesco Petrizzelli, Tommaso Biagini, Alessandro Barbieri, et al.
Evolutionary Bioinformatics Online
|
June 18, 2019
Are Gaming-Enabled Graphic Processing Unit Cards Convenient for Molecular Dynamics Simulation?
Tommaso Biagini, Francesco Petrizzelli, Mauro Truglio, et al.
International Journal of Molecular Sciences
|
August 7, 2021
A Novel Genetic Variant in the WFS1 Gene in a Patient with Partial Uniparental Mero-Isodisomy of Chromosome 4
Maurizio Delvecchio, Federica Ortolani, Orazio Palumbo, et al.
Oncotarget
|
December 30, 2017
A primary tumor gene expression signature identifies a crucial role played by tumor stroma myofibroblasts in lymph node involvement in oral squamous cell carcinoma
Gianluigi Mazzoccoli, Stefano Castellana, Massimo Carella, et al.
Pediatrics
|
June 22, 2017
Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome
Alessandro Mussa, Cristina Molinatto, Flavia Cerrato, et al.
European Journal of Human Genetics : EJHG
|
February 22, 2019
A novel dominant-negative FGFR1 variant causes Hartsfield syndrome by deregulating RAS/ERK1/2 pathway
Pietro Palumbo, Antonio Petracca, Roberto Maggi, et al.
Page
of 21