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Barbara Pasini

Showing results (41-50 of 96) with videos related to

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European Journal of Medical Genetics|February 5, 2017
A case of Feingold type 2 syndrome associated with keratoconus refines keratoconus type 7 locus on chromosome 13qFabio Sirchia, Eleonora Di Gregorio, Gabriella Restagno, et al.
Endocrine Pathology|February 18, 2026
From Tissue Architecture To Genetic Signature: Artificial intelligence-based Analysis of Reticulin Framework and Clinical Variables Predicts Molecular Cluster in ParagangliomasEleonora Duregon, Mirko Parasiliti-Caprino, Giulia Orlando, et al.
Clinical Genetics|July 7, 2019
Germline mutations and new copy number variants among 40 pediatric cancer patients suspected for genetic predispositionAntonella Gambale, Roberta Russo, Immacolata Andolfo, et al.
Journal of Human Genetics|February 8, 2006
Mutational screening of the RB1 gene in Italian patients with retinoblastoma reveals 11 novel mutationsKatia Sampieri, Theodora Hadjistilianou, Francesca Mari, et al.
Melanoma Research|June 23, 2023
Temporal correlation between the first melanoma and the first noncutaneous tumor in CKDN2A genotyped patientsLaura Cristina Gironi, Elia Esposto, Francesca Zottarelli, et al.
Familial Cancer|May 8, 2014
A founder MLH1 mutation in Lynch syndrome families from Piedmont, Italy, is associated with an increased risk of pancreatic tumours and diverse immunohistochemical patternsIolanda Borelli, Guido C Casalis Cavalchini, Serena Del Peschio, et al.
International Journal of Cancer|August 26, 2018
The expression of LINE1-MET chimeric transcript identifies a subgroup of aggressive breast cancersUmberto Miglio, Enrico Berrino, Mara Panero, et al.
Cancers|April 3, 2019
<i>TERT</i> Promoter Mutations are Associated with Visceral Spreading in Melanoma of the TrunkSimona Osella-Abate, Luca Bertero, Rebecca Senetta, et al.
The Journal of Pathology|August 12, 2009
Does chromosome 17 centromere copy number predict polysomy in breast cancer? A fluorescence in situ hybridization and microarray-based CGH analysisCaterina Marchiò, Maryou B Lambros, Patrizia Gugliotta, et al.
European Journal of Endocrinology|April 1, 2022
Development and internal validation of a predictive model for the estimation of pheochromocytoma recurrence risk after radical surgeryMirko Parasiliti-Caprino, Fabio Bioletto, Chiara Lopez, et al.
Pageof 10

Showing results (41-50 of 96) with videos related to

Sort By:
Pageof 10
European Journal of Medical Genetics|February 5, 2017
A case of Feingold type 2 syndrome associated with keratoconus refines keratoconus type 7 locus on chromosome 13qFabio Sirchia, Eleonora Di Gregorio, Gabriella Restagno, et al.
Endocrine Pathology|February 18, 2026
From Tissue Architecture To Genetic Signature: Artificial intelligence-based Analysis of Reticulin Framework and Clinical Variables Predicts Molecular Cluster in ParagangliomasEleonora Duregon, Mirko Parasiliti-Caprino, Giulia Orlando, et al.
Clinical Genetics|July 7, 2019
Germline mutations and new copy number variants among 40 pediatric cancer patients suspected for genetic predispositionAntonella Gambale, Roberta Russo, Immacolata Andolfo, et al.
Journal of Human Genetics|February 8, 2006
Mutational screening of the RB1 gene in Italian patients with retinoblastoma reveals 11 novel mutationsKatia Sampieri, Theodora Hadjistilianou, Francesca Mari, et al.
Melanoma Research|June 23, 2023
Temporal correlation between the first melanoma and the first noncutaneous tumor in CKDN2A genotyped patientsLaura Cristina Gironi, Elia Esposto, Francesca Zottarelli, et al.
Familial Cancer|May 8, 2014
A founder MLH1 mutation in Lynch syndrome families from Piedmont, Italy, is associated with an increased risk of pancreatic tumours and diverse immunohistochemical patternsIolanda Borelli, Guido C Casalis Cavalchini, Serena Del Peschio, et al.
International Journal of Cancer|August 26, 2018
The expression of LINE1-MET chimeric transcript identifies a subgroup of aggressive breast cancersUmberto Miglio, Enrico Berrino, Mara Panero, et al.
Cancers|April 3, 2019
<i>TERT</i> Promoter Mutations are Associated with Visceral Spreading in Melanoma of the TrunkSimona Osella-Abate, Luca Bertero, Rebecca Senetta, et al.
The Journal of Pathology|August 12, 2009
Does chromosome 17 centromere copy number predict polysomy in breast cancer? A fluorescence in situ hybridization and microarray-based CGH analysisCaterina Marchiò, Maryou B Lambros, Patrizia Gugliotta, et al.
European Journal of Endocrinology|April 1, 2022
Development and internal validation of a predictive model for the estimation of pheochromocytoma recurrence risk after radical surgeryMirko Parasiliti-Caprino, Fabio Bioletto, Chiara Lopez, et al.
Pageof 10