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Showing results (41-50 of 147) with videos related to

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Clinical Genetics|October 16, 2012
Hereditary trichilemmal cysts: a proposal for the assessment of diagnostic clinical criteriaS Seidenari, G Pellacani, S Nasti, et al.
Oncotarget|October 27, 2015
The 5'-untranslated region of p16INK4a melanoma tumor suppressor acts as a cellular IRES, controlling mRNA translation under hypoxia through YBX1 bindingAlessandra Bisio, Elisa Latorre, Virginia Andreotti, et al.
Human Pathology|August 7, 2004
Inverse correlation between p16INK4A expression and NF-kappaB activation in melanoma progressionPaola Ghiorzo, Michela Mantelli, Sara Gargiulo, et al.
European Journal of Endocrinology|February 27, 2008
Uncommon association of germline mutations of RET proto-oncogene and CDKN2A geneL Foppiani, F Forzano, I Ceccherini, et al.
Clinical Genetics|October 8, 2009
Five novel germline function-impairing mutations of CYLD in Italian patients with multiple cylindromasS Nasti, L Pastorino, W Bruno, et al.
Oncotarget|February 22, 2018
Combining molecular and immunohistochemical analyses of key drivers in primary melanomas: interplay between germline and somatic variationsWilliam Bruno, Claudia Martinuzzi, Bruna Dalmasso, et al.
Future Oncology (London, England)|February 25, 2014
Brooke-Spiegler syndrome tumor spectrum beyond the skin: a patient carrying germline R936X CYLD mutation and a somatic CYLD mutation in Brenner tumorGiovanni Ponti, Cristel Ruini, Giampiero Girolomoni, et al.
Human Pathology|January 28, 2004
Expression and localization of mutant p16 proteins in melanocytic lesions from familial melanoma patientsPaola Ghiorzo, Barbara Villaggio, Angela Rita Sementa, et al.
Oncotarget|July 10, 2018
Correction: Combining molecular and immunohistochemical analyses of key drivers in primary melanomas: interplay between germline and somatic variationsWilliam Bruno, Claudia Martinuzzi, Bruna Dalmasso, et al.
Children (Basel, Switzerland)|October 29, 2025
Synchronous Cardiac Fibroma and Medulloblastoma in Gorlin Syndrome: A Paradigmatic Case and Narrative ReviewMarta Molteni, Gianluca Trocchio, Antonio Verrico, et al.
Pageof 15

Showing results (41-50 of 147) with videos related to

Sort By:
Pageof 15
Clinical Genetics|October 16, 2012
Hereditary trichilemmal cysts: a proposal for the assessment of diagnostic clinical criteriaS Seidenari, G Pellacani, S Nasti, et al.
Oncotarget|October 27, 2015
The 5'-untranslated region of p16INK4a melanoma tumor suppressor acts as a cellular IRES, controlling mRNA translation under hypoxia through YBX1 bindingAlessandra Bisio, Elisa Latorre, Virginia Andreotti, et al.
Human Pathology|August 7, 2004
Inverse correlation between p16INK4A expression and NF-kappaB activation in melanoma progressionPaola Ghiorzo, Michela Mantelli, Sara Gargiulo, et al.
European Journal of Endocrinology|February 27, 2008
Uncommon association of germline mutations of RET proto-oncogene and CDKN2A geneL Foppiani, F Forzano, I Ceccherini, et al.
Clinical Genetics|October 8, 2009
Five novel germline function-impairing mutations of CYLD in Italian patients with multiple cylindromasS Nasti, L Pastorino, W Bruno, et al.
Oncotarget|February 22, 2018
Combining molecular and immunohistochemical analyses of key drivers in primary melanomas: interplay between germline and somatic variationsWilliam Bruno, Claudia Martinuzzi, Bruna Dalmasso, et al.
Future Oncology (London, England)|February 25, 2014
Brooke-Spiegler syndrome tumor spectrum beyond the skin: a patient carrying germline R936X CYLD mutation and a somatic CYLD mutation in Brenner tumorGiovanni Ponti, Cristel Ruini, Giampiero Girolomoni, et al.
Human Pathology|January 28, 2004
Expression and localization of mutant p16 proteins in melanocytic lesions from familial melanoma patientsPaola Ghiorzo, Barbara Villaggio, Angela Rita Sementa, et al.
Oncotarget|July 10, 2018
Correction: Combining molecular and immunohistochemical analyses of key drivers in primary melanomas: interplay between germline and somatic variationsWilliam Bruno, Claudia Martinuzzi, Bruna Dalmasso, et al.
Children (Basel, Switzerland)|October 29, 2025
Synchronous Cardiac Fibroma and Medulloblastoma in Gorlin Syndrome: A Paradigmatic Case and Narrative ReviewMarta Molteni, Gianluca Trocchio, Antonio Verrico, et al.
Pageof 15