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Sabina Barresi

Showing results (81-90 of 90) with videos related to

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Neuropathology and Applied Neurobiology|July 13, 2026
Utility of Optical Genome Mapping in the Characterisation of the Global Genomic Architecture of Paediatric Central Nervous System Tumours: A Pilot StudyViola Alesi, Silvia Genovese, Serena Russo, et al.
Gut|April 9, 2017
CHK1-targeted therapy to deplete DNA replication-stressed, p53-deficient, hyperdiploid colorectal cancer stem cellsGwenola Manic, Michele Signore, Antonella Sistigu, et al.
Pigment Cell & Melanoma Research|January 6, 2026
Melanomas and Mesenchymal Tumors Arising in Giant Congenital Melanocytic Nevi: Clinico-Pathological and Molecular Characterization of a Case SeriesSabrina Rossi, Sabina Barresi, Isabella Giovannoni, et al.
Haematologica|May 9, 2020
CD28.OX40 co-stimulatory combination is associated with long in vivo persistence and high activity of CAR.CD30 T-cellsMarika Guercio, Domenico Orlando, Stefano Di Cecca, et al.
Cancer Letters|February 29, 2024
Clinicopathological and molecular landscape of 5-year IDH-wild-type glioblastoma survivors: A multicentric retrospective studyEvelina Miele, Elena Anghileri, Chiara Calatozzolo, et al.
Cell Reports|March 5, 2020
The Interplay between CD27<sup>dull</sup> and CD27<sup>bright</sup> B Cells Ensures the Flexibility, Stability, and Resilience of Human B Cell MemoryOla Grimsholm, Eva Piano Mortari, Alexey N Davydov, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|November 25, 2023
PATZ1-Rearranged Tumors of the Central Nervous System: Characterization of a Pediatric Series of Seven CasesSabrina Rossi, Sabina Barresi, Giovanna Stefania Colafati, et al.
American Journal of Human Genetics|December 20, 2023
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndromeVincenzo Salpietro, Reza Maroofian, Maha S Zaki, et al.
Nature Communications|February 1, 2020
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathyHolger Hengel, Célia Bosso-Lefèvre, George Grady, et al.
Science Advances|December 3, 2020
Histone H3.3 beyond cancer: Germline mutations in <i>Histone 3 Family 3A and 3B</i> cause a previously unidentified neurodegenerative disorder in 46 patientsLaura Bryant, Dong Li, Samuel G Cox, et al.
Pageof 9

Showing results (81-90 of 90) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 90 results.
Neuropathology and Applied Neurobiology|July 13, 2026
Utility of Optical Genome Mapping in the Characterisation of the Global Genomic Architecture of Paediatric Central Nervous System Tumours: A Pilot StudyViola Alesi, Silvia Genovese, Serena Russo, et al.
Gut|April 9, 2017
CHK1-targeted therapy to deplete DNA replication-stressed, p53-deficient, hyperdiploid colorectal cancer stem cellsGwenola Manic, Michele Signore, Antonella Sistigu, et al.
Pigment Cell & Melanoma Research|January 6, 2026
Melanomas and Mesenchymal Tumors Arising in Giant Congenital Melanocytic Nevi: Clinico-Pathological and Molecular Characterization of a Case SeriesSabrina Rossi, Sabina Barresi, Isabella Giovannoni, et al.
Haematologica|May 9, 2020
CD28.OX40 co-stimulatory combination is associated with long in vivo persistence and high activity of CAR.CD30 T-cellsMarika Guercio, Domenico Orlando, Stefano Di Cecca, et al.
Cancer Letters|February 29, 2024
Clinicopathological and molecular landscape of 5-year IDH-wild-type glioblastoma survivors: A multicentric retrospective studyEvelina Miele, Elena Anghileri, Chiara Calatozzolo, et al.
Cell Reports|March 5, 2020
The Interplay between CD27<sup>dull</sup> and CD27<sup>bright</sup> B Cells Ensures the Flexibility, Stability, and Resilience of Human B Cell MemoryOla Grimsholm, Eva Piano Mortari, Alexey N Davydov, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|November 25, 2023
PATZ1-Rearranged Tumors of the Central Nervous System: Characterization of a Pediatric Series of Seven CasesSabrina Rossi, Sabina Barresi, Giovanna Stefania Colafati, et al.
American Journal of Human Genetics|December 20, 2023
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndromeVincenzo Salpietro, Reza Maroofian, Maha S Zaki, et al.
Nature Communications|February 1, 2020
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathyHolger Hengel, Célia Bosso-Lefèvre, George Grady, et al.
Science Advances|December 3, 2020
Histone H3.3 beyond cancer: Germline mutations in <i>Histone 3 Family 3A and 3B</i> cause a previously unidentified neurodegenerative disorder in 46 patientsLaura Bryant, Dong Li, Samuel G Cox, et al.
Pageof 9