Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Bernat Gel

Showing results (31-40 of 49) with videos related to

Pageof 5
Sort By:
Stem Cell Reports|February 5, 2019
Reprogramming Captures the Genetic and Tumorigenic Properties of Neurofibromatosis Type 1 Plexiform NeurofibromasMeritxell Carrió, Helena Mazuelas, Yvonne Richaud-Patin, et al.
Genes & Diseases|August 1, 2025
iPSC-based merlin-deficient Schwann cell-like spheroids as an <i>in vitro</i> system for studying <i>NF2</i> pathogenesisNúria Catasús, Gemma Casals-Sendra, Miguel Torres-Martin, et al.
Human Genetics|June 1, 2021
Chromosomal translocations inactivating CDKN2A support a single path for malignant peripheral nerve sheath tumor initiationMiriam Magallón-Lorenz, Juana Fernández-Rodríguez, Ernest Terribas, et al.
Neuro-Oncology Advances|July 10, 2020
KIF11 and KIF15 mitotic kinesins are potential therapeutic vulnerabilities for malignant peripheral nerve sheath tumorsErnest Terribas, Marco Fernández, Helena Mazuelas, et al.
Clinical Genetics|October 2, 2019
Mutational spectrum by phenotype: panel-based NGS testing of patients with clinical suspicion of RASopathy and children with multiple café-au-lait maculesElisabeth Castellanos, Inma Rosas, Alex Negro, et al.
Human Mutation|May 19, 2018
Analysis of intratumor heterogeneity in Neurofibromatosis type 1 plexiform neurofibromas and neurofibromas with atypical features: Correlating histological and genomic findingsMeritxell Carrió, Bernat Gel, Ernest Terribas, et al.
Scientific Reports|January 5, 2017
A comprehensive custom panel design for routine hereditary cancer testing: preserving control, improving diagnostics and revealing a complex variation landscapeElisabeth Castellanos, Bernat Gel, Inma Rosas, et al.
Journal of Translational Medicine|February 4, 2026
Personalized medicine strategy for MPNSTs: using precision oncology on PDOX models to inform tumor boardsSara Ortega-Bertran, Juana Fernández-Rodríguez, Miriam Magallón-Lorenz, et al.
Cell Reports|February 16, 2022
Modeling iPSC-derived human neurofibroma-like tumors in mice uncovers the heterogeneity of Schwann cells within plexiform neurofibromasHelena Mazuelas, Míriam Magallón-Lorenz, Juana Fernández-Rodríguez, et al.
Blood|September 6, 2008
Common variants in NLRP2 and NLRP3 genes are strong prognostic factors for the outcome of HLA-identical sibling allogeneic stem cell transplantationMiquel Granell, Alvaro Urbano-Ispizua, Aina Pons, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
Stem Cell Reports|February 5, 2019
Reprogramming Captures the Genetic and Tumorigenic Properties of Neurofibromatosis Type 1 Plexiform NeurofibromasMeritxell Carrió, Helena Mazuelas, Yvonne Richaud-Patin, et al.
Genes & Diseases|August 1, 2025
iPSC-based merlin-deficient Schwann cell-like spheroids as an <i>in vitro</i> system for studying <i>NF2</i> pathogenesisNúria Catasús, Gemma Casals-Sendra, Miguel Torres-Martin, et al.
Human Genetics|June 1, 2021
Chromosomal translocations inactivating CDKN2A support a single path for malignant peripheral nerve sheath tumor initiationMiriam Magallón-Lorenz, Juana Fernández-Rodríguez, Ernest Terribas, et al.
Neuro-Oncology Advances|July 10, 2020
KIF11 and KIF15 mitotic kinesins are potential therapeutic vulnerabilities for malignant peripheral nerve sheath tumorsErnest Terribas, Marco Fernández, Helena Mazuelas, et al.
Clinical Genetics|October 2, 2019
Mutational spectrum by phenotype: panel-based NGS testing of patients with clinical suspicion of RASopathy and children with multiple café-au-lait maculesElisabeth Castellanos, Inma Rosas, Alex Negro, et al.
Human Mutation|May 19, 2018
Analysis of intratumor heterogeneity in Neurofibromatosis type 1 plexiform neurofibromas and neurofibromas with atypical features: Correlating histological and genomic findingsMeritxell Carrió, Bernat Gel, Ernest Terribas, et al.
Scientific Reports|January 5, 2017
A comprehensive custom panel design for routine hereditary cancer testing: preserving control, improving diagnostics and revealing a complex variation landscapeElisabeth Castellanos, Bernat Gel, Inma Rosas, et al.
Journal of Translational Medicine|February 4, 2026
Personalized medicine strategy for MPNSTs: using precision oncology on PDOX models to inform tumor boardsSara Ortega-Bertran, Juana Fernández-Rodríguez, Miriam Magallón-Lorenz, et al.
Cell Reports|February 16, 2022
Modeling iPSC-derived human neurofibroma-like tumors in mice uncovers the heterogeneity of Schwann cells within plexiform neurofibromasHelena Mazuelas, Míriam Magallón-Lorenz, Juana Fernández-Rodríguez, et al.
Blood|September 6, 2008
Common variants in NLRP2 and NLRP3 genes are strong prognostic factors for the outcome of HLA-identical sibling allogeneic stem cell transplantationMiquel Granell, Alvaro Urbano-Ispizua, Aina Pons, et al.
Pageof 5