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

Brunangelo Falini

Showing results (141-150 of 246) with videos related to

Pageof 25
Sort By:
Blood|May 12, 2009
AML with mutated NPM1 carrying a normal or aberrant karyotype show overlapping biologic, pathologic, immunophenotypic, and prognostic featuresClaudia Haferlach, Cristina Mecucci, Susanne Schnittger, et al.
The Journal of Experimental Medicine|September 17, 2008
Origin and pathogenesis of nodular lymphocyte-predominant Hodgkin lymphoma as revealed by global gene expression analysisVerena Brune, Enrico Tiacci, Ines Pfeil, et al.
Cancer Research|July 10, 2007
Born to be exported: COOH-terminal nuclear export signals of different strength ensure cytoplasmic accumulation of nucleophosmin leukemic mutantsNiccolò Bolli, Ildo Nicoletti, M Felicetta De Marco, et al.
Haematologica|January 26, 2013
Constant activation of the RAF-MEK-ERK pathway as a diagnostic and therapeutic target in hairy cell leukemiaEnrico Tiacci, Gianluca Schiavoni, Maria Paola Martelli, et al.
Blood|October 27, 2011
Simple genetic diagnosis of hairy cell leukemia by sensitive detection of the BRAF-V600E mutationEnrico Tiacci, Gianluca Schiavoni, Francesco Forconi, et al.
European Journal of Ophthalmology|February 23, 2022
Choroidal vasculature analysis in MEK inhibitor-associated retinopathyAlessio Cerquaglia, Marco Lupidi, Jay Chhablani, et al.
Hemasphere|April 27, 2026
Neuroinflammatory changes in acute myeloid leukemia: Evidence for blood-brain barrier disruption and glial activationMarta Febo, Daniele Sorcini, Alessandra Mirarchi, et al.
Blood|February 26, 2013
The human NPM1 mutation A perturbs megakaryopoiesis in a conditional mouse modelPaolo Sportoletti, Emanuela Varasano, Roberta Rossi, et al.
Nucleic Acids Research|January 19, 2013
Nucleophosmin mutations alter its nucleolar localization by impairing G-quadruplex binding at ribosomal DNASara Chiarella, Antonella De Cola, Giovanni Luca Scaglione, et al.
Blood|July 26, 2003
Expression of the IRTA1 receptor identifies intraepithelial and subepithelial marginal zone B cells of the mucosa-associated lymphoid tissue (MALT)Brunangelo Falini, Enrico Tiacci, Alessandra Pucciarini, et al.
Pageof 25

Showing results (141-150 of 246) with videos related to

Sort By:
Pageof 25
Blood|May 12, 2009
AML with mutated NPM1 carrying a normal or aberrant karyotype show overlapping biologic, pathologic, immunophenotypic, and prognostic featuresClaudia Haferlach, Cristina Mecucci, Susanne Schnittger, et al.
The Journal of Experimental Medicine|September 17, 2008
Origin and pathogenesis of nodular lymphocyte-predominant Hodgkin lymphoma as revealed by global gene expression analysisVerena Brune, Enrico Tiacci, Ines Pfeil, et al.
Cancer Research|July 10, 2007
Born to be exported: COOH-terminal nuclear export signals of different strength ensure cytoplasmic accumulation of nucleophosmin leukemic mutantsNiccolò Bolli, Ildo Nicoletti, M Felicetta De Marco, et al.
Haematologica|January 26, 2013
Constant activation of the RAF-MEK-ERK pathway as a diagnostic and therapeutic target in hairy cell leukemiaEnrico Tiacci, Gianluca Schiavoni, Maria Paola Martelli, et al.
Blood|October 27, 2011
Simple genetic diagnosis of hairy cell leukemia by sensitive detection of the BRAF-V600E mutationEnrico Tiacci, Gianluca Schiavoni, Francesco Forconi, et al.
European Journal of Ophthalmology|February 23, 2022
Choroidal vasculature analysis in MEK inhibitor-associated retinopathyAlessio Cerquaglia, Marco Lupidi, Jay Chhablani, et al.
Hemasphere|April 27, 2026
Neuroinflammatory changes in acute myeloid leukemia: Evidence for blood-brain barrier disruption and glial activationMarta Febo, Daniele Sorcini, Alessandra Mirarchi, et al.
Blood|February 26, 2013
The human NPM1 mutation A perturbs megakaryopoiesis in a conditional mouse modelPaolo Sportoletti, Emanuela Varasano, Roberta Rossi, et al.
Nucleic Acids Research|January 19, 2013
Nucleophosmin mutations alter its nucleolar localization by impairing G-quadruplex binding at ribosomal DNASara Chiarella, Antonella De Cola, Giovanni Luca Scaglione, et al.
Blood|July 26, 2003
Expression of the IRTA1 receptor identifies intraepithelial and subepithelial marginal zone B cells of the mucosa-associated lymphoid tissue (MALT)Brunangelo Falini, Enrico Tiacci, Alessandra Pucciarini, et al.
Pageof 25