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Lidia Larizza

Showing results (11-20 of 150) with videos related to

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The Hematology Journal : the Official Journal of the European Haematology Association|July 12, 2002
Amplification of a novel c-Kit activating mutation Asn(822)-Lys in the Kasumi-1 cell line: a t(8;21)-Kit mutant model for acute myeloid leukemiaAlessandro Beghini, Ivana Magnani, Carla B Ripamonti, et al.
Journal of Human Genetics|February 26, 2003
Identification of two novel RECQL4exonic SNPs and genomic characterization of the IVS12 minisatelliteGaia Roversi, Alessandro Beghini, Giovanna Zambruno, et al.
The International Journal of Developmental Biology|January 21, 2003
KL/KIT co-expression in mouse fetal oocytesLuisa Doneda, Francesca-Gioia Klinger, Lidia Larizza, et al.
American Journal of Medical Genetics. Part A|July 3, 2003
RNA processing defects of the helicase gene RECQL4 in a compound heterozygous Rothmund-Thomson patientAlessandro Beghini, Pierangela Castorina, Gaia Roversi, et al.
Molecular and Cellular Probes|November 7, 2003
A fluorescent method for detecting low-grade 11patUPD mosaicism in Beckwith-Wiedemann syndromeSilvia Russo, Monica Mencarelli, Florinda Cavalleri, et al.
Cancer Genetics and Cytogenetics|January 29, 2003
Interphase fluorescence in situ hybridization analysis of del(11)(q23) and del(17)(p13) in chronic lymphocytic leukemia. a study of 40 early-onset patientsLuisa Doneda, Marco Montillo, Liliana Intropido, et al.
European Journal of Medical Genetics|February 5, 2019
A novel RAD21 mutation in a boy with mild Cornelia de Lange presentation: Further delineation of the phenotypeSarah Dorval, Maura Masciadri, Mikaël Mathot, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|May 29, 2004
Chronic myelogenous leukemia with acquired c-kit activating mutation and transient bone marrow mastocytosisRoberto Cairoli, Giovanni Grillo, Alessandro Beghini, et al.
Human Genetics|April 10, 2002
Tandem duplication of the NF1 gene detected by high-resolution FISH in the 17q11.2 regionCristina Gervasini, Angela Bentivegna, Marco Venturin, et al.
Cellular Oncology : the Official Journal of the International Society for Cellular Oncology|September 18, 2009
Multiple localization of endogenous MARK4L protein in human gliomaIvana Magnani, Chiara Novielli, Melissa Bellini, et al.
Pageof 15

Showing results (11-20 of 150) with videos related to

Sort By:
Pageof 15
The Hematology Journal : the Official Journal of the European Haematology Association|July 12, 2002
Amplification of a novel c-Kit activating mutation Asn(822)-Lys in the Kasumi-1 cell line: a t(8;21)-Kit mutant model for acute myeloid leukemiaAlessandro Beghini, Ivana Magnani, Carla B Ripamonti, et al.
Journal of Human Genetics|February 26, 2003
Identification of two novel RECQL4exonic SNPs and genomic characterization of the IVS12 minisatelliteGaia Roversi, Alessandro Beghini, Giovanna Zambruno, et al.
The International Journal of Developmental Biology|January 21, 2003
KL/KIT co-expression in mouse fetal oocytesLuisa Doneda, Francesca-Gioia Klinger, Lidia Larizza, et al.
American Journal of Medical Genetics. Part A|July 3, 2003
RNA processing defects of the helicase gene RECQL4 in a compound heterozygous Rothmund-Thomson patientAlessandro Beghini, Pierangela Castorina, Gaia Roversi, et al.
Molecular and Cellular Probes|November 7, 2003
A fluorescent method for detecting low-grade 11patUPD mosaicism in Beckwith-Wiedemann syndromeSilvia Russo, Monica Mencarelli, Florinda Cavalleri, et al.
Cancer Genetics and Cytogenetics|January 29, 2003
Interphase fluorescence in situ hybridization analysis of del(11)(q23) and del(17)(p13) in chronic lymphocytic leukemia. a study of 40 early-onset patientsLuisa Doneda, Marco Montillo, Liliana Intropido, et al.
European Journal of Medical Genetics|February 5, 2019
A novel RAD21 mutation in a boy with mild Cornelia de Lange presentation: Further delineation of the phenotypeSarah Dorval, Maura Masciadri, Mikaël Mathot, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|May 29, 2004
Chronic myelogenous leukemia with acquired c-kit activating mutation and transient bone marrow mastocytosisRoberto Cairoli, Giovanni Grillo, Alessandro Beghini, et al.
Human Genetics|April 10, 2002
Tandem duplication of the NF1 gene detected by high-resolution FISH in the 17q11.2 regionCristina Gervasini, Angela Bentivegna, Marco Venturin, et al.
Cellular Oncology : the Official Journal of the International Society for Cellular Oncology|September 18, 2009
Multiple localization of endogenous MARK4L protein in human gliomaIvana Magnani, Chiara Novielli, Melissa Bellini, et al.
Pageof 15