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C Bruno

Showing results (181-190 of 355) with videos related to

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European Journal of Immunology|April 15, 2010
Differential subcellular localization of the regulatory T-cell protein LAG-3 and the coreceptor CD4Seng-Ryong Woo, Nianyu Li, Tullia C Bruno, et al.
Annals of Neurology|January 1, 1993
Glycogen branching enzyme deficiency in adult polyglucosan body diseaseC Bruno, S Servidei, S Shanske, et al.
Digestive Diseases and Sciences|May 10, 2015
Correlation of Biomarker Expression in Colonic Mucosa with Disease Phenotype in Crohn's Disease and Ulcerative ColitisMaria E C Bruno, Eric W Rogier, Razvan I Arsenescu, et al.
Journal of Neurosurgical Sciences|November 24, 2004
Lymphoplasmacyte rich meningioma. A case report and review of the literatureM C Bruno, C Ginguené, M Santangelo, et al.
La Medicina Del Lavoro|May 1, 1993
[Mortality due to causes correlatable to asbestos in a cohort of workers in railway car construction]M Menegozzo, S Belli, C Bruno, et al.
Arquivos Brasileiros De Cardiologia|May 17, 2023
Prognosis Related to Reperfusion Therapy Post-Acute Coronary Syndrome in Secondary Care: Long-Term Survival Analysis in the ERICO StudyTatiana C Bruno, Márcio S Bittencourt, Alessandra V L Quidim, et al.
Journal of Interferon & Cytokine Research : the Official Journal of the International Society for Interferon and Cytokine Research|May 20, 1999
Antigenic characterization of recombinant, lymphoblastoid, and leukocyte IFN-alpha by monoclonal antibodiesG C Viscomi, G Antonelli, C Bruno, et al.
Human Mutation|April 11, 2001
Identification of novel WFS1 mutations in Italian children with Wolfram syndromeA Tessa, I Carbone, M C Matteoli, et al.
Human Reproduction (Oxford, England)|December 15, 2020
Do assisted reproductive technologies and in vitro embryo culture influence the epigenetic control of imprinted genes and transposable elements in children?J Barberet, C Binquet, M Guilleman, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Manifesting heterozygotes in a Japanese family with a novel mutation in the muscle-specific phosphoglycerate mutase (PGAM-M) geneG M Hadjigeorgiou, N Kawashima, C Bruno, et al.
Pageof 36

Showing results (181-190 of 355) with videos related to

Sort By:
Pageof 36
European Journal of Immunology|April 15, 2010
Differential subcellular localization of the regulatory T-cell protein LAG-3 and the coreceptor CD4Seng-Ryong Woo, Nianyu Li, Tullia C Bruno, et al.
Annals of Neurology|January 1, 1993
Glycogen branching enzyme deficiency in adult polyglucosan body diseaseC Bruno, S Servidei, S Shanske, et al.
Digestive Diseases and Sciences|May 10, 2015
Correlation of Biomarker Expression in Colonic Mucosa with Disease Phenotype in Crohn's Disease and Ulcerative ColitisMaria E C Bruno, Eric W Rogier, Razvan I Arsenescu, et al.
Journal of Neurosurgical Sciences|November 24, 2004
Lymphoplasmacyte rich meningioma. A case report and review of the literatureM C Bruno, C Ginguené, M Santangelo, et al.
La Medicina Del Lavoro|May 1, 1993
[Mortality due to causes correlatable to asbestos in a cohort of workers in railway car construction]M Menegozzo, S Belli, C Bruno, et al.
Arquivos Brasileiros De Cardiologia|May 17, 2023
Prognosis Related to Reperfusion Therapy Post-Acute Coronary Syndrome in Secondary Care: Long-Term Survival Analysis in the ERICO StudyTatiana C Bruno, Márcio S Bittencourt, Alessandra V L Quidim, et al.
Journal of Interferon & Cytokine Research : the Official Journal of the International Society for Interferon and Cytokine Research|May 20, 1999
Antigenic characterization of recombinant, lymphoblastoid, and leukocyte IFN-alpha by monoclonal antibodiesG C Viscomi, G Antonelli, C Bruno, et al.
Human Mutation|April 11, 2001
Identification of novel WFS1 mutations in Italian children with Wolfram syndromeA Tessa, I Carbone, M C Matteoli, et al.
Human Reproduction (Oxford, England)|December 15, 2020
Do assisted reproductive technologies and in vitro embryo culture influence the epigenetic control of imprinted genes and transposable elements in children?J Barberet, C Binquet, M Guilleman, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Manifesting heterozygotes in a Japanese family with a novel mutation in the muscle-specific phosphoglycerate mutase (PGAM-M) geneG M Hadjigeorgiou, N Kawashima, C Bruno, et al.
Pageof 36