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Garavelli

Showing results (361-370 of 609) with videos related to

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Journal of the American Chemical Society|October 22, 2016
Electron-Triggered Metamorphism in Porphyrin-Based Self-Assembled Coordination PolymersChristophe Kahlfuss, Sandrine Denis-Quanquin, Nathalie Calin, et al.
American Journal of Medical Genetics. Part A|April 2, 2004
Mental retardation, Robin sequence, and brachydactyly: further confirmation of a new syndromeFiorella Gurrieri, Gioacchino Scarano, Livia Garavelli, et al.
American Journal of Medical Genetics. Part A|November 14, 2008
Recurrence of Mowat-Wilson syndrome in siblings with a novel mutation in the ZEB2 geneMassimiliano Cecconi, Francesca Forzano, Livia Garavelli, et al.
American Journal of Hypertension|July 26, 2020
Short-Term but not Long-Term Blood Pressure Variability Is a Predictor of Adverse Cardiovascular Outcomes in Young Untreated HypertensivesFrancesca Saladini, Claudio Fania, Lucio Mos, et al.
The Journal of Chemical Physics|June 8, 2015
Ultra-broadband 2D electronic spectroscopy of carotenoid-bacteriochlorophyll interactions in the LH1 complex of a purple bacteriumMargherita Maiuri, Julien Réhault, Anne-Marie Carey, et al.
Proteomics|January 18, 2006
Autumn 2005 Workshop of the Human Proteome Organisation Proteomics Standards Initiative (HUPO-PSI) Geneva, September, 4-6, 2005Sandra Orchard, Henning Hermjakob, Chris Taylor, et al.
Journal of the American Chemical Society|March 25, 2009
Electrostatic control of the photoisomerization efficiency and optical properties in visual pigments: on the role of counterion quenchingGaia Tomasello, Gloria Olaso-González, Piero Altoè, et al.
Cancer|January 29, 2000
Lung carcinoma in 36 patients with human immunodeficiency virus infection. The Italian Cooperative Group on AIDS and TumorsU Tirelli, M Spina, S Sandri, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 6, 2003
Growth and pubertal disorders in neurofibromatosis type 1R Virdis, M E Street, M A Bandello, et al.
European Journal of Human Genetics : EJHG|October 16, 2003
Phenotypic and molecular characterisation of the Aarskog-Scott syndrome: a survey of the clinical variability in light of FGD1 mutation analysis in 46 patientsAlfredo Orrico, Lucia Galli, Maria Luigia Cavaliere, et al.
Pageof 61

Showing results (361-370 of 609) with videos related to

Sort By:
Pageof 61
Journal of the American Chemical Society|October 22, 2016
Electron-Triggered Metamorphism in Porphyrin-Based Self-Assembled Coordination PolymersChristophe Kahlfuss, Sandrine Denis-Quanquin, Nathalie Calin, et al.
American Journal of Medical Genetics. Part A|April 2, 2004
Mental retardation, Robin sequence, and brachydactyly: further confirmation of a new syndromeFiorella Gurrieri, Gioacchino Scarano, Livia Garavelli, et al.
American Journal of Medical Genetics. Part A|November 14, 2008
Recurrence of Mowat-Wilson syndrome in siblings with a novel mutation in the ZEB2 geneMassimiliano Cecconi, Francesca Forzano, Livia Garavelli, et al.
American Journal of Hypertension|July 26, 2020
Short-Term but not Long-Term Blood Pressure Variability Is a Predictor of Adverse Cardiovascular Outcomes in Young Untreated HypertensivesFrancesca Saladini, Claudio Fania, Lucio Mos, et al.
The Journal of Chemical Physics|June 8, 2015
Ultra-broadband 2D electronic spectroscopy of carotenoid-bacteriochlorophyll interactions in the LH1 complex of a purple bacteriumMargherita Maiuri, Julien Réhault, Anne-Marie Carey, et al.
Proteomics|January 18, 2006
Autumn 2005 Workshop of the Human Proteome Organisation Proteomics Standards Initiative (HUPO-PSI) Geneva, September, 4-6, 2005Sandra Orchard, Henning Hermjakob, Chris Taylor, et al.
Journal of the American Chemical Society|March 25, 2009
Electrostatic control of the photoisomerization efficiency and optical properties in visual pigments: on the role of counterion quenchingGaia Tomasello, Gloria Olaso-González, Piero Altoè, et al.
Cancer|January 29, 2000
Lung carcinoma in 36 patients with human immunodeficiency virus infection. The Italian Cooperative Group on AIDS and TumorsU Tirelli, M Spina, S Sandri, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 6, 2003
Growth and pubertal disorders in neurofibromatosis type 1R Virdis, M E Street, M A Bandello, et al.
European Journal of Human Genetics : EJHG|October 16, 2003
Phenotypic and molecular characterisation of the Aarskog-Scott syndrome: a survey of the clinical variability in light of FGD1 mutation analysis in 46 patientsAlfredo Orrico, Lucia Galli, Maria Luigia Cavaliere, et al.
Pageof 61