Výsledky vyhledávání - Emanuela V. Volpi

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  1. 1
    DNA damage in obesity: Initiator, promoter and predictor of cancer

    DNA damage in obesity: Initiator, promoter and predictor of cancer Autor Moonisah Usman, Emanuela V. Volpi

    Vydáno 2018
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  2. 2
    FISH Glossary: An Overview of the Fluorescence in Situ Hybridization Technique

    FISH Glossary: An Overview of the Fluorescence in Situ Hybridization Technique Autor Emanuela V. Volpi, Joanna M. Bridger

    Vydáno 2008
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  3. 3
    Comprehensive cytogenomic profile of the in vitro neuronal model SH-SY5Y

    Comprehensive cytogenomic profile of the in vitro neuronal model SH-SY5Y Autor Mohammed Yusuf, Kay Leung, Keith Morris, Emanuela V. Volpi

    Vydáno 2012
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  4. 4
    The role of CD180 in hematological malignancies and inflammatory disorders

    The role of CD180 in hematological malignancies and inflammatory disorders Autor Kurtis Edwards, Peter M. Lydyard, Nino Kulikova, Tamar Tsertsvadze, Emanuela V. Volpi, Nicholas Chiorazzi, Nino Porakishvili

    Vydáno 2023
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  5. 5
    The buccal micronucleus cytome assay: New horizons for its implementation in human studies

    The buccal micronucleus cytome assay: New horizons for its implementation in human studies Autor Michael Fenech, Siegfried Knasmueller, Armen Nersesyan, Claudia Bolognesi, Georg Wultsch, Christian Schunck, Emanuela V. Volpi, Stefano Bonassi

    Vydáno 2024
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  6. 6
    The Leukocyte Receptor Complex in Chicken Is Characterized by Massive Expansion and Diversification of Immunoglobulin-Like Loci

    The Leukocyte Receptor Complex in Chicken Is Characterized by Massive Expansion and Diversification of Immunoglobulin-Like Loci Autor Katja Laun, Penny Coggill, Sophie Palmer, Sarah Sims, Zemin Ning, Jiannis Ragoussis, Emanuela V. Volpi, Natalie Wilson, Stephan Beck, Andreas Ziegler, Armin Volz

    Vydáno 2006
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  7. 7
    Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection

    Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection Autor Nuala Sykes, Claudio Toma, Natalie Wilson, Emanuela V. Volpi, Inês Sousa, Alistair T. Pagnamenta, Raffaella Tancredi, Agatino Battaglia, Elena Maestrini, Anthony Bailey, Anthony P. Monaco

    Vydáno 2009
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  8. 8
    Integrated view of genome structure and sequence of a single DNA molecule in a nanofluidic device

    Integrated view of genome structure and sequence of a single DNA molecule in a nanofluidic device Autor Rodolphe Marie, Jonas N. Pedersen, David L.V. Bauer, Kristian H. Rasmussen, Mohammed Yusuf, Emanuela V. Volpi, Henrik Flyvbjerg, Anders Kristensen, Kalim U. Mir

    Vydáno 2013
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  9. 9
    Unexpected complexity in the haplotypes of commonly used inbred strains of laboratory mice

    Unexpected complexity in the haplotypes of commonly used inbred strains of laboratory mice Autor Binnaz Yalcin, Janice M. Fullerton, S J Miller, David A. Keays, Shannon C. Brady, Amarjit Bhomra, Andrew Jefferson, Emanuela V. Volpi, Richard R. Copley, Jonathan Flint, Richard Mott

    Vydáno 2004
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  10. 10
    An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism

    An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism Autor Michael R. Bowl, M. Andrew Nesbit, Brian Harding, Elaine R. Levy, Andrew Jefferson, Emanuela V. Volpi, Karine Rizzoti, Robin Lovell‐Badge, David Schlessinger, Michael P. Whyte, Rajesh V. Thakker

    Vydáno 2005
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  11. 11
    Structures of Lysenin Reveal a Shared Evolutionary Origin for Pore-Forming Proteins And Its Mode of Sphingomyelin Recognition

    Structures of Lysenin Reveal a Shared Evolutionary Origin for Pore-Forming Proteins And Its Mode of Sphingomyelin Recognition Autor Luigi De Colibus, Andreas F.‐P. Sonnen, Keith Morris, C. Alistair Siebert, Patrizia Abrusci, Jürgen M. Plitzko, Vesna Hodnik, Matthias Leippe, Emanuela V. Volpi, Gregor Anderluh, Robert J. C. Gilbert

    Vydáno 2012
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  12. 12
    Detailed Phenotypic and Genotypic Characterization of Bietti Crystalline Dystrophy

    Detailed Phenotypic and Genotypic Characterization of Bietti Crystalline Dystrophy Autor Stephanie Halford, Gerald Liew, Donna S. Mackay, Panagiotis I. Sergouniotis, Richard Holt, Suzanne Broadgate, Emanuela V. Volpi, Louise Ocaka, Anthony G. Robson, Graham E. Holder, Anthony T. Moore, Michel Michaelides, Andrew R. Webster

    Vydáno 2014
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  13. 13
    In vivo modeling of human neuron dynamics and Down syndrome

    In vivo modeling of human neuron dynamics and Down syndrome Autor Raquel Real, Manuel Peter, Antonio Trabalza, Shabana Khan, Mark A. Smith, Joana Dopp, Samuel J. Barnes, Ayiba Momoh, Alessio Strano, Emanuela V. Volpi, Graham Knott, Frederick J. Livesey, Vincenzo De Paola

    Vydáno 2018
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  14. 14
    Objectives and Achievements of the HUMN project on its 26th Anniversary

    Objectives and Achievements of the HUMN project on its 26th Anniversary Autor Michael Fenech, Nina Holland, Errol Zeiger, Peter Wushou Chang, Micheline Kirsch‐Volders, Claudia Bolognesi, Helga Stopper, Lisbeth E. Knudsen, Siegfried Knasmueller, Armen Nersesyan, Philip Thomas, Varinderpal S. Dhillon, Permal Deo, B. Franzke, Maria Grazia Andreassi, Blanca Laffón, Karl‐Heinz Wagner, Hannu Norppa, Juliana da Silva, Emanuela V. Volpi, Ruth C. Wilkins, Stefano Bonassi

    Vydáno 2024
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  15. 15
    Expression Profiling in Progressive Stages of Fumarate-Hydratase Deficiency: The Contribution of Metabolic Changes to Tumorigenesis

    Expression Profiling in Progressive Stages of Fumarate-Hydratase Deficiency: The Contribution of Metabolic Changes to Tumorigenesis Autor Houman Ashrafian, Linda O′Flaherty, Julie Adam, Violetta Steeples, Yuen‐Li Chung, Philip East, Sakari Vanharanta, Heli Lehtonen, Emma Nye, Emine Hatipoglu, Melroy Miranda, Kimberley Howarth, Deepa Shukla, Helen Troy, John Griffiths, Bradley Spencer‐Dene, Mohammed Yusuf, Emanuela V. Volpi, Patrick H. Maxwell, Gordon Stamp, Richard Poulsom, Christopher W. Pugh, Barbara Costa, Chiara Bardella, Maria Flavia Di Renzo, Michael I. Kotlikoff, Virpi Launonen, Lauri A. Aaltonen, Mona El‐Bahrawy, Ian Tomlinson, Patrick J. Pollard

    Vydáno 2010
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  16. 16
    Patient-specific Alzheimer-like pathology in trisomy 21 cerebral organoids reveals BACE2 as a gene dose-sensitive AD suppressor in human brain

    Patient-specific Alzheimer-like pathology in trisomy 21 cerebral organoids reveals BACE2 as a gene dose-sensitive AD suppressor in human brain Autor Ivan Alić, Pollyanna Goh, Aoife Murray, Erik Portelius, Eleni Gkanatsiou, Gillian Gough, Kin Y. Mok, David Koschut, Reinhard Brunmeir, Yee Jie Yeap, Niamh L. O’Brien, Jürgen Groet, Xiaowei Shao, Steven Havlicek, N. Ray Dunn, Hlin Kvartsberg, Gunnar Brinkmalm, Rosalyn Hithersay, Carla M. Startin, Sarah Hamburg, Margaret Phillips, Konstantin Pervushin, Mark Turmaine, David Wallon, Anne Rovelet‐Lecrux, Hilkka Soininen, Emanuela V. Volpi, Joanne E. Martin, Jia Nee Foo, David L. Becker, Agueda Rostagno, Jorge Ghiso, Željka Krsnik, Goran Šimić, Ivica Kostović, Dinko Mitrečić, André Strydom, Elizabeth Fisher, Frances K. Wiseman, Dean Nižetić, John Hardy, Victor L. J. Tybulewicz, Annette Karmiloff‐Smith, Paul T. Francis, Kaj Blennow, André Strydom, John Hardy, Henrik Zetterberg, Dean Nižetić

    Vydáno 2020
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