نتائج البحث - Michael Gonzalez
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<strong>Precision Medicine: Carbon Nanotubes as Potential Treatment for Human Brain Disorders-Based Mitochondrial Dysfunctions with a First Principles DFT-Study</strong>... حسب Patrícia de Oliveira, Michael Gonzàlez-Durruhty, José María Monserrat, Solange Binotto Fagan
منشور في 2018Artigo -
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Targeting Beta-Blocker Drug–Drug Interactions with Fibrinogen Blood Plasma Protein: A Computational and Experimental Study حسب Michael González‐Durruthy, Riccardo Concu, Laura Vendrame, Ivana Zanella, Juan M. Ruso, M. Natália D. S. Cordeiro
منشور في 2020Artigo -
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Geminin Escapes Degradation in G1 of Mouse Pluripotent Cells and Mediates the Expression of Oct4, Sox2, and Nanog حسب Valerie Shiwen Yang, Stephanie A. Carter, Sarah J. Hyland, Kikuë Tachibana-Konwalski, Ronald A. Laskey, Michael Gonzalez
منشور في 2011Artigo -
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Geminin is essential to prevent endoreduplication and to form pluripotent cells during mammalian development حسب Michael Gonzalez, Kikuë Tachibana, David J. Adams, Louise van der Weyden, Myriam Hemberger, Nicholas Coleman, Allan Bradley, Ronald A. Laskey
منشور في 2006Artigo -
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<i>Insulin-like growth factor-binding protein 5</i> ( <i>Igfbp5</i> ) compromises survival, growth, muscle development, and fertility in mice حسب Derviş A. Salih, Gyanendra Tripathi, Cathy Holding, Tadge Szestak, Michael Gonzalez, Emma Carter, Laura J. Cobb, Joan E. Eisemann, Jennifer M. Pell
منشور في 2004Artigo -
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GEnomes Management Application (GEM.app): A New Software Tool for Large-Scale Collaborative Genome Analysis حسب Michael Gonzalez, Rafael F. Acosta Lebrigio, Derek Van Booven, Rick H. Ulloa, Eric Powell, Fiorella Speziani, Mustafa Tekin, Rebecca Schüle, Stephan Züchner
منشور في 2013Artigo -
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The IGF-1/PI3K/Akt Pathway Prevents Expression of Muscle Atrophy-Induced Ubiquitin Ligases by Inhibiting FOXO Transcription Factors حسب Trevor N. Stitt, Doreen Drujan, Brian Clarke, Frank J. Panaro, Yekatarina Timofeyva, William O. Kline, Michael Gonzalez, George D. Yancopoulos, David J. Glass
منشور في 2004Artigo -
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Mutations in phospholipase DDHD2 cause autosomal recessive hereditary spastic paraplegia (SPG54) حسب Michael Gonzalez, Sheela Nampoothiri, Cornelia Kornblum, Andrés Caballero-Oteyza, Jochen Walter, Ioanna Konidari, William Hulme, Fiorella Speziani, Lüdger Schöls, Stephan Züchner, Rebecca Schüle
منشور في 2013Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Genetics
Medicine
Gene
Mutation
Phenotype
Internal medicine
Disease
Pathology
Cell biology
Biochemistry
Hereditary spastic paraplegia
Neuroscience
Exome sequencing
Endocrinology
Chemistry
Missense mutation
Ataxia
Computational biology
Exome
Cancer
Mitochondrion
Spinal cord
Atrophy
Compound heterozygosity
Computer science
Diabetes mellitus
Immunology
Motor neuron
Receptor