Torthaí cuardaigh - G. Lefèvre

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  1. 1
    EVIDENCE OF ACTIVE TRANSFER OF CERTAIN NON-ELECTROLYTES ACROSS THE HUMAN RED CELL MEMBRANE

    EVIDENCE OF ACTIVE TRANSFER OF CERTAIN NON-ELECTROLYTES ACROSS THE HUMAN RED CELL MEMBRANE de réir Paul G. LeFevre

    Foilsithe / Cruthaithe 1948
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  2. 2
    The Attachment of Phloretin and Analogues to Human Erythrocytes in Connection with Inhibition of Sugar Transport

    The Attachment of Phloretin and Analogues to Human Erythrocytes in Connection with Inhibition of Sugar Transport de réir Paul G. LeFevre, J Marshall

    Foilsithe / Cruthaithe 1959
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  3. 3
    ACTIVE TRANSPORT INTO THE HUMAN ERYTHROCYTE: EVIDENCE FROM COMPARATIVE KINETICS AND COMPETITION AMONG MONOSACCHARIDES

    ACTIVE TRANSPORT INTO THE HUMAN ERYTHROCYTE: EVIDENCE FROM COMPARATIVE KINETICS AND COMPETITION AMONG MONOSACCHARIDES de réir Paul G. LeFevre, R. I. Davies

    Foilsithe / Cruthaithe 1951
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  4. 4
    Tracer Exchange <i>vs</i>. Net Uptake of Glucose through Human Red Cell Surface

    Tracer Exchange <i>vs</i>. Net Uptake of Glucose through Human Red Cell Surface de réir Paul G. LeFevre, G. F. McGinniss

    Foilsithe / Cruthaithe 1960
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  5. 5
    Mutation of B-Raf in Human Choroidal Melanoma Cells Mediates Cell Proliferation and Transformation through the MEK/ERK Pathway

    Mutation of B-Raf in Human Choroidal Melanoma Cells Mediates Cell Proliferation and Transformation through the MEK/ERK Pathway de réir Armelle Calipel, G. Lefèvre, Célio Pouponnot, F. Mouriaux, Alain Eychène, Frédéric Mascarelli

    Foilsithe / Cruthaithe 2003
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  6. 6
    Altering a Histone H3K4 Methylation Pathway in Glomerular Podocytes Promotes a Chronic Disease Phenotype

    Altering a Histone H3K4 Methylation Pathway in Glomerular Podocytes Promotes a Chronic Disease Phenotype de réir G. Lefèvre, Sanjeevkumar R. Patel, Doyeob Kim, Lino Tessarollo, Gregory R. Dressler

    Foilsithe / Cruthaithe 2010
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  7. 7
    A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth

    A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth de réir G. Lefèvre, Vincent Michel, Dominique Weil, Léa Lepelletier, Emilie Bizard, Uwe Wolfrum, Jean‐Pierre Hardelin, Christine Petit

    Foilsithe / Cruthaithe 2008
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  8. 8
    Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells

    Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells de réir Avital Adato, G. Lefèvre, Benjamin Delprat, Vincent Michel, Nicolas Michalski, Sébastien Chardenoux, Dominique Weil, A. Amraoui, Christine Petit

    Foilsithe / Cruthaithe 2005
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  9. 9
    Roles of Stem Cell Factor/c-Kit and Effects of Glivec®/STI571 in Human Uveal Melanoma Cell Tumorigenesis

    Roles of Stem Cell Factor/c-Kit and Effects of Glivec®/STI571 in Human Uveal Melanoma Cell Tumorigenesis de réir G. Lefèvre, Anne‐Lise Glotin, Armelle Calipel, F. Mouriaux, Trần Thị Hiền, Zoulika Kherrouche, Claude‐Alain Maurage, Christian Auclair, Frédéric Mascarelli

    Foilsithe / Cruthaithe 2004
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  10. 10
    Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing

    Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing de réir Fatima Ammar‐Khodja, Crystel Bonnet, Malika Dahmani, Sofiane Ouhab, G. Lefèvre, Hassina Ibrahim, Jean‐Pierre Hardelin, Dominique Weil, Malek Louha, Christine Petit

    Foilsithe / Cruthaithe 2015
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  11. 11
    Molecular Characterization of the Ankle-Link Complex in Cochlear Hair Cells and Its Role in the Hair Bundle Functioning

    Molecular Characterization of the Ankle-Link Complex in Cochlear Hair Cells and Its Role in the Hair Bundle Functioning de réir Nicolas Michalski, Vincent Michel, Amel Bahloul, G. Lefèvre, Jérémie Barral, Hideshi Yagi, S. Chardenoux, Dominique Weil, Pascal Martin, Jean-Pierre Hardelin, Makoto Sato, Christine Petit

    Foilsithe / Cruthaithe 2007
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  12. 12
    Stereocilin-deficient mice reveal the origin of cochlear waveform distortions

    Stereocilin-deficient mice reveal the origin of cochlear waveform distortions de réir Elisabeth Verpy, Dominique Weil, Michel Leibovici, Richard J. Goodyear, Ghislaine Hamard, Carine Houdon, G. Lefèvre, Jean‐Pierre Hardelin, Guy P. Richardson, Paul Avan, Christine Petit

    Foilsithe / Cruthaithe 2008
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  13. 13
    Harmonin-b, an actin-binding scaffold protein, is involved in the adaptation of mechanoelectrical transduction by sensory hair cells

    Harmonin-b, an actin-binding scaffold protein, is involved in the adaptation of mechanoelectrical transduction by sensory hair cells de réir Nicolas Michalski, Vincent Michel, Elisa Caberlotto, G. Lefèvre, Alexander F. J. van Aken, Jean-Yves Tinévez, Emilie Bizard, Christophe Houbron, Dominique Weil, Jean‐Pierre Hardelin, Guy P. Richardson, Corné J. Kros, Pascal Martin, Christine Petit

    Foilsithe / Cruthaithe 2009
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  14. 14
    Mannose-coupled AAV2: A second-generation AAV vector for increased retinal gene therapy efficiency

    Mannose-coupled AAV2: A second-generation AAV vector for increased retinal gene therapy efficiency de réir Mathieu Mével, Virginie Pichard, Mohammed Bouzelha, Dimitri Álvarez‐Dorta, Pierre-Alban Lalys, Nathalie Provost, Marine Allais, Alexandra Mendes, Elodie Landagaray, Jean‐Baptiste Ducloyer, Estelle Toublanc, Anne Galy, Nicole Brument, G. Lefèvre, Sébastien G. Gouin, Carolina Isiegas, Guylène Le Meur, Thérèse Cronin, Caroline Le Guiner, Michel Weber, Philippe Moullier, Eduard Ayuso, David Deniaud, Oumeya Adjali

    Foilsithe / Cruthaithe 2024
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  15. 15
    Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis

    Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis de réir Sophie Boucher, Fabienne Wong Jun Tai, Sedigheh Delmaghani, Andrea Lelli, Amrit Singh‐Estivalet, Typhaine Dupont, Magali Niasme-Grare, Vincent Michel, Nicolas Wolff, Amel Bahloul, Yosra Bouyacoub, D. Bouccara, Bernard Fraysse, Olivier Déguine, Lionel Collet, Hung Thaï-Van, E. Ionescu, Jean-Louis Kémény, Fabrice Giraudet, Jean‐Pierre Lavieille, Arnaud Devèze, Anne-Laure Roudevitch-Pujol, C. Vincent, Christian Renard, V. Franco‐Vidal, Claire Thibult-Apt, Vincent Darrouzet, Éric Bizaguet, Arnaud Coëz, Hugues Aschard, Nicolas Michalski, G. Lefèvre, Anne Aubois, Paul Avan, Crystel Bonnet, Christine Petit

    Foilsithe / Cruthaithe 2020
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  16. 16
    An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients

    An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients de réir Crystel Bonnet, Zied Riahi, Sandra Chantot‐Bastaraud, Luce Smagghe, Mélanie Letexier, Charles Marcaillou, G. Lefèvre, Jean‐Pierre Hardelin, A. Amraoui, Amrit Singh‐Estivalet, Saddek Mohand‐Saïd, Susanne Kohl, Anne Kurtenbach, Ieva Sliesoraitytė, Ditta Zobor, Souad Gherbi, Francesco Testa, Francesca Simonelli, Sandro Banfi, Ana Fakin, Damjan Glavač, Martina Jarc-Vidmar, Andrej Zupan, Saba Battelino, Loreto Martorell, M.A. Clavería, Jaume Catalá‐Mora, Shzeena Dad, Lisbeth Birk Møller, Jesus Rodriguez Jorge, Marko Hawlina, Alberto Auricchio, José‐Alain Sahel, Sandrine Marlin, Eberhart Zrenner, Isabelle Audo, Christine Petit

    Foilsithe / Cruthaithe 2016
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