檢索結果 - Arnold Münnich

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  1. 1
    Genetic Features of Mitochondrial Respiratory Chain Disorders

    Genetic Features of Mitochondrial Respiratory Chain Disorders 由 Agnès Rötig, Arnold Münnich

    出版 2003
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  2. 2
    Succinate dehydrogenase and human diseases: new insights into a well-known enzyme

    Succinate dehydrogenase and human diseases: new insights into a well-known enzyme 由 Pierre Rustin, Arnold Münnich, Agnès Rötig

    出版 2002
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  3. 3
    TAB2, TRAF6 and TAK1 are involved in NF-κB activation induced by the TNF-receptor, Edar and its adaptator Edaradd

    TAB2, TRAF6 and TAK1 are involved in NF-κB activation induced by the TNF-receptor, Edar and its adaptator Edaradd 由 Aurore Morlon, Arnold Münnich, Asma Smahi

    出版 2005
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  4. 4
    The CLDN5 gene at the blood-brain barrier in health and disease

    The CLDN5 gene at the blood-brain barrier in health and disease 由 Yosuke Hashimoto, Chris Greene, Arnold Münnich, Matthew Campbell

    出版 2023
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  5. 5
    Transcriptional and post-transcriptional regulation of L-type pyruvate kinase gene expression in rat liver.

    Transcriptional and post-transcriptional regulation of L-type pyruvate kinase gene expression in rat liver. 由 Sophie Vaulont, Arnold Münnich, Jean‐François Decaux, A Kahn

    出版 1986
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  6. 6
    Fate and expression of the deleted mitochondrial DNA differ between human heteroplasmic skin fibroblast and Epstein-Barr virus-transformed lymphocyte cultures.

    Fate and expression of the deleted mitochondrial DNA differ between human heteroplasmic skin fibroblast and Epstein-Barr virus-transformed lymphocyte cultures. 由 Thomas Bourgeron, Dominique Chrétien, Agnès Rötig, Arnold Münnich, Pierre Rustin

    出版 1993
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  7. 7
    Redistribution of accumulated cell iron: a modality of chelation with therapeutic implications

    Redistribution of accumulated cell iron: a modality of chelation with therapeutic implications 由 Yang‐Sung Sohn, William Breuer, Arnold Münnich, Z. Ioav Cabantchik

    出版 2007
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  8. 8
    Activation of Peroxisome Proliferator-Activated Receptor Pathway Stimulates the Mitochondrial Respiratory Chain and Can Correct Deficiencies in Patients’ Cells Lacking Its Components

    Activation of Peroxisome Proliferator-Activated Receptor Pathway Stimulates the Mitochondrial Respiratory Chain and Can Correct Deficiencies in Patients’ Cells Lacking Its Componen... 由 Jean Bastin, Flore Aubey, Agnès Rötig, Arnold Münnich, Fatima Djouadi

    出版 2008
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  9. 9
    Nonsyndromic X‐linked intellectual deficiency in three brothers with a novel <i><scp>MED</scp>12</i> missense mutation [c.5922G&gt;T (p.Glu1974His)]

    Nonsyndromic X‐linked intellectual deficiency in three brothers with a novel <i><scp>MED</scp>12</i> missense mutation [c.5922G&gt;T (p.Glu1974His)] 由 Habib Bouazzi, Gaëtan Lesca, Carlos Trujillo, Mohammad Khalid Alwasiyah, Arnold Munnich

    出版 2015
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  10. 10
    miR-122, a paradigm for the role of microRNAs in the liver

    miR-122, a paradigm for the role of microRNAs in the liver 由 M Girard, Emmanuel Jacquemin, Arnold Münnich, Stanislas Lyonnet, Alexandra Henrion‐Caude

    出版 2008
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  11. 11
    Regional siderosis: a new challenge for iron chelation therapy

    Regional siderosis: a new challenge for iron chelation therapy 由 Z. Ioav Cabantchik, Arnold Münnich, Moussa B. H. Youdim, David Devos

    出版 2013
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  12. 12
    Transcriptionally Repressive Chromatin Remodelling and CpG Methylation in the Presence of Expanded CTG-Repeats at the DM1 Locus

    Transcriptionally Repressive Chromatin Remodelling and CpG Methylation in the Presence of Expanded CTG-Repeats at the DM1 Locus 由 Judith R. Brouwer, Aline Huguet, Annie Nicole, Arnold Münnich, Geneviève Gourdon

    出版 2013
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  13. 13
    Stabilization of RNA during laser capture microdissection by performing experiments under argon atmosphere or using ethanol as a solvent in staining solutions

    Stabilization of RNA during laser capture microdissection by performing experiments under argon atmosphere or using ethanol as a solvent in staining solutions 由 Mathieu Clément‐Ziza, Arnold Münnich, Stanislas Lyonnet, Francis Jaubert, Claude Besmond

    出版 2008
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  14. 14
    Inborn errors of the Krebs cycle: a group of unusual mitochondrial diseases in human

    Inborn errors of the Krebs cycle: a group of unusual mitochondrial diseases in human 由 Pierre Rustin, Thomas Bourgeron, Béatrice Parfait, Dominique Chrétien, Arnold Münnich, Agnès Rötig

    出版 1997
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  15. 15
    Fibroblast Growth Factor Receptor 3 Mutations Promote Apoptosis but Do Not Alter Chondrocyte Proliferation in Thanatophoric Dysplasia

    Fibroblast Growth Factor Receptor 3 Mutations Promote Apoptosis but Do Not Alter Chondrocyte Proliferation in Thanatophoric Dysplasia 由 Laurence Legeai‐Mallet, Catherine Benoist-Lasselin, Anne‐Lise Delezoide, Arnold Münnich, Jacky Bonaventure

    出版 1998
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  16. 16
    FGFR2 mutations in Pfeiffer syndrome

    FGFR2 mutations in Pfeiffer syndrome 由 Elisabeth Lajeunie, Hong Wei, Jacky Bonaventure, Arnold Münnich, Martine Le Merrer, Dominique Rénier

    出版 1995
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  17. 17
    Large scale deletions of the 5q13 region are specific to Werdnig-Hoffmann disease.

    Large scale deletions of the 5q13 region are specific to Werdnig-Hoffmann disease. 由 P Burlet, Lydie Bürglen, Olivier Clermont, S. Lefebvre, Louis Viollet, Arnold Münnich, Judith Melki

    出版 1996
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  18. 18
    In vivo hormonal control of L-type pyruvate kinase gene expression. Effects of glucagon, cyclic AMP, insulin, cortisone, and thyroid hormones on the dietary induction of mRNAs in the liver.

    In vivo hormonal control of L-type pyruvate kinase gene expression. Effects of glucagon, cyclic AMP, insulin, cortisone, and thyroid hormones on the dietary induction of mRNAs in t... 由 Arnold Münnich, Joëlle Marie, G. Reach, Sophie Vaulont, Marie‐Pierre Simon, A Kahn

    出版 1984
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  19. 19
    TP63 gene mutation in ADULT syndrome

    TP63 gene mutation in ADULT syndrome 由 Jeanne Amiel, Gaëlle Bougeard, Christine Francannet, Valérie Raclin, Arnold Münnich, Stanislas Lyonnet, Thierry Frébourg

    出版 2001
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  20. 20
    Incidence and clinical features of X-linked Cornelia de Lange syndrome due toSMC1L1 mutations

    Incidence and clinical features of X-linked Cornelia de Lange syndrome due toSMC1L1 mutations 由 Guntram Borck, Mohamed Zarhrate, Jean‐Paul Bonnefont, Arnold Münnich, Valérie Cormier‐Daire, Laurence Colleaux

    出版 2007
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