Hasil Pencarian - David Coelho

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  1. 1
    Sirt1-PPARS Cross-Talk in Complex Metabolic Diseases and Inherited Disorders of the One Carbon Metabolism

    Sirt1-PPARS Cross-Talk in Complex Metabolic Diseases and Inherited Disorders of the One Carbon Metabolism oleh Viola J. Kosgei, David Coelho, Rosa-Maria Guéant-Rodriguez, Jean-Louis Guéant

    Diterbitkan 2020-08-01
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  2. 2
    Glycine Receptor Activation Impairs ATP-Induced Calcium Transients in Cultured Cortical Astrocytes

    Glycine Receptor Activation Impairs ATP-Induced Calcium Transients in Cultured Cortical Astrocytes oleh Tatiana P. Morais, Tatiana P. Morais, David Coelho, David Coelho, Sandra H. Vaz, Sandra H. Vaz, Ana M. Sebastião, Ana M. Sebastião, Cláudia A. Valente, Cláudia A. Valente

    Diterbitkan 2018-01-01
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  3. 3
    Ressecção minimamente invasiva por broncoscopia de tumores brônquicos benignos Minimally invasive bronchoscopic resection of benign tumors of the bronchi

    Ressecção minimamente invasiva por broncoscopia de tumores brônquicos benignos Minimally invasive bronchoscopic resection of benign tumors of the bronchi oleh Ascedio Jose Rodrigues, David Coelho, Sérvulo Azevedo Dias Júnior, Márcia Jacomelli, Paulo Rogério Scordamaglio, Viviane Rossi Figueiredo

    Diterbitkan 2011-12-01
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  4. 4
    Check-Bit Region Exploration in Two-Dimensional Error Correction Codes

    Check-Bit Region Exploration in Two-Dimensional Error Correction Codes oleh David Freitas, David Mota, David Coelho, Humberto Fontinele, Alexandre Coelho, Jarbas Silveira, Lirida Naviner, Joao Mota, Cesar Marcon

    Diterbitkan 2024-01-01
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  5. 5
    Solução oral escalonada de misoprostol para indução do parto: estudo piloto Titrated oral solution of misoprostol for labour induction: a pilot study

    Solução oral escalonada de misoprostol para indução do parto: estudo piloto Titrated oral solution of misoprostol for labour induction: a pilot study oleh Alex Sandro Rolland Souza, Adriana Scavuzzi, David Coelho Rodrigues, Roberta Dantas de Oliveira, Francisco Edson Lucena Feitosa, Melania Maria Ramos Amorim

    Diterbitkan 2010-05-01
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  6. 6
    Cognitive Impairment Is Associated with AMPAR Glutamatergic Dysfunction in a Mouse Model of Neuronal Methionine Synthase Deficiency

    Cognitive Impairment Is Associated with AMPAR Glutamatergic Dysfunction in a Mouse Model of Neuronal Methionine Synthase Deficiency oleh Ziad Hassan, David Coelho, Carine Bossenmeyer-Pourié, Karim Matmat, Carole Arnold, Aurélie Savladori, Jean-Marc Alberto, Rémy Umoret, Jean-Louis Guéant, Grégory Pourié

    Diterbitkan 2023-04-01
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  7. 7
    A transgenic mice model of retinopathy of cblG-type inherited disorder of one-carbon metabolism highlights epigenome-wide alterations related to cone photoreceptor cells development and retinal metabolism

    A transgenic mice model of retinopathy of cblG-type inherited disorder of one-carbon metabolism highlights epigenome-wide alterations related to cone photoreceptor cells developmen... oleh Karim Matmat, Jean-Baptiste Conart, Paul-Henri Graindorge, Sandra El Kouche, Ziad Hassan, Youssef Siblini, Rémy Umoret, Ramia Safar, Okan Baspinar, Aurélie Robert, Jean-Marc Alberto, Abderrahim Oussalah, David Coelho, Jean-Louis Guéant, Rosa-Maria Guéant-Rodriguez

    Diterbitkan 2023-10-01
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  8. 8
    Correction: A transgenic mice model of retinopathy of cblG‑type inherited disorder of one‑carbon metabolism highlights epigenome‑wide alterations related to cone photoreceptor cells development and retinal metabolism

    Correction: A transgenic mice model of retinopathy of cblG‑type inherited disorder of one‑carbon metabolism highlights epigenome‑wide alterations related to cone photoreceptor cell... oleh Karim Matmat, Jean-Baptiste Conart, Paul-Henri Graindorge, Sandra El Kouche, Ziad Hassan, Youssef Siblini, Rémy Umoret, Ramia Safar, Okan Baspinar, Aurélie Robert, Jean-Marc Alberto, Abderrahim Oussalah, Sébastien Hergalant, David Coelho, Jean-Louis Guéant, Rosa-Maria Guéant-Rodriguez

    Diterbitkan 2024-02-01
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  9. 9
    Multiomic analysis in fibroblasts of patients with inborn errors of cobalmin metabolism reveals concordance with clinical and metabolic variabilityResearch in context

    Multiomic analysis in fibroblasts of patients with inborn errors of cobalmin metabolism reveals concordance with clinical and metabolic variabilityResearch in context oleh Arnaud Wiedemann, Abderrahim Oussalah, Rosa-Maria Guéant Rodriguez, Elise Jeannesson, Marc Mertens, Irina Rotaru, Jean-Marc Alberto, Okan Baspinar, Charif Rashka, Ziad Hassan, Youssef Siblini, Karim Matmat, Manon Jeandel, Celine Chery, Aurélie Robert, Guillaume Chevreux, Laurent Lignières, Jean-Michel Camadro, François Feillet, David Coelho, Jean-Louis Guéant

    Diterbitkan 2024-01-01
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  10. 10
    Dose-dependent effects of siRNA-mediated inhibition of SCAP on PCSK9, LDLR, and plasma lipids in mouse and rhesus monkey[S]

    Dose-dependent effects of siRNA-mediated inhibition of SCAP on PCSK9, LDLR, and plasma lipids in mouse and rhesus monkey[S] oleh Kristian K. Jensen, Marija Tadin-Strapps, Sheng-ping Wang, James Hubert, Yanqing Kan, Yong Ma, David G. McLaren, Stephen F. Previs, Kithsiri B. Herath, Ablatt Mahsut, Andy Liaw, Shubing Wang, Steven J. Stout, CarolAnn Keohan, Gail Forrest, David Coelho, Satya Yendluri, Stephanie Williams, Martin Koser, Steven Bartz, Karen O. Akinsanya, Shirly Pinto

    Diterbitkan 2016-12-01
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  11. 11
    Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients

    Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients oleh Jean-Louis Guéant, Céline Chéry, Abderrahim Oussalah, Javad Nadaf, David Coelho, Thomas Josse, Justine Flayac, Aurélie Robert, Isabelle Koscinski, Isabelle Gastin, Pierre Filhine-Tresarrieu, Mihaela Pupavac, Alison Brebner, David Watkins, Tomi Pastinen, Alexandre Montpetit, Fadi Hariri, David Tregouët, Benjamin A Raby, Wendy K. Chung, Pierre-Emmanuel Morange, D. Sean Froese, Matthias R. Baumgartner, Jean-François Benoist, Can Ficicioglu, Virginie Marchand, Yuri Motorin, Chrystèle Bonnemains, François Feillet, Jacek Majewski, David S. Rosenblatt

    Diterbitkan 2018-02-01
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  12. 12
    A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients

    A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients oleh Jean-Louis Guéant, Céline Chéry, Abderrahim Oussalah, Javad Nadaf, David Coelho, Thomas Josse, Justine Flayac, Aurélie Robert, Isabelle Koscinski, Isabelle Gastin, Pierre Filhine-Tresarrieu, Mihaela Pupavac, Alison Brebner, David Watkins, Tomi Pastinen, Alexandre Montpetit, Fadi Hariri, David Tregouët, Benjamin A Raby, Wendy K. Chung, Pierre-Emmanuel Morange, D. Sean Froese, Matthias R. Baumgartner, Jean-François Benoist, Can Ficicioglu, Virginie Marchand, Yuri Motorin, Chrystèle Bonnemains, François Feillet, Jacek Majewski, David S. Rosenblatt

    Diterbitkan 2018-01-01
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