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	Pour les 40 documents Envoyer sur ORCID RSS ATOM Exporter BibTeX XML-TEI CSV RTF EndNote PDF HTML Export avancé	Page : Page précédente 1 2 Page suivante	triés par Pertinence Auteur A→Z Auteur Z→A Titre A→Z Titre Z→A Date de publication croissante Date de publication décroissante Date de dépôt croissante Date de dépôt décroissante

		KCNQ1 gain-of-function mutation in familial atrial fibrillation Y.H. Chen , S.J. Xu , S. Bendahhou , X.L. Wang , Y. Wang , et al. Science, 2003, 299, pp.251-254 Article dans une revue hal-00091098v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation. M. Xia , Q. Jin , S. Bendahhou , Y. He , Mm Larroque , et al. Biochemical and Biophysical Research Communications, 2005, 332, pp.1012-1019 Article dans une revue hal-00094521v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		TWIK1, a unique background channel with variable ion selectivity. Franck C Chatelain , Delphine Bichet , Dominique Douguet , Sylvain Feliciangeli , Saïd Bendahhou , et al. Proceedings of the National Academy of Sciences of the United States of America, 2012, 109 (14), pp.5499-504. ⟨10.1073/pnas.1201132109⟩ Article dans une revue hal-00731871v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Potassium Channel Silencing by Constitutive Endocytosis and Intracellular Sequestration Sylvain Feliciangeli , Magalie Tardy , Guillaume Sandoz , Franck Claude Chatelain , Richard Warth , et al. Journal of Biological Chemistry, 2010, 285 (7), pp.4798-4805. ⟨10.1074/jbc.M109.078535⟩ Article dans une revue hal-02390573v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Revisiting CFTR inhibition: a comparative study of CFTR inh -172 and GlyH-101 inhibitors N Melis , M. Tauc , M. Cougnon , S. Bendahhou , S. Giuliano , et al. British Journal of Pharmacology, 2014, 171 (15), pp.3716-3727. ⟨10.1111/bph.12726⟩ Article dans une revue hal-02918173v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		ARF6-dependent interaction of the TWIK1 K(+) channel with EFA6, a GDP/GTP exchange factor for ARF6. S. Decressac , M. Franco , S. Bendahhou , R. Warth , S. Knauer , et al. EMBO Reports, 2004, 5, pp.1171-1175 Article dans une revue hal-00091459v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		In vivo and in vitro functional characterization of Andersen's syndrome mutations. S. Bendahhou , E. Fournier , D. Sternberg , G. Bassez , A. Furby , et al. The Journal of Physiology, 2005, 565, pp.731-741 Article dans une revue hal-00094518v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Does sumoylation control K2P1/TWIK1 background K+ channels? Sylvain Feliciangeli , Saïd Bendahhou , Guillaume Sandoz , Pierre Gounon , Markus Reichold , et al. Cell, 2007, 130 (3), pp.563-9. ⟨10.1016/j.cell.2007.06.012⟩ Article dans une revue hal-00171463v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Defective potassium channel Kir2.1 trafficking underlies andersen-tawil syndrome S. Bendahhou , M.R. Donaldson , N.M. Plaster , M. Tristani-Firouzi , Y.H. Fu , et al. Journal of Biological Chemistry, 2003, xxx Article dans une revue hal-00091313v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Role of hydrophobic residues in the voltage sensors of the voltage-gated sodium channel. Saïd Bendahhou , Andrias O O'Reilly , Hervé Duclohier Biochimica et Biophysica Acta - Molecular Cell Research, 2007, 1768 (6), pp.1440-7. ⟨10.1016/j.bbamem.2007.03.002⟩ Article dans une revue hal-00171469v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Dkk3 is a component of the genetic circuitry regulating aldosterone biosynthesis in the adrenal cortex. Abeer El Wakil , Sascha Bandulik , Nicolas Guy , Saïd Bendahhou , Maria-Christina Zennaro , et al. Human Molecular Genetics, 2012, epub ahead of print. ⟨10.1093/hmg/dds333⟩ Article dans une revue hal-00727703v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Integrative Study of the Structural and Dynamical Properties of a KirBac3.1 Mutant: Functional Implication of a Highly Conserved Tryptophan in the Transmembrane Domain Charline Fagnen , Ludovic Bannwarth , Iman Oubella , Dania Zuniga , Ahmed Haouz , et al. International Journal of Molecular Sciences, 2022, 23 (1), pp.335. ⟨10.3390/ijms23010335⟩ Article dans une revue hal-03529811v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Task2 potassium channels set central respiratory CO 2 and O 2 sensitivity Christian Gestreau , Dirk Heitzmann , Joerg Thomas , V. Dubreuil , Sascha Bandulik , et al. Proceedings of the National Academy of Sciences of the United States of America, 2010, 107 (5), pp.2325-2330. ⟨10.1073/pnas.0910059107⟩ Article dans une revue hal-01229488v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		In vitro molecular interactions and distribution of KCNE family with KCNQ1 in the human heart. S. Bendahhou , C. Marionneau , K. Haurogne , Mm Larroque , R. Derand , et al. Cardiovascular Research, 2005, 67, pp.529-538 Article dans une revue hal-00094530v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome) M. Tristani-Firouzi , J.L. Jensen , M.R. Donaldson , V. Sansone , G. Meola , et al. Journal of Clinical Investigation, 2002, xxx, pp.381-388 Article dans une revue hal-00091062v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Proximal renal tubular acidosis in TASK2 K+ channel-deficient mice reveals a mechanism for stabilizing bicarbonate transport. Richard Warth , Hervé Barrière , Pierre Meneton , May Bloch , Jörg Thomas , et al. Proceedings of the National Academy of Sciences of the United States of America, 2004, 101 (21), pp.8215-20. ⟨10.1073/pnas.0400081101⟩ Article dans une revue hal-00320811v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patients. Heidi Fodstad , Saïd Bendahhou , Jean-Sébastien Rougier , Päivi J Laitinen-Forsblom , Jacques Barhanin , et al. Annals of Medicine, 2006, 38 (4), pp.294-304. ⟨10.1080/07853890600756065⟩ Article dans une revue hal-00171493v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		First Evidence of Kv3.1b Potassium Channel Subtype Expression during Neuronal Serotonergic 1C11 Cell Line Development Hager Tabka , Amani Cheikh , Sonia Maatoug , Mohamed El Ayeb , Saïd Bendahhou , et al. International Journal of Molecular Sciences, 2020, 21 (19), pp.7175. ⟨10.3390/ijms21197175⟩ Article dans une revue hal-03455296v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Double Trouble Mutations Underlie Mitochondrial Dynamics Disorders in a Severe Form of Charcot-Marie-Tooth Disease Angela Puma , Samuel Guilbault , Emmanuelle C Genin , Christophe Duranton , Isabelle Rubera , et al. Journal of Biotechnology and Biomedicine, 2023, 06 (04), pp.468-475. ⟨10.26502/jbb.2642-91280109⟩ Article dans une revue hal-04275405v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		New Structural insights into Kir channel gating from molecular simulations, HDX-MS and functional studies Charline Fagnen , Ludovic Bannwarth , Iman Oubella , Eric Forest , Rita de Zorzi , et al. Scientific Reports, 2020, 10 (1), ⟨10.1038/s41598-020-65246-z⟩ Article dans une revue hal-02946682v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Corticosteroid-exacerbated symptoms in an Andersen's syndrome kindred. Saïd Bendahhou , Emmanuel Fournier , Serge Gallet , Dominique Ménard , Marie-Madeleine Larroque , et al. Human Molecular Genetics, 2007, 16 (8), pp.900-6. ⟨10.1093/hmg/ddm034⟩ Article dans une revue hal-00171483v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		TWIK1, a unique background channel with variable ion selectivity Franck Claude Chatelain , D. Bichet , D. Douguet , S. Feliciangeli , S. Bendahhou , et al. Proceedings of the National Academy of Sciences of the United States of America, 2012, 109 (14), pp.5499-5504. ⟨10.1073/pnas.1201132109⟩ Article dans une revue hal-02390554v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		In vivo and in vitro functional characterization of Andersen's syndrome mutations. Saïd Bendahhou , Emmanuel Fournier , Damien Sternberg , Guillaume Bassez , Alain Furby , et al. The Journal of Physiology, 2005, 565 (Pt 3), pp.731-41. ⟨10.1113/jphysiol.2004.081620⟩ Article dans une revue hal-00272219v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Potassium channel silencing by constitutive endocytosis and intracellular sequestration. Sylvain Feliciangeli , Magalie P Tardy , Guillaume Sandoz , Franck C Chatelain , Richard Warth , et al. Journal of Biological Chemistry, 2010, 285 (7), pp.4798-805. ⟨10.1074/jbc.M109.078535⟩ Article dans une revue hal-00497748v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Proximal renal tubular acidosis in TASK2 K+ channel-deficient mice reveals a mechanism for stabilizing bicarbonate transport. R. Warth , H. Barriere , P. Meneton , M. Bloch , J. Thomas , et al. Proceedings of the National Academy of Sciences of the United States of America, 2004, 101, pp.8215-8220 Article dans une revue hal-00092326v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Proximal renal tubular acidosis in TASK2 K+ channel-deficient mice reveals a mechanism for stabilizing bicarbonate transport R. Warth , H. Barriere , P. Meneton , M. Bloch , J. Thomas , et al. Proceedings of the National Academy of Sciences of the United States of America, 2004, 1017, pp.8215-8220 Article dans une revue hal-00094493v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Biological fractionation of lithium isotopes by cellular Na + /H + exchangers unravels fundamental transport mechanisms Mallorie Poet , Nathalie Vigier , Yann Bouret , Gisele Jarretou , Romain Gautier , et al. iScience, 2023, 26 (6), ⟨10.1016/j.isci.2023.106887⟩ Article dans une revue hal-04275505v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		A recessive Na v 1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis Karima Habbout , Hugo Poulin , Francois Rivier , Serena Giuliano , Damien Sternberg , et al. Neurology, 2016, 86 (2), pp.161-169. ⟨10.1212/WNL.0000000000002264⟩ Article dans une revue hal-01817830v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		The K+ channel TASK1 modulates β-adrenergic response in brown adipose tissue through the mineralocorticoid receptor pathway. Didier F Pisani , Guillaume E Beranger , Alain Corinus , Maude Giroud , Rayane A Ghandour , et al. FASEB Journal, 2015 Article dans une revue hal-01252963v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		TWIK1, a unique background channel with variable ion selectivity Franck Claude Chatelain , D. Bichet , D. Douguet , S. Feliciangeli , S. Bendahhou , et al. Proceedings of the National Academy of Sciences of the United States of America, 2012, 109 (14), pp.5499-5504. ⟨10.1073/pnas.1201132109⟩ Article dans une revue hal-03813655v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More

Filtrer vos résultats

KCNQ1 gain-of-function mutation in familial atrial fibrillation

A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation.

TWIK1, a unique background channel with variable ion selectivity.

Potassium Channel Silencing by Constitutive Endocytosis and Intracellular Sequestration

Revisiting CFTR inhibition: a comparative study of CFTR inh -172 and GlyH-101 inhibitors

ARF6-dependent interaction of the TWIK1 K(+) channel with EFA6, a GDP/GTP exchange factor for ARF6.

In vivo and in vitro functional characterization of Andersen's syndrome mutations.

Does sumoylation control K2P1/TWIK1 background K+ channels?

Defective potassium channel Kir2.1 trafficking underlies andersen-tawil syndrome

Role of hydrophobic residues in the voltage sensors of the voltage-gated sodium channel.

Dkk3 is a component of the genetic circuitry regulating aldosterone biosynthesis in the adrenal cortex.

Integrative Study of the Structural and Dynamical Properties of a KirBac3.1 Mutant: Functional Implication of a Highly Conserved Tryptophan in the Transmembrane Domain

Task2 potassium channels set central respiratory CO 2 and O 2 sensitivity

In vitro molecular interactions and distribution of KCNE family with KCNQ1 in the human heart.

Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)

Proximal renal tubular acidosis in TASK2 K+ channel-deficient mice reveals a mechanism for stabilizing bicarbonate transport.

Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patients.

First Evidence of Kv3.1b Potassium Channel Subtype Expression during Neuronal Serotonergic 1C11 Cell Line Development

Double Trouble Mutations Underlie Mitochondrial Dynamics Disorders in a Severe Form of Charcot-Marie-Tooth Disease

New Structural insights into Kir channel gating from molecular simulations, HDX-MS and functional studies

Corticosteroid-exacerbated symptoms in an Andersen's syndrome kindred.

TWIK1, a unique background channel with variable ion selectivity

In vivo and in vitro functional characterization of Andersen's syndrome mutations.

Potassium channel silencing by constitutive endocytosis and intracellular sequestration.

Proximal renal tubular acidosis in TASK2 K+ channel-deficient mice reveals a mechanism for stabilizing bicarbonate transport.

Proximal renal tubular acidosis in TASK2 K+ channel-deficient mice reveals a mechanism for stabilizing bicarbonate transport

Biological fractionation of lithium isotopes by cellular Na + /H + exchangers unravels fundamental transport mechanisms

A recessive Na v 1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis

The K+ channel TASK1 modulates β-adrenergic response in brown adipose tissue through the mineralocorticoid receptor pathway.

TWIK1, a unique background channel with variable ion selectivity