Search - Université de Nantes

	1 2 3 4 5 6 7 Suivant Dernière	Relevance Author A→Z Author Z→A Title A→Z Title Z→A Date de publication croissante Date de publication décroissante Date de dépôt croissante Date de dépôt décroissante 30 results per page 50 results per page 100 results per page Merci d'indiquer la raison de votre demande o Export XML-TEI BibTeX EndNote CSV PDF HTML Advanced export... Syndicated feeds RSS ATOM
	hal-01064298v1 Journal articles Pierre Charles, Antoine Néel, Nathalie Tieulié, Arnaud Hot, Gregory Pugnet et al. Rituximab for induction and maintenance treatment of ANCA-associated vasculitides: a multicentre retrospective study on 80 patients Rheumatology, Oxford University Press (OUP), 2014, 53 (3), pp.532--539. ⟨10.1093/rheumatology/ket381⟩
	hal-01064343v1 Journal articles Marjolaine Morgand, Marc Buffet, Marc Busson, Pascale Loiseau, Sandrine Malot et al. High prevalence of infectious events in thrombotic thrombocytopenic purpura and genetic relationship with toll-like receptor 9 polymorphisms: experience of the French Thrombotic Microangiopathies Reference Center Transfusion, Wiley, 2014, 54 (2), pp.389--397. ⟨10.1111/trf.12263⟩
	hal-01064489v1 Journal articles Marion Chapal, Agnes Debout, Alexandre Dufay, Remi Salomon, Gwenaelle Roussey et al. Kidney and liver transplantation in patients with autosomal recessive polycystic kidney disease: a multicentric study Nephrology Dialysis Transplantation, Oxford University Press (OUP), 2012, 27 (5), pp.2083-2088. ⟨10.1093/ndt/gfr588⟩
	inserm-01072525v1 Journal articles Cédric Rat, Gaëlle Penhouet, Aurélie Gaultier, Anicet Chaslerie, Jacques Pivette et al. Did the new French pay-for-performance system modify benzodiazepine prescribing practices? BMC Health Services Research, BioMed Central, 2014, 14, pp.301. ⟨10.1186/1472-6963-14-301⟩
	inserm-01073774v1 Journal articles Kafia Belhocine, Fabienne Vavasseur, Christelle Volteau, Laurent Flet, Yann Touchefeu et al. Controlling on-demand gastric acidity in obese subjects: a randomized, controlled trial comparing a single dose of 20 mg rabeprazole and 20 mg omeprazole. BMC Gastroenterology, BioMed Central, 2014, 14, pp.128. ⟨10.1186/1471-230X-14-128⟩
	hal-02393752v1 Journal articles Mathilde Nizon, Vincent Laugel, Kevin Flanigan, Matthew Pastore, Megan Waldrop et al. Correction: Variants in MED12L, encoding a subunit of the Mediator kinase module, are responsible for intellectual disability associated with transcriptional defect Genetics in Medicine, Nature Publishing Group, 2019, 21 (11), pp.2663-2663. ⟨10.1038/s41436-019-0590-2⟩
	hal-01659629v1 Journal articles A. Faucon, H. Benhelli-Mokrani, F. Fleury, S. Dutertre, M. Tramier et al. Bioconjugated fluorescent organic nanoparticles targeting EGFR-overexpressing cancer cells Nanoscale, Royal Society of Chemistry, 2017, 9 (45), pp.18094-18106. ⟨10.1039/c7nr06533g⟩
	hal-01414464v1 Journal articles Vincent Portero, Solena Le Scouarnec, Zeineb Es-Salah-Lamoureux, Sophie Burel, Jean-Baptiste Gourraud et al. Dysfunction of the Voltage-Gated K+ Channel beta 2 Subunit in a Familial Case of Brugada Syndrome Journal of the American Heart Association, Wiley-Blackwell, 2016, 5 (6), pp.e003122. ⟨10.1161/JAHA.115.003122⟩
	hal-01340106v1 Journal articles Christel Gentil, Caroline Le Guiner, Sestina Falcone, Jean-Yves Hogrel, Cecile Peccate et al. Dystrophin threshold level necessary for normalisation of nNOS, iNOS and RyR1 nitrosylation in GRMD dystrophinopathy Human Gene Therapy, Mary Ann Liebert, 2016, 27 (9), pp.712-726. ⟨10.1089/hum.2016.041⟩
	hal-01801793v1 Journal articles Elodie Persyn, Matilde Karakachoff, Solena Le Scouarnec, Camille Le Clézio, Dominique Campion et al. An association test to detect clustered disease-risk rare variants PLoS ONE, Public Library of Science, 2017, 12 (7), pp.e0179364. ⟨10.1371/journal.pone.0179364⟩
	hal-01259225v1 Journal articles Bertrand Isidor, Sébastien Küry, Jill A. Rosenfeld, Thomas Besnard, Sébastien Schmitt et al. De Novo Truncating Mutations in the kinetochore-microtubules attachment gene CHAMP1 Cause Syndromic Intellectual Disability Human Mutation, Wiley, 2016, 37 (4), pp.354-358. ⟨10.1002/humu.22952⟩
	hal-01168658v1 Books Christine Sinoquet, Raphaël Mourad. Probabilistic graphical models for genetics, genomics and postgenomics Keith Mansfield. Oxford University Press, 480 p., 2014, 978-0-19-870902-2
	hal-01168755v1 Book sections Christine Sinoquet, Raphaël Mourad. Modeling linkage disequilibrium and performing association studies through probabilistic graphical models: a visiting tour of recent advances. Probabilistic graphical models for genetics, genomics, and postgenomics, Oxford University Press, pp.217-246, 2014
	hal-01439368v1 Journal articles Alice Polat, Sébastien Barbarot, Amandine Bellanger, Carine Lallemant, Henri Adamski et al. Congenital Erosive and Vesicular Dermatosis Healing with Reticulated Scarring Journal of Pediatrics, Elsevier, 2016, 176, pp.212-212.e1. ⟨10.1016/j.jpeds.2016.05.074⟩
	hal-02084404v1 Journal articles Xavier Puéchal, Thierry Bienvenu, Emmanuelle Genin, Jean-Marie Berthelot, Jean Sibilia et al. Mutations of the Cystic Fibrosis Gene in Patients with Bronchiectasis Associated with Rheumatoid Arthritis Annals of the Rheumatic Diseases, BMJ Publishing Group, 2011, 70 (4), pp.653--659. ⟨10.1136/ard.2010.142760⟩
	pasteur-01758726v1 Journal articles Stéphanie Kilens, Dimitri Meistermann, Diego Moreno, Caroline Chariau, Anne Gaignerie et al. Parallel derivation of isogenic human primed and naive induced pluripotent stem cells Nature Communications, Nature Publishing Group, 2018, 9 (1), pp.302 - 314. ⟨10.1038/s41467-017-02107-w⟩
	hal-02878329v1 Master thesis Amandine Le Roy. Étude fonctionnelle de variants génétiques identifiés chez des patients atteints d’érythrocytoses héréditaires Sciences du Vivant [q-bio]. 2020
	hal-03049072v1 Book sections Anne Camus, Aitana Perea-Gomez, Jérôme Collignon. Origin, Early Patterning, and Fate of the Mouse Epiblast Handbook of Stem Cells, Elsevier, pp.129-142, 2004, ⟨10.1016/B978-012436643-5/50020-1⟩
	hal-03515293v1 Journal articles Gilles Salbert, Aurélien Sérandour, Bart Staels, Philippe Lefebvre, Jérôme Eeckhoute. The conundrum of the functional relationship between transcription factors and chromatin Epigenomics, Future Medicine, 2022, ⟨10.2217/epi-2021-0509⟩
	hal-01764655v1 Preprints, Working Papers, ... Philippe Carmona. Some deterministic structured population models which are limit of stochastic individual based models 2018
	hal-01553450v1 Journal articles Amandine Baurand, Sylvie Falcon-Eicher,, Gabriel Laurent, Elisabeth Villain, Caroline Bonnet et al. Incomplete Timothy syndrome secondary to a mosaic mutation of the CACNA1C gene diagnosed using next-generation sequencing American Journal of Medical Genetics Part A, Wiley, 2017, 173 (2), pp.531-536. ⟨10.1002/ajmg.a.38045⟩
	hal-01812518v1 Journal articles Judith Lorant, Thibaut Larcher, Nicolas Jaulin, Benoit Hedan, Aurélie Lardenois et al. Vascular Delivery of Allogeneic MuStem Cells in Dystrophic Dogs Requires Only Short-Term Immunosuppression to Avoid Host Immunity and Generate Clinical/Tissue Benefits Cell Transplantation, Cognizant Communication Corporation, 2018, 27 (7), pp.1096-1110. ⟨10.1177/0963689718776306⟩
	hal-02044435v1 Journal articles Guntram Borck, Anahi Mollà-Herman, Nathalie Boddaert, Ferechte Encha-Razavi, Anne Philippe et al. Clinical, cellular, and neuropathological consequences of AP1S2 mutations: further delineation of a recognizable X-linked mental retardation syndrome Human Mutation, Wiley, 2008, 29 (7), pp.966-974. ⟨10.1002/humu.20531⟩
	hal-01986017v1 Journal articles Marielle Margier, Xavier Collet, Cédric Le May, Charles Desmarchelier, François André et al. ABCB1 (P-glycoprotein) regulates vitamin D absorption and contributes to its transintestinal efflux FASEB Journal, Federation of American Society of Experimental Biology, 2019, 33 (2), pp.2084-2094. ⟨10.1096/fj.201800956R⟩
	hal-01986673v1 Conference papers Vittorio Perduca, Raphaël Mourad, Christine Sinoquet, Gregory Nuel. Waffect: a method to simulate case-control samples in genome-wide association studies. JOBIM, Jun 2011, Paris, France. 7 p
	hal-01952641v1 Journal articles Chloé Angelini, Julien van Gils, Antoine Bigourdan, Pierre-Simon Jouk, Didier Lacombe et al. Major intra-familial phenotypic heterogeneity and incomplete penetrance due to a CACNA1A pathogenic variant European Journal of Medical Genetics, Elsevier, In press, ⟨10.1016/j.ejmg.2018.08.011⟩
	hal-01905989v1 Journal articles Dorothée Hermann, Fadoumo Egue, Emmanuelle Tastard, Duc-Hung Nguyen, Nathalie Casse et al. An introduction to the vast world of transposable elements – what about the diatoms? Diatom Research, Biopress Limited, 2013, 29 (1), pp.91 - 104. ⟨10.1080/0269249X.2013.877083⟩
	hal-01915128v1 Journal articles Duc Nguyen, Claude Lemieux, Monique Turmel, Vân Duy Nguyen, Jean-Luc Mouget et al. Complete mitogenome of Cerithidea obtusa , the red chut-chut snail from the Cần Giờ Mangrove in Vietnam Mitochondrial DNA Part B Resources, Taylor & Francis Online, 2018, 3 (2), pp.1267 - 1269. ⟨10.1080/23802359.2018.1532832⟩
	hal-01905441v1 Journal articles Benoît Chénais. Transposable Elements in Cancer and Other Human Diseases Current Cancer Drug Targets, Bentham Science Publishers, 2015, 15 (3), pp.227 - 242. ⟨10.2174/1568009615666150317122506⟩
	hal-01906235v1 Journal articles Benoît Chénais. Transposable elements and human cancer: A causal relationship? Biochimica et Biophysica Acta (BBA) - Reviews on Cancer, Elsevier, 2013, 1835 (1), pp.28 - 35. ⟨10.1016/j.bbcan.2012.09.001⟩
	1 2 3 4 5 6 7 Suivant Dernière	Relevance Author A→Z Author Z→A Title A→Z Title Z→A Date de publication croissante Date de publication décroissante Date de dépôt croissante Date de dépôt décroissante 30 results per page 50 results per page 100 results per page o Export XML-TEI BibTeX EndNote CSV PDF HTML Advanced export... Syndicated feeds RSS ATOM

hal-01064298v1 Journal articles
Pierre Charles, Antoine Néel, Nathalie Tieulié, Arnaud Hot, Gregory Pugnet et al. Rituximab for induction and maintenance treatment of ANCA-associated vasculitides: a multicentre retrospective study on 80 patients
Rheumatology, Oxford University Press (OUP), 2014, 53 (3), pp.532--539. ⟨10.1093/rheumatology/ket381⟩

hal-01064343v1 Journal articles
Marjolaine Morgand, Marc Buffet, Marc Busson, Pascale Loiseau, Sandrine Malot et al. High prevalence of infectious events in thrombotic thrombocytopenic purpura and genetic relationship with toll-like receptor 9 polymorphisms: experience of the French Thrombotic Microangiopathies Reference Center
Transfusion, Wiley, 2014, 54 (2), pp.389--397. ⟨10.1111/trf.12263⟩

hal-01064489v1 Journal articles
Marion Chapal, Agnes Debout, Alexandre Dufay, Remi Salomon, Gwenaelle Roussey et al. Kidney and liver transplantation in patients with autosomal recessive polycystic kidney disease: a multicentric study
Nephrology Dialysis Transplantation, Oxford University Press (OUP), 2012, 27 (5), pp.2083-2088. ⟨10.1093/ndt/gfr588⟩

inserm-01072525v1 Journal articles
Cédric Rat, Gaëlle Penhouet, Aurélie Gaultier, Anicet Chaslerie, Jacques Pivette et al. Did the new French pay-for-performance system modify benzodiazepine prescribing practices?
BMC Health Services Research, BioMed Central, 2014, 14, pp.301. ⟨10.1186/1472-6963-14-301⟩

inserm-01073774v1 Journal articles
Kafia Belhocine, Fabienne Vavasseur, Christelle Volteau, Laurent Flet, Yann Touchefeu et al. Controlling on-demand gastric acidity in obese subjects: a randomized, controlled trial comparing a single dose of 20 mg rabeprazole and 20 mg omeprazole.
BMC Gastroenterology, BioMed Central, 2014, 14, pp.128. ⟨10.1186/1471-230X-14-128⟩

hal-02393752v1 Journal articles
Mathilde Nizon, Vincent Laugel, Kevin Flanigan, Matthew Pastore, Megan Waldrop et al. Correction: Variants in MED12L, encoding a subunit of the Mediator kinase module, are responsible for intellectual disability associated with transcriptional defect
Genetics in Medicine, Nature Publishing Group, 2019, 21 (11), pp.2663-2663. ⟨10.1038/s41436-019-0590-2⟩

hal-01659629v1 Journal articles
A. Faucon, H. Benhelli-Mokrani, F. Fleury, S. Dutertre, M. Tramier et al. Bioconjugated fluorescent organic nanoparticles targeting EGFR-overexpressing cancer cells
Nanoscale, Royal Society of Chemistry, 2017, 9 (45), pp.18094-18106. ⟨10.1039/c7nr06533g⟩

hal-01414464v1 Journal articles
Vincent Portero, Solena Le Scouarnec, Zeineb Es-Salah-Lamoureux, Sophie Burel, Jean-Baptiste Gourraud et al. Dysfunction of the Voltage-Gated K+ Channel beta 2 Subunit in a Familial Case of Brugada Syndrome
Journal of the American Heart Association, Wiley-Blackwell, 2016, 5 (6), pp.e003122. ⟨10.1161/JAHA.115.003122⟩

hal-01340106v1 Journal articles
Christel Gentil, Caroline Le Guiner, Sestina Falcone, Jean-Yves Hogrel, Cecile Peccate et al. Dystrophin threshold level necessary for normalisation of nNOS, iNOS and RyR1 nitrosylation in GRMD dystrophinopathy
Human Gene Therapy, Mary Ann Liebert, 2016, 27 (9), pp.712-726. ⟨10.1089/hum.2016.041⟩

hal-01801793v1 Journal articles
Elodie Persyn, Matilde Karakachoff, Solena Le Scouarnec, Camille Le Clézio, Dominique Campion et al. An association test to detect clustered disease-risk rare variants
PLoS ONE, Public Library of Science, 2017, 12 (7), pp.e0179364. ⟨10.1371/journal.pone.0179364⟩

hal-01259225v1 Journal articles
Bertrand Isidor, Sébastien Küry, Jill A. Rosenfeld, Thomas Besnard, Sébastien Schmitt et al. De Novo Truncating Mutations in the kinetochore-microtubules attachment gene CHAMP1 Cause Syndromic Intellectual Disability
Human Mutation, Wiley, 2016, 37 (4), pp.354-358. ⟨10.1002/humu.22952⟩

hal-01168658v1 Books
Christine Sinoquet, Raphaël Mourad. Probabilistic graphical models for genetics, genomics and postgenomics
Keith Mansfield. Oxford University Press, 480 p., 2014, 978-0-19-870902-2

hal-01168755v1 Book sections
Christine Sinoquet, Raphaël Mourad. Modeling linkage disequilibrium and performing association studies through probabilistic graphical models: a visiting tour of recent advances.
Probabilistic graphical models for genetics, genomics, and postgenomics, Oxford University Press, pp.217-246, 2014

hal-01439368v1 Journal articles
Alice Polat, Sébastien Barbarot, Amandine Bellanger, Carine Lallemant, Henri Adamski et al. Congenital Erosive and Vesicular Dermatosis Healing with Reticulated Scarring
Journal of Pediatrics, Elsevier, 2016, 176, pp.212-212.e1. ⟨10.1016/j.jpeds.2016.05.074⟩

hal-02084404v1 Journal articles
Xavier Puéchal, Thierry Bienvenu, Emmanuelle Genin, Jean-Marie Berthelot, Jean Sibilia et al. Mutations of the Cystic Fibrosis Gene in Patients with Bronchiectasis Associated with Rheumatoid Arthritis
Annals of the Rheumatic Diseases, BMJ Publishing Group, 2011, 70 (4), pp.653--659. ⟨10.1136/ard.2010.142760⟩

pasteur-01758726v1 Journal articles
Stéphanie Kilens, Dimitri Meistermann, Diego Moreno, Caroline Chariau, Anne Gaignerie et al. Parallel derivation of isogenic human primed and naive induced pluripotent stem cells
Nature Communications, Nature Publishing Group, 2018, 9 (1), pp.302 - 314. ⟨10.1038/s41467-017-02107-w⟩

hal-02878329v1 Master thesis
Amandine Le Roy. Étude fonctionnelle de variants génétiques identifiés chez des patients atteints d’érythrocytoses héréditaires
Sciences du Vivant [q-bio]. 2020

hal-03049072v1 Book sections
Anne Camus, Aitana Perea-Gomez, Jérôme Collignon. Origin, Early Patterning, and Fate of the Mouse Epiblast
Handbook of Stem Cells, Elsevier, pp.129-142, 2004, ⟨10.1016/B978-012436643-5/50020-1⟩

hal-03515293v1 Journal articles
Gilles Salbert, Aurélien Sérandour, Bart Staels, Philippe Lefebvre, Jérôme Eeckhoute. The conundrum of the functional relationship between transcription factors and chromatin
Epigenomics, Future Medicine, 2022, ⟨10.2217/epi-2021-0509⟩

hal-01764655v1 Preprints, Working Papers, ...
Philippe Carmona. Some deterministic structured population models which are limit of stochastic individual based models
2018

hal-01553450v1 Journal articles
Amandine Baurand, Sylvie Falcon-Eicher,, Gabriel Laurent, Elisabeth Villain, Caroline Bonnet et al. Incomplete Timothy syndrome secondary to a mosaic mutation of the CACNA1C gene diagnosed using next-generation sequencing
American Journal of Medical Genetics Part A, Wiley, 2017, 173 (2), pp.531-536. ⟨10.1002/ajmg.a.38045⟩

hal-01812518v1 Journal articles
Judith Lorant, Thibaut Larcher, Nicolas Jaulin, Benoit Hedan, Aurélie Lardenois et al. Vascular Delivery of Allogeneic MuStem Cells in Dystrophic Dogs Requires Only Short-Term Immunosuppression to Avoid Host Immunity and Generate Clinical/Tissue Benefits
Cell Transplantation, Cognizant Communication Corporation, 2018, 27 (7), pp.1096-1110. ⟨10.1177/0963689718776306⟩

hal-02044435v1 Journal articles
Guntram Borck, Anahi Mollà-Herman, Nathalie Boddaert, Ferechte Encha-Razavi, Anne Philippe et al. Clinical, cellular, and neuropathological consequences of AP1S2 mutations: further delineation of a recognizable X-linked mental retardation syndrome
Human Mutation, Wiley, 2008, 29 (7), pp.966-974. ⟨10.1002/humu.20531⟩

hal-01986017v1 Journal articles
Marielle Margier, Xavier Collet, Cédric Le May, Charles Desmarchelier, François André et al. ABCB1 (P-glycoprotein) regulates vitamin D absorption and contributes to its transintestinal efflux
FASEB Journal, Federation of American Society of Experimental Biology, 2019, 33 (2), pp.2084-2094. ⟨10.1096/fj.201800956R⟩

hal-01986673v1 Conference papers
Vittorio Perduca, Raphaël Mourad, Christine Sinoquet, Gregory Nuel. Waffect: a method to simulate case-control samples in genome-wide association studies.
JOBIM, Jun 2011, Paris, France. 7 p

hal-01952641v1 Journal articles
Chloé Angelini, Julien van Gils, Antoine Bigourdan, Pierre-Simon Jouk, Didier Lacombe et al. Major intra-familial phenotypic heterogeneity and incomplete penetrance due to a CACNA1A pathogenic variant
European Journal of Medical Genetics, Elsevier, In press, ⟨10.1016/j.ejmg.2018.08.011⟩

hal-01905989v1 Journal articles
Dorothée Hermann, Fadoumo Egue, Emmanuelle Tastard, Duc-Hung Nguyen, Nathalie Casse et al. An introduction to the vast world of transposable elements – what about the diatoms?
Diatom Research, Biopress Limited, 2013, 29 (1), pp.91 - 104. ⟨10.1080/0269249X.2013.877083⟩

hal-01915128v1 Journal articles
Duc Nguyen, Claude Lemieux, Monique Turmel, Vân Duy Nguyen, Jean-Luc Mouget et al. Complete mitogenome of Cerithidea obtusa , the red chut-chut snail from the Cần Giờ Mangrove in Vietnam
Mitochondrial DNA Part B Resources, Taylor & Francis Online, 2018, 3 (2), pp.1267 - 1269. ⟨10.1080/23802359.2018.1532832⟩

hal-01905441v1 Journal articles
Benoît Chénais. Transposable Elements in Cancer and Other Human Diseases
Current Cancer Drug Targets, Bentham Science Publishers, 2015, 15 (3), pp.227 - 242. ⟨10.2174/1568009615666150317122506⟩

hal-01906235v1 Journal articles
Benoît Chénais. Transposable elements and human cancer: A causal relationship?
Biochimica et Biophysica Acta (BBA) - Reviews on Cancer, Elsevier, 2013, 1835 (1), pp.28 - 35. ⟨10.1016/j.bbcan.2012.09.001⟩

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