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	Pour les 23 documents Envoyer sur ORCID RSS ATOM Exporter BibTeX XML-TEI CSV RTF EndNote PDF HTML Export avancé	Page :	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

		Generation of immortalized human chromaffin cell lines for clinical applications. M.J. Eaton , L. Vaysse , J.P. Herman , J.C. Sol , S. Jozan , et al. IRPC Recent avances and Research Updates, 2007, 8, pp.161-170 Article dans une revue hal-00193108v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Impaired expression of the COSMOC/MOCOS gene unit in ASD patient stem cells Pauline Rontani , Olivier Perche , Louise Greetham , Nicolas Jullien , Bruno Gepner , et al. Molecular Psychiatry, 2020, ⟨10.1038/s41380-020-0728-2⟩ Article dans une revue hal-02869315v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Deficit in Anterior Pituitary Function and Variable Immune Deficiency (DAVID) in Children Presenting with Adrenocorticotropin Deficiency and Severe Infections Marie-Helene Quentien , Brigitte Delemer , Dimitris Papadimitriou , Pierre-François Souchon , Roland Jaussaud , et al. Journal of Clinical Endocrinology and Metabolism, 2012, 97 (1), pp.E121 - E128. ⟨10.1210/jc.2011-0407⟩ Article dans une revue hal-01775020v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Regulation of Cre recombinase by ligand-induced complementation of inactive fragments Nicolas Jullien , François Sampieri , Alain Enjalbert , Jean-Paul Herman Nucleic Acids Research, 2003, 31 (21), pp.131e - 131. ⟨10.1093/nar/gng131⟩ Article dans une revue hal-01775207v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		LUEGO: a cost and time saving gel shift procedure. Nicolas Jullien , Jean-Paul Herman Biotechniques, 2011, 51 (4), pp.267-9. ⟨10.2144/000113751⟩ Article dans une revue hal-00755675v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Identifying the Deleterious Effect of Rare LHX4 Allelic Variants, a Challenging Issue Claire Rochette , Nicolas Jullien , Alexandru Saveanu , Emmanuelle Caldagues , Ignacio Bergada , et al. PLoS ONE, 2015, 10 (e0126648), ⟨10.1371/journal.pone.0126648⟩ Article dans une revue hal-01211758v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Research Resource: A Genome-Wide Study Identifies Potential New Target Genes for POU1F1 Jean-Paul Herman , Nicolas Jullien , Séverine Guillen , Alain Enjalbert , Isabelle Pellegrini , et al. Molecular Endocrinology -Baltimore-, 2012, 26 (8), pp.1455 - 1463. ⟨10.1210/me.2011-1308⟩ Article dans une revue hal-01775005v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Use of ERT2-iCre-ERT2 for conditional transgenesis N. Jullien , I. Goddard , S. Selmi-Ruby , J.L. Fina , H. Cremer , et al. Genesis, 2008, 46, pp.193-199 Article dans une revue hal-00408753v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Presynapses contain distinct actin nanostructures Dominic Bingham , Channa Elise Jakobs , Florian Wernert , Fanny Boroni-Rueda , Nicolas Jullien , et al. Journal of Cell Biology, 2023, 222 (10), ⟨10.1083/jcb.202208110⟩ Article dans une revue hal-04220784v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Conditional genome engineering in Toxoplasma gondii uncovers alternative invasion mechanisms Nicole Andenmatten , Saskia Egarter , Allison J Jackson , Nicolas Jullien , Jean-Paul Herman , et al. Nature Methods, 2013, 10 (2), pp.125-127. ⟨10.1038/nmeth.2301⟩ Article dans une revue hal-01772103v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		SARS, ARSS, AND A,T-RICH REGIONS EVIDENCED BY RESTRICTION MAPPING ON AN 835-KB DNA FRAGMENT FROM DROSOPHILA C. Brun , N Jullien , M Jacobzone , Et Al. Experimental Cell Research, 1995, 220 (2), pp.338-347 Article dans une revue hal-01596335v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Dose-Dependent Dual Role of PIT-1 (POU1F1) in Somatolactotroph Cell Proliferation and Apoptosis Nicolas Jullien , Catherine Roche , Thierry Brue , Dominique Figarella-Branger , Thomas Graillon , et al. PLoS ONE, 2015, 10 (e0120010), ⟨10.1371/journal.pone.0120010.t001⟩ Article dans une revue hal-01217093v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		GPR101 Mutations are not a Frequent Cause of Congenital Isolated Growth Hormone Deficiency Frederic Castinetti , A. F. Daly , C. A. Stratakis , J.-H. Caberg , E. Castermans , et al. Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme, 2016, 48 (6), pp.389--393. ⟨10.1055/s-0042-100733⟩ Article dans une revue hal-01474293v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		MECHANISMS IN ENDOCRINOLOGY: An update in the genetic aetiologies of combined pituitary hormone deficiency Frederic Castinetti , Rachel Reynaud , Alexandru Saveanu , Nicolas Jullien , Marie Helene Quentien , et al. European Journal of Endocrinology, 2016, 174 (6), pp.R239--247. ⟨10.1530/EJE-15-1095⟩ Article dans une revue hal-01473968v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Clinical lessons learned in constitutional hypopituitarism from two decades of experience in a large international cohort Nicolas Jullien , Alexandru Saveanu , Julia Vergier , Emeline Marquant , Marie Helene Quentien , et al. Clinical Endocrinology, 2021, 94 (2), pp.277-289. ⟨10.1111/cen.14355⟩ Article dans une revue hal-03225618v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Human iPSCs-derived astrocytes reveal APOE as a critical modulator of inflammation that could underlie Alzheimer’s disease pathogenesis Laurie Arnaud , Louise Greetham , Laura García-González , Delphine Stephan , Nicolas Jullien , et al. International Astrocyte School (IAS), Apr 2021, Bertinoro, Italy Communication dans un congrès hal-03866310v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Heterozygous LHX3 mutations may lead to a mild phenotype of combined pituitary hormone deficiency Nicolas Jullien , Mélanie Philippon , Marie-Hélène Quentien , Paolo Beck-Peccoz , Ignacio Bergada , et al. European Journal of Human Genetics, 2019, 27 (2), pp.216-225. ⟨10.1038/s41431-018-0264-6⟩ Article dans une revue hal-01903170v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Conditional Transgenesis Using Dimerizable Cre (DiCre) Nicolas Jullien , Isabelle Goddard , Samia Selmi-Ruby , Jean-Luc Fina , Harold Cremer , et al. PLoS ONE, 2007, 2 (12), pp.e1355. ⟨10.1371/journal.pone.0001355⟩ Article dans une revue hal-00202654v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		MT5-MMP controls APP and β-CTF/C99 metabolism through proteolytic-dependent and -independent mechanisms relevant for Alzheimer’s disease Laura García-González , Jean-Michel Paumier , Laurence Louis , Dominika Pilat , Anne Bernard , et al. 2020 Pré-publication, Document de travail hal-03064994v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		APOE4 primes inflammation in human astrocytes through the downregulation of a newly discovered target candidatevv Laurie Arnaud , Phillipe Benech , Louise Greetham , Delphine Stephan , Angelique Jimenez , et al. Alzheimer's & Parkinson's Diseases Congress (AD/PD), Mar 2021, Barcelona, Spain. pp.251-262 Communication dans un congrès hal-03866284v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Lessons from monogenic causes of growth hormone deficiency Thierry Brue , Alexandru Saveanu , Nicolas Jullien , Teddy Fauquier , Frederic Castinetti , et al. Annales d'Endocrinologie, 2017, 78 (2), pp.77 - 79. ⟨10.1016/j.ando.2017.04.001⟩ Article dans une revue hal-01731589v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports Thi Thom Mac , Frédéric Castinetti , Celine Bar , Sophie Julia , Marlene Pasquet , et al. Journal of Neuroendocrinology, 2023, ⟨10.1111/jne.13287⟩ Article dans une revue hal-04254098v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		[Genetic aspects of growth hormone deficiency]. Rachel Reynaud , Frederic Castinetti , N. Galon-Faure , F. Albarel-Loy , Alexandru Saveanu , et al. Archives de Pédiatrie, 2011, 18 (6), pp.696-706. ⟨10.1016/j.arcped.2011.03.005⟩ Article dans une revue istex hal-00625440v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More

Filtrer vos résultats

Generation of immortalized human chromaffin cell lines for clinical applications.

Impaired expression of the COSMOC/MOCOS gene unit in ASD patient stem cells

Deficit in Anterior Pituitary Function and Variable Immune Deficiency (DAVID) in Children Presenting with Adrenocorticotropin Deficiency and Severe Infections

Regulation of Cre recombinase by ligand-induced complementation of inactive fragments

LUEGO: a cost and time saving gel shift procedure.

Identifying the Deleterious Effect of Rare LHX4 Allelic Variants, a Challenging Issue

Research Resource: A Genome-Wide Study Identifies Potential New Target Genes for POU1F1

Use of ERT2-iCre-ERT2 for conditional transgenesis

Presynapses contain distinct actin nanostructures

Conditional genome engineering in Toxoplasma gondii uncovers alternative invasion mechanisms

SARS, ARSS, AND A,T-RICH REGIONS EVIDENCED BY RESTRICTION MAPPING ON AN 835-KB DNA FRAGMENT FROM DROSOPHILA

Dose-Dependent Dual Role of PIT-1 (POU1F1) in Somatolactotroph Cell Proliferation and Apoptosis

GPR101 Mutations are not a Frequent Cause of Congenital Isolated Growth Hormone Deficiency

MECHANISMS IN ENDOCRINOLOGY: An update in the genetic aetiologies of combined pituitary hormone deficiency

Clinical lessons learned in constitutional hypopituitarism from two decades of experience in a large international cohort

Human iPSCs-derived astrocytes reveal APOE as a critical modulator of inflammation that could underlie Alzheimer’s disease pathogenesis

Heterozygous LHX3 mutations may lead to a mild phenotype of combined pituitary hormone deficiency

Conditional Transgenesis Using Dimerizable Cre (DiCre)

MT5-MMP controls APP and β-CTF/C99 metabolism through proteolytic-dependent and -independent mechanisms relevant for Alzheimer’s disease

APOE4 primes inflammation in human astrocytes through the downregulation of a newly discovered target candidatevv

Lessons from monogenic causes of growth hormone deficiency

Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports

[Genetic aspects of growth hormone deficiency].