Olivier Lahuna

Inserm — France

Medicine · Health Sciences

23h-index1.4kcitations40works0.02yr avg
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Research Topics

Pancreatic function and diabetes(8), Growth Hormone and Insulin-like Growth Factors(7), Amino Acid Enzymes and Metabolism(7), Receptor Mechanisms and Signaling(5), Digestive system and related health(5)

Publications40 total

SAT025 Characterization Of The Melatonin Type 1 Receptor / Cannabinoid Type 1 Receptor (MT1/CB1) Heteromers
Journal of the Endocrine Society·2023Open Access
Hétérodimérisation des récepteurs de la mélatonine et des cannabinoïdes de type 1
Annales d Endocrinologie·2022
Heterodimerization and Subcellular Distribution of Melatonin and Cannabinoid Type 1 Receptors
Journal of the Endocrine Society·2021· 1 citedOpen Access
GPR50-Ctail cleavage and nuclear translocation: a new signal transduction mode for G protein-coupled receptors
Cellular and Molecular Life Sciences·2020· 17 citedOpen Access
Defective bicarbonate reabsorption in Kir4.2 potassium channel deficient mice impairs acid-base balance and ammonia excretion
Kidney International·2019· 38 citedOpen Access
L’inactivation du gène Kcnj15 encodant la protéine Kir4.2 provoque chez la souris une acidose tubulaire proximale isolée associée à une ammoniurie inadaptée
Néphrologie & Thérapeutique·2018
A novel <i>CLCN5</i> pathogenic mutation supports Dent disease with normal endosomal acidification
Human Mutation·2018· 25 citedOpen Access
The orphan GPR50 receptor promotes constitutive TGFβ receptor signaling and protects against cancer development
Nature Communications·2018· 37 citedOpen Access
Signalisation mitochondriale des récepteurs couplés aux protéines G
Biologie Aujourd hui·2018· 3 cited
Orphan GPR61, GPR62 and GPR135 receptors and the melatonin MT2 receptor reciprocally modulate their signaling functions
Scientific Reports·2017· 42 citedOpen Access
Functional analysis of a novel pathogenic mutation affecting the gating glutamate of the 2Cl <sup>−</sup> /H <sup>+</sup> exchanger ClC‐5 in patients with Dent's disease type 1
The FASEB Journal·2017
Identification of human telomerase assembly inhibitors enabled by a novel method to produce hTERT
Nucleic Acids Research·2015· 14 citedOpen Access
Novel<i>CLCNKB</i>Mutations Causing Bartter Syndrome Affect Channel Surface Expression
Human Mutation·2013· 29 citedOpen Access
Spermatogenèse normale chez un homme avec défaut génétique de la LH
médecine/sciences·2010· 2 citedOpen Access
Normal Spermatogenesis in a Man with Mutant Luteinizing Hormone
New England Journal of Medicine·2009· 72 cited
Moleular pathology of the FSH receptor
8th European Congress of Endocrinology incorporating the British Endocrine Societies·2006
Involvement of β-catenin and unusual behavior of CBP and p300 in glucocorticosteroid signaling in Schwann cells
Proceedings of the National Academy of Sciences·2005· 30 citedOpen Access
Thyrotropin receptor trafficking relies on the hScrib–βPIX–GIT1–ARF6 pathway
The EMBO Journal·2005· 74 citedOpen Access
Delayed Puberty and Primary Amenorrhea Associated with a Novel Mutation of the Human Follicle-Stimulating Hormone Receptor: Clinical, Histological, and Molecular Studies
The Journal of Clinical Endocrinology & Metabolism·2003· 184 citedOpen Access
Involvement of STAT5 (Signal Transducer and Activator of Transcription 5) and HNF-4 (Hepatocyte Nuclear Factor 4) in the Transcriptional Control of the hnf6 Gene by Growth Hormone
Molecular Endocrinology·2000· 23 citedOpen Access
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Frequent Co-authors

Yannick Laperche(8), Mojtaba Darbouy(7), Agneta Mode(6), Ralf Jockers(6), Geri Méduri(5), Micheline Misrahi(5), Marie-Noële Chobert(5), Stéphane Lourdel(5), Yohan Bignon(4), Nadia Frachon(4), Jacques Teulon(4), Arthur Brouillet(4), Philippe Touraine(3), Leandro Fernández‐Pérez(3), Jan-Ακε Gustafsson(3), Georges Guellaën(3), Raise Ahmad(3), Rosa Vargas‐Poussou(3), F Kuttenn(2), Dominique Maiter(2)