About: Yves Le Bouc

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An Entity of Type : foaf:Person, within Data Space : data.idref.fr associated with source document(s)

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type	Person
sameAs	Le Bouc, Yves (19..-.... ; professeur de physiologie) Le Bouc, Yves (19..-.... ; professeur de physiologie) Le Bouc, Yves (19..-.... ; professeur de physiologie) Le Bouc, Yves (19..-.... ; professeur de physiologie)
Life Event	http://www.idref.fr/098392352/birth
preferred label	Le Bouc, Yves (19..-.... ; professeur de physiologie)
name	Yves Le Bouc
dbpedia-owl:citizenship	http://sws.geonames.org/3017382/
Language	http://lexvo.org/id/iso639-3/fra
isni:identifierValid	0000000141033069
Given name	Yves
familyName	Le Bouc
has biographical i...tion (Deprecated)	Directeur de thèse à l'Université Pierre et Marie Curie - Paris 6 en 2008, 2009 et 2013 Professeur de Physiologie à l'Université Pierre et Marie Curie (Paris VI) Professeur émérite, Sorbonne Université, en poste à l'Hopital St Antoine (en 2023)
gender	male
ORCID iD	0000-0002-1017-5002
Scopus ID	7006826905
is sameAs of	Le Bouc, Yves (19..-.... ; professeur de physiologie) Le Bouc, Yves (19..-.... ; professeur de physiologie) Le Bouc, Yves (19..-.... ; professeur de physiologie) Le Bouc, Yves (19..-.... ; professeur de physiologie)
is Thesis advisor of	http://www.sudoc.fr/198535732/id http://www.sudoc.fr/136797202/id Suivi endocrininen des sportifs de haut niveau, axes hypothalamo-hypophyso-surrénalien et somatotrope et remodelage osseux http://www.sudoc.fr/059982055/id http://www.sudoc.fr/142897906/id http://www.sudoc.fr/098391267/id http://www.sudoc.fr/059981911/id http://www.sudoc.fr/066777542/id http://www.sudoc.fr/178159506/id http://www.sudoc.fr/22329974X/id http://www.sudoc.fr/104608587/id http://www.sudoc.fr/043908640/id http://www.sudoc.fr/041360443/id Implication du système des insulin-like growth factors (IGF) dans la pathogénie et la réponse thérapeutique des tumeurs corticosurrénaliennes humaines, étude de deux modèles expérimentaux http://www.sudoc.fr/247120162/id Régulation épigénétique de la région chromosomique 11p15 et croissance fœtale ETUDE PHYSIOPATHOGENIQUE DES TUMEURS DE L'AXE CORTICOTROPE http://www.sudoc.fr/246602139/id http://www.sudoc.fr/246561858/id http://www.sudoc.fr/248671316/id Analyse du système des insulin-like growth factors (IGF) et du fibroblast growth factor-2 (FGF-2) dans la tumorigenèse corticosurrenalienne Physiopathologie des troubles de la croissance foetale, approche génétique et épigénétique http://www.sudoc.fr/246899948/id http://www.sudoc.fr/248050524/id Rôles respectifs de l'axe hormone de croissance (GH) / insulin like growth factor-I (IGF-I) et de la somatostatine dans le développement de l'inflammation et de la fibrose glomérulaires http://www.sudoc.fr/247158933/id Pathologies de la croissance fœtale (syndromes de Beckwith Wiedemann et Silver Russell), implication de la protéine CDKN1C et autres mécanismes moléculaires LE SYSTEME DES INSULIN-LIKE GROWTH FACTORS AU COURS DU VIEILLISSEMENT, INFLUENCE DE LA DENUTRITION ET DE L'INFLAMMATION http://www.sudoc.fr/24656170X/id Etude des voies de signalisation impliquées dans les effets anti-apoptotique et prolifératif de l'hormone de croissance http://www.sudoc.fr/245831436/id
is Author of	Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci IGF-1 receptor regulates lifespan and resistance to oxidative stress in mice New insights into the pathogenesis of Beckwith-Wiedemann and Silver-Russell syndromes: contribution of small copy number variations to 11p15 imprinting defects. Recessive Isolated Growth Hormone Deficiency and Mutations in the Ghrelin Receptor The epigenetic imprinting defect of patients with Beckwith—Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region Insulin-Like Growth Factor-I and Insulin-Like Growth Factor Binding Protein-3 in Alzheimer's Disease Régulation de la croissance : des mécanismes épigénétiques ? https://hal.archives-ouvertes.fr/hal-02376096#id The functional development of the somatotropic axis depends on hypothalamic IGF-1R in mice Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders Serum GH concentration must now be expressed in mass units in France like in the rest of the world Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences Brain IGF-1 receptors control mammalian growth and lifespan through a neuroendocrine mechanism. Coupling Complete Blood Count and Steroidomics to Track Low Doses Administration of Recombinant Growth Hormone: An Anti-Doping Perspective Hepatocyte proliferation during liver regeneration is impaired in mice with liver-specific IGF-1R knockout IGF-1 Induces GHRH Neuronal Axon Elongation during Early Postnatal Life in Mice CDKN1C mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndrome Genetic variants within the second intron of the KCNQ1 gene effect CTCF binding and confer a risk of Beckwith-Wiedemann syndrome upon maternal transmission Early Postnatal Nutrition Determines Somatotropic Function in Mice Impact of Age-Adjusted Insulin-Like Growth Factor 1 on Major Cardiovascular Events After Acute Myocardial Infarction: Results From the Fast-MI Registry https://orbi.uliege.be/handle/2268/11791#id Combining metabolomics and machine learning models as a tool to distinguish non-classic 21-hydroxylase deficiency from polycystic ovary syndrome without adrenocorticotropic hormone testing ALLELE-SPECIFIC METHYLATED MULTIPLEX REAL TIME QUANTITATIVE PCR (ASMM RTQ-PCR), A POWERFUL METHOD FOR DIAGNOSING LOSS OF IMPRINTING OF THE 11p15 REGION IN RUSSELL SILVER AND BECKWITH WIEDEMANN SYNDROMES Epigenetic abnormalities of the mannose-6-phosphate/IGF2 receptor gene are uncommon in human overgrowth syndromes IGF2 promotes growth of adrenocortical carcinoma cells, but its overexpression does not modify phenotypic and molecular features of adrenocortical carcinoma. Metabolomic signatures in Elite cyclists: differential characterization of a seeming normal endocrine status regarding three serum hormones Evolution of IGF-1 in children born small for gestational age and with growth retardation, treated by growth hormone adapted to IGF-1 levels after 1 year https://archive-ouverte.unige.ch/unige:47083#id Insulin-Like Growth Factor-I, Insulin-Like Growth factor Binding Protein-3 and Blood Hemoglobin Concentration in an Elderly Population Increasing knowledge in IGF1R defects: lessons from 35 new patients Imprinted disorders and growth Growth pattern from birth to adulthood in African pygmies of known age Mutations of the Imprinted CDKN1C Gene as a Cause of the Overgrowth Beckwith–Wiedemann Syndrome: Clinical Spectrum and Functional Characterization Child health, developmental plasticity, and epigenetic programming Genetic disruption of the oncogenic HMGA2–PLAG1–IGF2 pathway causes fetal growth restriction The role of GHR and IGF1 genes in the genetic determination of African pygmies’ short stature Deleting IGF-1 receptor from forebrain neurons confers neuroprotection during stroke and upregulates endocrine somatotropin Changes in circulating miRNA19a-3p precede insulin resistance programmed by intra-uterine growth retardation in mice https://orbi.uliege.be/handle/2268/11754#id https://orbi.uliege.be/handle/2268/20100#id Normal Growth despite Combined Pituitary Hormone Deficiency https://serval.unil.ch/notice/serval:BIB_EB1304FA1D94#id http://id.erudit.org/iderudit/012779ar#id Low Maternal DLK1 Levels at 26 Weeks Is Associated With Small for Gestational Age at Birth 11p15 ICR1 Partial Deletions Associated with IGF2/H19 DMR Hypomethylation and Silver-Russell Syndrome
is primary topic of	http://www.idref.fr/098392352

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