About: Jacques Young

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	ikertzailea (eu) researcher (en) 연구원 (ko) 研究者 (ja) investigador (es) wetenschapper (nl) дослідник (uk) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy)
rdfs:label	Jacques Young (en) Jacques Young (nl)
skos:prefLabel	Jacques Young (en) Jacques Young (nl)
name	Jacques Young (en) Jacques Young (nl)
given name	wds:Q79281866-C69587AE-F85C-4D2A-A84E-38595E3133B0
given name	Jacques
instance of	wds:Q79281866-B61C16C7-637B-4682-AD24-40553294D849
instance of	Homo sapiens
doctoral advisor	wds:Q79281866-0E963742-DEBE-4077-A0FC-793A329796F5
doctoral student	wds:Q79281866-E496E663-91E6-44E8-8D7D-86FA0AFCED7C
doctoral advisor	Étienne-Émile Baulieu
doctoral student	Lavinia Vija
occupation	wds:Q79281866-1A180973-568D-47D4-B332-1E31EE99E191
employer	wds:Q79281866-4D052D59-1448-449A-B254-398544E16397 wds:Q79281866-7CBBC610-6648-4D9C-B054-8B9786E70799
sex or gender	wds:Q79281866-81811a1a-1b2f-42a4-ab67-7fafbcbbcb27
VIAF ID	wds:Q79281866-83F61252-FB11-49DA-8A09-9FED9154FC88
Bibliothèque nationale de France ID	wds:Q79281866-A68D7117-C514-4C99-83DD-7A70C76E7766
IdRef ID	wds:Q79281866-A2FF38C1-83F0-4303-8F1E-DECD1DD41101
educated at	wds:Q79281866-13F0F7FE-8D5F-4BF9-8FBE-6B6721F6F175
family name	wds:Q79281866-5818CAF0-8449-4D2E-B2DC-DCB4B8A39ECB
VIAF ID	http://viaf.org/viaf/54320835
Bibliothèque nationale de France ID	http://data.bnf.fr/ark:/12148/cb136105424#about
IdRef ID	http://www.idref.fr/055812120/id
occupation	researcher
employer	Assistance Publique – Hôpitaux de Paris University of Paris-Sud
sex or gender	male
VIAF ID	54320835
Bibliothèque nationale de France ID	136105424
IdRef ID	055812120
educated at	University of Paris-Sud
family name	Young
ORCID iD	wds:Q79281866-9E8243BC-3257-4A66-87C5-B706BF4E653A
ORCID iD	https://orcid.org/0000-0001-9286-5631
ORCID iD	0000-0001-9286-5631
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q79281866
is author of	Intraadrenal corticotropin in bilateral macronodular adrenal hyperplasia A family with hypogonadotropic hypogonadism and mutations in the gonadotropin-releasing hormone receptor Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2 Genetics defects in GNRH1: a paradigm of hypothalamic congenital gonadotropin deficiency Phage-induced expression of CRISPR-associated proteins is revealed by shotgun proteomics in Streptococcus thermophilus Normosmic congenital hypogonadotropic hypogonadism due to TAC3/TACR3 mutations: characterization of neuroendocrine phenotypes and novel mutations Non-syndromic congenital hypogonadotropic hypogonadism: clinical presentation and genotype-phenotype relationships Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism SDHBmutations are associated with response to temozolomide in patients with metastatic pheochromocytoma or paraganglioma Neurosteroids: pregnenolone in human sciatic nerves Hyperprolactinemia-induced ovarian acyclicity is reversed by kisspeptin administration. Ketoconazole in Cushing's disease: is it worth a try? Clinical Outcome, Hormonal Status, Gonadotrope Axis, and Testicular Function in 219 Adult Men Born With Classic 21-Hydroxylase Deficiency. A French National Survey SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development Neonatal gonadotropin therapy in male congenital hypogonadotropic hypogonadism. Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatment One-Year Progression-Free Survival of Therapy-Naive Patients With Malignant Pheochromocytoma and Paraganglioma [HAS report on vitamin D measurement: don't go from an extreme situation to another as extreme situation] Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian Insufficiency. Metaproteomics reveals functional shifts in microbial and human proteins during a preterm infant gut colonization case Prevalence of KISS1 Receptor mutations in a series of 603 patients with normosmic congenital hypogonadotrophic hypogonadism and characterization of novel mutations: a single-centre study. An ancient founder mutation in PROKR2 impairs human reproduction Mitotane for 21-hydroxylase deficiency in an infertile man Cardiac structure and function in Cushing's syndrome: a cardiac magnetic resonance imaging study Clinical Management of Congenital Hypogonadotropic Hypogonadism Selective modification of a native protein in a patient tissue homogenate using palladium nanoparticles Insulin-like peptide 3 (INSL3) in men with congenital hypogonadotropic hypogonadism/Kallmann syndrome and effects of different modalities of hormonal treatment: a single-center study of 281 patients Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism New NOBOX mutations identified in a large cohort of women with primary ovarian insufficiency decrease KIT-L expression PKA regulatory subunit 1A inactivating mutation induces serotonin signaling in primary pigmented nodular adrenal disease. Effects of cortisol on the heart: characterization of myocardial involvement in cushing's disease by longitudinal cardiac MRI T1 mapping Prolactin - a pleiotropic factor in health and disease Congenital hypogonadotropic hypogonadism and Kallmann syndrome as models for studying hormonal regulation of human testicular endocrine functions Similarities and differences in the reproductive phenotypes of women with congenital hypogonadotrophic hypogonadism caused by GNRHR mutations and women with polycystic ovary syndrome [Weakening osteopathies, chronic kidney disease, malabsorption, biological anomalies of calium/phosphorus metabolism: appropriate indications for a reasoned reimbursment of serum vitamin D measurement] French law: what about a reasoned reimbursement of serum vitamin D assays? Illicit Upregulation of Serotonin Signaling Pathway in Adrenals of Patients With High Plasma or Intra-Adrenal ACTH Levels
is author of	wds:Q34059565-531FB369-F77C-467B-B747-F69D92170B78 wds:Q41141599-99D5FCCD-6F95-497A-85D6-F95AF405DE41 wds:Q87120692-A613769F-9FFA-483E-8C53-326527D500BD wds:Q91542042-BAFB3F1D-79F8-4AFC-837C-38613CEFF62E wds:Q34486033-F5E33675-EA8F-470E-9DEA-3FBABCF87A31 wds:Q34446712-697D5FF2-FA59-4BC9-A0CE-18437B5EDDEF wds:Q35664605-B39C85FE-10CF-4BF7-952C-C152C7FA53AD wds:Q42450040-AF59F6F2-BAC7-49F7-9486-59EC4361AB34 wds:Q86303712-E3B39641-8A4C-4AD3-AC46-DFA2C13FB0AC wds:Q37713556-191CC19A-EBCA-405C-BA93-AABADEFAF13C wds:Q86022117-263EB1D3-18D5-4403-AD72-993708490EE7 wds:Q87179331-53FABDFC-405E-4E74-9991-5DA60D5CF7E8 wds:Q28316500-DE511D9F-D2F9-49D8-8E86-058C539C6A2B

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