Articles with public access mandates - Thierry BrueLearn more
Not available anywhere: 3
Characterization of the ability of a, second-generation SST-DA chimeric molecule, TBR-065, to suppress GH secretion from human GH-secreting adenoma cells
T Cuny, T Graillon, C Defilles, R Datta, S Zhang, D Figarella-Branger, ...
Pituitary 24, 351-358, 2021
Mandates: National Institute of Health and Medical Research, France
Novel mechanism of pituitary hormone deficiency: genetic variants shift splicing to produce a dominant negative transcription factor isoform
T Brue, SA Camper
European Journal of Endocrinology 185 (6), C19-C25, 2021
Mandates: US National Institutes of Health
Gonadotropic status in adult women with pituitary stalk interruption syndrome
A Terray, B Baussart, M Zins, M Goldberg, S Kab, L Cazabat, M Brière, ...
European Journal of Endocrinology 190 (6), 501-508, 2024
Mandates: Agence Nationale de la Recherche
Available somewhere: 33
A new prognostic clinicopathological classification of pituitary adenomas: a multicentric case–control study of 410 patients with 8 years post-operative follow-up
J Trouillas, P Roy, N Sturm, E Dantony, C Cortet-Rudelli, G Viennet, ...
Acta neuropathologica 126, 123-135, 2013
Mandates: National Institute of Health and Medical Research, France
Clinical and genetic characterization of pituitary gigantism: an international collaborative study in 208 patients
L Rostomyan, AF Daly, P Petrossians, E Nachev, AR Lila, AL Lecoq, ...
Endocrine-related cancer 22 (5), 745-757, 2015
Mandates: US National Institutes of Health
Prognostic factors in prolactin pituitary tumors: clinical, histological, and molecular data from a series of 94 patients with a long postoperative follow-up
G Raverot, A Wierinckx, E Dantony, C Auger, G Chapas, L Villeneuve, ...
The Journal of Clinical Endocrinology & Metabolism 95 (4), 1708-1716, 2010
Mandates: National Institute of Health and Medical Research, France
Molecular mechanisms of pituitary organogenesis: in search of novel regulatory genes
SW Davis, F Castinetti, LR Carvalho, BS Ellsworth, MA Potok, RH Lyons, ...
Molecular and cellular endocrinology 323 (1), 4-19, 2010
Mandates: US National Institutes of Health
Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population …
F Castinetti, XP Qi, MK Walz, AL Maia, G Sansó, M Peczkowska, ...
The Lancet Oncology 15 (6), 648-655, 2014
Mandates: Government of Italy
The selector gene Pax7 dictates alternate pituitary cell fates through its pioneer action on chromatin remodeling
L Budry, A Balsalobre, Y Gauthier, K Khetchoumian, A L'honoré, ...
Genes & development 26 (20), 2299-2310, 2012
Mandates: Canadian Institutes of Health Research, Genome Canada
Natural history, treatment, and long-term follow up of patients with multiple endocrine neoplasia type 2B: an international, multicentre, retrospective study
F Castinetti, SG Waguespack, A Machens, S Uchino, K Hasse-Lazar, ...
The lancet Diabetes & endocrinology 7 (3), 213-220, 2019
Mandates: US National Institutes of Health
Pituitary stem cell update and potential implications for treating hypopituitarism
F Castinetti, SW Davis, T Brue, SA Camper
Endocrine reviews 32 (4), 453-471, 2011
Mandates: US National Institutes of Health
Cooperation between Cyclin E and p27Kip1 in Pituitary Tumorigenesis
A Roussel-Gervais, S Bilodeau, S Vallette, F Berthelet, A Lacroix, ...
Molecular Endocrinology 24 (9), 1835-1845, 2010
Mandates: Canadian Institutes of Health Research
Mutations in NFKB2and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficiencies
T Brue, MH Quentien, K Khetchoumian, M Bensa, JM Capo-Chichi, ...
BMC medical genetics 15, 1-7, 2014
Mandates: Canadian Institutes of Health Research, Genome Canada
Phenotypic Homogeneity and Genotypic Variability in a Large Series of Congenital Isolated ACTH-Deficiency Patients with TPIT Gene Mutations
C Couture, A Saveanu, A Barlier, JC Carel, M Fassnacht, CE Flück, ...
The Journal of Clinical Endocrinology & Metabolism 97 (3), E486-E495, 2012
Mandates: Canadian Institutes of Health Research
High mortality within 90 days of diagnosis in patients with Cushing’s syndrome: results from the ERCUSYN registry
E Valassi, A Tabarin, T Brue, RA Feelders, M Reincke, R Netea-Maier, ...
European journal of endocrinology 181 (5), 461-472, 2019
Mandates: National Institute of Health and Medical Research, France
Bilateral adrenalectomy in the 21st century: when to use it for hypercortisolism?
C Guerin, D Taieb, G Treglia, T Brue, A Lacroix, F Sebag, F Castinetti
Endocrine-Related Cancer 23 (2), R131-R142, 2016
Mandates: Fundação para a Ciência e a Tecnologia, Portugal
The Cables1 Gene in Glucocorticoid Regulation of Pituitary Corticotrope Growth and Cushing Disease
A Roussel-Gervais, C Couture, D Langlais, S Takayasu, A Balsalobre, ...
The Journal of Clinical Endocrinology & Metabolism 101 (2), 513-522, 2016
Mandates: Canadian Cancer Society, Canadian Institutes of Health Research, Fonds de …
Diagnostic tests for Cushing's syndrome differ from published guidelines: data from ERCUSYN
E Valassi, H Franz, T Brue, RA Feelders, R Netea-Maier, S Tsagarakis, ...
European Journal of Endocrinology 176 (5), 613-624, 2017
Mandates: National Institute of Health and Medical Research, France
Prevalence of KISS1 Receptor mutations in a series of 603 patients with normosmic congenital hypogonadotrophic hypogonadism and characterization of novel …
B Francou, C Paul, L Amazit, A Cartes, C Bouvattier, F Albarel, D Maiter, ...
Human Reproduction 31 (6), 1363-1374, 2016
Mandates: European Commission
Pasireotide and octreotide antiproliferative effects and sst2 trafficking in human pancreatic neuroendocrine tumor cultures
A Mohamed, MP Blanchard, M Albertelli, F Barbieri, T Brue, P Niccoli, ...
Endocrine-related cancer 21 (5), 691-704, 2014
Mandates: Danish Council for Independent Research, Cancer Research UK
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