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Anna Maria Barbieri
Anna Maria Barbieri
Università degli Studi di Milano - Dip. di Scienze Cliniche e di Comunità Fondazione IRCCS Ca
在 unimi.it 的电子邮件经过验证
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引用次数
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Eukaryotic initiation factor 6 is rate-limiting in translation, growth and transformation
V Gandin, A Miluzio, AM Barbieri, A Beugnet, H Kiyokawa, PC Marchisio, ...
Nature 455 (7213), 684-688, 2008
2452008
A homeobox gene, vax2, controls the patterning of the eye dorsoventral axis
AM Barbieri, G Lupo, A Bulfone, M Andreazzoli, M Mariani, ...
Proceedings of the National Academy of Sciences 96 (19), 10729-10734, 1999
1861999
Pseudohypoparathyroidism and GNAS Epigenetic Defects: Clinical Evaluation of Albright Hereditary Osteodystrophy and Molecular Analysis in 40 Patients
G Mantovani, L de Sanctis, AM Barbieri, FM Elli, V Bollati, V Vaira, ...
The Journal of Clinical Endocrinology & Metabolism 95 (2), 651-658, 2010
1852010
Vax2 inactivation in mouse determines alteration of the eye dorsal-ventral axis, misrouting of the optic fibres and eye coloboma
AM Barbieri, V Broccoli, P Bovolenta, G Alfano, A Marchitiello, C Mocchetti, ...
Oxford University Press for The Company of Biologists Limited 129 (3), 805-813, 2002
1652002
The limited role of midnight salivary cortisol levels in the diagnosis of subclinical hypercortisolism in patients with adrenal incidentaloma
B Masserini, V Morelli, S Bergamaschi, F Ermetici, C Eller-Vainicher, ...
European Journal of Endocrinology 160 (1), 87-92, 2009
1292009
Pseudohypoparathyroidism Type Ia and Pseudo‐Pseudohypoparathyroidism: The Growing Spectrum of GNAS Inactivating Mutations
FM Elli, L deSanctis, B Ceoloni, AM Barbieri, P Bordogna, P Beck‐Peccoz, ...
Human mutation 34 (3), 411-416, 2013
862013
Quantitative analysis of methylation defects and correlation with clinical characteristics in patients with pseudohypoparathyroidism type I and GNAS epigenetic alterations
FM Elli, L de Sanctis, V Bollati, L Tarantini, M Filopanti, AM Barbieri, ...
The Journal of Clinical Endocrinology & Metabolism 99 (3), E508-E517, 2014
582014
Dopamine D2 receptor gene polymorphisms and response to cabergoline therapy in patients with prolactin-secreting pituitary adenomas
M Filopanti, AM Barbieri, AR Angioni, A Colao, V Gasco, S Grottoli, A Peri, ...
The pharmacogenomics journal 8 (5), 357-363, 2008
522008
Two novel nonsense mutations in GALNT3 gene are responsible for familial tumoral calcinosis
AM Barbieri, M Filopanti, G Bua, P Beck-Peccoz
Journal of Human Genetics 52 (5), 464-468, 2007
442007
Screening for GNAS genetic and epigenetic alterations in progressive osseous heteroplasia: first Italian series
FM Elli, AM Barbieri, P Bordogna, P Ferrari, R Bufo, E Ferrante, ...
Bone 56 (2), 276-280, 2013
402013
Pharmacology of the calcium sensing receptor
M Filopanti, S Corbetta, AM Barbieri, A Spada
Clinical Cases in Mineral and Bone Metabolism 10 (3), 162, 2013
342013
Peripheral insulin-like factor 3 concentrations are reduced in men with type 2 diabetes mellitus: effect of glycemic control and visceral adiposity on Leydig cell function
F Ermetici, F Donadio, L Iorio, AE Malavazos, A Dolci, E Peverelli, ...
European journal of endocrinology 161 (6), 853-859, 2009
342009
Seven novel additional small mutations and a new alternative splicing in the human dystrophin gene detected by heteroduplex analysis and restricted RT-PCR heteroduplex analysis …
AM Barbieri, N Soriani, A Ferlini, A Michelato, M Ferrari, P Carrera
European Journal of Human Genetics 4 (3), 183-187, 1996
321996
In postmenopausal female subjects with type 2 diabetes mellitus, vertebral fractures are independently associated with cortisol secretion and sensitivity
VV Zhukouskaya, C Eller-Vainicher, A Gaudio, E Cairoli, FM Ulivieri, ...
The Journal of Clinical Endocrinology & Metabolism 100 (4), 1417-1425, 2015
292015
Calcimimetic R-568 effects on activity of R990G polymorphism of calcium-sensing receptor
A Terranegra, A Ferraretto, E Dogliotti, M Scarpellini, S Corbetta, ...
Journal of Molecular Endocrinology 45 (4), 245, 2010
282010
Cortisol secretion, sensitivity, and activity are associated with hypertension in postmenopausal eucortisolemic women
I Chiodini, A Gaudio, C Eller-Vainicher, V Morelli, C Aresta, ...
The Journal of Clinical Endocrinology & Metabolism 104 (10), 4441-4448, 2019
202019
Suppressive effects of tenofovir disoproxil fumarate, an antiretroviral prodrug, on mineralization and type II and type III sodium‐dependent phosphate transporters expression …
AM Barbieri, I Chiodini, E Ragni, G Colaianni, F Gadda, M Locatelli, ...
Journal of cellular biochemistry 119 (6), 4855-4866, 2018
182018
Role of UGT1A1 and ADH gene polymorphisms in pegvisomant-induced liver toxicity in acromegalic patients
M Filopanti, AM Barbieri, G Mantovani, S Corbetta, V Gasco, M Ragonese, ...
European journal of endocrinology 170 (2), 247-254, 2014
182014
Rapid detection of 21-hydroxylase deficiency mutations by allele-specific in vitro amplification and capillary zone electrophoresis
P Carrera, AM Barbieri, M Ferrari, PG Righetti, M Perego, C Gelfi
Clinical chemistry 43 (11), 2121-2127, 1997
151997
Cofilin is a mediator of RET-promoted medullary thyroid carcinoma cell migration, invasion and proliferation
E Giardino, R Catalano, AM Barbieri, D Treppiedi, F Mangili, A Spada, ...
Molecular and cellular endocrinology 495, 110519, 2019
72019
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