A. Barbieri

发表

Calcimimetic R-568 effects on activity of R990G polymorphism of calcium-sensing receptor.

D. Cusi, G. Vezzoli, L. Soldati, 2010, Journal of molecular endocrinology.

Dopamine D2 receptor gene polymorphisms and response to cabergoline therapy in patients with prolactin-secreting pituitary adenomas

A. Peri, S. Grottoli, S. Brogioni, 2008, The Pharmacogenomics Journal.

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.

I. Chiodini, P. Beck‐Peccoz, B. Ambrosi, 2009, European journal of endocrinology.

Two novel nonsense mutations in GALNT3 gene are responsible for familial tumoral calcinosis

P. Beck‐Peccoz, A. Barbieri, M. Filopanti, 2007, Journal of Human Genetics.

P720R USP8 Mutation Is Associated with a Better Responsiveness to Pasireotide in ACTH-Secreting PitNETs

M. Arosio, E. Esposito, F. Bravi, 2022, Cancers.

TMPRSS2 Expression and Activity Modulation by Sex-Related Hormones in Lung Calu-3 Cells: Impact on Gender-Specific SARS-CoV-2 Infection

M. Arosio, E. Esposito, E. Peverelli, 2022, Frontiers in Endocrinology.

Adrenalectomy Improves Blood Pressure and Metabolic Control in Patients With Possible Autonomous Cortisol Secretion: Results of a RCT

S. Fustinoni, I. Chiodini, A. Scillitani, 2022, Frontiers in Endocrinology.

The limited role of midnight salivary cortisol levels in the diagnosis of subclinical hypercortisolism in patients with adrenal incidentaloma.

I. Chiodini, A. Scillitani, V. Morelli, 2009, European journal of endocrinology.

Pharmacology of the calcium sensing receptor.

A. Spada, S. Corbetta, A. Barbieri, 2013, Clinical cases in mineral and bone metabolism : the official journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases.

Suppressive effects of tenofovir disoproxil fumarate, an antiretroviral prodrug, on mineralization and type II and type III sodium‐dependent phosphate transporters expression in primary human osteoblasts

P. Lampertico, I. Chiodini, C. Eller-Vainicher, 2018, Journal of cellular biochemistry.

Quantitative analysis of methylation defects and correlation with clinical characteristics in patients with pseudohypoparathyroidism type I and GNAS epigenetic alterations.

V. Bollati, P. Beck‐Peccoz, E. Peverelli, 2014, The Journal of clinical endocrinology and metabolism.

Pseudohypoparathyroidism type Ia and GNAS epigenetic defects: clinical evaluation and molecular analysis in 40 patients with Albright's hereditary osteodystrophy

P. Beck‐Peccoz, A. Lania, E. Peverelli, 2009 .

Genetic Profiling of a Cohort of Italian Patients with ACTH-Secreting Pituitary Tumors and Characterization of a Novel USP8 Gene Variant

M. Arosio, E. Esposito, M. Locatelli, 2021, Cancers.

DRD2 Agonist Cabergoline Abolished the Escape Mechanism Induced by mTOR Inhibitor Everolimus in Tumoral Pituitary Cells

M. Arosio, E. Esposito, M. Locatelli, 2022, Frontiers in Endocrinology.

SAT-566 Cofilin Is a Mediator of RET-Promoted Medullary Thyroid Carcinoma Cell Migration, Invasion and Proliferation

M. Arosio, E. Peverelli, A. Barbieri, 2019, Molecular and Cellular Endocrinology.

Octreotide and pasireotide effects on medullary thyroid carcinoma (MTC) cells growth, migration and invasion

M. Arosio, E. Peverelli, A. Barbieri, 2020, Molecular and Cellular Endocrinology.

Rapid detection of 21-hydroxylase deficiency mutations by allele-specific in vitro amplification and capillary zone electrophoresis.

M. Ferrari, P. Righetti, C. Gelfi, 1997, Clinical chemistry.

Screening for GNAS genetic and epigenetic alterations in progressive osseous heteroplasia: first Italian series.

P. Beck‐Peccoz, P. Ferrari, A. Spada, 2013, Bone.

Vax2 inactivation in mouse determines alteration of the eye dorsal-ventral axis, misrouting of the optic fibres and eye coloboma.

P. Bovolenta, A. Ballabio, V. Broccoli, 2002, Development.

Patients with macroprolactinaemia: clinical and radiological features

P. Beck‐Peccoz, A. Lania, A. Spada, 2007, European journal of clinical investigation.

Eukaryotic initiation factor 6 is rate-limiting in translation, growth and transformation

H. Kiyokawa, S. Biffo, V. Gandin, 2008, Nature.

Pseudohypoparathyroidism Type Ia and Pseudo‐Pseudohypoparathyroidism: The Growing Spectrum of GNAS Inactivating Mutations

P. Beck‐Peccoz, A. Spada, A. Barbieri, 2013, Human mutation.

Pseudohypoparathyroidism and GNAS epigenetic defects: clinical evaluation of albright hereditary osteodystrophy and molecular analysis in 40 patients.

V. Bollati, V. Vaira, P. Beck‐Peccoz, 2010, The Journal of clinical endocrinology and metabolism.

Bone involvement and mineral metabolism in Williams’ syndrome

I. Chiodini, A. Scillitani, V. Morelli, 2018, Journal of Endocrinological Investigation.

Variability of hemispheric scale energy parameters

E. Reiter, A. Barbieri, J. P. Mcguirk, 1974 .

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 of Illegitimate Transcripts

P. Carrera, A. Michelato, A. Barbieri, 1996, European journal of human genetics : EJHG.

A homeobox gene, vax2, controls the patterning of the eye dorsoventral axis.

G. Borsani, A. Ballabio, F. Fougerousse, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Impact of IGF(CA)19 gene polymorphism on the metabolic response to GH therapy in adult GH-deficient patients.

P. Beck‐Peccoz, B. Ambrosi, M. Arosio, 2014, European journal of endocrinology.

Cortisol secretion, sensitivity, and activity are associated with hypertension in postmenopausal eucortisolemic women.

S. Fustinoni, I. Chiodini, A. Scillitani, 2019, The Journal of clinical endocrinology and metabolism.

In postmenopausal female subjects with type 2 diabetes mellitus, vertebral fractures are independently associated with cortisol secretion and sensitivity.

S. Fustinoni, C. Fiore, I. Chiodini, 2015, The Journal of clinical endocrinology and metabolism.

Filamin A is required for somatostatin receptor type 5 expression and pasireotide-mediated signaling in pituitary corticotroph tumor cells

M. Arosio, M. Locatelli, E. Peverelli, 2021, Molecular and Cellular Endocrinology.

Role of IGF1‐(CA)19 promoter microsatellite in the clinical presentation of acromegaly

P. Beck‐Peccoz, M. Arosio, A. Lania, 2014, European journal of clinical investigation.

Beta-Arrestin 2 Is Required for Dopamine Receptor Type 2 Inhibitory Effects on AKT Phosphorylation and Cell Proliferation in Pituitary Tumors

M. Arosio, M. Locatelli, A. Lania, 2020, Neuroendocrinology.

Role of UGT1A1 and ADH gene polymorphisms in pegvisomant-induced liver toxicity in acromegalic patients.

M. Ragonese, A. Peri, F. Bogazzi, 2014, European journal of endocrinology.

USP8 inhibitor RA-9 reduces ACTH release and cell growth in tumor corticotrophs.

M. Arosio, M. Locatelli, A. Lania, 2021, Endocrine-Related Cancer.

A new polymorphism in exon 14 of the dystrophin gene detected by RT-PCR and DGGE.

P. Carrera, A. Barbieri, N. Soriani, 1997, Molecular and cellular probes.

The Novel SSTR3 Agonist ITF2984 Exerts Antimitotic and Proapoptotic Effects in Human Non-Functioning Pituitary Neuroendocrine Tumor (NF-PitNET) Cells

A. Lania, E. Peverelli, A. Barbieri, 2024, International Journal of Molecular Sciences.

A β-Arrestin 2-Biased Dopamine Receptor Type 2 (DRD2) Agonist Is More Efficacious Than Cabergoline in Reducing Cell Proliferation in PRL-Secreting but Not in Non-Functioning Pituitary Tumor Cells

M. Arosio, E. Esposito, M. Locatelli, 2023, Cancers.