G. Marco

发表

Ras homolog enriched in striatum inhibits the functional activity of wild type thyrotropin, follicle-stimulating hormone, luteinizing hormone receptors and activating thyrotropin receptor mutations by altering their expression in COS-7 cells

A. Pinchera, P. Vitti, J. Bernal, 2007, Journal of endocrinological investigation.

Patients affected by vitiligo and autoimmune diseases do not show antibodies interfering with the activity of the melanocortin 1 receptor

A. Pinchera, P. Vitti, A. Dimida, 2010, Journal of endocrinological investigation.

Frequency and effect on serum TSH of phosphodiesterase 8B (PDE8B) gene polymorphisms in patients with sporadic nonautoimmune subclinical hypothyroidism

P. Vitti, P. Agretti, M. Tonacchera, 2014, Journal of Endocrinological Investigation.

Sporadic congenital nonautoimmune hyperthyroidism caused by P639S mutation in thyrotropin receptor gene

A. Pinchera, P. Vitti, P. Agretti, 2012, European Journal of Pediatrics.

Study of potential inhibitors of thyroid iodide uptake by using CHO cells stably expressing the human sodium/iodide symporter (hNIS) protein

A. Pinchera, F. Santini, P. Vitti, 2011 .

In vitro effects of natural phytoestrogens on sodium/iodide symporter mediated thyroid iodide uptake by using a differentiated TSH-dependent cell line

A. Dimida, P. Agretti, M. Tonacchera, 2018 .

Characterization of a novel mutation V136L in bone morphogenetic protein 15 identified in a woman affected by POI

P. Agretti, M. Tonacchera, T. Simoncini, 2021, Journal of Ovarian Research.

TSH receptor and Gsα genetic analysis in children with Down’s syndrome and subclinical hypothyroidism

Elena S. Di Martino, A. Pinchera, L. Chiovato, 2003, Journal of endocrinological investigation.

Prevalence of activating thyrotropin receptor and Gsα gene mutations in paediatric thyroid toxic adenomas: a multicentric Italian study

M. Pelizzo, M. Segni, D. Larizza, 2013, Clinical endocrinology.

The different requirement of L-T4 therapy in congenital athyreosis compared with adult-acquired hypothyroidism suggests a persisting thyroid hormone resistance at the hypothalamic-pituitary level.

P. Vitti, P. Agretti, M. Tonacchera, 2014, European journal of endocrinology.

Absence of interference of serum IgGs from patients with breast cancer and thyroid autoimmunity on the function of human iodide symporter gene stably transfected in CHO cells

P. Agretti, M. Tonacchera, E. Seregni, 2004, Journal of endocrinological investigation.

Genetic markers to discriminate benign and malignant thyroid nodules with undetermined cytology in an area of borderline iodine deficiency

R. Musmanno, A. Pinchera, T. Rago, 2011, Journal of Endocrinological Investigation.

THEME 2 GENETICS AND GENOMICS GEN-01 A case of an uncommon late onset of ALS associated with an undescribed SOD1 mutation GEN-02 A novel mutation in ZFYVE26 gene (c.195-1G > A) in a young man affected by spastic paraplegia

A. Calvo, G. Siciliano, A. Fogli, 2022 .

BRAF mutation analysis in thyroid nodules with indeterminate cytology: our experience on surgical management of patients with thyroid nodules from an area of borderline iodine deficiency

T. Rago, M. Scutari, P. Agretti, 2014, Journal of Endocrinological Investigation.

Theme 02 - Genetics and Genomics

A. Calvo, G. Siciliano, A. Fogli, 2022, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Measurement of urinary free cortisol by LC–MS–MS: adoption of a literature reference range and comparison with our current immunometric method

C. Marcocci, P. Vitti, P. Agretti, 2019, Journal of Endocrinological Investigation.

Genetic interaction analysis of VEGF-A rs3025039 and VEGFR-2 rs2071559 identifies a genetic profile at higher risk to develop nodular goiter

P. Vitti, P. Agretti, M. Tonacchera, 2019, Journal of Endocrinological Investigation.

Electric and magnetic fields do not modify the biochemical properties of FRTL-5 cells

A. Dimida, P. Agretti, M. Tonacchera, 2011, Journal of endocrinological investigation.