Patrizia Agretti


Ontology type: schema:Person     


Person Info

NAME

Patrizia

SURNAME

Agretti

Publications in SciGraph latest 50 shown

  • 2016-10 Papillary thyroid cancer in a patient with congenital goitrous hypothyroidism due to a novel deletion in NIS gene in ENDOCRINE
  • 2014-12 Identification of a novel pax8 gene sequence variant in four members of the same family: from congenital hypothyroidism with thyroid hypoplasia to mild subclinical hypothyroidism in BMC ENDOCRINE DISORDERS
  • 2014-10 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 in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2014-02 Frequency and effect on serum TSH of phosphodiesterase 8B (PDE8B) gene polymorphisms in patients with sporadic nonautoimmune subclinical hypothyroidism in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2013-12 Non-autoimmune subclinical hypothyroidism due to a mutation in TSH receptor: report on two brothers in ITALIAN JOURNAL OF PEDIATRICS
  • 2013-10 The W520X mutation in the TSHR gene brings on subclinical hypothyroidism through an haploinsufficiency mechanism in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2013-07 Congenital hypothyroidism caused by a novel homozygous mutation in the thyroglobulin gene in EUROPEAN JOURNAL OF PEDIATRICS
  • 2012-12 Metabolic engineering of the iodine content in Arabidopsis in SCIENTIFIC REPORTS
  • 2012-07 Sporadic congenital nonautoimmune hyperthyroidism caused by P639S mutation in thyrotropin receptor gene in EUROPEAN JOURNAL OF PEDIATRICS
  • 2011-03 Electric and magnetic fields do not modify the biochemical properties of FRTL-5 cells in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2011-03 Study of potential inhibitors of thyroid iodide uptake by using CHO cells stably expressing the human sodium/iodide symporter (hNIS) protein in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2010-12 Patients affected by vitiligo and autoimmune diseases do not show antibodies interfering with the activity of the melanocortin 1 receptor in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2007-04 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 in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2006-12 Genetic analysis of the follicle stimulating hormone receptor gene in women with polycystic ovary syndrome in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2005-07 Poorly specific binding of thyroglobulin to orbital fibroblasts from patients with Graves’ ophthalmopathy in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2004-10 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 in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2003-10 TSH receptor and Gsα genetic analysis in children with Down’s syndrome and subclinical hypothyroidism in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2003-10 In vitro assay of thyroid disruptors affecting TSH-stimulated adenylate cyclase activity in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 1996-04 Transfection with the cDNA of the human thyrotropin receptor of a poorly differentiated rat thyroid cell line (FRT) in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • Affiliations

  • University of Pisa (current)
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