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Journal of Endocrinological Investigation
|
June 9, 2007
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
P Agretti, G De Marco, A Pinchera, et al.
Journal of Endocrinological Investigation
|
August 4, 2005
Poorly specific binding of thyroglobulin to orbital fibroblasts from patients with Graves' ophthalmopathy
S Lisi, R Botta, P Agretti, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 11, 2001
Thyroid resistance to TSH complicated by autoimmune thyroiditis
M Tonacchera, P Agretti, G De Marco, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 17, 2000
Congenital hypothyroidism with impaired thyroid response to thyrotropin (TSH) and absent circulating thyroglobulin: evidence for a new inactivating mutation of the TSH receptor gene
M Tonacchera, P Agretti, A Pinchera, et al.
Journal of Endocrinological Investigation
|
June 1, 2020
Importance of total and measured free testosterone in diagnosis of male hypogonadism: immunoassay versus mass spectrometry in a population of healthy young/middle-aged blood donors
P Agretti, C Pelosini, L Bianchi, et al.
Journal of Endocrinological Investigation
|
May 24, 2003
Gain of function TSH receptor mutations and iodine deficiency: implications in iodine prophylaxis
M Tonacchera, P Vitti, M De Servi, et al.
Journal of Endocrinological Investigation
|
February 6, 2014
Frequency and effect on serum TSH of phosphodiesterase 8B (PDE8B) gene polymorphisms in patients with sporadic nonautoimmune subclinical hypothyroidism
P Agretti, G De Marco, C Di Cosmo, et al.
Journal of Endocrinological Investigation
|
August 18, 2021
Gene expression profile in functioning and non-functioning nodules of autonomous multinodular goiter from an area of iodine deficiency: unexpected common characteristics between the two entities
P Agretti, G De Marco, E Ferrarini, et al.
European Journal of Endocrinology
|
May 29, 2001
Autoantibodies from patients with autoimmune thyroid disease do not interfere with the activity of the human iodide symporter gene stably transfected in CHO cells
M Tonacchera, P Agretti, G Ceccarini, et al.
Journal of Endocrinological Investigation
|
December 1, 2021
Screening for drugs potentially interfering with MCT8-mediated T<sub>3</sub> transport in vitro identifies dexamethasone and some commonly used drugs as inhibitors of MCT8 activity
C Di Cosmo, G De Marco, P Agretti, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 31) with videos related to
Sort By:
Page
of 4
Journal of Endocrinological Investigation
|
June 9, 2007
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
P Agretti, G De Marco, A Pinchera, et al.
Journal of Endocrinological Investigation
|
August 4, 2005
Poorly specific binding of thyroglobulin to orbital fibroblasts from patients with Graves' ophthalmopathy
S Lisi, R Botta, P Agretti, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 11, 2001
Thyroid resistance to TSH complicated by autoimmune thyroiditis
M Tonacchera, P Agretti, G De Marco, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 17, 2000
Congenital hypothyroidism with impaired thyroid response to thyrotropin (TSH) and absent circulating thyroglobulin: evidence for a new inactivating mutation of the TSH receptor gene
M Tonacchera, P Agretti, A Pinchera, et al.
Journal of Endocrinological Investigation
|
June 1, 2020
Importance of total and measured free testosterone in diagnosis of male hypogonadism: immunoassay versus mass spectrometry in a population of healthy young/middle-aged blood donors
P Agretti, C Pelosini, L Bianchi, et al.
Journal of Endocrinological Investigation
|
May 24, 2003
Gain of function TSH receptor mutations and iodine deficiency: implications in iodine prophylaxis
M Tonacchera, P Vitti, M De Servi, et al.
Journal of Endocrinological Investigation
|
February 6, 2014
Frequency and effect on serum TSH of phosphodiesterase 8B (PDE8B) gene polymorphisms in patients with sporadic nonautoimmune subclinical hypothyroidism
P Agretti, G De Marco, C Di Cosmo, et al.
Journal of Endocrinological Investigation
|
August 18, 2021
Gene expression profile in functioning and non-functioning nodules of autonomous multinodular goiter from an area of iodine deficiency: unexpected common characteristics between the two entities
P Agretti, G De Marco, E Ferrarini, et al.
European Journal of Endocrinology
|
May 29, 2001
Autoantibodies from patients with autoimmune thyroid disease do not interfere with the activity of the human iodide symporter gene stably transfected in CHO cells
M Tonacchera, P Agretti, G Ceccarini, et al.
Journal of Endocrinological Investigation
|
December 1, 2021
Screening for drugs potentially interfering with MCT8-mediated T<sub>3</sub> transport in vitro identifies dexamethasone and some commonly used drugs as inhibitors of MCT8 activity
C Di Cosmo, G De Marco, P Agretti, et al.
Page
of 4