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Biochimie
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July 14, 1999
Mutation of the Secys residue 266 in human type 2 selenodeiodinase alters 75Se incorporation without affecting its biochemical properties
D Salvatore, J W Harney, P R Larsen
Clinical Genetics
|
February 10, 2016
Salt depletion syndrome as the initial presentation of cystic fibrosis in a toddler with the rare p.Ala309Gly (A309G) CFTR variant
D Salvatore, D Dell'Edera, C Colangelo, et al.
Journal of Endocrinological Investigation
|
January 11, 2019
Local ablative therapy of oligoprogressive TKI-treated thyroid cancer
T Porcelli, F Sessa, C Luongo, et al.
Enzyme
|
January 1, 1985
Biosynthesis of alpha-N-acetylglucosaminidase in cultured human kidney carcinoma cells
P Di Natale, D Salvatore, A Daniele, et al.
Veterinary Research Communications
|
July 12, 2023
Antimicrobial resistance genes in a golden jackal (Canis aureus L. 1758) from Central Italy
A Di Francesco, D Salvatore, M Gobbi, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
March 1, 1993
Growth dynamics in cystic fibrosis
L Greco, F Santamaria, D Salvatore, et al.
Endocrinology
|
August 1, 1996
Molecular biological and biochemical characterization of the human type 2 selenodeiodinase
D Salvatore, T Bartha, J W Harney, et al.
Journal of Endocrinological Investigation
|
October 21, 2024
Rebound effect of hypothalamic-pituitary thyreotropic activity: a new model to better understand hypothyroidism
T Piticchio, C Luongo, P Trimboli, et al.
The Journal of Clinical Investigation
|
August 15, 1996
Type 2 iodothyronine deiodinase is highly expressed in human thyroid
D Salvatore, H Tu, J W Harney, et al.
Human Genetics
|
September 1, 1990
The delta F508 mutation in cystic fibrosis patients of southern Italy
G Sebastio, O Castiglione, B Incerti, et al.
Page
of 35
Search research articles
Search
Showing results (11-20 of 346) with videos related to
Sort By:
Page
of 35
Biochimie
|
July 14, 1999
Mutation of the Secys residue 266 in human type 2 selenodeiodinase alters 75Se incorporation without affecting its biochemical properties
D Salvatore, J W Harney, P R Larsen
Clinical Genetics
|
February 10, 2016
Salt depletion syndrome as the initial presentation of cystic fibrosis in a toddler with the rare p.Ala309Gly (A309G) CFTR variant
D Salvatore, D Dell'Edera, C Colangelo, et al.
Journal of Endocrinological Investigation
|
January 11, 2019
Local ablative therapy of oligoprogressive TKI-treated thyroid cancer
T Porcelli, F Sessa, C Luongo, et al.
Enzyme
|
January 1, 1985
Biosynthesis of alpha-N-acetylglucosaminidase in cultured human kidney carcinoma cells
P Di Natale, D Salvatore, A Daniele, et al.
Veterinary Research Communications
|
July 12, 2023
Antimicrobial resistance genes in a golden jackal (Canis aureus L. 1758) from Central Italy
A Di Francesco, D Salvatore, M Gobbi, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
March 1, 1993
Growth dynamics in cystic fibrosis
L Greco, F Santamaria, D Salvatore, et al.
Endocrinology
|
August 1, 1996
Molecular biological and biochemical characterization of the human type 2 selenodeiodinase
D Salvatore, T Bartha, J W Harney, et al.
Journal of Endocrinological Investigation
|
October 21, 2024
Rebound effect of hypothalamic-pituitary thyreotropic activity: a new model to better understand hypothyroidism
T Piticchio, C Luongo, P Trimboli, et al.
The Journal of Clinical Investigation
|
August 15, 1996
Type 2 iodothyronine deiodinase is highly expressed in human thyroid
D Salvatore, H Tu, J W Harney, et al.
Human Genetics
|
September 1, 1990
The delta F508 mutation in cystic fibrosis patients of southern Italy
G Sebastio, O Castiglione, B Incerti, et al.
Page
of 35