Page last updated: 2024-09-03

chymosin and Chronic Illness

chymosin has been researched along with Chronic Illness in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Adams, JN; Bleyer, AJ; Cornell, LD; Elleder, M; Hart, PS; Hart, TC; Haws, R; Hodanová, K; Hulková, H; Kapp, K; Kmoch, S; Sikora, J; Sovová, J; Vyletal, P; Zivná, M; Zivný, J	1

Other Studies

1 other study(ies) available for chymosin and Chronic Illness

Article	Year
Clinical and molecular characterization of a family with a dominant renin gene mutation and response to treatment with fludrocortisone. Clinical nephrology, 2010, Volume: 74, Issue:6 Topics: Adult; Amino Acid Sequence; Anemia; Base Sequence; Biopsy; Blood Pressure; Cell Line; Child; Chronic Disease; Chymosin; Cytoplasm; DNA Mutational Analysis; Endoplasmic Reticulum; Enzyme Precursors; Female; Fludrocortisone; Genes, Dominant; Genetic Predisposition to Disease; Glomerular Filtration Rate; Glycosylation; Heterozygote; Humans; Hyperuricemia; Hypoaldosteronism; Kidney Concentrating Ability; Kidney Diseases; Male; Molecular Sequence Data; Mutation; Pedigree; Phenotype; Polyuria; Protein Processing, Post-Translational; Protein Sorting Signals; Protein Transport; Renin; Transfection; Treatment Outcome	2010

Article

Year

Clinical and molecular characterization of a family with a dominant renin gene mutation and response to treatment with fludrocortisone.

Clinical nephrology, 2010, Volume: 74, Issue:6

Topics: Adult; Amino Acid Sequence; Anemia; Base Sequence; Biopsy; Blood Pressure; Cell Line; Child; Chronic Disease; Chymosin; Cytoplasm; DNA Mutational Analysis; Endoplasmic Reticulum; Enzyme Precursors; Female; Fludrocortisone; Genes, Dominant; Genetic Predisposition to Disease; Glomerular Filtration Rate; Glycosylation; Heterozygote; Humans; Hyperuricemia; Hypoaldosteronism; Kidney Concentrating Ability; Kidney Diseases; Male; Molecular Sequence Data; Mutation; Pedigree; Phenotype; Polyuria; Protein Processing, Post-Translational; Protein Sorting Signals; Protein Transport; Renin; Transfection; Treatment Outcome

2010