adenine and c-peptide

adenine has been researched along with c-peptide in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	2 (100.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Babazono, T; Iwasaki, N; Ohgawara, H; Omori, Y; Takahashi, Y; Wasada, T	1
Blanché, H; Byrne, MM; Clément, K; Fiet, J; Froguel, P; Passa, P; Polonsky, KS; Pueyo, ME; Robert, JJ; Sturis, J; Velho, G; Vionnet, N	1

Other Studies

2 other study(ies) available for adenine and c-peptide

Article	Year
Insulin sensitivity in patients with NIDDM and the A-to-G mutation at nucleotide 3,243 of the mitochondrial tRNALeu(UUR) gene. Diabetes care, 1995, Volume: 18, Issue:6 Topics: Adenine; Adult; Blood Glucose; Body Mass Index; C-Peptide; Diabetes Mellitus, Type 2; Family; Female; Glucose Clamp Technique; Glycated Hemoglobin; Guanine; Hearing Loss; Humans; Insulin; Male; Middle Aged; Point Mutation; Polymerase Chain Reaction; Proteinuria; RNA; RNA, Mitochondrial; RNA, Transfer, Leu	1995
Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation. Diabetes, 1996, Volume: 45, Issue:4 Topics: Adenine; Adolescent; Adult; Aged; Arginine; Blood Glucose; Body Mass Index; C-Peptide; Child; Child, Preschool; Deafness; Diabetes Mellitus, Type 2; Female; Genomic Imprinting; Glucose Tolerance Test; Glycated Hemoglobin; Guanine; Humans; Insulin; Insulin Secretion; Male; Middle Aged; Pedigree; Periodicity; Phenotype; Point Mutation; Reference Values; RNA, Transfer, Leu; Sex Characteristics	1996

Article

Year

Insulin sensitivity in patients with NIDDM and the A-to-G mutation at nucleotide 3,243 of the mitochondrial tRNALeu(UUR) gene.

Diabetes care, 1995, Volume: 18, Issue:6

Topics: Adenine; Adult; Blood Glucose; Body Mass Index; C-Peptide; Diabetes Mellitus, Type 2; Family; Female; Glucose Clamp Technique; Glycated Hemoglobin; Guanine; Hearing Loss; Humans; Insulin; Male; Middle Aged; Point Mutation; Polymerase Chain Reaction; Proteinuria; RNA; RNA, Mitochondrial; RNA, Transfer, Leu

1995

Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation.

Diabetes, 1996, Volume: 45, Issue:4

Topics: Adenine; Adolescent; Adult; Aged; Arginine; Blood Glucose; Body Mass Index; C-Peptide; Child; Child, Preschool; Deafness; Diabetes Mellitus, Type 2; Female; Genomic Imprinting; Glucose Tolerance Test; Glycated Hemoglobin; Guanine; Humans; Insulin; Insulin Secretion; Male; Middle Aged; Pedigree; Periodicity; Phenotype; Point Mutation; Reference Values; RNA, Transfer, Leu; Sex Characteristics

1996