Page last updated: 2024-10-17

cytosine and ADPKD

cytosine has been researched along with ADPKD in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (33.33)18.2507
2000's0 (0.00)29.6817
2010's2 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Musetti, C1
Babu, D1
Fusco, I1
Mellone, S1
Zonta, A1
Quaglia, M1
Cantaluppi, V1
Stratta, P1
Giordano, M1
Kirby, A1
Gnirke, A1
Jaffe, DB1
Barešová, V1
Pochet, N1
Blumenstiel, B1
Ye, C1
Aird, D1
Stevens, C1
Robinson, JT1
Cabili, MN1
Gat-Viks, I1
Kelliher, E1
Daza, R1
DeFelice, M1
Hůlková, H1
Sovová, J1
Vylet'al, P1
Antignac, C1
Guttman, M1
Handsaker, RE1
Perrin, D1
Steelman, S1
Sigurdsson, S1
Scheinman, SJ1
Sougnez, C1
Cibulskis, K1
Parkin, M1
Green, T1
Rossin, E1
Zody, MC1
Xavier, RJ1
Pollak, MR1
Alper, SL1
Lindblad-Toh, K1
Gabriel, S1
Hart, PS1
Regev, A1
Nusbaum, C1
Kmoch, S1
Bleyer, AJ1
Lander, ES1
Daly, MJ1
Xenophontos, S1
Constantinides, R1
Hayashi, T1
Mochizuki, T1
Somlo, S1
Pierides, A1
Deltas, CC1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Study of the Effect of Ergocalciferol on Plasma and Urinary Mucin-1 Levels in Healthy Individuals and Individuals With Autosomal Dominant Tubulo-Interstitial Kidney Disease Due to MUC1 Mutations (ADTKD-MUC1)[NCT03747523]Early Phase 144 participants (Actual)Interventional2019-03-12Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Other Studies

3 other studies available for cytosine and ADPKD

ArticleYear
Testing for the cytosine insertion in the VNTR of the MUC1 gene in a cohort of Italian patients with autosomal dominant tubulointerstitial kidney disease.
    Journal of nephrology, 2016, Volume: 29, Issue:3

    Topics: Adult; Cohort Studies; Cytosine; Humans; Male; Middle Aged; Minisatellite Repeats; Mucin-1; Mutagene

2016
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing.
    Nature genetics, 2013, Volume: 45, Issue:3

    Topics: Cytosine; Female; Genetic Linkage; Haplotypes; High-Throughput Nucleotide Sequencing; Humans; Male;

2013
A translation frameshift mutation induced by a cytosine insertion in the polycystic kidney disease 2 gene (PDK2).
    Human molecular genetics, 1997, Volume: 6, Issue:6

    Topics: Cytosine; Female; Humans; Male; Membrane Proteins; Mutagenesis, Insertional; Pedigree; Polycystic Ki

1997