Page last updated: 2024-10-17

creatine and Glycosuria, Renal

creatine has been researched along with Glycosuria, Renal in 1 studies

Glycosuria, Renal: An autosomal inherited disorder due to defective reabsorption of GLUCOSE by the PROXIMAL RENAL TUBULES. The urinary loss of glucose can reach beyond 50 g/day. It is attributed to the mutations in the SODIUM-GLUCOSE TRANSPORTER 2 encoded by the SLC5A2 gene.

Research Excerpts

ExcerptRelevanceReference
"Creatine transport has been assigned to creatine transporter 1 (CRT1), encoded by mental retardation associated SLC6A8."5.39The cataract and glucosuria associated monocarboxylate transporter MCT12 is a new creatine transporter. ( Abplanalp, J; Berger, W; Braun, P; Camargo, SM; Kloeckener-Gruissem, B; Laczko, E; Munier, FL; Neidhardt, J; Philp, NJ; Schorderet, DF; Verrey, F; Zuercher, J, 2013)
"Creatine transport has been assigned to creatine transporter 1 (CRT1), encoded by mental retardation associated SLC6A8."1.39The cataract and glucosuria associated monocarboxylate transporter MCT12 is a new creatine transporter. ( Abplanalp, J; Berger, W; Braun, P; Camargo, SM; Kloeckener-Gruissem, B; Laczko, E; Munier, FL; Neidhardt, J; Philp, NJ; Schorderet, DF; Verrey, F; Zuercher, J, 2013)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Abplanalp, J1
Laczko, E1
Philp, NJ1
Neidhardt, J1
Zuercher, J1
Braun, P1
Schorderet, DF1
Munier, FL1
Verrey, F1
Berger, W1
Camargo, SM1
Kloeckener-Gruissem, B1

Other Studies

1 other study available for creatine and Glycosuria, Renal

ArticleYear
The cataract and glucosuria associated monocarboxylate transporter MCT12 is a new creatine transporter.
    Human molecular genetics, 2013, Aug-15, Volume: 22, Issue:16

    Topics: Animals; Cataract; Creatine; Female; Glycosuria, Renal; Humans; Kidney; Male; Membrane Transport Pro

2013