Cultured skin fibroblasts as an in vitro model to assess phenotypic features in subjects with diabetic nephropathy

American Journal of Kidney Diseases

Volumn 38, Issue 3, 2001, Pages 646-648

  LaPointe, Michael S ^a   Batlle, Daniel ^a  

^a NORTHWESTERN UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM); CALCIUM; GLUCOSE; HEMOGLOBIN A1C;

CALCIUM TRANSPORT; CELL CULTURE; CULTURE MEDIUM; CYTOLOGY; DIABETES CONTROL; DIABETIC NEPHROPATHY; EDITORIAL; HUMAN; IN VITRO STUDY; INSULIN DEPENDENT DIABETES MELLITUS; MODEL; PHENOTYPE; SKIN FIBROBLAST;

EID: 0034861909     PISSN: 02726386     EISSN: None     Source Type: Journal    
DOI: 10.1053/ajkd.2001.28026     Document Type: Article

References (28)

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8. Is diabetic nephropathy an inherited complication?
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11. + antiport activity and cell growth in cultured skin fibroblasts of IDDM patients with nephropathy
12. Temporal profile of serum induced S phase entry and pRB phosphorylation in human skin fibroblasts
13. Cyclin dependent kinase inhibitor p16 is decreased in cultured skin fibroblasts from type 1 diabetic patients with nephropathy (DN). A marker of diabetic nephropathy?
14. + antiport activity in cultured fibroblasts from NIDDM patients with hypertension and microalbuminuria
15. 2+ pump activity in diabetic nephropathy
16. 2+ exchange in vascular smooth muscle cells
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18. Mechanisms of chloride transport in thymic lymphocytes
19. Abnormal Na+/H+ antiporter phenotype and turnover of immortalized lymphoblasts from type 1 diabetic patients with nephropathy
20. + exchanger of immortalized lymphoblasts from type I diabetic patients with nephropathy
21. + exchange
22. + antiporter (NHE-1 isoform) in cultured vascular smooth muscle from the spontaneously hypertensive rat
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26. Genetic susceptibility to nephropathy in insulin-dependent diabetes: From epidemiology to molecular genetics
27. + exchanger isoform- 1 abundance in skin fibroblasts of type I diabetic patients with nephropathy
28. 2+ ATPase in vascular smooth muscle cells