Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Romy Lambrecht"'
Publikováno v:
Nephrology Dialysis Transplantation. 17:1218-1227
Background. Alport syndrome (AS) is a hereditary nephropathy characterized by progressive renal failure, hearing loss and ocular lesions. Numerous mutations of the COL4A5 gene encoding the a5-chain of type IV collagen have been described, establishin
Publikováno v:
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 18(6)
Background. Alport syndrome (AS) is a common hereditary cause for end-stage renal failure due to a defect in type IV collagen genes. The molecular pathogenesis of benign familial haematuria (BFH) is not fully understood. Evidence from linkage analyse
Publikováno v:
Kidney international. 50(4)
Alport syndrome [1] is a genetic renal disease characterized by hematuria and varying degrees of proteinuria, sensorineural hearing loss, and less frequently ocular lesions (lenticonus, macular lesions). Diverse mutations of the COL4A5 gene encoding
Autor:
Romy Lambrecht, Renate Ulbrich-Hofmann
Publikováno v:
Biotechnology and bioengineering. 41(8)
Immobilization of phospholipase D from cabbage was studied with the aim of stabilizing the enzyme for its use in synthesis of phospholipids. It was shown that phospholipase D can be immobilized by adsorption to polymeric carriers containing long chai
Autor:
Renate Ulbrich-Hofmann, Romy Lambrecht
Publikováno v:
Biological chemistry Hoppe-Seyler. 373(2)
Phospholipase D (PLD), an enzyme predestined for the preparation of new phospholipids, was isolated from cabbage and purified in a highly efficient way by using a combination of hydrophobic chromatography and a specific calcium effect. In the presenc