Zobrazeno 1 - 10
of 56
pro vyhledávání: '"K O Netzer"'
Publikováno v:
Clinical Research in Cardiology Supplements. 2:S67-S74
Role of the L-arginine/NO-pathway in acute renal failure ■ Summary Regulation of renal hemodynamics – in particular intraglomerluar hemodynamics -is closely related to the L-arginine/ NO-pathway. Almost all forms of acute renal failure (ARF) are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca5ce99616f76b2e130bf6ba2664db8a
https://doi.org/10.1007/s11789-006-0041-x
https://doi.org/10.1007/s11789-006-0041-x
Publikováno v:
Klinische Monatsblätter für Augenheilkunde. 224:207-209
The oculo-cerebro-renal syndrome of Lowe (OCRL) is a rare X-chromosomal disorder characterised by the triad of congenital cataracts, renal tubular dysfunction, and mental retardation. Typically complete opacification and discoid deformation of the le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::610c709170952363abd336d355ed9fe2
https://doi.org/10.1055/s-2007-962947
https://doi.org/10.1055/s-2007-962947
Publikováno v:
Kidney and Blood Pressure Research. 19:298-304
The mechanisms of glomerular injury are multiple: one aspect is cell-mediated immunity in inflammatory kidney disease. Its fundamental role has been established within the last decade. T cells seem to play a regulatory role in the course of inflammat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2ba01e584c34366d9b634aa64b870d3
https://doi.org/10.1159/000174090
https://doi.org/10.1159/000174090
Publikováno v:
Kidney International. 43(2):486-492
COL4A5 splice site mutation and α5(IV) collagen mRNA in Alport syndrome. Mutations affecting the COL4A5 gene encoding the α5 chain of type IV collagen, are involved in the pathogenesis of X-linked Alport syndrome. We used denaturing gradient gel el
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec736154d248c15932300b7b19b46c3f
Publikováno v:
Klinische Monatsblatter fur Augenheilkunde. 224(3)
The oculo-cerebro-renal syndrome of Lowe (OCRL) is a rare X-chromosomal disorder characterised by the triad of congenital cataracts, renal tubular dysfunction, and mental retardation. Typically complete opacification and discoid deformation of the le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b587e22ef70900070f9f03bcdba603a9
https://pubmed.ncbi.nlm.nih.gov/17385124
https://pubmed.ncbi.nlm.nih.gov/17385124
Publikováno v:
Journal of nephrology. 18(4)
The regulation of renal hemodynamics is closely related to the L-arginine (L-Arg)/nitric oxide (NO) pathway. NO - metabolized from L-Arg - is capable of improving renal function in ischemic and toxic acute renal failure (ARF), while NO synthase (NOS)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bee487598d3f63afd5510a18b4980725
https://pubmed.ncbi.nlm.nih.gov/16245240
https://pubmed.ncbi.nlm.nih.gov/16245240
Autor:
A, Boutaud, D B, Borza, O, Bondar, S, Gunwar, K O, Netzer, N, Singh, Y, Ninomiya, Y, Sado, M E, Noelken, B G, Hudson
Publikováno v:
The Journal of biological chemistry. 275(39)
The ultrafiltration function of the glomerular basement membrane (GBM) of the kidney is impaired in genetic and acquired diseases that affect type IV collagen. The GBM is composed of five (alpha1 to alpha5) of the six chains of type IV collagen, orga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2b2bee06598cbf43f9ba6a21a5c0d9da
https://pubmed.ncbi.nlm.nih.gov/10896941
https://pubmed.ncbi.nlm.nih.gov/10896941
Publikováno v:
The Journal of biological chemistry. 275(8)
Goodpasture (GP) disease is an autoimmune disorder in which autoantibodies against the alpha3(IV) chain of type IV collagen bind to the glomerular and alveolar basement membranes, causing progressive glomerulonephritis and pulmonary hemorrhage. Two m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b328f8aa9bda4ecf46e510f99e47a832
https://pubmed.ncbi.nlm.nih.gov/10681598
https://pubmed.ncbi.nlm.nih.gov/10681598
Autor:
K O, Netzer, A, Leinonen, A, Boutaud, D B, Borza, P, Todd, S, Gunwar, J P, Langeveld, B G, Hudson
Publikováno v:
The Journal of biological chemistry. 274(16)
The Goodpasture (GP) autoantigen has been identified as the alpha3(IV) collagen chain, one of six homologous chains designated alpha1-alpha6 that comprise type IV collagen (Hudson, B. G., Reeders, S. T., and Tryggvason, K. (1993) J. Biol. Chem. 268,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8619057f7b8e577f15d2c45e939d2e1a
https://pubmed.ncbi.nlm.nih.gov/10196215
https://pubmed.ncbi.nlm.nih.gov/10196215
Publikováno v:
Kidney international. Supplement. 64
Systemic lupus erythematosus is a chronic disease with many clinical features, while Goodpasture's syndrome usually becomes manifest with progressive glomerulonephritis and pulmonary hemorrhage. Rapidly declining renal function and even pulmonary hem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::26eecbf11ff80df94f19b63253ab1742
https://pubmed.ncbi.nlm.nih.gov/9475486
https://pubmed.ncbi.nlm.nih.gov/9475486