Distribution of the α1 and α2 chains of collagen IV and of collagens V and VI in Alport syndrome

This publication has 35 references indexed in Scilit:

• Characterization of the 3′ half of the human type IV collagen α5 gene that is affected in the Alport syndrome
  Genomics, 1991
• Single base mutation in α5(IV) collagen chain gene converting a conserved cysteine to serine in Alport syndrome
  Genomics, 1991
• Identification of variant Alport phenotypes using an Alport-specific antibody probe
  Kidney International, 1989
• Basement membrane collagen in the kidney: Regional localization of novel chains related to collagen IV
  Kidney International, 1989
• Completion of the amino acid sequence of the α1 chain of human basement membrane collagen (type IV) reveals 21 non‐triplet interruptions located within the collagenous domain
  European Journal of Biochemistry, 1987
• Alport familial nephritis. Absence of 28 kilodalton non-collagenous monomers of type IV collagen in glomerular basement membrane.
  Journal of Clinical Investigation, 1987
• Biosynthesis and Properties of Procollagens Va
  Annals of the New York Academy of Sciences, 1985
• Retardation of fading and enhancement of intensity of immunofluorescence by p-phenylenediamine.
  Journal of Histochemistry & Cytochemistry, 1983
• Diagnosis of hereditary nephritis by failure of glomeruli to bind anti-glomerular basement membrane antibodies
  The Journal of Pediatrics, 1980
• Isolation of three collagenous components of probable basement membrane origin from several tissues
  Biochemical and Biophysical Research Communications, 1976