Results 201 to 210 of about 140,913 (263)

Osteogenesis imperfecta: a registry-based study of the clinical symptoms of disease in a large cohort of Italian patients. [PDF]

open access: yesFront Endocrinol (Lausanne)
Mordenti M   +7 more
europepmc   +1 more source

Human iPSC-Derived Blood Vessel Organoids for Studying Chronic Hypoxia-Induced Microvascular Dysfunction. [PDF]

open access: yesJ Histochem Cytochem
Serrano Martinez P   +5 more
europepmc   +1 more source

Biological functions of type IV collagen

open access: yesBiological functions of type IV collagen
openaire  
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Type-IV collagen related diseases

Journal of Nephrology, 2003
  Alport syndrome (ATS) is a progressive inherited glomerulonephritis accounting for 1-2% of all patients who start renal replacement therapy, with an estimated gene frequency of approximately 1 in 5000. ATS is a genetically heterogeneous disease, commonly inherited as an X-linked semi-dominant trait, caused by mutations in COL4A5, on
PESCUCCI C.   +4 more
openaire   +3 more sources

Difference in interaction of fibronectin with type I collagen and type IV collagen

Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1997
In our studies on fibronectin, difference in binding to type I collagen and type IV collagen was observed and analysed. Four different fragments, which consist of I6-II1-II2-I7-I8-I9, I6-II1-II2-I7, I6-II1-II2, and I8-I9 within the collagen binding domain, have been isolated from proteolytic digests of fibronectin.
M, Shimizu   +3 more
openaire   +2 more sources

Basement membrane (type IV) collagen

Matrix Biology, 1995
The collagen IV molecule is 400 nm long and consists of two alpha 1 (IV) and one alpha 2 (IV) chains. Their genes COL4A1 and COL4A2 form a transcription unit in which they are arranged head-to-head and connected by a short common promoter region. Recently, four additional genes have been discovered.
openaire   +2 more sources

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