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Tryggvason Karl
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http://hub.abes.fr/acs/periodical/bichaw/1980/volume_19/issue_7/101021bi00548a003/authorship/1
http://hub.abes.fr/oup/periodical/hmg/2002/volume_11/issue_4/101093hmg114379/authorship/6
http://hub.abes.fr/oup/periodical/ndt/2009/volume_24/issue_7/101093ndtgfn758/authorship/4
http://hub.abes.fr/oup/periodical/hmg/2001/volume_10/issue_23/101093hmg10232637/authorship/7
http://hub.abes.fr/oup/periodical/ndt/2002/volume_17/issue_3/101093ndt173478/authorship/7
http://hub.abes.fr/oup/periodical/ndt/2009/volume_24/issue_3/101093ndtgfn722/authorship/20
http://hub.abes.fr/oup/periodical/hmg/2001/volume_10/issue_1/101093hmg1011/authorship/5
http://hub.abes.fr/oup/periodical/ndt/2008/volume_23/issue_8/101093ndtgfn100/authorship/7
http://hub.abes.fr/acs/periodical/bichaw/1981/volume_20/issue_1/101021bi00504a017/authorship/2
http://hub.abes.fr/acs/periodical/bichaw/1982/volume_21/issue_24/101021bi00267a025/authorship/5
http://hub.abes.fr/springer/periodical/439/1991/volume_88/issue_2/B9280FB2F3025EE6E053120B220A60AA/authorship/8
http://hub.abes.fr/springer/periodical/10549/1993/volume_24/issue_3/B8D03D2D93737918E053120B220AE83D/authorship/1
http://hub.abes.fr/acs/periodical/bichaw/1995/volume_34/issue_9/101021bi00009a011/authorship/4
http://hub.abes.fr/springer/periodical/439/1992/volume_90/issue_4/B927DD9E88945D90E053120B220A1EA8/authorship/11
http://hub.abes.fr/acs/periodical/bichaw/1993/volume_32/issue_6/101021bi00057a024/authorship/3
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Partial purification and characterization of a neutral protease which cleaves type IV collagen
Stability analysis of latent and active 72-kDa type IV collagenase: The role of tissue inhibitor of metalloproteinases-2 (TIMP-2)
Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration
Dendrin expression in glomerulogenesis and in human minimal change nephrotic syndrome
The murine nephrin gene is specifically expressed in kidney, brain and pancreas: inactivation of the gene leads to massive proteinuria and neonatal death
Expression of nephrin in acquired human glomerular disease
Stem cell therapy for Alport syndrome: the hope beyond the hype
Defective nephrin trafficking caused by missense mutations in the NPHS1 gene: insight into the mechanisms of congenital nephrotic syndrome
Glomerular filtration is normal in the absence of both agrin and perlecan-heparan sulfate from the glomerular basement membrane
Biosynthesis of type IV procollagens
Isolation and characterization of type IV procollagen, laminin, and heparan sulfate proteoglycan from the EHS sarcoma
Type IV collagenases in invasive tumors
High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers
Alport syndrome: a genetic study of 31 families
Autolytic Activation of Recombinant Human 72 Kilodalton Type IV Collagenase
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