Zobrazeno 1 - 10
of 179
pro vyhledávání: '"Alfred F. Michael"'
Autor:
N. Gunnar Westberg, Alfred F. Michael
Publikováno v:
Acta Medica Scandinavica. 194:39-47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a5a13592302cd18cfc1d357b6f43c8a
https://doi.org/10.1111/j.0954-6820.1973.tb19411.x
https://doi.org/10.1111/j.0954-6820.1973.tb19411.x
Autor:
Clifford E. Kashtan, Elizabeth A. Wayner, Bing Zhou, Youngki Kim, Wei-Wei Fan, Effie C. Tsilibary, Uma Krishnamurti, Alfred F. Michael
Publikováno v:
Journal of the American Society of Nephrology. 12:758-766
Puromycin aminonucleoside (PAN)-induced nephrosis is a well-described model of human idiopathic nephrotic syndrome, but the mechanism of PAN's effect is not completely understood. Because PAN injection into rats results in retraction of glomerular ep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec0e4292d2a26790a7b418470df0d917
https://doi.org/10.1681/asn.v124758
https://doi.org/10.1681/asn.v124758
Autor:
Aristidis S. Charonis, Bill Gleason, Bing Zhou, Todd R. Nelson, Metaxia Vlassi, Alfred F. Michael, Clifford E. Kashtan
Publikováno v:
Journal of the American Society of Nephrology. 11:658-668
Tubulointerstitial nephritis antigen (TIN-Ag) is a recently described basement membrane glycoprotein reactive with autoantibodies in some forms of immunologically mediated human tubulointerstitial nephritis. This report presents the complete cDNA and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29f1a924d1c05f63503c0ea4a92f2b04
https://doi.org/10.1681/asn.v114658
https://doi.org/10.1681/asn.v114658
Autor:
Curtis L. Atkin, Joyce C. Denison, Yoav Segal, Yoshikazu Sado, Satoshi Sasaki, Yoshifumi Ninomiya, Clifford E. Kashtan, David F. Barker, Martin C. Gregory, Jing Zhou, Youngki Kim, Bing Zhou, Alfred F. Michael, Wei Wei Fan
Publikováno v:
Matrix Biology. 17:279-291
COL4A5 mutations causing X-linked Alport syndrome (XLAS) are frequently associated with absence of the alpha3, alpha4,alpha5 and alpha6 chains of type IV collagen from basement membranes and increased amounts of the alpha1(IV) and alpha2(IV) chains i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::151b10315fc7b87163723a2b32447d44
https://doi.org/10.1016/s0945-053x(98)90081-6
https://doi.org/10.1016/s0945-053x(98)90081-6
Publikováno v:
Connective Tissue Research. 37:53-60
Tubulointerstitial nephritis antigen (TIN-ag) is a 58 kDa glycoprotein restricted within the kidney to basement membranes underlying the epithelium of Bowman's capsule and proximal and distal tubules. Autoantibody formation against this component has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8722df3682668f6d2d16eb8ff8643c3d
https://doi.org/10.3109/03008209809028899
https://doi.org/10.3109/03008209809028899
Immunochemical and biochemical evidence for distinct basement membrane heparan sulfate proteoglycans
Publikováno v:
Journal of Biological Chemistry. 268:7261-7269
Two antigenically and structurally related heparan sulfate proteoglycans (HSPG), with masses of 200 and 350 kDa, have been isolated and characterized from bovine renal tubular basement membranes (BTBM) using DEAE-Sephacel, octyl-Sepharose CL-4B, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bad52f7d0cd3c3a8f5dec4139097b11
https://doi.org/10.1016/s0021-9258(18)53171-9
https://doi.org/10.1016/s0021-9258(18)53171-9
Publikováno v:
Kidney International. 41:1629-1637
Immunochemical studies of the Alport antigen. The Alport antigen, a component of normal glomerular basement membranes (GBM) which is absent in Alport familial nephritis, is characterized as a 26 kD non-collagenous (NCI) peptide identified by a monocl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::269939814d9d268f67bbd6ef297baede
https://doi.org/10.1038/ki.1992.235
https://doi.org/10.1038/ki.1992.235
Publikováno v:
Kidney International. 38:925-930
Gene mapping in Alport families with different basement membrane antigenic phenotypes. The present study was undertaken to determine whether differences among Alport kindreds in the antigenic phenotypes of their basement membranes result from defects
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f14d2b5b339e35c7dacd41b44ff44983
https://doi.org/10.1038/ki.1990.292
https://doi.org/10.1038/ki.1990.292
Publikováno v:
Pediatric Nephrology. 4:523-532
Alport syndrome, an inherited disorder of the kidney, eye and ear, has fascinated nephrologists, pathologists, and geneticists for nearly a century. With the recent application of molecular biochemical and genetic techniques, this mysterious disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01cbd7adce6a753859f6f5ca5ddf619b
https://doi.org/10.1007/bf00869840
https://doi.org/10.1007/bf00869840
Autor:
Bing Zhou, Paraskevi V. Kitsiou, Alfred F. Michael, Effie C. Tsilibary, William G. Stetler-Stevenson, Wei Wei Fan, Athina K. Tzinia
Publikováno v:
American journal of physiology. Renal physiology. 284(4)
In cultured human glomerular epithelial cells (HGEC), 25 mM glucose resulted in decreased expression of α3-, α2-, and β1-integrins and increased expression of α5- and αvβ3-integrins. This change was accompanied by decreased binding of HGEC to t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af41afb9695fc4eee8bb530a18863220
https://pubmed.ncbi.nlm.nih.gov/12620921
https://pubmed.ncbi.nlm.nih.gov/12620921