Alport's syndrome. Emphasizing electron microscopic studies of the glomerulus
about
Canine X chromosome-linked hereditary nephritis: a genetic model for human X-linked hereditary nephritis resulting from a single base mutation in the gene encoding the alpha 5 chain of collagen type IVSamoyed hereditary glomerulopathy (SHG). Evolution of splitting of glomerular capillary basement membranesMammalian collagen IVHereditary nephritis (with unusual renal histology): report of a first case from the West Indies.Genetic linkage of autosomal-dominant Alport syndrome with leukocyte inclusions and macrothrombocytopenia (Fechtner syndrome) to chromosome 22q11-13Alport's syndrome.The effect of progressive glomerular disease on megalin-mediated endocytosis in the kidneyNephritogenic antigen determinants in epidermal and renal basement membranes of kindreds with Alport-type familial nephritis.Urinary excretion of glomerular basement membrane antigens in Alport's syndrome. A new diagnostic approach.Alport familial nephritis. Absence of 28 kilodalton non-collagenous monomers of type IV collagen in glomerular basement membraneThe investigation of haematuriaAbsence of the alpha6(IV) chain of collagen type IV in Alport syndrome is related to a failure at the protein assembly level and does not result in diffuse leiomyomatosis.Human tissue distribution of novel basement membrane collagen.Renal disease in carrier female dogs with X-linked hereditary nephritis. Implications for female patients with this diseaseGlomerular basement membrane and related glomerular diseaseGlomerular pathology in Alport syndrome: a molecular perspective.A Novel COL4A4 Mutation Identified in a Chinese Family with Thin Basement Membrane Nephropathy.Challenge in pathologic diagnosis of Alport syndrome: evidence from correction of previous misdiagnosis.Acquired and heritable defects in collagen synthesis and fibrogenesis.Benign familial hematuria due to mutation of the type IV collagen alpha4 gene.The Chemical Chaperone, PBA, Reduces ER Stress and Autophagy and Increases Collagen IV α5 Expression in Cultured Fibroblasts From Men With X-Linked Alport Syndrome and Missense Mutations.
P2860
Q24563403-5D4ED64B-3CB6-402E-90D8-EBB094B03060Q24675978-73C85927-26BB-46FB-B75F-35603B6699B3Q28265884-0AA86337-059C-46A1-9644-DEC0CAD7B217Q30493435-4ECA6142-A9B7-4D10-8162-B4781AFCCB3BQ33330773-BFE1A634-8A48-47FB-BFD1-6E90CD673953Q33678707-C18A1C59-9545-40AD-B37A-9FC265D7BBCDQ34021381-F82E8AE1-A09A-4F0C-88A5-E8F2169AE1CDQ34542988-AAD81CD1-ED4F-49CE-998A-1FE20DDBA40BQ34986248-3A45FB30-E325-4AF7-9D67-985AE1936C32Q35576226-08F99863-C8DE-49B8-93B6-B26A244D6E5EQ35624170-7DF61F4C-43EC-4C52-87EF-163148D76F1EQ35787141-F6A89887-D144-4F69-97E3-B6D2BD2B339CQ35816565-CE321FC0-58E0-4932-9429-CE4688642814Q35831141-61F8BCC0-4486-426B-868D-7301BE675B6CQ36336238-45CCF0A3-17DA-4885-87B5-1B14217E6ADFQ36359599-431BC639-CB0D-443F-9A45-54D4319587E2Q36528259-8A0C201C-62CA-42AE-B4CD-FE4C09F6984BQ36556406-FA2861BD-43FD-427C-B01D-F8AE25081838Q36739096-E80BF5AD-1CC0-4CB4-955F-C78656595C55Q37359117-9EC5CBC0-C0D9-486D-9C28-098AE9C5BFCBQ47094043-F405FA00-EC70-470A-B921-FFC0632E28B6
P2860
Alport's syndrome. Emphasizing electron microscopic studies of the glomerulus
description
1972 nî lūn-bûn
@nan
1972年の論文
@ja
1972年論文
@yue
1972年論文
@zh-hant
1972年論文
@zh-hk
1972年論文
@zh-mo
1972年論文
@zh-tw
1972年论文
@wuu
1972年论文
@zh
1972年论文
@zh-cn
name
Alport's syndrome. Emphasizing electron microscopic studies of the glomerulus
@ast
Alport's syndrome. Emphasizing electron microscopic studies of the glomerulus
@en
type
label
Alport's syndrome. Emphasizing electron microscopic studies of the glomerulus
@ast
Alport's syndrome. Emphasizing electron microscopic studies of the glomerulus
@en
prefLabel
Alport's syndrome. Emphasizing electron microscopic studies of the glomerulus
@ast
Alport's syndrome. Emphasizing electron microscopic studies of the glomerulus
@en
P1476
Alport's syndrome. Emphasizing electron microscopic studies of the glomerulus
@en
P2093
P2860
P304
P407
P577
1972-11-01T00:00:00Z