Glomerular Basement Membrane Protein Expression and the Diagnosis and Prognosis of Autosomal Dominant Alport Syndrome
暂无分享,去创建一个
T. Mochizuki | K. Nitta | E. Sohara | S. Uchida | Takayasu Mori | S. Horita | H. Kataoka | Masayo Sato | Taro Akihisa | Shiho Makabe | Orie Hirose | S. Taneda | Yoshie Wakayama
[1] K. Ohashi,et al. Autosomal dominant form of type IV collagen nephropathy exists among patients with hereditary nephritis difficult to diagnose clinicopathologically , 2018, Nephrology.
[2] Jie Ding,et al. Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working Group. , 2018, Kidney international.
[3] Ituro Inoue,et al. Comprehensive genetic testing approach for major inherited kidney diseases, using next-generation sequencing with a custom panel , 2017, Clinical and Experimental Nephrology.
[4] E. Ars,et al. X-Linked and Autosomal Recessive Alport Syndrome: Pathogenic Variant Features and Further Genotype-Phenotype Correlations , 2016, PloS one.
[5] K. Nakanishi,et al. Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome. , 2016, Clinical journal of the American Society of Nephrology : CJASN.
[6] D. Abrahamson. Steps on the Alport path to proteinuria. , 2016, Kidney international.
[7] L. Maquat,et al. Nonsense-mediated mRNA decay in humans at a glance , 2016, Journal of Cell Science.
[8] K. Voskarides,et al. Frequency of COL4A3/COL4A4 Mutations amongst Families Segregating Glomerular Microscopic Hematuria and Evidence for Activation of the Unfolded Protein Response. Focal and Segmental Glomerulosclerosis Is a Frequent Development during Ageing , 2014, PloS one.
[9] K. Nakanishi,et al. Milder clinical aspects of X-linked Alport syndrome in men positive for the collagen IV α5 chain. , 2014, Kidney international.
[10] R. Korstanje,et al. A mouse collagen4α4 mutation causing Alport glomerulosclerosis with abnormal collagen α3α4α5(IV) trimers , 2013, Kidney international.
[11] M. Gubler,et al. The renal lesions of Alport syndrome. , 2009, Journal of the American Society of Nephrology : JASN.
[12] A. Amoroso,et al. Autosomal dominant Alport syndrome: molecular analysis of the COL4A4 gene and clinical outcome. , 2009, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[13] K. Kyriacou,et al. COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy. , 2007, Journal of the American Society of Nephrology : JASN.
[14] P. S. St. John,et al. Laminin compensation in collagen alpha3(IV) knockout (Alport) glomeruli contributes to permeability defects. , 2007, Journal of the American Society of Nephrology : JASN.
[15] C. Kashtan. Alport syndrome and the X chromosome: implications of a diagnosis of Alport syndrome in females. , 2007, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[16] B. Beirowski,et al. Chronic renal failure and shortened lifespan in COL4A3+/- mice: an animal model for thin basement membrane nephropathy. , 2006, Journal of the American Society of Nephrology : JASN.
[17] A. Renieri,et al. Autosomal-dominant Alport syndrome: natural history of a disease due to COL4A3 or COL4A4 gene. , 2004, Kidney international.
[18] K. Tryggvason,et al. Alport's syndrome, Goodpasture's syndrome, and type IV collagen. , 2003, The New England journal of medicine.
[19] P. Thorner,et al. Abnormal glomerular basement membrane laminins in murine, canine, and human Alport syndrome: aberrant laminin alpha2 deposition is species independent. , 2001, Journal of the American Society of Nephrology : JASN.
[20] R. Kalluri,et al. Isoform switching of type IV collagen is developmentally arrested in X-linked Alport syndrome leading to increased susceptibility of renal basement membranes to endoproteolysis. , 1997, The Journal of clinical investigation.