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0030457613
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Molecular and functional defects in kidneys of mice lacking collagen a3(IV): Implications for Alport syndrome
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••] describe the production of knockout mice with a targeted mutation in Col4a3, which causes a disease with many similarities to human Alport syndrome, including absence of the collagen α3-α5(IV) chains in kidney. Both studies make use of the ability to look at renal structure and various GBM components before and during the onset of disease, which is rarely possible in humans. RNA analyses show that the α4 and α5(IV) mRNAs are not down-regulated as they are in the dog model.
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(1996)
J Cell Biol
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Miner, J.H.1
Sanes, J.R.2
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57
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0030828898
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Diabetes induces changes in glomerular development and laminin β2 (s-laminin) expression
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Abrass CK, Spicer D, Berfield AK, St. John PL, Abrahamson DR. Diabetes induces changes in glomerular development and laminin β2 (s-laminin) expression. Am J Pathol 1997; 151:1131-1140. This study makes use of the ability of embryonic rat kidney to develop and become vascularized when transplanted into the anterior eye chamber of an adult rat. Normal metanephroi are implanted into diabetic, control, and insulin-treated hosts to determine the effects of these states both on GBM and on mesangial development.
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(1997)
Am J Pathol
, vol.151
, pp. 1131-1140
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Abrass, C.K.1
Spicer, D.2
Berfield, A.K.3
St. John, P.L.4
Abrahamson, D.R.5
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58
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0028863565
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Fine mapping and haplotype analysis of the locus for congenital nephrotic syndrome on chromosome 19q13.1
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Mannikko M, Kestaila M, Holmberg C, Norio R, Ryynanen M, Olsen A, et al. Fine mapping and haplotype analysis of the locus for congenital nephrotic syndrome on chromosome 19q13.1. Am J Hum Genet 1995; 57:1377-1383.
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(1995)
Am J Hum Genet
, vol.57
, pp. 1377-1383
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Mannikko, M.1
Kestaila, M.2
Holmberg, C.3
Norio, R.4
Ryynanen, M.5
Olsen, A.6
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59
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0028792063
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Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis
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Fuchshuber A, Jean G, Gribouval O, Gubler MC, Broyer M, Beckmann JS, et al. Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis. Hum Mol Genet 1395; 4:2155-2158.
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(1395)
Hum Mol Genet
, vol.4
, pp. 2155-2158
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Fuchshuber, A.1
Jean, G.2
Gribouval, O.3
Gubler, M.C.4
Broyer, M.5
Beckmann, J.S.6
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