-
1
-
-
0013589201
-
The proteinuria of renal tubular disorders
-
1. Butler EA, Flynn FV: The proteinuria of renal tubular disorders. Lancet 2:978-981, 1958
-
(1958)
Lancet
, vol.2
, pp. 978-981
-
-
Butler, E.A.1
Flynn, F.V.2
-
2
-
-
0029806197
-
Biology and genetics of inherited renal tubular disorders
-
2. Van't Hoff WG: Biology and genetics of inherited renal tubular disorders. Exp Nephrol 4:253-262, 1996
-
(1996)
Exp Nephrol
, vol.4
, pp. 253-262
-
-
Van't Hoff, W.G.1
-
4
-
-
0000329219
-
Renal handling of proteins and polypeptides
-
edited by Windhager EE, New York, Oxford University Press
-
4. Maack T: Renal handling of proteins and polypeptides, in Handbook of Physiology, Renal Physiology (2nd ed), edited by Windhager EE, New York, Oxford University Press, 1992, pp 2039-2082
-
(1992)
Handbook of Physiology, Renal Physiology (2nd Ed)
, pp. 2039-2082
-
-
Maack, T.1
-
6
-
-
0020662255
-
Alpha-1-microglobulin: An indicator protein for renal tubular function
-
6. Yu H, Yanagisawa Y, Forbes MA, Cooper EH, Crockson RA, MacLennan ICM: Alpha-1-microglobulin: An indicator protein for renal tubular function. J Clin Pathol 36:253-259, 1983
-
(1983)
J Clin Pathol
, vol.36
, pp. 253-259
-
-
Yu, H.1
Yanagisawa, Y.2
Forbes, M.A.3
Cooper, E.H.4
Crockson, R.A.5
MacLennan, I.C.M.6
-
7
-
-
0020461240
-
2-microglobulin determination in urine for the early detection of tubular proteinuria
-
2-microglobulin determination in urine for the early detection of tubular proteinuria. Clin Chim Acta 126:1-7, 1982
-
(1982)
Clin Chim Acta
, vol.126
, pp. 1-7
-
-
Bernard, A.M.1
Moreau, D.2
Lauwerys, R.3
-
8
-
-
0024433331
-
Urine protein 1: A sex-dependent marker of tubular or glomerular dysfunction
-
8. Bernard AM, Lauwerys RR, Noël A, Vandeleene B, Lambert A: Urine protein 1: A sex-dependent marker of tubular or glomerular dysfunction. Clin Chem 35:2141-2142, 1989
-
(1989)
Clin Chem
, vol.35
, pp. 2141-2142
-
-
Bernard, A.M.1
Lauwerys, R.R.2
Noël, A.3
Vandeleene, B.4
Lambert, A.5
-
9
-
-
0031023145
-
Characterization of proteinuria in primary glomerulonephritides: SDS-PAGE patterns: Clinical significance and prognostic value of low molecular weight ("tubular") proteins
-
9. Bazzi C, Petrini C, Rizza V, Arrigo G, Beltrame A, D'Amico G: Characterization of proteinuria in primary glomerulonephritides: SDS-PAGE patterns: Clinical significance and prognostic value of low molecular weight ("tubular") proteins. Am J Kidney Dis 29:27-35, 1997
-
(1997)
Am J Kidney Dis
, vol.29
, pp. 27-35
-
-
Bazzi, C.1
Petrini, C.2
Rizza, V.3
Arrigo, G.4
Beltrame, A.5
D'Amico, G.6
-
10
-
-
0031006238
-
Low molecular weight protein excretion in glomerular disease: A comparative analysis
-
10. Tomlinson PA, Dalton RN, Hartley B, Haycock GB, Chantler C: Low molecular weight protein excretion in glomerular disease: A comparative analysis. Paediatr Nephrol 11:285-290, 1997
-
(1997)
Paediatr Nephrol
, vol.11
, pp. 285-290
-
-
Tomlinson, P.A.1
Dalton, R.N.2
Hartley, B.3
Haycock, G.B.4
Chantler, C.5
-
11
-
-
0026694339
-
2-glycoprotein-1 (apolipoprotein H) and other markers of tubular malfunction in "non-tubular" renal disease
-
2-glycoprotein-1 (apolipoprotein H) and other markers of tubular malfunction in "non-tubular" renal disease. J Clin Pathol 45:561-567, 1992
-
(1992)
J Clin Pathol
, vol.45
, pp. 561-567
-
-
Flynn, F.V.1
Lapsley, M.2
Sansom, P.A.3
Cohen, S.L.4
-
12
-
-
0031888274
-
X-linked hypercalciuric nephrolithiasis: Clinical syndromes and chloride channel mutations
-
12. Scheinman SJ: X-linked hypercalciuric nephrolithiasis: Clinical syndromes and chloride channel mutations. Kidney Int 53:3-17, 1998
-
(1998)
Kidney Int
, vol.53
, pp. 3-17
-
-
Scheinman, S.J.1
-
13
-
-
0028038212
-
Dent's disease; a familial proximal renal tubular syndrome with low-molecular-weight proteinuria, hypercalciuria, nephrocalcinosis, metabolic bone disease, progressive renal failure and a marked male predominance
-
13. Wrong OM, Norden AGW, Feest TG: Dent's disease; a familial proximal renal tubular syndrome with low-molecular-weight proteinuria, hypercalciuria, nephrocalcinosis, metabolic bone disease, progressive renal failure and a marked male predominance. Q J Med 87:473-493, 1994
-
(1994)
Q J Med
, vol.87
, pp. 473-493
-
-
Wrong, O.M.1
Norden, A.G.W.2
Feest, T.G.3
-
14
-
-
0027716372
-
Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DSX255 and maps to Xp11.22
-
14. Pook MA, Wrong O, Wooding C, Norden AGW, Feest TG, Thakker RV: Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DSX255 and maps to Xp11.22. Hum Mol Genet 2:2129-2134, 1993
-
(1993)
Hum Mol Genet
, vol.2
, pp. 2129-2134
-
-
Pook, M.A.1
Wrong, O.2
Wooding, C.3
Norden, A.G.W.4
Feest, T.G.5
Thakker, R.V.6
-
15
-
-
0025896089
-
X-linked recessive nephrolithiasis with renal failure
-
15. Frymoyer PA, Scheinman SJ, Dunham PB, Jones DB, Hueber P, Schroeder ET: X-linked recessive nephrolithiasis with renal failure. N Engl J Med 325:681-686, 1991
-
(1991)
N Engl J Med
, vol.325
, pp. 681-686
-
-
Frymoyer, P.A.1
Scheinman, S.J.2
Dunham, P.B.3
Jones, D.B.4
Hueber, P.5
Schroeder, E.T.6
-
16
-
-
13344286321
-
A common molecular basis for three inherited kidney stone diseases
-
16. Lloyd SE, Pearce SHS, Fisher SE, Steinmeyer K, Schwappach B, Scheinman SJ, Harding B, Bolino A, Devoto M, Goodyer P, Rigden SPA, Wrong O, Jentsch TJ, Craig IW, Thakker RV: A common molecular basis for three inherited kidney stone diseases. Nature 379:445-449, 1996
-
(1996)
Nature
, vol.379
, pp. 445-449
-
-
Lloyd, S.E.1
Pearce, S.H.S.2
Fisher, S.E.3
Steinmeyer, K.4
Schwappach, B.5
Scheinman, S.J.6
Harding, B.7
Bolino, A.8
Devoto, M.9
Goodyer, P.10
Rigden, S.P.A.11
Wrong, O.12
Jentsch, T.J.13
Craig, I.W.14
Thakker, R.V.15
-
17
-
-
0031708210
-
CLCN5 chloride-channel mutations in six new North American families with X-linked nephrolithiasis
-
17. Hoopes RR Jr, Hueber PA, Reid RJ Jr, Braden GL, Goodyer PR, Melnyk AR, Midgley JP, Moel DI, Neu AM, Vanwhy SK, Scheinman SJ: CLCN5 chloride-channel mutations in six new North American families with X-linked nephrolithiasis. Kidney Int 54:698-705, 1998
-
(1998)
Kidney Int
, vol.54
, pp. 698-705
-
-
Hoopes R.R., Jr.1
Hueber, P.A.2
Reid R.J., Jr.3
Braden, G.L.4
Goodyer, P.R.5
Melnyk, A.R.6
Midgley, J.P.7
Moel, D.I.8
Neu, A.M.9
Vanwhy, S.K.10
Scheinman, S.J.11
-
18
-
-
0027829385
-
Genetic mapping in the Xp11.2 region of a new form of X-linked hypophosphataemic rickets
-
18. Bolino A, Devoto M, Enia G, Zoccali C, Weissenbach J, Romeo G: Genetic mapping in the Xp11.2 region of a new form of X-linked hypophosphataemic rickets. Eur J Hum Genet 1:269-279, 1993
-
(1993)
Eur J Hum Genet
, vol.1
, pp. 269-279
-
-
Bolino, A.1
Devoto, M.2
Enia, G.3
Zoccali, C.4
Weissenbach, J.5
Romeo, G.6
-
19
-
-
0028957547
-
Hypercalciuria and nephrocalcinosis in patients with idiopathic low-molecular-weight proteinuria in Japan: Is the disease identical to Dent's disease in United Kingdom?
-
19. Igarashi T, Hayakawa H, Shiraga H, Kawato H, Yan K, Kawaguchi H, Yamanaka T, Tsuchida S, Akagi K: Hypercalciuria and nephrocalcinosis in patients with idiopathic low-molecular-weight proteinuria in Japan: Is the disease identical to Dent's disease in United Kingdom? Nephron 69:242-247, 1995
-
(1995)
Nephron
, vol.69
, pp. 242-247
-
-
Igarashi, T.1
Hayakawa, H.2
Shiraga, H.3
Kawato, H.4
Yan, K.5
Kawaguchi, H.6
Yamanaka, T.7
Tsuchida, S.8
Akagi, K.9
-
20
-
-
0030907872
-
Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5)
-
20. Lloyd SE, Pearce SHS, Günther W, Kawaguchi H, Igarashi T, Jentsch TJ, Thakker RV: Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5). J Clin Invest 99:967-974, 1997
-
(1997)
J Clin Invest
, vol.99
, pp. 967-974
-
-
Lloyd, S.E.1
Pearce, S.H.S.2
Günther, W.3
Kawaguchi, H.4
Igarashi, T.5
Jentsch, T.J.6
Thakker, R.V.7
-
21
-
-
0030874882
-
Mutations of CLCN5 in Japanese children with idiopathic low molecular weight proteinuria, hypercalciuria and nephrocalcinosis
-
21. Akuta N, Lloyd SE, Igarashi T, Shiraga H, Matsuyama T, Yokoro S, Cox JPD, Thakker RV: Mutations of CLCN5 in Japanese children with idiopathic low molecular weight proteinuria, hypercalciuria and nephrocalcinosis. Kidney Int 52:911-916, 1997
-
(1997)
Kidney Int
, vol.52
, pp. 911-916
-
-
Akuta, N.1
Lloyd, S.E.2
Igarashi, T.3
Shiraga, H.4
Matsuyama, T.5
Yokoro, S.6
Cox, J.P.D.7
Thakker, R.V.8
-
22
-
-
0030801334
-
Mutations in the CLCN5 gene in Japanese patients with familial idiopathic low molecular weight proteinuria
-
22. Nakazato H, Hattori S, Furuse A, Kawano T, Karashima S, Tsuruta M, Toshimuta J, Endo F, Matsuda I: Mutations in the CLCN5 gene in Japanese patients with familial idiopathic low molecular weight proteinuria. Kidney Int 52:895-900, 1997
-
(1997)
Kidney Int
, vol.52
, pp. 895-900
-
-
Nakazato, H.1
Hattori, S.2
Furuse, A.3
Kawano, T.4
Karashima, S.5
Tsuruta, M.6
Toshimuta, J.7
Endo, F.8
Matsuda, I.9
-
23
-
-
0021863972
-
Tubular proteinuria in children without other defects of renal function
-
23. Geary DF, Dillon MJ, Gammon K, Barratt TM: Tubular proteinuria in children without other defects of renal function. Nephron 40:329-331, 1985
-
(1985)
Nephron
, vol.40
, pp. 329-331
-
-
Geary, D.F.1
Dillon, M.J.2
Gammon, K.3
Barratt, T.M.4
-
24
-
-
8544254724
-
Characterisation of renal chloride channel CLCN5 mutations in hypercalciuric nephrolithiasis (kidney stones) disorders
-
24. Lloyd SE, Gunther W, Pearce SHS, Thomson A, Bianchi ML, Bosio M, Craig IW, Fisher SE, Scheinman SJ, Wrong O, Jentsch TJ, Thakker RV: Characterisation of renal chloride channel CLCN5 mutations in hypercalciuric nephrolithiasis (kidney stones) disorders. Hum Mol Genet 6:1233-1239, 1997
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1233-1239
-
-
Lloyd, S.E.1
Gunther, W.2
Pearce, S.H.S.3
Thomson, A.4
Bianchi, M.L.5
Bosio, M.6
Craig, I.W.7
Fisher, S.E.8
Scheinman, S.J.9
Wrong, O.10
Jentsch, T.J.11
Thakker, R.V.12
-
25
-
-
0031909863
-
CLCN5 mutation Ser244-Leu is associated with X-linked renal failure without X-linked recessive hypophosphatemic rickets
-
25. Kelleher CL, Buckalew VM, Frederickson ED, Rhodes DJ, Conner DA, Seidman JG, Seidman CE: CLCN5 mutation Ser244-Leu is associated with X-linked renal failure without X-linked recessive hypophosphatemic rickets. Kidney Int 53:31-37, 1998
-
(1998)
Kidney Int
, vol.53
, pp. 31-37
-
-
Kelleher, C.L.1
Buckalew, V.M.2
Frederickson, E.D.3
Rhodes, D.J.4
Conner, D.A.5
Seidman, J.G.6
Seidman, C.E.7
-
26
-
-
0016158212
-
Hereditary renal tubular acidosis
-
26. Buckalew VM, Mattox MD, Purvis ML, Shulman MG, Herndon CN, Rudman D: Hereditary renal tubular acidosis. Medicine (Baltimore) 53:229-253, 1974
-
(1974)
Medicine (Baltimore)
, vol.53
, pp. 229-253
-
-
Buckalew, V.M.1
Mattox, M.D.2
Purvis, M.L.3
Shulman, M.G.4
Herndon, C.N.5
Rudman, D.6
-
27
-
-
0029015415
-
Characterization of carrier females and affected males with X-linked recessive nephrolithiasis
-
27. Reinhart SC, Norden AGW, Lapsley M, Thakker RV, Pang J, Moses AM, Frymoyer PA, Favus MJ, Hoepner JA, Scheinman SJ: Characterization of carrier females and affected males with X-linked recessive nephrolithiasis. J Am Soc Nephrol 5:1451-1461, 1995
-
(1995)
J Am Soc Nephrol
, vol.5
, pp. 1451-1461
-
-
Reinhart, S.C.1
Norden, A.G.W.2
Lapsley, M.3
Thakker, R.V.4
Pang, J.5
Moses, A.M.6
Frymoyer, P.A.7
Favus, M.J.8
Hoepner, J.A.9
Scheinman, S.J.10
-
28
-
-
0034001447
-
Isolated hypercalciuria with mutation in CLCN5: Relevance to idiopathic hypercalciuria
-
28. Scheinman SJ, Cox JPD, Lloyd SE, Pearce SHS, Salenger PV, Hoopes RR Jr, Bushinsky DA, Wrong O, Asplin J, Langman CB, Norden AGW, Thakker RV: Isolated hypercalciuria with mutation in CLCN5: Relevance to idiopathic hypercalciuria. Kidney Int 57:232-239, 2000
-
(2000)
Kidney Int
, vol.57
, pp. 232-239
-
-
Scheinman, S.J.1
Cox, J.P.D.2
Lloyd, S.E.3
Pearce, S.H.S.4
Salenger, P.V.5
Hoopes R.R., Jr.6
Bushinsky, D.A.7
Wrong, O.8
Asplin, J.9
Langman, C.B.10
Norden, A.G.W.11
Thakker, R.V.12
-
29
-
-
0019854294
-
The adult presenting idiopathic Fanconi syndrome
-
29. Brenton DP, Isenberg DA, Cusworth DC, Garrod P, Krywawych S, Stamp TCB: The adult presenting idiopathic Fanconi syndrome. J Inherit Metab Dis 4:211-215, 1981
-
(1981)
J Inherit Metab Dis
, vol.4
, pp. 211-215
-
-
Brenton, D.P.1
Isenberg, D.A.2
Cusworth, D.C.3
Garrod, P.4
Krywawych, S.5
Stamp, T.C.B.6
-
30
-
-
0019833067
-
A family with a dominant form of idiopathic Fanconi syndrome leading to renal failure in adult life
-
30. Patrick A, Cameron JS, Ogg CS: A family with a dominant form of idiopathic Fanconi syndrome leading to renal failure in adult life. Clin Nephrol 16:289-292, 1981
-
(1981)
Clin Nephrol
, vol.16
, pp. 289-292
-
-
Patrick, A.1
Cameron, J.S.2
Ogg, C.S.3
-
31
-
-
0000623605
-
Organic aciduria, decreased renal ammonia production, hydropthalmos and mental retardation: A clinical entity
-
31. Lowe CU, Terrey M, MacLachlan EA: Organic aciduria, decreased renal ammonia production, hydropthalmos and mental retardation: A clinical entity. Am J Dis Child 83:164-184, 1952
-
(1952)
Am J Dis Child
, vol.83
, pp. 164-184
-
-
Lowe, C.U.1
Terrey, M.2
MacLachlan, E.A.3
-
32
-
-
0027326953
-
Immune-related potassium-losing interstitial nephritis: A comparison with distal renal tubular acidosis
-
32. Wrong, OM, Feest TG, MacIver AG: Immune-related potassium-losing interstitial nephritis: A comparison with distal renal tubular acidosis. Q J Med 86:513-534, 1993
-
(1993)
Q J Med
, vol.86
, pp. 513-534
-
-
Wrong, O.M.1
Feest, T.G.2
MacIver, A.G.3
-
33
-
-
0030923557
-
Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene
-
33. Bruce LJ, Cope DL, Jones DK, Schofield AE, Burley M, Povey S, Unwin RJ, Wrong O, Tanner MJA: Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene. J Clin Invest 100:1693-1707, 1997
-
(1997)
J Clin Invest
, vol.100
, pp. 1693-1707
-
-
Bruce, L.J.1
Cope, D.L.2
Jones, D.K.3
Schofield, A.E.4
Burley, M.5
Povey, S.6
Unwin, R.J.7
Wrong, O.8
Tanner, M.J.A.9
-
34
-
-
13144262840
-
Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis
-
34. Karet FE, Gainza FJ, Györy AZ, Unwin RJ, Wrong O, Tanner MJA, Nayir A, Alpay H, Santos F, Hulton SA, Bakkaloglu A, Ozen S, Cunningham MJ, Dipietro A, Walker WG, Lifton RP: Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis. Proc Natl Acad Sci USA 95:6337-6342, 1998
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 6337-6342
-
-
Karet, F.E.1
Gainza, F.J.2
Györy, A.Z.3
Unwin, R.J.4
Wrong, O.5
Tanner, M.J.A.6
Nayir, A.7
Alpay, H.8
Santos, F.9
Hulton, S.A.10
Bakkaloglu, A.11
Ozen, S.12
Cunningham, M.J.13
Dipietro, A.14
Walker, W.G.15
Lifton, R.P.16
-
35
-
-
0023859098
-
Effect of renal insufficiency on the concentration of free retinol-binding protein in urine and serum
-
35. Bernard A, Vyskocyl A, Mahieu P, Lauwerys R: Effect of renal insufficiency on the concentration of free retinol-binding protein in urine and serum. Clin Chim Acta 171:85-94, 1988
-
(1988)
Clin Chim Acta
, vol.171
, pp. 85-94
-
-
Bernard, A.1
Vyskocyl, A.2
Mahieu, P.3
Lauwerys, R.4
-
36
-
-
8044235655
-
Proximal tubular injury in Chinese herbs nephropathy: Monitoring by neutral endopeptidase enzymuria
-
36. Nortier JL, Deschodt-Lanckman MM, Simon S, Thielemans NO, Deprez EG, Depierreux MF, Tielemans CL, Richard C, Lauwerys RR, Bernard AM, Vanherweghem J-L: Proximal tubular injury in Chinese herbs nephropathy: Monitoring by neutral endopeptidase enzymuria. Kidney Int 51:288-293, 1997
-
(1997)
Kidney Int
, vol.51
, pp. 288-293
-
-
Nortier, J.L.1
Deschodt-Lanckman, M.M.2
Simon, S.3
Thielemans, N.O.4
Deprez, E.G.5
Depierreux, M.F.6
Tielemans, C.L.7
Richard, C.8
Lauwerys, R.R.9
Bernard, A.M.10
Vanherweghem, J.-L.11
-
38
-
-
0032576744
-
X inactivation in females with X-linked disease
-
38. Puck JM, Willard HF: X inactivation in females with X-linked disease. N Engl J Med 338:325-328, 1998
-
(1998)
N Engl J Med
, vol.338
, pp. 325-328
-
-
Puck, J.M.1
Willard, H.F.2
-
39
-
-
0029035255
-
A mathematical equation to differentiate overload proteinuria from tubulo-interstitial involvement in glomerular diseases
-
39. Hofmann W, Edel H, Guder WG: A mathematical equation to differentiate overload proteinuria from tubulo-interstitial involvement in glomerular diseases. Clin Nephrol 44:28-31, 1995
-
(1995)
Clin Nephrol
, vol.44
, pp. 28-31
-
-
Hofmann, W.1
Edel, H.2
Guder, W.G.3
-
40
-
-
0013590214
-
Haematuria in the adult
-
edited by Coe FL, Favus MJ, Pak CYC, Parks JH, Preminger GM, Philadelphia, Lippincott-Raven
-
40. Bagley DH: Haematuria in the adult, in Kidney Stones: Medical and Surgical Management (2nd ed), edited by Coe FL, Favus MJ, Pak CYC, Parks JH, Preminger GM, Philadelphia, Lippincott-Raven, 1996, pp 521-528
-
(1996)
Kidney Stones: Medical and Surgical Management (2nd Ed)
, pp. 521-528
-
-
Bagley, D.H.1
-
41
-
-
0031682667
-
Measurement of the kinetics of protein uptake by proximal tubular cells using an optical biosensor
-
41. Thakkar H, Lowe PA, Price CP, Newman DJ: Measurement of the kinetics of protein uptake by proximal tubular cells using an optical biosensor. Kidney Int 54:1197-1205, 1998
-
(1998)
Kidney Int
, vol.54
, pp. 1197-1205
-
-
Thakkar, H.1
Lowe, P.A.2
Price, C.P.3
Newman, D.J.4
-
42
-
-
0023070346
-
The effect of a synthetic polypeptide on the renal handling of protein in man
-
42. Beetham R, Dawnay A, Cattell W: The effect of a synthetic polypeptide on the renal handling of protein in man. Clin Sci 72:245-249, 1987
-
(1987)
Clin Sci
, vol.72
, pp. 245-249
-
-
Beetham, R.1
Dawnay, A.2
Cattell, W.3
-
43
-
-
0031773081
-
Molecular interactions between albumin and proximal tubular cells
-
43. Brunskill NJ: Molecular interactions between albumin and proximal tubular cells. Exp Nephrol 6:491-495, 1998
-
(1998)
Exp Nephrol
, vol.6
, pp. 491-495
-
-
Brunskill, N.J.1
-
44
-
-
0032953770
-
Intra-renal and subcellular distribution of the human chloride channel, CLC-5, reveals a pathophysiological basis for Dent's disease
-
44. Devuyst O, Christie PT, Courtoy PJ, Beauwens R, Thakker RV: Intra-renal and subcellular distribution of the human chloride channel, CLC-5, reveals a pathophysiological basis for Dent's disease. Hum Mol Genet 8:247-257, 1999
-
(1999)
Hum Mol Genet
, vol.8
, pp. 247-257
-
-
Devuyst, O.1
Christie, P.T.2
Courtoy, P.J.3
Beauwens, R.4
Thakker, R.V.5
-
45
-
-
0032493276
-
C1C5, the chloride channel mutated in Dent's disease, colocalizes with the proton pump in endocytically active kidney cells
-
45. Günther W, Lüchow A, Cluzeaud F, Vandewalle A, Jentsch TJ: C1C5, the chloride channel mutated in Dent's disease, colocalizes with the proton pump in endocytically active kidney cells. Proc Natl Acad Sci USA 95:8075-8080, 1998
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 8075-8080
-
-
Günther, W.1
Lüchow, A.2
Cluzeaud, F.3
Vandewalle, A.4
Jentsch, T.J.5
|