Low molecular weight ('tubular') proteinuria in patients with mutations of the CLCN5 renal chloride channel gene.

Low molecular weight ('tubular') proteinuria in patients with mutations of the CLCN5 renal chloride channel gene.

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Norden, A, Asplin, J, Deschodt-Lanckman, M, Langman, C, Lapsley, M, Nortier, J, Scheinman, S, Thakker, R, Unwin, R, Wrong, O
التنسيق:	Journal article
منشور في:	1999

مواد مشابهة

Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases.
حسب: Norden, A, وآخرون
منشور في: (2000)

Isolated hypercalciuria with mutation in CLCN5: relevance to idiopathic hypercalciuria.
حسب: Scheinman, S, وآخرون
منشور في: (2000)

Mutations in the chloride channel gene (CLCN5) are associated with hypercalciuric rickets and nephrolithiasis.
حسب: Lloyd, SE, وآخرون
منشور في: (1996)

Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.
حسب: Lloyd, SE, وآخرون
منشور في: (1997)

Renal chloride channel, CLCN5, mutations in Dent's disease.
حسب: Cox, J, وآخرون
منشور في: (1999)

Characterization of renal chloride channel (CLCN5) mutations in Dent's disease.
حسب: Yamamoto, K, وآخرون
منشور في: (2000)

Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5).
حسب: Lloyd, SE, وآخرون
منشور في: (1997)

Hypercalciuric nephrocalcinosis in Japanese children due to mutations of the renal chloride channel (CLCN5).
حسب: Lloyd, SE, وآخرون
منشور في: (1996)

Mutations of CLCN5 in Japanese children with idiopathic low molecular weight proteinuria, hypercalciuria and nephrocalcinosis.
حسب: Akuta, N, وآخرون
منشور في: (1997)

Functional characterization of renal chloride channel, CLCN5, mutations associated with Dent'sJapan disease.
حسب: Igarashi, T, وآخرون
منشور في: (1998)

Fragmentation of filtered proteins and implications for glomerular protein sieving in Fanconi syndrome.
حسب: Norden, A, وآخرون
منشور في: (2002)

Glomerular protein sieving and implications for renal failure in Fanconi syndrome.
حسب: Norden, A, وآخرون
منشور في: (2001)

HEREDITARY NEPHROLITHIASIS IS ASSOCIATED WITH MUTATIONS IN AN X-LINKED CHLORIDE CHANNEL GENE
حسب: Lloyd, S, وآخرون
منشور في: (1995)

Autosomal dominant osteopetrosis associated with renal tubular acidosis is due to a CLCN7 mutation
حسب: Piret, S, وآخرون
منشور في: (2016)

Urinary megalin deficiency implicates abnormal tubular endocytic function in Fanconi syndrome.
حسب: Norden, A, وآخرون
منشور في: (2002)

Cloning and characterization of CLCN5, the human kidney chloride channel gene implicated in Dent disease (an X-linked hereditary nephrolithiasis).
حسب: Fisher, S, وآخرون
منشور في: (1995)

MAPPING OF 2 HEREDITARY RENAL TUBULAR DISORDERS ASSOCIATED WITH KIDNEY-STONES, AND REFERRED TO AS DENT-DISEASE AND X-LINKED RECESSIVE NEPHROLITHIASIS, TO CHROMOSOME-XP11
حسب: Thakker, R, وآخرون
منشور في: (1994)

In memoriam: Oliver M. Wrong.
حسب: Scheinman, S, وآخرون
منشور في: (2012)

Clinical and genetic studies of CLCN5 mutations in Japanese families with Dent's disease.
حسب: Igarashi, T, وآخرون
منشور في: (2000)

Channel and tubular electrodes
حسب: Compton, R, وآخرون
منشور في: (1986)

ANALYSIS OF THE GENE ENCODING AN X-LINKED VOLTAGE-GATED CHLORIDE CHANNEL IN IDIOPATHIC HYPERCALIURIA
حسب: Scheinman, S, وآخرون
منشور في: (1995)

Chloride channels in renal disease.
حسب: Thakker, R
منشور في: (1999)

Chloride channels cough up.
حسب: Thakker, R
منشور في: (1997)

ROLE OF A VOLTAGE-GATED CHLORIDE-CHANNEL GENE CLC-5 IN HUMAN AND RAT HYPERCALCIURIA
حسب: Scheinman, S, وآخرون
منشور في: (1995)

The role of renal chloride channel mutations in kidney stone disease and nephrocalcinosis.
حسب: Thakker, R
منشور في: (1998)

Dent's disease.
حسب: Neild, G, وآخرون
منشور في: (2005)

Proteinuria and proximal tubular epithelial cells: correlation between immunofluorescence, histology, and degree of proteinuria
حسب: Maria Bernadette CY Chow, وآخرون
منشور في: (2024-10-01)

Isolation and partial characterization of a chloride channel gene which is expressed in kidney and is a candidate for Dent's disease (an X-linked hereditary nephrolithiasis).
حسب: Fisher, S, وآخرون
منشور في: (1994)

Characterization of carrier females and affected males with X-linked recessive nephrolithiasis.
حسب: Reinhart, S, وآخرون
منشور في: (1995)

Molecular pathology of renal chloride channels and calcium metabolism
حسب: Thakker, R
منشور في: (2003)

The influence of proteinuria on tubular transport of Na+, K+, CL
حسب: Petrović Dejan, وآخرون
منشور في: (2002-01-01)

MASS-TRANSPORT TO CHANNEL AND TUBULAR ELECTRODES - THE SINGH AND DUTT APPROXIMATION
حسب: Compton, R, وآخرون
منشور في: (1987)

Proximal tubular hypertrophy and enlarged glomerular and proximal tubular urinary space in obese subjects with proteinuria.
حسب: Ana Tobar, وآخرون
منشور في: (2013-01-01)

Molecular pathology of renal chloride channels in Dent's disease and Bartter's syndrome.
حسب: Thakker, R
منشور في: (2000)

Long-Term Follow-Up of Proteinuria and Estimated Glomerular Filtration Rate in HIV-Infected Patients with Tubular Proteinuria.
حسب: Hélène Peyriere, وآخرون
منشور في: (2015-01-01)

A novel mutation in CLCN1 associated with feline myotonia congenita.
حسب: Barbara Gandolfi, وآخرون
منشور في: (2014-01-01)

Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22.
حسب: Pook, M, وآخرون
منشور في: (1993)

THE GENE CAUSING DENTS DISEASE, A RENAL FANCONI SYNDROME WITH NEPHROCALCINOSIS AND KIDNEY-STONES, IS ON THE SHORT ARM OF THE X-CHROMOSOME (XP11.22)
حسب: Thakker, R, وآخرون
منشور في: (1993)

Proteinuria.
حسب: Haynes, J, وآخرون
منشور في: (2006)

Screening for CLCN5 mutation in renal calcium stone formers patients
حسب: Maria Alice P. Rebelo, وآخرون
منشور في: (2005-03-01)