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.

書目詳細資料
Main Authors:	Norden, A, Asplin, J, Deschodt-Lanckman, M, Langman, C, Lapsley, M, Nortier, J, Scheinman, S, Thakker, R, Unwin, R, Wrong, O
格式:	Journal article
出版:	1999

相似書籍

Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases.
由: Norden, A, et al.
出版: (2000)

Isolated hypercalciuria with mutation in CLCN5: relevance to idiopathic hypercalciuria.
由: Scheinman, S, et al.
出版: (2000)

Mutations in the chloride channel gene (CLCN5) are associated with hypercalciuric rickets and nephrolithiasis.
由: Lloyd, SE, et al.
出版: (1996)

Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.
由: Lloyd, SE, et al.
出版: (1997)

Renal chloride channel, CLCN5, mutations in Dent's disease.
由: Cox, J, et al.
出版: (1999)

Characterization of renal chloride channel (CLCN5) mutations in Dent's disease.
由: Yamamoto, K, et al.
出版: (2000)

Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5).
由: Lloyd, SE, et al.
出版: (1997)

Hypercalciuric nephrocalcinosis in Japanese children due to mutations of the renal chloride channel (CLCN5).
由: Lloyd, SE, et al.
出版: (1996)

Mutations of CLCN5 in Japanese children with idiopathic low molecular weight proteinuria, hypercalciuria and nephrocalcinosis.
由: Akuta, N, et al.
出版: (1997)

Functional characterization of renal chloride channel, CLCN5, mutations associated with Dent'sJapan disease.
由: Igarashi, T, et al.
出版: (1998)

Fragmentation of filtered proteins and implications for glomerular protein sieving in Fanconi syndrome.
由: Norden, A, et al.
出版: (2002)

Glomerular protein sieving and implications for renal failure in Fanconi syndrome.
由: Norden, A, et al.
出版: (2001)

HEREDITARY NEPHROLITHIASIS IS ASSOCIATED WITH MUTATIONS IN AN X-LINKED CHLORIDE CHANNEL GENE
由: Lloyd, S, et al.
出版: (1995)

Autosomal dominant osteopetrosis associated with renal tubular acidosis is due to a CLCN7 mutation
由: Piret, S, et al.
出版: (2016)

Urinary megalin deficiency implicates abnormal tubular endocytic function in Fanconi syndrome.
由: Norden, A, et al.
出版: (2002)

Cloning and characterization of CLCN5, the human kidney chloride channel gene implicated in Dent disease (an X-linked hereditary nephrolithiasis).
由: Fisher, S, et al.
出版: (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
由: Thakker, R, et al.
出版: (1994)

In memoriam: Oliver M. Wrong.
由: Scheinman, S, et al.
出版: (2012)

Clinical and genetic studies of CLCN5 mutations in Japanese families with Dent's disease.
由: Igarashi, T, et al.
出版: (2000)

Channel and tubular electrodes
由: Compton, R, et al.
出版: (1986)

ANALYSIS OF THE GENE ENCODING AN X-LINKED VOLTAGE-GATED CHLORIDE CHANNEL IN IDIOPATHIC HYPERCALIURIA
由: Scheinman, S, et al.
出版: (1995)

Chloride channels in renal disease.
由: Thakker, R
出版: (1999)

Chloride channels cough up.
由: Thakker, R
出版: (1997)

ROLE OF A VOLTAGE-GATED CHLORIDE-CHANNEL GENE CLC-5 IN HUMAN AND RAT HYPERCALCIURIA
由: Scheinman, S, et al.
出版: (1995)

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

Dent's disease.
由: Neild, G, et al.
出版: (2005)

Proteinuria and proximal tubular epithelial cells: correlation between immunofluorescence, histology, and degree of proteinuria
由: Maria Bernadette CY Chow, et al.
出版: (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).
由: Fisher, S, et al.
出版: (1994)

Characterization of carrier females and affected males with X-linked recessive nephrolithiasis.
由: Reinhart, S, et al.
出版: (1995)

Molecular pathology of renal chloride channels and calcium metabolism
由: Thakker, R
出版: (2003)

The influence of proteinuria on tubular transport of Na+, K+, CL
由: Petrović Dejan, et al.
出版: (2002-01-01)

MASS-TRANSPORT TO CHANNEL AND TUBULAR ELECTRODES - THE SINGH AND DUTT APPROXIMATION
由: Compton, R, et al.
出版: (1987)

Proximal tubular hypertrophy and enlarged glomerular and proximal tubular urinary space in obese subjects with proteinuria.
由: Ana Tobar, et al.
出版: (2013-01-01)

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

Long-Term Follow-Up of Proteinuria and Estimated Glomerular Filtration Rate in HIV-Infected Patients with Tubular Proteinuria.
由: Hélène Peyriere, et al.
出版: (2015-01-01)

A novel mutation in CLCN1 associated with feline myotonia congenita.
由: Barbara Gandolfi, et al.
出版: (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.
由: Pook, M, et al.
出版: (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)
由: Thakker, R, et al.
出版: (1993)

Proteinuria.
由: Haynes, J, et al.
出版: (2006)

Screening for CLCN5 mutation in renal calcium stone formers patients
由: Maria Alice P. Rebelo, et al.
出版: (2005-03-01)