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.

Библиографические подробности
Главные авторы:	Norden, A, Asplin, J, Deschodt-Lanckman, M, Langman, C, Lapsley, M, Nortier, J, Scheinman, S, Thakker, R, Unwin, R, Wrong, O
Формат:	Journal article
Опубликовано:	1999

Схожие документы

Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases.
по: Norden, A, и др.
Опубликовано: (2000)

Isolated hypercalciuria with mutation in CLCN5: relevance to idiopathic hypercalciuria.
по: Scheinman, S, и др.
Опубликовано: (2000)

Mutations in the chloride channel gene (CLCN5) are associated with hypercalciuric rickets and nephrolithiasis.
по: Lloyd, SE, и др.
Опубликовано: (1996)

Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.
по: Lloyd, SE, и др.
Опубликовано: (1997)

Renal chloride channel, CLCN5, mutations in Dent's disease.
по: Cox, J, и др.
Опубликовано: (1999)

Characterization of renal chloride channel (CLCN5) mutations in Dent's disease.
по: Yamamoto, K, и др.
Опубликовано: (2000)

Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5).
по: Lloyd, SE, и др.
Опубликовано: (1997)

Hypercalciuric nephrocalcinosis in Japanese children due to mutations of the renal chloride channel (CLCN5).
по: Lloyd, SE, и др.
Опубликовано: (1996)

Mutations of CLCN5 in Japanese children with idiopathic low molecular weight proteinuria, hypercalciuria and nephrocalcinosis.
по: Akuta, N, и др.
Опубликовано: (1997)

Functional characterization of renal chloride channel, CLCN5, mutations associated with Dent'sJapan disease.
по: Igarashi, T, и др.
Опубликовано: (1998)

Fragmentation of filtered proteins and implications for glomerular protein sieving in Fanconi syndrome.
по: Norden, A, и др.
Опубликовано: (2002)

Glomerular protein sieving and implications for renal failure in Fanconi syndrome.
по: Norden, A, и др.
Опубликовано: (2001)

HEREDITARY NEPHROLITHIASIS IS ASSOCIATED WITH MUTATIONS IN AN X-LINKED CHLORIDE CHANNEL GENE
по: Lloyd, S, и др.
Опубликовано: (1995)

Autosomal dominant osteopetrosis associated with renal tubular acidosis is due to a CLCN7 mutation
по: Piret, S, и др.
Опубликовано: (2016)

Urinary megalin deficiency implicates abnormal tubular endocytic function in Fanconi syndrome.
по: Norden, A, и др.
Опубликовано: (2002)

Cloning and characterization of CLCN5, the human kidney chloride channel gene implicated in Dent disease (an X-linked hereditary nephrolithiasis).
по: Fisher, S, и др.
Опубликовано: (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
по: Thakker, R, и др.
Опубликовано: (1994)

In memoriam: Oliver M. Wrong.
по: Scheinman, S, и др.
Опубликовано: (2012)

Clinical and genetic studies of CLCN5 mutations in Japanese families with Dent's disease.
по: Igarashi, T, и др.
Опубликовано: (2000)

Channel and tubular electrodes
по: Compton, R, и др.
Опубликовано: (1986)

ANALYSIS OF THE GENE ENCODING AN X-LINKED VOLTAGE-GATED CHLORIDE CHANNEL IN IDIOPATHIC HYPERCALIURIA
по: Scheinman, S, и др.
Опубликовано: (1995)

Chloride channels in renal disease.
по: Thakker, R
Опубликовано: (1999)

Chloride channels cough up.
по: Thakker, R
Опубликовано: (1997)

ROLE OF A VOLTAGE-GATED CHLORIDE-CHANNEL GENE CLC-5 IN HUMAN AND RAT HYPERCALCIURIA
по: Scheinman, S, и др.
Опубликовано: (1995)

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

Dent's disease.
по: Neild, G, и др.
Опубликовано: (2005)

Proteinuria and proximal tubular epithelial cells: correlation between immunofluorescence, histology, and degree of proteinuria
по: Maria Bernadette CY Chow, и др.
Опубликовано: (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).
по: Fisher, S, и др.
Опубликовано: (1994)

Characterization of carrier females and affected males with X-linked recessive nephrolithiasis.
по: Reinhart, S, и др.
Опубликовано: (1995)

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

The influence of proteinuria on tubular transport of Na+, K+, CL
по: Petrović Dejan, и др.
Опубликовано: (2002-01-01)

MASS-TRANSPORT TO CHANNEL AND TUBULAR ELECTRODES - THE SINGH AND DUTT APPROXIMATION
по: Compton, R, и др.
Опубликовано: (1987)

Proximal tubular hypertrophy and enlarged glomerular and proximal tubular urinary space in obese subjects with proteinuria.
по: Ana Tobar, и др.
Опубликовано: (2013-01-01)

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

Long-Term Follow-Up of Proteinuria and Estimated Glomerular Filtration Rate in HIV-Infected Patients with Tubular Proteinuria.
по: Hélène Peyriere, и др.
Опубликовано: (2015-01-01)

A novel mutation in CLCN1 associated with feline myotonia congenita.
по: Barbara Gandolfi, и др.
Опубликовано: (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.
по: Pook, M, и др.
Опубликовано: (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)
по: Thakker, R, и др.
Опубликовано: (1993)

Proteinuria.
по: Haynes, J, и др.
Опубликовано: (2006)

Screening for CLCN5 mutation in renal calcium stone formers patients
по: Maria Alice P. Rebelo, и др.
Опубликовано: (2005-03-01)