Literature DB >> 10444339

Mutations of CTNS causing intermediate cystinosis.

J Thoene1, R Lemons, Y Anikster, J Mullet, K Paelicke, C Lucero, W Gahl, J Schneider, S G Shu, H T Campbell.   

Abstract

Six patients with the intermediate form of cystinosis are described. Two have new mutations not previously described. The disease occurs due either to the combination of one mild mutation and one which is known to cause nephropathic cystinosis or to homozygosity for a predicted mild mutation. Partial phenotypic correction of cystinotic fibroblasts by transfection with normal cDNA or a cDNA derived from a mutation causing intermediate cystinosis is demonstrated. Copyright 1999 Academic Press.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10444339     DOI: 10.1006/mgme.1999.2876

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  26 in total

Review 1.  Mitochondrial energetics and therapeutics.

Authors:  Douglas C Wallace; Weiwei Fan; Vincent Procaccio
Journal:  Annu Rev Pathol       Date:  2010       Impact factor: 23.472

2.  Cystinosin, the protein defective in cystinosis, is a H(+)-driven lysosomal cystine transporter.

Authors:  V Kalatzis; S Cherqui; C Antignac; B Gasnier
Journal:  EMBO J       Date:  2001-11-01       Impact factor: 11.598

3.  Slow progression of renal failure in a child with infantile cystinosis.

Authors:  Maria Bitsori; Eleni Vergadi; Emmanouil Galanakis
Journal:  CEN Case Rep       Date:  2018-02-14

4.  Cystinosis as a lysosomal storage disease with multiple mutant alleles: Phenotypic-genotypic correlations.

Authors:  Mohammad Al-Haggar
Journal:  World J Nephrol       Date:  2013-11-06

5.  Two novel CTNS mutations in cystinosis patients in Thailand.

Authors:  Patra Yeetong; Siraprapa Tongkobpetch; Pornchai Kingwatanakul; Tawatchai Deekajorndech; Isa M Bernardini; Kanya Suphapeetiporn; William A Gahl; Vorasuk Shotelersuk
Journal:  Gene       Date:  2012-03-16       Impact factor: 3.688

6.  Natural history of adolescent-onset cystinosis.

Authors:  Julian P Midgley; Reyhan El-Kares; François Mathieu; Paul Goodyer
Journal:  Pediatr Nephrol       Date:  2011-05-08       Impact factor: 3.714

7.  Intralysosomal cystine accumulation in mice lacking cystinosin, the protein defective in cystinosis.

Authors:  Stéphanie Cherqui; Caroline Sevin; Ghislaine Hamard; Vasiliki Kalatzis; Mireille Sich; Marie O Pequignot; Karïn Gogat; Marc Abitbol; Michel Broyer; Marie-Claire Gubler; Corinne Antignac
Journal:  Mol Cell Biol       Date:  2002-11       Impact factor: 4.272

Review 8.  New aspects of the pathogenesis of cystinosis.

Authors:  Vasiliki Kalatzis; Corinne Antignac
Journal:  Pediatr Nephrol       Date:  2003-02-27       Impact factor: 3.714

Review 9.  Nephropathic cystinosis: late complications of a multisystemic disease.

Authors:  Galina Nesterova; William Gahl
Journal:  Pediatr Nephrol       Date:  2008-06       Impact factor: 3.714

10.  Late-onset nephropathic cystinosis: clinical presentation, outcome, and genotyping.

Authors:  Aude Servais; Vincent Morinière; Jean-Pierre Grünfeld; Laure-Hélène Noël; Jean-Michel Goujon; Bernadette Chadefaux-Vekemans; Corinne Antignac
Journal:  Clin J Am Soc Nephrol       Date:  2008-01       Impact factor: 8.237

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.