Literature DB >> 9099838

Mitochondrial mutation as a probable causative factor in familial progressive tubulointerstitial nephritis.

G Zsurka1, J Ormos, B Iványi, S Túri, E Endreffy, M Magyari, S Sonkodi, P Venetianer.   

Abstract

Renal biopsy of two children and a maternal relative, diagnosed with severe progressive tubulointerstitial nephritis, has shown the presence of distorted mitochondria. Mitochondrial DNA from the blood of these patients was analysed. No major deletions were found, but an A to G mutation was detected in position 5656. It is proposed that this mutation might play a causative role in the renal disease of the patients.

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Year:  1997        PMID: 9099838     DOI: 10.1007/s004390050393

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  7 in total

1.  The mitochondrial and kidney disease phenotypes of kd/kd mice under germfree conditions.

Authors:  Troy M Hallman; Min Peng; Ray Meade; Wayne W Hancock; Michael P Madaio; David L Gasser
Journal:  J Autoimmun       Date:  2005-12-06       Impact factor: 7.094

2.  Mitochondrial DNA and Alzheimer's disease: a first case-control study of the Tunisian population.

Authors:  Nesrine Ben Salem; Sami Boussetta; Itziar de Rojas; Sonia Moreno-Grau; Laura Montrreal; Narjes Mokni; Imene Mahmoud; Samia Younes; Nizar Daouassi; Mahbouba Frih-Ayed; Afef Hammami; Amel Ben Ammar Elgaaied; Agustín Ruiz; Lotfi Cherni
Journal:  Mol Biol Rep       Date:  2021-12-01       Impact factor: 2.316

3.  Mutant prenyltransferase-like mitochondrial protein (PLMP) and mitochondrial abnormalities in kd/kd mice.

Authors:  Min Peng; Leonard Jarett; Ray Meade; Michael P Madaio; Wayne W Hancock; Alfred L George; Eric G Neilson; David L Gasser
Journal:  Kidney Int       Date:  2004-07       Impact factor: 10.612

4.  Focal segmental glomerulosclerosis is associated with a PDSS2 haplotype and, independently, with a decreased content of coenzyme Q10.

Authors:  David L Gasser; Cheryl A Winkler; Min Peng; Ping An; Louise M McKenzie; Gregory D Kirk; Yuchen Shi; Letian X Xie; Beth N Marbois; Catherine F Clarke; Jeffrey B Kopp
Journal:  Am J Physiol Renal Physiol       Date:  2013-08-07

5.  Focal segmental glomerulosclerosis associated with mitochondrial disease.

Authors:  Kenneth Lim; David Steele; Andrew Fenves; Ravi Thadhani; Eliot Heher; Amel Karaa
Journal:  Clin Nephrol Case Stud       Date:  2017-03-03

Review 6.  Mitochondrial DNA mutations in renal disease: an overview.

Authors:  Larissa P Govers; Hakan R Toka; Ali Hariri; Stephen B Walsh; Detlef Bockenhauer
Journal:  Pediatr Nephrol       Date:  2020-01-10       Impact factor: 3.714

Review 7.  Renal manifestations of genetic mitochondrial disease.

Authors:  John F O'Toole
Journal:  Int J Nephrol Renovasc Dis       Date:  2014-01-31
  7 in total

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