Focal segmental glomerulosclerosis is associated with a PDSS2 haplotype and, independently, with a decreased content of coenzyme Q10. - Test2 - elhamkhani - TriplyDB

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

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

http://www.wikidata.org/entity/Q37234710

about

Mitochondrial dysfunction in inherited renal disease and acute kidney injury Defining nephrotic syndrome from an integrative genomics perspective.The podocyte power-plant disaster and its contribution to glomerulopathy.Resveratrol and para-coumarate serve as ring precursors for coenzyme Q biosynthesis.Mitochondrial and cytoskeletal alterations are involved in the pathogenesis of hydronephrosis in ICR/Mlac-hydro mice The Genetics of Nephrotic Syndrome.Coenzyme Q supplementation or over-expression of the yeast Coq8 putative kinase stabilizes multi-subunit Coq polypeptide complexes in yeast coq null mutants.Renal manifestations of genetic mitochondrial disease.Genetic bases and clinical manifestations of coenzyme Q10 (CoQ 10) deficiency.Molecular diagnosis of coenzyme Q10 deficiency.Focal Segmental Glomerulosclerosis.Rescue of primary ubiquinone deficiency due to a novel COQ7 defect using 2,4-dihydroxybensoic acid.Increasing the level of peroxisome proliferator-activated receptor γ coactivator-1α in podocytes results in collapsing glomerulopathy.Osmotic stress: Is CoQ a membrane stabilizer?A Personalized Model of COQ2 Nephropathy Rescued by the Wild-Type COQ2 Allele or Dietary Coenzyme Q10 Supplementation.Coenzyme Q10 supplementation therapy for 2 children with proteinuria renal disease and ADCK4 mutation: Case reports and literature review.Diffuse mesangial sclerosis in a PDSS2 mutation-induced coenzyme Q10 deficiency.Biochemistry of Mitochondrial Coenzyme Q Biosynthesis.Oxidative Stress, Apoptosis, and Mitochondrial Function in Diabetic Nephropathy.

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

http://www.wikidata.org/entity/Q37234710

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 07 August 2013

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Focal segmental glomeruloscler ...... eased content of coenzyme Q10.

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Focal segmental glomeruloscler ...... eased content of coenzyme Q10.

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Focal segmental glomeruloscler ...... eased content of coenzyme Q10.

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Focal segmental glomeruloscler ...... eased content of coenzyme Q10.

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Focal segmental glomeruloscler ...... eased content of coenzyme Q10.

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Focal segmental glomeruloscler ...... eased content of coenzyme Q10.

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AJPRENAL.00143.2013

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American Journal of Physiology - Renal Physiology

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Focal segmental glomeruloscler ...... eased content of coenzyme Q10.

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Beth N Marbois

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Catherine F Clarke

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Cheryl A Winkler

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David L Gasser

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Gregory D Kirk

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Letian X Xie

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Louise M McKenzie

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Min Peng

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Yuchen Shi

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P2860

Characterization of solanesyl and decaprenyl diphosphate synthases in mice and humans

A mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiency

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.

Association of trypanolytic ApoL1 variants with kidney disease in African Americans

APOL1 genetic variants in focal segmental glomerulosclerosis and HIV-associated nephropathy

A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease

Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders

A New Statistical Method for Haplotype Reconstruction from Population Data

Haploview: analysis and visualization of LD and haplotype maps

Yeast COQ4 encodes a mitochondrial protein required for coenzyme Q synthesis.

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