Results 281 to 290 of about 248,926 (292)

The Cardiac Copper Chaperone Proteins Sco1 and CCS are Up-Regulated, but Cox 1 and Cox4 are Down-Regulated, by Copper Deficiency

Biological Trace Element Research, 2010
Dingbo Lin, Denis M Medeiros
exaly  

The pathomechanism of COX deficiency includes nuclear DNA damage and replicative stress

Biochimica et Biophysica Acta (BBA) - Bioenergetics, 2018
Ann Saada (Reisch), Liza Douiev
openaire   +1 more source

Mutations in theSURF1gene associated with Leigh syndrome and cytochromecoxidase deficiency

Human Mutation, 2001
Massimo Zeviani, Valeria Tiranti
exaly  

Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency

Human Molecular Genetics, 2003
Hana Antonicka, Scot C Leary, Rita Horvath   +2 more
exaly  

Prevention of upper aerodigestive tract cancer in zinc‐deficient rodents: Inefficacy of genetic or pharmacological disruption of COX‐2

International Journal of Cancer, 2008
Louise Y Y Fong, Karl J Smalley
exaly  

Saguenay Lac Saint Jean cytochrome oxidase deficiency: sequence analysis of nuclear encoded COX subunits, chromosomal localization and a sequence anomaly in subunit VIc

Biochimica Et Biophysica Acta - Molecular Basis of Disease, 1998
exaly  

Inherited bleeding disorder due to familial type 2 platelet cyclo-oxygenase deficiency

Thrombosis Research, 2005
Yesim Dargaud
exaly  

Mitochondrial Encephalomyopathy with COX Deficiency

2018
Corrado Angelini
exaly  

A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgroup with syndromal encephalopathy.

Journal of Medical Genetics, 1998
exaly  

Leigh Syndrome due to COX Deficiency

2018
exaly