Pages that link to "Q39668671"

The following pages link to Maternal genes: mitochondrial diseases. (Q39668671):

Displaying 23 items.

• Detection of the G to A mitochondrial DNA mutation at position 11778 in German families with Leber's hereditary optic neuropathy (Q28251896) (← links)
• Effect of 'binary mitochondrial heteroplasmy' on respiration and ATP synthesis: implications for mitochondrial diseases (Q28344441) (← links)
• Mitochondrial involvement in bladder function and dysfunction (Q33677398) (← links)
• Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome (Q34323823) (← links)
• The mitochondrial genome of the sea anemone Metridium senile (Cnidaria): introns, a paucity of tRNA genes, and a near-standard genetic code. (Q34603529) (← links)
• Pedigree models for complex human traits involving the mitochondrial genome (Q35195183) (← links)
• Does the mitochondrial DNA play a role in the pathogenesis of diabetes? (Q35654346) (← links)
• Nucleus-driven mutations of human mitochondrial DNA (Q35848666) (← links)
• Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome (Q35950795) (← links)
• X chromosome-linked and mitochondrial gene control of Leber hereditary optic neuropathy: evidence from segregation analysis for dependence on X chromosome inactivation (Q37594930) (← links)
• Renal involvement in mitochondrial cytopathies (Q41101804) (← links)
• Evolution of human mitochondrial DNA: evidence for departure from a pure neutral model of populations at equilibrium (Q41173410) (← links)
• Preliminary exclusion of an X-linked gene in Leber optic atrophy by linkage analysis (Q41312203) (← links)
• Disorders of nuclear-mitochondrial intergenomic signalling. (Q41547365) (← links)
• Mitochondrial disorders and the kidney (Q43102825) (← links)
• Control over the contribution of the mitochondrial membrane potential (DeltaPsi) and proton gradient (DeltapH) to the protonmotive force (Deltap). In silico studies (Q43154648) (← links)
• Muscle carnitine acetyltransferase and carnitine deficiency in a case of mitochondrial encephalomyopathy (Q48092166) (← links)
• Visual dysfunction in patients with mitochondrial myopathies (Q57252399) (← links)
• Chronic intestinal pseudoobstruction with myopathy and ophthalmoplegia. A muscular biochemical study of a mitochondrial disorder (Q67742824) (← links)
• Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes (Q68453563) (← links)
• X-linked myoclonus epilepsy explained as a maternally inherited mitochondrial disorder (Q70613475) (← links)
• No evidence for 'skewed' inactivation of the X-chromosome as cause of Leber's hereditary optic neuropathy in female carriers (Q71599227) (← links)
• Partial outlet obstruction of the rabbit bladder results in changes in the mitochondrial genetic system (Q72596270) (← links)