Pages that link to "Q30986717"
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The following pages link to Oxidative stress and disturbed glutamate transport in hereditary nucleotide repair disorders (Q30986717):
Displaying 28 items.
- Senataxin, defective in ataxia oculomotor apraxia type 2, is involved in the defense against oxidative DNA damage (Q24309516) (← links)
- Increased apoptosis, p53 up-regulation, and cerebellar neuronal degeneration in repair-deficient Cockayne syndrome mice (Q24682525) (← links)
- Early postnatal ataxia and abnormal cerebellar development in mice lacking Xeroderma pigmentosum Group A and Cockayne syndrome Group B DNA repair genes (Q30759755) (← links)
- Cockayne syndrome in adults: review with clinical and pathologic study of a new case (Q31075490) (← links)
- Brainstem and basal ganglia lesions in xeroderma pigmentosum group A. (Q31126310) (← links)
- Convulsive episodes in patients with group A xeroderma pigmentosum (Q33222912) (← links)
- Cockayne syndrome group B cellular and biochemical functions (Q33905274) (← links)
- Involvement of oxidatively damaged DNA and repair in cancer development and aging. (Q33942077) (← links)
- DNA repair on the brain (Q33948860) (← links)
- Changes in cerebrospinal fluid biomarkers in human herpesvirus-6-associated acute encephalopathy/febrile seizures. (Q34256876) (← links)
- Neuropathology of the limbic system and brainstem in West syndrome (Q34432737) (← links)
- Disorders of nucleotide excision repair: the genetic and molecular basis of heterogeneity (Q35006896) (← links)
- Cockayne Syndrome B Protects Against Methamphetamine-Enhanced Oxidative DNA Damage in Murine Fetal Brain and Postnatal Neurodevelopmental Deficits (Q35049796) (← links)
- Cockayne syndrome group B protein is engaged in processing of DNA adducts of lipid peroxidation product trans-4-hydroxy-2-nonenal (Q36101169) (← links)
- Cockayne syndrome exhibits dysregulation of p21 and other gene products that may be independent of transcription-coupled repair (Q36178025) (← links)
- Do all of the neurologic diseases in patients with DNA repair gene mutations result from the accumulation of DNA damage? (Q36690915) (← links)
- Clinical implications of the basic defects in Cockayne syndrome and xeroderma pigmentosum and the DNA lesions responsible for cancer, neurodegeneration and aging (Q36839881) (← links)
- The influence of DNA repair on neurological degeneration, cachexia, skin cancer and internal neoplasms: autopsy report of four xeroderma pigmentosum patients (XP-A, XP-C and XP-D). (Q37180228) (← links)
- Oxidative stress in developmental brain disorders (Q37372745) (← links)
- Damage of DNA and proteins by major lipid peroxidation products in genome stability (Q37976880) (← links)
- Cockayne syndrome: Clinical features, model systems and pathways (Q38923380) (← links)
- Evidence of Oxidative Stress and Secondary Mitochondrial Dysfunction in Metabolic and Non-Metabolic Disorders (Q41161393) (← links)
- Oxidative stress and disturbed glutamate transport in spinal muscular atrophy (Q44230702) (← links)
- Cancer in xeroderma pigmentosum and related disorders of DNA repair (Q46465906) (← links)
- Mechanisms of neurodegeneration in mucopolysaccharidoses II and IIIB: analysis of human brain tissue (Q46865312) (← links)
- Mechanisms of neurodegeneration in neuronal ceroid-lipofuscinoses (Q46933595) (← links)
- A 35-year-old female with growth and developmental retardation, progressive ataxia, dementia and visual loss (Q48933397) (← links)
- Rare single nucleotide polymorphisms in the regulatory regions of the superoxide dismutase genes in autism spectrum disorder (Q50309573) (← links)