Pages that link to "Q34535168"
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The following pages link to Mitochondrial dysfunction in the neuronal ceroid-lipofuscinoses (Batten disease). (Q34535168):
Displaying 30 items.
- Autophagy, mitochondria and oxidative stress: cross-talk and redox signalling (Q24608960) (← links)
- The Role of Autophagy, Mitophagy and Lysosomal Functions in Modulating Bioenergetics and Survival in the Context of Redox and Proteotoxic Damage: Implications for Neurodegenerative Diseases (Q26750137) (← links)
- Neurodegeneration and Epilepsy in a Zebrafish Model of CLN3 Disease (Batten Disease) (Q27339580) (← links)
- Autophagy is disrupted in a knock-in mouse model of juvenile neuronal ceroid lipofuscinosis (Q28591948) (← links)
- Alterations in ROS activity and lysosomal pH account for distinct patterns of macroautophagy in LINCL and JNCL fibroblasts (Q31110961) (← links)
- Aberrant Ca2+ handling in lysosomal storage disorders (Q33727058) (← links)
- Lysosomal function in macromolecular homeostasis and bioenergetics in Parkinson's disease (Q33843073) (← links)
- An atypical case of neuronal ceroid lipofuscinosis with co-inheritance of a variably penetrant POLG1 mutation (Q34315263) (← links)
- Aging in the canine and feline brain (Q34625739) (← links)
- The cell biology of lysosomal storage disorders (Q35825859) (← links)
- Nitric oxide signaling is disrupted in the yeast model for Batten disease (Q35901877) (← links)
- Mitochondrial Ca2+ homeostasis in lysosomal storage diseases (Q37074786) (← links)
- Pathophysiology of neuropathic lysosomal storage disorders (Q37739318) (← links)
- Lysosomal storage disorders and Parkinson's disease: Gaucher disease and beyond (Q37880734) (← links)
- Neuronal ceroid lipofuscinosis: impact of recent genetic advances and expansion of the clinicopathologic spectrum (Q38115191) (← links)
- Neuronopathic lysosomal storage diseases: clinical and pathologic findings. (Q38116812) (← links)
- Genetic convergence of Parkinson's disease and lysosomal storage disorders (Q38237560) (← links)
- Mining for mitochondrial mechanisms: linking known syndromes to mitochondrial function (Q38689523) (← links)
- Mitochondrial adventures at the organelle society (Q39272436) (← links)
- Mitochondrial Dysfunction in Lysosomal Storage Disorders (Q41970073) (← links)
- Proteomic mapping of differentially vulnerable pre-synaptic populations identifies regulators of neuronal stability in vivo (Q42069362) (← links)
- Enhanced expression of manganese-dependent superoxide dismutase in human and sheep CLN6 tissues (Q42251158) (← links)
- Neuronal ceroid lipofuscinosis genes, CLN2, CLN3 and CLN5 are spatially and temporally co-expressed in a developing mouse brain (Q43851305) (← links)
- A278C mutation of dihydropteridine reductase decreases autophagy via mTOR signaling (Q46347228) (← links)
- Neuronal ceroid-lipofuscinosis in a Holstein steer (Q46433870) (← links)
- Neuronal ceroid-lipofuscinosis in Borderdale sheep (Q46609453) (← links)
- Mitochondrial aberrations in mucolipidosis Type IV. (Q48390239) (← links)
- The problematic issue of Kufs disease diagnosis as performed on rectal biopsies: a case report (Q51033513) (← links)
- Mitochondrial biogenesis is transcriptionally repressed in lysosomal lipid storage diseases (Q61795799) (← links)
- Proteomic and functional analyses in disease models reveal CLN5 protein involvement in mitochondrial dysfunction (Q91644975) (← links)