Maternal transmission of Alzheimer's disease: prodromal metabolic phenotype and the search for genes. - Test2 - elhamkhani - TriplyDB

Maternal transmission of Alzheimer's disease: prodromal metabolic phenotype and the search for genes.

Maternal transmission of Alzheimer's disease: prodromal metabolic phenotype and the search for genes.

http://www.wikidata.org/entity/Q34552263

about

Common defects of mitochondria and iron in neurodegeneration and diabetes (MIND): a paradigm worth exploring Mitochondrial abnormalities in Alzheimer's disease: possible targets for therapeutic intervention Mitochondria-Derived Damage-Associated Molecular Patterns in Neurodegeneration.New Therapeutics to Modulate Mitochondrial Function in Neurodegenerative Disorders.Oxidative stress and amyloid-beta pathology in normal individuals with a maternal history of Alzheimer's.Alzheimer's and ABC transporters--new opportunities for diagnostics and treatment.Mitochondrial genomic analysis of late onset Alzheimer's disease reveals protective haplogroups H6A1A/H6A1B: the Cache County Study on Memory in Aging Progressive regional atrophy in normal adults with a maternal history of Alzheimer disease.FDG and Amyloid PET in Cognitively Normal Individuals at Risk for Late-Onset Alzheimer's Disease.Mitochondria, Amyloid β, and Alzheimer's Disease Structural brain changes in normal individuals with a maternal history of Alzheimer's.Maternal age affects brain metabolism in adult children of mothers affected by Alzheimer's disease.Using biomarkers to improve detection of Alzheimer's disease.Alcohol-induced blackouts and maternal family history of problematic alcohol use.Genetic and epigenetic underpinnings of sex differences in the brain and in neurological and psychiatric disease susceptibility FDG- and amyloid-PET in Alzheimer's disease: is the whole greater than the sum of the parts?Reduced mitochondria cytochrome oxidase activity in adult children of mothers with Alzheimer's disease.Mitochondria and cell bioenergetics: increasingly recognized components and a possible etiologic cause of Alzheimer's disease.Role and treatment of mitochondrial DNA-related mitochondrial dysfunction in sporadic neurodegenerative diseases.Maternal transmission of Alzheimer disease.Amyloid and metabolic positron emission tomography imaging of cognitively normal adults with Alzheimer's parents Estrogen receptor β in Alzheimer's disease: From mechanisms to therapeutics.Maternal family history is associated with Alzheimer's disease biomarkers Mitochondrial DNA polymorphisms specifically modify cerebral β-amyloid proteostasis Impaired mitochondrial energy production and ABC transporter function-A crucial interconnection in dementing proteopathies of the brain.Brain imaging of cognitively normal individuals with 2 parents affected by late-onset AD.The Alzheimer's disease mitochondrial cascade hypothesis: progress and perspectives.Pre-clinical detection of Alzheimer's disease using FDG-PET, with or without amyloid imaging.The concept of FDG-PET endophenotype in Alzheimer's disease.Rethinking on the concept of biomarkers in preclinical Alzheimer's disease.Antioxidant modulation in restoring mitochondrial function in neurodegeneration.Mitochondria, Cybrids, Aging, and Alzheimer's Disease.Influence of family history of dementia in the development and progression of late-onset Alzheimer's disease.Sex differences in metabolic aging of the brain: insights into female susceptibility to Alzheimer's disease.Mild cognitive impairment, risk factors and magnetic resonance volumetry: role of probable Alzheimer's disease in the family.Maternal imprinting on cognition markers of wild type and transgenic Alzheimer's disease model mice.Molecular mechanisms of long noncoding RNAs and their role in disease pathogenesis.

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Maternal transmission of Alzheimer's disease: prodromal metabolic phenotype and the search for genes.

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2010 nî lūn-bûn

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2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2010 թվականի փետրվարին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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Maternal transmission of Alzhe ...... type and the search for genes.

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Lisa Mosconi

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Ranjan Duara

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Russell H Swerdlow

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P2860

Chronic Parkinsonism in humans due to a product of meperidine-analog synthesis

Neurotrophic and neurotoxic effects of amyloid beta protein: reversal by tachykinin neuropeptides

Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease

APP binds DR6 to trigger axon pruning and neuron death via distinct caspases

Role of Genes and Environments for Explaining Alzheimer Disease

Cytochrome c oxidase and mitochondrial F1F0-ATPase (ATP synthase) activities in platelets and brain from patients with Alzheimer's disease

Evidence for an association between KIBRA and late-onset Alzheimer's disease

Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease

GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers

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Alzheimer's disease

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3033750

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