Somatic mitochondrial DNA mutations in early parkinson and incidental lewy body disease

التفاصيل البيبلوغرافية
العنوان: Somatic mitochondrial DNA mutations in early parkinson and incidental lewy body disease
المؤلفون: David Simon, Rebecca A. Betensky, Thomas Arzberger, Ippolita Cantuti-Castelvetri, Yong B. Tan, Michael T. Lin, Kangni Zheng, Andrew J. Lees, M. Flint Beal, Katie E. Jackson
المصدر: Annals of Neurology. 71:850-854
بيانات النشر: Wiley, 2012.
سنة النشر: 2012
مصطلحات موضوعية: Lewy Body Disease, Male, Pathology, medicine.medical_specialty, Mitochondrial DNA, Somatic cell, DNA Mutational Analysis, Substantia nigra, Laser Capture Microdissection, Disease, Biology, medicine.disease_cause, DNA, Mitochondrial, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, medicine, Humans, Aged, 030304 developmental biology, Laser capture microdissection, Aged, 80 and over, Neurons, 0303 health sciences, Mutation, Brain, Parkinson Disease, Middle Aged, medicine.anatomical_structure, Neurology, chemistry, Neuroglia, Female, Neurology (clinical), 030217 neurology & neurosurgery, DNA
الوصف: Somatic mutations in mitochondrial DNA (mtDNA) are hypothesized to play a role in Parkinson disease (PD), but large increases in mtDNA mutations have not previously been found in PD, potentially because neurons with high mutation levels degenerate and thus are absent in late stage tissue. To address this issue, we studied early stage PD cases and cases of incidental Lewy body disease (ILBD), which is thought to represent presymptomatic PD. We show for the first time that mtDNA mutation levels in substantia nigra neurons are significantly elevated in this group of early PD and ILBD cases.
تدمد: 0364-5134
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::066bbb120815cbb0de9decc5d262ff67
https://doi.org/10.1002/ana.23568
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....066bbb120815cbb0de9decc5d262ff67
قاعدة البيانات: OpenAIRE