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Frontiers in Bioscience (Elite Edition)|December 29, 2011
Sex, death and the (nerve) cellKatarzyna Tonska, Ewa BartnikToxicology Mechanisms and Methods|December 22, 2009
Mitochondrial DNA in polish centenariansAnna Lorenc, Katarzyna Tonska, Dagmara Kabzinska, et al.Experimental Eye Research|October 13, 2018
Investigation of whole mitochondrial genome variation in normal tension glaucomaAgnieszka Piotrowska-Nowak, Ewa Kosior-Jarecka, Aleksandra Schab, et al.Mitochondrion|September 20, 2008
A family with 3460G>A and 11778G>A mutations and haplogroup analysis of Polish Leber hereditary optic neuropathy patientsKatarzyna Tonska, Marzena Kurzawa, Anna M Ambroziak, et al.Human Molecular Genetics|August 14, 2003
Investigation of a pathogenic mtDNA microdeletion reveals a translation-dependent deadenylation decay pathway in human mitochondriaRichard J Temperley, Sara H Seneca, Katarzyna Tonska, et al.Frontiers in Genetics|January 24, 2019
New mtDNA Association Model, MutPred Variant Load, Suggests Individuals With Multiple Mildly Deleterious mtDNA Variants Are More Likely to Suffer From AtherosclerosisAgnieszka Piotrowska-Nowak, Joanna L Elson, Agnieszka Sobczyk-Kopciol, et al.Folia Neuropathologica|January 8, 2008
G8363A mitochondrial DNA mutation is not a rare cause of Leigh syndrome - clinical, biochemical and pathological study of an affected childMaciej Pronicki, Jolanta Sykut-Cegielska, Ewa Matyja, et al.Neurologia I Neurochirurgia Polska|February 8, 2017
Identification of the first in Poland CACNA1A gene mutation in familial hemiplegic migraine. Case reportBiruta Kierdaszuk, Dorota Dziewulska, Ewa Pronicka, et al.Journal of Biomedical Science|September 10, 2010
Mitochondrial genotype in vulvar carcinoma - cuckoo in the nestAleksandra Klemba, Magdalena Kowalewska, Wojciech Kukwa, et al.Postepy Biochemii|August 20, 2014
[The role of reactive oxygen species and mitochondria in aging]Agnieszka Piotrowska, Ewa BartnikPageof 9