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Mechanisms of Ageing and Development, ISSN 0047-6374, 01/2015, Volume 145, pp. 13 - 17
Journal Article
Current aging science, 2013, Volume 6, Issue 3, pp. 244 - 250
Journal Article
Current aging science, 12/2013, Volume 6, Issue 3, p. 244
The shortening of telomeres with ageing is a well-documented observation; however, the reported number of nucleotides in telomeres varies between different... 
Leukocytes, Mononuclear - metabolism | Age Factors | Humans | Middle Aged | Male | Telomere Homeostasis | Case-Control Studies | Aging - blood | Young Adult | Latvia | Telomere Shortening | Aging - genetics | Time Factors | Cellular Senescence | Aged, 80 and over | Adult | Female | Aged | Telomere - metabolism
Journal Article
Proceedings of the Latvian Academy of Sciences. Section B. Natural, Exact, and Applied Sciences, ISSN 1407-009X, 06/2018, Volume 72, Issue 3, pp. 131 - 151
This article presents a review on population genetics of Latvians, which alongside Lithuanians are the two extant Baltic speaking populations. The article... 
population genetics | Latvians | autosomes | mitochondrial DNA | Y chromosome | Subpopulations | Territory | Populations | Admixtures | Gene pool | Population studies | Genomes | Mitochondrial DNA | Single-nucleotide polymorphism | Minority & ethnic groups | Population genetics | Gene flow | Genetic markers | Genetics | Stone Age | Y Chromosomes | Deoxyribonucleic acid--DNA | Polymorphism
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 2004, Volume 74, Issue 4, pp. 661 - 682
Journal Article
European Journal of Oral Sciences, ISSN 0909-8836, 12/2011, Volume 119, Issue 6, pp. 413 - 417
Journal Article
Mitochondrion, ISSN 1567-7249, 2011, Volume 11, Issue 2, pp. 357 - 359
Latvia has one of the highest prevalence of isolated cleft lip with or without cleft palate (CL/P) in Europe. To clarify the genetic origins of the Latvian... 
Cleft lip/palate | Mitochondrial haplogroups | WESTERN | PALATE | REGION | CELL BIOLOGY | CHROMOSOME 8Q24 | EUROPE | LIP | MTDNA | GENETICS & HEREDITY | DUPLICATION | SUSCEPTIBILITY LOCUS | ASSOCIATION | Genetics, Population | Cleft Lip - genetics | Latvia | Cleft Palate - genetics | DNA, Mitochondrial - genetics | Humans | Index Medicus
Journal Article
Proceedings of the Latvian Academy of Sciences. Section B. Natural, Exact, and Applied Sciences, ISSN 1407-009X, 04/2015, Volume 69, Issue 1, pp. 8 - 13
Sex determination is one of the most important and initial steps in human profile identification from archaeological material. The aim of the current study was... 
anthropological characteristics | ancient DNA | amelogenin | archaeological material | Ancient DNA | Anthropological characteristics | SRY | Amelogenin | Archaeological material
Journal Article
Mitochondrial DNA Part A, ISSN 2470-1394, 04/2018, Volume 29, Issue 3, pp. 431 - 438
We studied telomere length (TL) and mitochondrial DNA (mtDNA) copy number variations in individuals from Latvian Caucasian population in different age groups.... 
heteroplasmy | Mitochondria | haplogroups | nonagenarians | mtDNA copy number | telomeres | European Continental Ancestry Group - genetics | Age Distribution | Humans | Middle Aged | Male | Telomere Homeostasis | Young Adult | Latvia | DNA, Mitochondrial - genetics | Aging - genetics | Mitochondria - genetics | Aged, 80 and over | Adult | Female | Aged | Telomere - genetics | Index Medicus
Journal Article
Proceedings of the Latvian Academy of Sciences. Section B. Natural, Exact, and Applied Sciences, ISSN 1407-009X, 1/2008, Volume 62, Issue 6, pp. 193 - 198
Atrial natriuretic peptide (ANP) appears to have a physiological role in volume and pressure homeostasis. Increased cardiac expression and synthesis of ANP... 
polymorphic restriction sites | ANP gene | primary open-angle glaucoma | pro-ANP level
Journal Article
Mitochondrial DNA Part A, ISSN 2470-1394, 10/2018, Volume 29, Issue 7, pp. 1115 - 1120
The most common mitochondrial disorder in children is Leigh syndrome, which is a progressive and genetically heterogeneous neurodegenerative disorder caused by... 
brain MRI | Leigh syndrome | mitochondrial DNA | MITOCHONDRIAL-DNA MUTATIONS | MTATP6 GENE | GENETICS & HEREDITY | MUSCLE | mitochondria DNA | DISEASE PHENOTYPES | MELAS | COMMON-CAUSE | I-DEFICIENCY | CHILDREN | DNA, Mitochondrial - genetics | Humans | Child, Preschool | Female | Infant | Male | Mutation | Leigh Disease - genetics | Leigh Disease - pathology | Index Medicus
Journal Article