| scholarly article | Q13442814 |
| P50 | author | Alessandro Achilli | Q28468771 |
| Antonio Salas | Q30504065 | ||
| Yong-Gang Yao | Q47667115 | ||
| Hans-Jürgen Bandelt | Q102165184 | ||
| P2093 | author name string | Antonio Torroni | |
| Ya-Ping Zhang | |||
| Chang Sun | |||
| Shi-Fang Wu | |||
| Li Zhong | |||
| Qing-Peng Kong | |||
| Cheng-Ye Wang | |||
| Chun-Ling Zhu | |||
| P2860 | cites work | Traces of archaic mitochondrial lineages persist in Austronesian-speaking Formosan populations | Q21092807 |
| Major genomic mitochondrial lineages delineate early human expansions | Q21093396 | ||
| Single, Rapid Coastal Settlement of Asia Revealed by Analysis of Complete Mitochondrial Genomes | Q22065802 | ||
| The effects of human population structure on large genetic association studies | Q22337233 | ||
| Saami and Berbers--an unexpected mitochondrial DNA link | Q24531584 | ||
| Phylogeny of east Asian mitochondrial DNA lineages inferred from complete sequences | Q24532849 | ||
| Phylogenetic network for European mtDNA. | Q24533541 | ||
| The molecular dissection of mtDNA haplogroup H confirms that the Franco-Cantabrian glacial refuge was a major source for the European gene pool | Q24534129 | ||
| Phylogeny of mitochondrial DNA macrohaplogroup N in India, based on complete sequencing: implications for the peopling of South Asia | Q24534168 | ||
| The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs | Q24540081 | ||
| The matrilineal ancestry of Ashkenazi Jewry: portrait of a recent founder event | Q24540769 | ||
| Natural selection shaped regional mtDNA variation in humans | Q24541289 | ||
| Mitochondrial genome variation in eastern Asia and the peopling of Japan | Q24562348 | ||
| Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups | Q24563892 | ||
| Analysis of mitochondrial DNA diversity in the aleuts of the commander islands and its implications for the genetic history of beringia | Q24612500 | ||
| Phylogeographic differentiation of mitochondrial DNA in Han Chinese | Q24632824 | ||
| More evidence for non-maternal inheritance of mitochondrial DNA? | Q24674207 | ||
| A critical reassessment of the role of mitochondria in tumorigenesis | Q24810557 | ||
| Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA | Q27860870 | ||
| Mitochondrial genome variation and the origin of modern humans | Q28141023 | ||
| An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy | Q28156628 | ||
| Mitochondrial genome variation and evolutionary history of Australian and New Guinean aborigines | Q28184498 | ||
| Mitochondrial DNA sequence polymorphisms of five ethnic populations from northern China | Q28203371 | ||
| Reconstructing the evolutionary history of China: a caveat about inferences drawn from ancient DNA | Q28211204 | ||
| Expanding Southwest Pacific mitochondrial haplogroups P and Q | Q28243842 | ||
| Genetic origins of the Ainu inferred from combined DNA analyses of maternal and paternal lineages | Q28248069 | ||
| Reconstructing the origin of Andaman Islanders | Q28250416 | ||
| Mitochondrial DNA diversity in indigenous populations of the southern extent of Siberia, and the origins of Native American haplogroups | Q28301593 | ||
| Sequence polymorphisms of the mitochondrial DNA control region and phylogenetic analysis of mtDNA lineages in the Japanese population | Q29040386 | ||
| Population structure, differential bias and genomic control in a large-scale, case-control association study | Q29614945 | ||
| Detecting errors in mtDNA data by phylogenetic analysis | Q30666169 | ||
| A call for mtDNA data quality control in forensic science | Q30919522 | ||
| Association mapping in structured populations | Q33903172 | ||
| Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy | Q33904852 | ||
| Ancient mitochondrial M haplogroups identified in the Southwest Pacific | Q33948044 | ||
| Different matrilineal contributions to genetic structure of ethnic groups in the silk road region in china | Q33980765 | ||
| Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees. | Q34507282 | ||
| mtDNA mutations and common neurodegenerative disorders | Q36254228 | ||
| Mechanism of somatic mitochondrial DNA mutations associated with age and diseases | Q40437270 | ||
| Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNA(Lys) gene. | Q40489976 | ||
| The A8296G mtDNA mutation associated with several mitochondrial diseases does not cause mitochondrial dysfunction in cybrid cell lines. | Q40749197 | ||
| Attenuation of free radical production and paracrystalline inclusions by creatine supplementation in a patient with a novel cytochrome b mutation | Q42459462 | ||
| A reappraisal of complete mtDNA variation in East Asian families with hearing impairment | Q42491866 | ||
| Genetic relationship of Chinese ethnic populations revealed by mtDNA sequence diversity | Q42674284 | ||
| To trust or not to trust an idiosyncratic mitochondrial data set. | Q42927562 | ||
| Errors, phantoms and otherwise, in human mtDNA sequences | Q42927620 | ||
| 'Racial' differences in genetic effects for complex diseases | Q44586727 | ||
| Mitochondrial DNA 3644T-->C mutation associated with bipolar disorder | Q45144296 | ||
| Palaeoanthropology. Coasting out of Africa | Q46627973 | ||
| A case of CPT deficiency, homoplasmic mtDNA mutation and ragged red fibers at muscle biopsy | Q46707830 | ||
| Sequence polymorphism in the mtDNA HV1 region in Japanese and Chinese | Q47668938 | ||
| Association of the mitochondrial DNA 15497G/A polymorphism with obesity in a middle-aged and elderly Japanese population | Q47707199 | ||
| Mitochondrial DNA variation in Koryaks and Itel'men: population replacement in the Okhotsk Sea-Bering Sea region during the Neolithic | Q47730304 | ||
| Frontotemporal dementia and mitochondrial DNA transitions | Q47986294 | ||
| Low "penetrance" of phylogenetic knowledge in mitochondrial disease studies | Q48133900 | ||
| A new database of mitochondrial DNA hypervariable regions I and II sequences from 162 Japanese individuals | Q48299045 | ||
| Atypical MELAS associated with mitochondrial tRNA(Lys) gene A8296G mutation | Q48418646 | ||
| Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation. | Q50476427 | ||
| Leber's hereditary optic neuropathy: the spectrum of mitochondrial DNA mutations in Iranian patients. | Q51679328 | ||
| Detection of mitochondrial DNA mutations in gestational trophoblastic disease. | Q54764043 | ||
| Mitochondrial genes and schizophrenia | Q57305100 | ||
| Genomic Control to the extreme | Q58047101 | ||
| Mitochondrial DNA 5178A polymorphism and longevity | Q59295608 | ||
| P433 | issue | 13 | |
| P921 | main subject | phylogenetics | Q171184 |
| P304 | page(s) | 2076-2086 | |
| P577 | publication date | 2006-05-19 | |
| P1433 | published in | Human Molecular Genetics | Q2720965 |
| P1476 | title | Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations | |
| P478 | volume | 15 |
| Q38752245 | A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNAGlu and Mitochondrial Dysfunction. |
| Q37073167 | A Hypertension-Associated tRNAAla Mutation Alters tRNA Metabolism and Mitochondrial Function. |
| Q37184894 | A MELAS syndrome family harboring two mutations in mitochondrial genome |
| Q33800122 | A Protocol for mtGenome Analysis on Large Sample Numbers. |
| Q28277415 | A counter-clockwise northern route of the Y-chromosome haplogroup N from Southeast Asia towards Europe |
| Q35070116 | A genetic contribution from the Far East into Ashkenazi Jews via the ancient Silk Road |
| Q39889927 | A genetic investigation of Korean mummies from the Joseon Dynasty. |
| Q39938178 | A great diversity of Amerindian mitochondrial DNA ancestry is present in the Mexican mestizo population. |
| Q24681638 | A mitochondrial stratigraphy for island southeast Asia |
| Q21283743 | A new deep branch of eurasian mtDNA macrohaplogroup M reveals additional complexity regarding the settlement of Madagascar |
| Q50526524 | A new mitochondria-related disease showing myopathy with episodic hyper-creatine kinase-emia. |
| Q30479483 | A six-generation Chinese family in haplogroup B4C1C exhibits high penetrance of 1555A > G-induced hearing Loss |
| Q34997395 | Amerindian mitochondrial DNA haplogroups predominate in the population of Argentina: towards a first nationwide forensic mitochondrial DNA sequence database |
| Q46639265 | Analysis of mitochondrial genome diversity identifies new and ancient maternal lineages in Cambodian aborigines |
| Q35233693 | Ancient inland human dispersals from Myanmar into interior East Asia since the Late Pleistocene |
| Q33513243 | Applications of MALDI-TOF MS to large-scale human mtDNA population-based studies |
| Q54655780 | Are ATPase6 polymorphisms associated with primary ovarian insufficiency? |
| Q24606584 | Autosomal and uniparental portraits of the native populations of Sakha (Yakutia): implications for the peopling of Northeast Eurasia |
| Q46515103 | Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation. |
| Q46244123 | Breast cancer-associated mitochondrial DNA haplogroup promotes neoplastic growth via ROS-mediated AKT activation. |
| Q57265539 | Bulgarians vs the other European populations: a mitochondrial DNA perspective |
| Q33655597 | Cancer type-specific modulation of mitochondrial haplogroups in breast, colorectal and thyroid cancer. |
| Q43948751 | Challenging views on the peopling history of East Asia: the story according to HLA markers |
| Q60296943 | Chapter 29 Mitochondrial DNA: future challenges in forensic genetics |
| Q28273717 | Climate change and postglacial human dispersals in southeast Asia |
| Q52628983 | Clinical and molecular characterization of a Han Chinese family with high penetrance of essential hypertension. |
| Q92839200 | Clinical and molecular features of a Han Chinese family with maternally transmitted hypertension |
| Q21090943 | Complete mitochondrial DNA analysis of eastern Eurasian haplogroups rarely found in populations of northern Asia and eastern Europe |
| Q36511591 | Complete mitochondrial DNA genome sequence variation of Chinese families with mutation m.3635G>A and Leber hereditary optic neuropathy |
| Q41436208 | Complete mitochondrial DNA sequences provide new insights into the Polynesian motif and the peopling of Madagascar |
| Q53101980 | Comprehensive analysis of common and rare mitochondrial DNA variants in elite Japanese athletes: a case-control study. |
| Q47804057 | Consistent treatment of length variants in the human mtDNA control region: a reappraisal |
| Q33430993 | Contamination and sample mix-up can best explain some patterns of mtDNA instabilities in buccal cells and oral squamous cell carcinoma |
| Q91712161 | Contribution of Mitochondrial DNA Variation to Chronic Disease in East Asian Populations |
| Q47653533 | Contribution of the tRNAIle 4317A>G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A>G mutation |
| Q37193896 | Coronary heart disease is associated with a mutation in mitochondrial tRNA. |
| Q22252552 | Correcting for purifying selection: an improved human mitochondrial molecular clock |
| Q28709064 | DNA analysis of an early modern human from Tianyuan Cave, China |
| Q46358704 | Deciphering the signature of selective constraints on cancerous mitochondrial genome |
| Q28728930 | Decrypting the mitochondrial gene pool of modern Panamanians |
| Q45776742 | Detecting the somatic mutations spectrum of Chinese lung cancer by analyzing the whole mitochondrial DNA genomes |
| Q54185676 | Developing a multiplex mtSNP assay for forensic application in Han Chinese based on mtDNA phylogeny and hot spot. |
| Q36148241 | Development of a multiplex single base extension assay for mitochondrial DNA haplogroup typing. |
| Q33361663 | Distilling artificial recombinants from large sets of complete mtDNA genomes |
| Q28270040 | East Asian mtDNA haplogroup determination in Koreans: haplogroup-level coding region SNP analysis and subhaplogroup-level control region sequence analysis |
| Q36334137 | Effects of mitochondrial haplogroup N9a on type 2 diabetes mellitus and its associated complications |
| Q79796179 | Enrichment of longevity phenotype in mtDNA haplogroups D4b2b, D4a, and D5 in the Japanese population |
| Q84417029 | Evaluating mitochondrial DNA in patients with breast cancer and benign breast disease |
| Q34636458 | Evaluating self-declared ancestry of U.S. Americans with autosomal, Y-chromosomal and mitochondrial DNA. |
| Q21136190 | Evidence for sub-haplogroup h5 of mitochondrial DNA as a risk factor for late onset Alzheimer's disease |
| Q33883640 | Evolutionary analyses of entire genomes do not support the association of mtDNA mutations with Ras/MAPK pathway syndromes |
| Q54190674 | Exploring the maternal history of the Tai people. |
| Q33292683 | External contamination in single cell mtDNA analysis |
| Q45733943 | Forensic and phylogeographic characterization of mtDNA lineages from northern Thailand (Chiang Mai). |
| Q34531549 | Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics |
| Q42659457 | Gender bias in the multiethnic genetic composition of central Argentina |
| Q46270458 | Generation and Bioenergetic Profiles of Cybrids with East Asian mtDNA Haplogroups |
| Q33807738 | Genetic affinities between the Yami tribe people of Orchid Island and the Philippine Islanders of the Batanes archipelago |
| Q28244277 | Genetic diversity and evidence for population admixture in Batak Negritos from Palawan |
| Q34345228 | Genetic evidence of paleolithic colonization and neolithic expansion of modern humans on the tibetan plateau |
| Q47251222 | Genetic features of ancient West Siberian people of the Middle Ages, revealed by mitochondrial DNA haplogroup analysis |
| Q21283882 | Genetic origin, admixture, and asymmetry in maternal and paternal human lineages in Cuba |
| Q38039842 | Haplogrouping mitochondrial DNA sequences in Legal Medicine/Forensic Genetics |
| Q55396033 | Hi-MC: a novel method for high-throughput mitochondrial haplogroup classification. |
| Q35080298 | High-throughput sequencing of a South American Amerindian |
| Q21284115 | Human evolution in Siberia: from frozen bodies to ancient DNA |
| Q29300605 | Identification of kinship and occupant status in Mongolian noble burials of the Yuan Dynasty through a multidisciplinary approach |
| Q38003304 | Impaired mitochondrial function in psychiatric disorders |
| Q21284051 | In search of the genetic footprints of Sumerians: a survey of Y-chromosome and mtDNA variation in the Marsh Arabs of Iraq |
| Q33789588 | Inland post-glacial dispersal in East Asia revealed by mitochondrial haplogroup M9a'b |
| Q24288726 | Investigating the role of mitochondrial haplogroups in genetic predisposition to meningococcal disease |
| Q30570775 | Large-scale mitochondrial DNA analysis in Southeast Asia reveals evolutionary effects of cultural isolation in the multi-ethnic population of Myanmar |
| Q40511873 | Leber Hereditary Optic Neuropathy: A Mitochondrial Disease Unique in Many Ways |
| Q34735172 | Leber's hereditary optic neuropathy affects only female matrilineal relatives in two Chinese families |
| Q34000675 | Leber's hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation |
| Q37445425 | Leber's hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutation |
| Q33679205 | Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation |
| Q54251109 | Maternal genetic backgrounds contribute to the genetic susceptibility of tongue cancer patients in Hunan, central of China. |
| Q50357935 | Maternally transmitted aminoglycoside-induced and non-syndromic hearing loss caused by the 1494C > T mutation in the mitochondrial 12S rRNA gene in two Chinese families. |
| Q43525882 | Median network analysis of defectively sequenced entire mitochondrial genomes from early and contemporary disease studies |
| Q33325729 | Minisequencing mitochondrial DNA pathogenic mutations |
| Q30950224 | MitoVariome: a variome database of human mitochondrial DNA. |
| Q41644724 | Mitochondrial DNA Haplogroup A may confer a genetic susceptibility to AIDS group from Southwest China |
| Q47127732 | Mitochondrial DNA Mutations Associated with Type 2 Diabetes Mellitus in Chinese Uyghur Population |
| Q34219889 | Mitochondrial DNA analysis of Hokkaido Jomon skeletons: remnants of archaic maternal lineages at the southwestern edge of former Beringia |
| Q47447579 | Mitochondrial DNA analysis of Yayoi period human skeletal remains from the Doigahama site |
| Q31067787 | Mitochondrial DNA copy number, but not haplogroup, confers a genetic susceptibility to leprosy in Han Chinese from Southwest China |
| Q43510173 | Mitochondrial DNA depletion, mitochondrial mutations and high TFAM expression in hepatocellular carcinoma |
| Q21562568 | Mitochondrial DNA haplogroup D4a is a marker for extreme longevity in Japan |
| Q48946315 | Mitochondrial DNA haplogroup R in the Han population and recovery from septic encephalopathy |
| Q45147836 | Mitochondrial DNA haplogroup R predicts survival advantage in severe sepsis in the Han population |
| Q21562287 | Mitochondrial DNA haplogroup analysis reveals no association between the common genetic lineages and prostate cancer in the Korean population |
| Q37436981 | Mitochondrial DNA haplogroup associated with sperm motility in the Han population |
| Q37539168 | Mitochondrial DNA haplogroup confers genetic susceptibility to nasopharyngeal carcinoma in Chaoshanese from Guangdong, China. |
| Q33694079 | Mitochondrial DNA haplogroup distribution in Chaoshanese with and without myopia. |
| Q37156232 | Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation |
| Q35627196 | Mitochondrial DNA haplogroups and short-term neurological outcomes of ischemic stroke |
| Q36023873 | Mitochondrial DNA mutation m.10680G > A is associated with Leber hereditary optic neuropathy in Chinese patients |
| Q33728325 | Mitochondrial DNA sequence variation and haplogroup distribution in Chinese patients with LHON and m.14484T>C |
| Q41592993 | Mitochondrial DNA sequencing and large-scale genotyping identifies MT-ND4 gene mutation m.11696G>A associated with idiopathic oligoasthenospermia |
| Q24682875 | Mitochondrial DNA variation of modern Tuscans supports the near eastern origin of Etruscans |
| Q42944161 | Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese families |
| Q21283848 | Mitochondrial and Y-chromosome diversity of the Tharus (Nepal): a reservoir of genetic variation |
| Q35837338 | Mitochondrial diversity within modern human populations |
| Q35015676 | Mitochondrial genome evidence reveals successful Late Paleolithic settlement on the Tibetan Plateau. |
| Q35064864 | Mitochondrial genomes and exceptional longevity in a Chinese population: the Rugao longevity study |
| Q40682178 | Mitochondrial haplogroup D4j specific variant m.11696G > a(MT-ND4) may increase the penetrance and expressivity of the LHON-associated m.11778G > a mutation in Chinese pedigrees |
| Q42930492 | Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation |
| Q53072695 | Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated ND1 G3460A mutation in Chinese families. |
| Q37455749 | Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation |
| Q53675482 | Mitochondrial intergenic COII/tRNA(Lys) 9-bp deletion, a biomarker for hepatocellular carcinoma? |
| Q54337155 | Mitochondrial nt3010G-nt3970C haplotype is implicated in high-altitude adaptation of Tibetans. |
| Q45738904 | Mitochondrial tRNA mutations are associated with maternally inherited hypertension in two Han Chinese pedigrees |
| Q37648407 | Mitochondrial tRNA variants in Chinese subjects with coronary heart disease |
| Q92654743 | Mitochondrial tRNAAla 5601C>T variant may affect the clinical expression of the LHON‑related ND4 11778G>A mutation in a family |
| Q51700019 | Mitochondrial tRNAThr 15891C>G mutation was not associated with Leber's hereditary optic neuropathy in Han Chinese patients. |
| Q82674539 | Mitochondrial variants may influence the phenotypic manifestation of Leber's hereditary optic neuropathy-associated ND4 G11778A mutation |
| Q46315226 | Molecular characterization of a pedigree carrying the hypertension‑associated mitochondrial tRNAGln T4363C mutation |
| Q51577298 | Molecular characterization of six Chinese families with m.3460G>A and Leber hereditary optic neuropathy. |
| Q84077035 | MtDNA control region sequence polymorphisms and phylogenetic analysis of Malay population living in or around Kuala Lumpur in Malaysia |
| Q33503932 | MtSNPscore: a combined evidence approach for assessing cumulative impact of mitochondrial variations in disease |
| Q21562443 | New population and phylogenetic features of the internal variation within mitochondrial DNA macro-haplogroup R0 |
| Q92198280 | Obesity associated with a novel mitochondrial tRNACys 5802A>G mutation in a Chinese family |
| Q33784755 | Origin and post-glacial dispersal of mitochondrial DNA haplogroups C and D in northern Asia |
| Q44474323 | PCA and clustering reveal alternate mtDNA phylogeny of N and M clades |
| Q39025075 | Phylogenetic and population-based approaches to mitogenome variation do not support association with male infertility |
| Q48071982 | Phylogenetic classification of Japanese mtDNA assisted by complete mitochondrial DNA sequences |
| Q24655534 | Phylogeographic analysis of mitochondrial DNA in northern Asian populations |
| Q28240166 | Population history of the Red Sea--genetic exchanges between the Arabian Peninsula and East Africa signaled in the mitochondrial DNA HV1 haplogroup |
| Q28752107 | Population increase and environmental deterioration correspond with microlithic innovations in South Asia ca. 35,000 years ago |
| Q36481986 | Population phylogenomic analysis of mitochondrial DNA in wild boars and domestic pigs revealed multiple domestication events in East Asia |
| Q33733649 | Potential pitfalls in MitoChip detected tumor-specific somatic mutations: a call for caution when interpreting patient data |
| Q33864259 | Reassessing the role of mitochondrial DNA mutations in autism spectrum disorder |
| Q28752054 | Reconstructing Indian-Australian phylogenetic link |
| Q24678187 | Revealing the prehistoric settlement of Australia by Y chromosome and mtDNA analysis |
| Q42866235 | Revision of the mtDNA tree and corresponding haplogroup nomenclature |
| Q47215650 | Revisiting the role of the Himalayas in peopling Nepal: insights from mitochondrial genomes |
| Q37645263 | Role of mtDNA haplogroups in the prevalence of knee osteoarthritis in a southern Chinese population |
| Q90712112 | Screening for mitochondrial 12S rRNA C1494T mutation in 655 patients with non-syndromic hearing loss: An observational study |
| Q41391890 | Simultaneous Whole Mitochondrial Genome Sequencing with Short Overlapping Amplicons Suitable for Degraded DNA Using the Ion Torrent Personal Genome Machine |
| Q33824192 | Southeast Asian diversity: first insights into the complex mtDNA structure of Laos |
| Q24603025 | Strong maternal Khoisan contribution to the South African coloured population: a case of gender-biased admixture |
| Q47886390 | Subhaplogroup D4b1 enhances the risk of cervical cancer initiation: A case-control study in southern China |
| Q36093490 | Survival and mitochondrial function in septic patients according to mitochondrial DNA haplogroup. |
| Q34046457 | Systematic analysis of mitochondrial genes associated with hearing loss in the Japanese population: dHPLC reveals a new candidate mutation |
| Q34268156 | Targeting mitochondrially mediated plasticity to develop improved therapeutics for bipolar disorder |
| Q44845428 | The Himalayas: barrier and conduit for gene flow |
| Q47322474 | The Soliga, an isolated tribe from Southern India: genetic diversity and phylogenetic affinities. |
| Q42179831 | The Use and Effectiveness of Triple Multiplex System for Coding Region Single Nucleotide Polymorphism in Mitochondrial DNA Typing of Archaeologically Obtained Human Skeletons from Premodern Joseon Tombs of Korea |
| Q56874049 | The acquisition of an inheritable 50-bp deletion in the human mtDNA control region does not affect the mtDNA copy number in peripheral blood cells |
| Q34389694 | The case for the continuing use of the revised Cambridge Reference Sequence (rCRS) and the standardization of notation in human mitochondrial DNA studies |
| Q36470441 | The creation of cybrids harboring mitochondrial haplogroups in the Taiwanese population of ethnic Chinese background: an extensive in vitro tool for the study of mitochondrial genomic variations |
| Q24647197 | The first Korean genome sequence and analysis: full genome sequencing for a socio-ethnic group |
| Q34634474 | The genetic legacy of the pre-colonial period in contemporary Bolivians |
| Q21133751 | The history of Slavs inferred from complete mitochondrial genome sequences |
| Q41399798 | The mitochondrial tRNA(Gln) T4353C mutation may not be associated with essential hypertension in Han Chinese population |
| Q21144337 | The phylogeny of the four pan-American MtDNA haplogroups: implications for evolutionary and disease studies |
| Q79451011 | The role of climate in human mitochondrial DNA evolution: a reappraisal |
| Q36183037 | The role of mitochondrial tRNA mutations in lung cancer |
| Q34267442 | The saga of the many studies wrongly associating mitochondrial DNA with breast cancer |
| Q38857934 | The tRNA(Gly) T10003C mutation in mitochondrial haplogroup M11b in a Chinese family with diabetes decreases the steady-state level of tRNA(Gly), increases aberrant reactive oxygen species production, and reduces mitochondrial membrane potential |
| Q28649774 | Toward a mtDNA locus-specific mutation database using the LOVD platform |
| Q24632852 | Traces of sub-Saharan and Middle Eastern lineages in Indian Muslim populations |
| Q21284038 | Tracing the legacy of the early Hainan Islanders--a perspective from mitochondrial DNA |
| Q84427617 | Typing of 24 mtDNA SNPs in a Chinese population using SNaPshot minisequencing |
| Q33955150 | Uncovering the profile of somatic mtDNA mutations in Chinese colorectal cancer patients |
| Q50434325 | Unique penetrance of hearing loss in a five-generation Chinese family with the mitochondrial 12S rRNA 1555A > G mutation. |
| Q21091177 | Updating phylogeny of mitochondrial DNA macrohaplogroup m in India: dispersal of modern human in South Asian corridor |
| Q34005399 | Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation |
| Q33729752 | Very low penetrance of Leber's hereditary optic neuropathy in five Han Chinese families carrying the ND1 G3460A mutation |
| Q50461556 | What is a 'novel' mtDNA mutation--and does 'novelty' really matter? |
| Q47994847 | mtDNA Heteroplasmy in Monozygotic Twins Discordant for Schizophrenia |
| Q51167618 | mtDNA lineage expansions in Sherpa population suggest adaptive evolution in Tibetan highlands. |
| Q43559138 | mtDNA variation in the Buryat population of the Barguzin Valley: New insights into the micro-evolutionary history of the Baikal area. |
| Q33384977 | mtDNAmanager: a Web-based tool for the management and quality analysis of mitochondrial DNA control-region sequences |
Search more.