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1994 1
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2002 1
2004 2
2005 3
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2008 2
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2010 3
2011 2
2012 4
2013 3
2014 4
2015 2
2017 4
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2020 2
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Mitochondrial Haplogroups Affect Severity But Not Prevalence of Diabetic Retinopathy.
Bregman JA, Herren DJ, Estopinal CB, Chocron IM, Harlow PA, Warden C, Brantley MA Jr, Samuels DC. Bregman JA, et al. Invest Ophthalmol Vis Sci. 2017 Feb 1;58(2):1346-1351. doi: 10.1167/iovs.16-20616. Invest Ophthalmol Vis Sci. 2017. PMID: 28245487 Free PMC article.
PURPOSE: We previously reported European mitochondrial haplogroup H to be a risk factor for and haplogroup UK to be protective against proliferative diabetic retinopathy (PDR) among Caucasian patients with diabetic retinopathy (DR) …
PURPOSE: We previously reported European mitochondrial haplogroup H to be a risk factor for and haplogroup UK to be pro …
Mitochondrial haplogroups are associated with severity of diabetic retinopathy.
Estopinal CB, Chocron IM, Parks MB, Wade EA, Roberson RM, Burgess LG, Brantley MA Jr, Samuels DC. Estopinal CB, et al. Invest Ophthalmol Vis Sci. 2014 Aug 12;55(9):5589-95. doi: 10.1167/iovs.14-15149. Invest Ophthalmol Vis Sci. 2014. PMID: 25118268 Free PMC article.
PURPOSE: To determine if specific mitochondrial haplogroups associate with nonproliferative diabetic retinopathy (NPDR) and proliferative diabetic retinopathy (PDR). ...The association was independent of the major clinical variables af
PURPOSE: To determine if specific mitochondrial haplogroups associate with nonproliferative diabetic retinopathy
Differential effects of cisplatin on cybrid cells with varying mitochondrial DNA haplogroups.
Abedi S, Yung G, Atilano SR, Thaker K, Chang S, Chwa M, Schneider K, Udar N, Bota D, Kenney MC. Abedi S, et al. PeerJ. 2020 Oct 1;8:e9908. doi: 10.7717/peerj.9908. eCollection 2020. PeerJ. 2020. PMID: 33062421 Free PMC article.
There is accumulating evidence that an individual's mitochondrial (mt) DNA may play a role in their response to medications. ...CONCLUSION: Our findings suggest that an individual's mtDNA background may be associated with variations in their response to cispl …
There is accumulating evidence that an individual's mitochondrial (mt) DNA may play a role in their response to medications. . …
Mitochondrial DNA haplogroups modulate the radiographic progression of Spanish patients with osteoarthritis.
Soto-Hermida A, Fernández-Moreno M, Pértega-Díaz S, Oreiro N, Fernández-López C, Blanco FJ, Rego-Pérez I. Soto-Hermida A, et al. Rheumatol Int. 2015 Feb;35(2):337-44. doi: 10.1007/s00296-014-3104-1. Epub 2014 Aug 3. Rheumatol Int. 2015. PMID: 25086630
Taking into account the incidence of the mitochondria and the mtDNA haplogroups in the pathogenesis of OA, the main objective of this work was to evaluate the incidence of the mtDNA haplogroups in the radiographic progression of the OA disease in a well-chara …
Taking into account the incidence of the mitochondria and the mtDNA haplogroups in the pathogenesis of OA, the main objective …
Mitochondrial DNA levels in Huntington disease leukocytes and dermal fibroblasts.
Jędrak P, Krygier M, Tońska K, Drozd M, Kaliszewska M, Bartnik E, Sołtan W, Sitek EJ, Stanisławska-Sachadyn A, Limon J, Sławek J, Węgrzyn G, Barańska S. Jędrak P, et al. Metab Brain Dis. 2017 Aug;32(4):1237-1247. doi: 10.1007/s11011-017-0026-0. Epub 2017 May 16. Metab Brain Dis. 2017. PMID: 28508341 Free PMC article.
Here, samples of blood from 84 HD patients and 79 controls, and dermal fibroblasts from 10 HD patients and 9 controls were analysed for mtDNA levels. Although the type of mitochondrial haplogroup had no influence on the mtDNA level, and there was no correlation betw …
Here, samples of blood from 84 HD patients and 79 controls, and dermal fibroblasts from 10 HD patients and 9 controls were analysed for mtDN …
Whole Mitochondrial Genome Analysis in Serbian Cases of Leber's Hereditary Optic Neuropathy.
Dawod PGA, Jancic J, Marjanovic A, Brankovic M, Jankovic M, Samardzic J, Potkonjak D, Djuric V, Mesaros S, Novakovic I, Abdel Motaleb FI, Kostic VS, Nikolic D. Dawod PGA, et al. Genes (Basel). 2020 Sep 2;11(9):1037. doi: 10.3390/genes11091037. Genes (Basel). 2020. PMID: 32887465 Free PMC article.
Leber's hereditary optic neuropathy (LHON) is a maternally inherited disorder that affects central vision in young adults and is typically associated with mitochondrial DNA (mtDNA) mutations. ...MITOMASTER analysis showed that the two well-known primary mutat …
Leber's hereditary optic neuropathy (LHON) is a maternally inherited disorder that affects central vision in young adults and …
Mitochondrial haplotype and phenotype of 13 Chinese families may suggest multi-original evolution of mitochondrial C1494T mutation.
Zhu Y, Li Q, Chen Z, Kun Y, Liu L, Liu X, Yuan H, Zhai S, Han D, Dai P. Zhu Y, et al. Mitochondrion. 2009 Nov;9(6):418-28. doi: 10.1016/j.mito.2009.07.006. Epub 2009 Aug 12. Mitochondrion. 2009. PMID: 19682603
Mutations in mitochondrial DNA (mtDNA) are associated with sensorineural hearing loss. ...These results suggested that both T 5628C and A5836G mutations might not significantly modify the manifestation of the C1494T mutation. Sequencing analysis of the whole mitochondri
Mutations in mitochondrial DNA (mtDNA) are associated with sensorineural hearing loss. ...These results suggested that both T 5628C a …
What is influencing the phenotype of the common homozygous polymerase-γ mutation p.Ala467Thr?
Neeve VC, Samuels DC, Bindoff LA, van den Bosch B, Van Goethem G, Smeets H, Lombès A, Jardel C, Hirano M, Dimauro S, De Vries M, Smeitink J, Smits BW, de Coo IF, Saft C, Klopstock T, Keiling BC, Czermin B, Abicht A, Lochmüller H, Hudson G, Gorman GG, Turnbull DM, Taylor RW, Holinski-Feder E, Chinnery PF, Horvath R. Neeve VC, et al. Brain. 2012 Dec;135(Pt 12):3614-26. doi: 10.1093/brain/aws298. Brain. 2012. PMID: 23250882 Free PMC article.
Polymerase-gamma (POLG) is a major human disease gene and may account for up to 25% of all mitochondrial diseases in the UK and in Italy. To date, >150 different pathogenic mutations have been described in POLG. ...Patients with mitochondrial DNA haplog
Polymerase-gamma (POLG) is a major human disease gene and may account for up to 25% of all mitochondrial diseases in the UK an …
[The influence of mitochondrial haplogroup on Leber's hereditary optic neuropathy].
Mao YJ, Qu J, Guan MX. Mao YJ, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Feb;25(1):45-9. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 18247303 Review. Chinese.
Leber's hereditary optic neuropathy (LHON) is a maternally inherited disorder leading to rapid, painless, bilateral and usually permanent central vision loss in young adults, males are preferentially affected. ...In particular, the mitochondrial haplotypes ma …
Leber's hereditary optic neuropathy (LHON) is a maternally inherited disorder leading to rapid, painless, bilateral and usually perma …
Unravelling the Genetic Diversity among Cassava Bemisia tabaci Whiteflies Using NextRAD Sequencing.
Wosula EN, Chen W, Fei Z, Legg JP. Wosula EN, et al. Genome Biol Evol. 2017 Nov 1;9(11):2958-2973. doi: 10.1093/gbe/evx219. Genome Biol Evol. 2017. PMID: 29096025 Free PMC article.
Comparison of the mtCOI and SNP identities of sampled insects provided a strong indication that hybrid populations are emerging in parts of Africa recently affected by the severe CMD pandemic. This study reveals that mtCOI is not an effective marker at distinguishin …
Comparison of the mtCOI and SNP identities of sampled insects provided a strong indication that hybrid populations are emerging in parts of …
43 results