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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 11, 2023. (Total: 223939Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Disease and ATP8[original query]
Investigation on mitochondrial tRNA(Leu/Lys), NDI and ATPase 6/8 in Iranian multiple sclerosis patients.
Cellular and molecular neurobiology 2007 Sep 27 (6): 695-700.
Ahari Solmaz Etemad, Houshmand Massoud, Panahi Mehdi Shafa Shariat, Kasraie Sadaf, Moin Mostafa, Bahar Mohammad A
Evidence for the presence of somatic mitochondrial DNA mutations in right atrial appendage tissues of coronary artery disease patients.
Molecular genetics and genomics : MGG 2014 Aug 289 (4): 533-40.
Matam Kavitha, Shaik Noor Ahmad, Aggarwal Sunil, Diwale Sameer, Banaganapalli Babajan, Al-Aama Jumana Yousuf, Elango Ramu, Rao Pragna, Hasan Qurratula
Mitochondrial DNA variant discovery in normal-tension glaucoma patients by next-generation sequencing.
Investigative ophthalmology & visual science 2014 Feb 55 (2): 986-92.
Jeoung Jin Wook, Seong Moon-Woo, Park Sung Sup, Kim Dong Myung, Kim Seok Hwan, Park Ki
Mitochondrial genome mutations in 13 subunits of respiratory chain complexes in Chinese Han and Mongolian hypertensive individuals.
Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis 2017 11 29 (7): 1090-1099.
Zhao Ying, Chen Xi, Li Haide, Zhu Chao, Li Yang, Liu Yu
Next-generation sequencing of the whole mitochondrial genome identifies functionally deleterious mutations in patients with multiple sclerosis.
PloS one 2022 17 (2): e0263606.
Al-Kafaji Ghada, Bakheit Halla F, AlAli Faisal, Fattah Mina, Alhajeri Saad, Alharbi Maram A, Daif Abdulqader, Alsabbagh Manahel Mahmood, Alwehaidah Materah Salem, Bakhiet Mo
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