Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Syndrome and ND1[original query] |
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Mutational analysis of the mitochondrial tRNALeu(UUR) gene in Tunisian patients with mitochondrial diseases. Biochemical and biophysical research communications 2007 Apr 355 (4): 1031-7. Mkaouar-Rebai Emna, Tlili Abdelaziz, Masmoudi Saber, Belguith Neila, Charfeddine Ilhem, Mnif Mouna, Triki Chahnez, Fakhfakh Fai |
Mitochondrial DNA associations with East Asian metabolic syndrome. Biochimica et biophysica acta. Bioenergetics 2018 7 1859 (9): 878-892. Chalkia Dimitra, Chang Yi-Cheng, Derbeneva Olga, Lvova Maria, Wang Ping, Mishmar Dan, Liu Xiaogang, Singh Larry N, Chuang Lee-Ming, Wallace Douglas |
Multisystem mitochondrial diseases due to mutations in mtDNA-encoded subunits of complex I. BMC pediatrics 2020 1 20 (1): 41. Danhelovska Tereza, Kolarova Hana, Zeman Jiri, Hansikova Hana, Vaneckova Manuela, Lambert Lukas, Kucerova-Vidrova Vendula, Berankova Kamila, Honzik Tomas, Tesarova Marke |
NGS-based mtDNA Profiling Could Reveal Genetic Alterations in Schizophrenia. Current topics in medicinal chemistry 2021 6 21 (11): 938-948. Ivanova Elena Mihailova, Kandilarova Snezhina Mihailova, Lukanov Tzvetelin Ivanov, Naumova Elissaveta Jordanova, Akabalieva Katerina Valentinova, Milanova Vihra Krumo |
Association of Mitochondrial Variants with the Joint Occurrence of Polycystic Ovary Syndrome and Hashimoto's Thyroiditis. Antioxidants (Basel, Switzerland) 2023 11 12 (11): . Natalia Zeber-Lubecka, Maria Kulecka, Katarzyna Suchta, Michalina D?browska, Micha? Ciebiera, Ewa E Henn |
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