Results 71 to 80 of about 5,286 (150)

The complete mitochondrial genome and phylogenetic analysis of Tipula (Yamatotipula) nova Walker, 1848 (Diptera, Tipulidae) from Qingdao, Shandong, China

Mitochondrial DNA. Part B. Resources, 2019
The genus Tipula Linnaeus, is a large group of crane flies with more than 2400 known species from 41 subgenera. In this study, we report the first complete mitochondrial (mt) genome sequence of the subgenus Tipula (Yamatotipula), which is a circular ...
Chuande Zhao, Xingyang Qian, Sifang Wang, Yan Li, Xiao Zhang   +4 more
doaj   +1 more source

Identification of key genes and long non‑coding RNA expression profiles in osteoporosis with rheumatoid arthritis based on bioinformatics analysis

BMC Musculoskeletal Disorders
Background Although rheumatoid arthritis (RA) is a chronic systemic tissue disease often accompanied by osteoporosis (OP), the molecular mechanisms underlying this association remain unclear. This study aimed to elucidate the pathogenesis of RA and OP by
Jin-yu An, Xing-na Ma, Hui-long Wen, Hui-dong Hu   +3 more
doaj   +1 more source

ATP Synthase Diseases of Mitochondrial Genetic Origin

Frontiers in Physiology, 2018
Devastating human neuromuscular disorders have been associated to defects in the ATP synthase. This enzyme is found in the inner mitochondrial membrane and catalyzes the last step in oxidative phosphorylation, which provides aerobic eukaryotes with ATP ...
Alain Dautant, Thomas Meier, Alexander Hahn, Déborah Tribouillard-Tanvier, Jean-Paul di Rago, Roza Kucharczyk   +5 more
doaj   +1 more source

Clinical and genetic spectrum of pediatric mitochondrial disorders in China: insights from a 47-case genetically confirmed cohort

Orphanet Journal of Rare Diseases
Background Primary mitochondrial disorders (MDs) are genetically and clinically heterogeneous metabolic diseases caused by mitochondrial DNA (mtDNA) or nuclear DNA (nDNA) mutations.
Fan Yang, Ruen Yao, Guoying Chang, Jiayue Hu, Biyun Feng, Libo Wang, Feihan Hu, Yiguo Huang, Shuo Wu, Tingting Yu, Yu Ding, Xiumin Wang   +11 more
doaj   +1 more source

Effects of mitochondrial gene mutation 8923 (A→G) on inflammatory indicators and blood pressure after acute high-altitude exposure

Frontiers in Physiology
BackgroundIn recent years, an increasing number of individuals have traveled to or resided in plateau regions for various reasons. The hypobaric hypoxia characteristics of plateau environments represents a key risk factor for acute mountain sickness (AMS)
Minglei Zhang, Minglei Zhang, Ruizhe Li, Yining Liu, Zongbin Li, Zongbin Li, Zongbin Li   +6 more
doaj   +1 more source

A Mutation in Mouse MT-ATP6 Gene Induces Respiration Defects and Opposed Effects on the Cell Tumorigenic Phenotype. [PDF]

Int J Mol Sci, 2023
Moreno-Loshuertos R, Movilla N, Marco-Brualla J, Soler-Agesta R, Ferreira P, Enríquez JA, Fernández-Silva P.   +6 more
europepmc   +1 more source

Detection and quantification of pork and rat DNA in processed meats using multiplex quantitative Real‐Time PCR (m‐qPCR)

Indonesian Journal of Biotechnology
In addition to the issue of pork contamination, processed meats frequently contain traces of rat meat. Therefore, detection and quantification of the pork and rat DNA in cases of meat and processed meat adulteration are necessary.
Nurul Azmah Nikmatullah, Etin Diah Permanasari   +1 more
doaj   +1 more source

Keragaman Genetik Sekuen Gen ATP Synthase FO Subunit 6 (ATP6) Monyet Hantu (Tarsius) Indonesia (GENETIC DIVERSITY STUDY OF ATP6 GENE SEQUENCES OF TARSIERS FROM INDONESIA)

Jurnal Veteriner, 2013
In a conservation effort, the identification of Tarsier species, on the bases of the morphological andmolecular characteristic is necessary. Up to now, the identification of the animals were based on themorphology and vocalizations, which is extremely ...
Rini Widayanti, Niken Satuti Nur Handayani, Hery Wijayanto   +2 more
doaj  

Spontaneous mutation in 2310061I04Rik results in reduced expression of mitochondrial genes and impaired brain myelination.

PLoS ONE
Here, we describe a spontaneous mouse mutant with a deletion in a predicted gene 2310061I04Rik (Rik) of unknown function located on chromosome 17. A 59 base pair long deletion occurred in the first intron of the Rik gene and disrupted its expression ...
Erdyni N Tsitsikov, Khanh P Phan, Yufeng Liu, Alla V Tsytsykova, Rosalia Paterno, David M Sherry, Anthony C Johnson, Ian F Dunn   +7 more
doaj   +1 more source

A lack of a definite correlation between male sub-fertility and single nucleotide polymorphisms in sperm mitochondrial genes MT-CO3, MT-ATP6 and MT-ATP8. [PDF]

Mol Biol Rep, 2022
Saleh Jaweesh M, Hammadeh ME, Dahadhah FW, Al Smadi MA, Al Zoubi MS, Alarjah MIA, Amor H.   +6 more
europepmc   +1 more source