| Single nucleotide polymorphism rs527236194 of the cytochrome B gene (MT-CYB) is associated with alterations in sperm parameters. | Single nucleotide polymorphism rs527236194 of the cytochrome B gene (MT-CYB) is associated with alterations in sperm parameters.
Gromenko YY, Galimov KS, Gilyazova IR, Galimova EF, Bulygin KV, Ryagin SN, Galimov SN, Litvitskiy PF, Piavchenko GA, Pavlov VN. | 11/28/2023 |
| Mitochondrial Genome-Encoded Long Noncoding RNA Cytochrome B and Mitochondrial Dysfunction in Diabetic Retinopathy. | Mitochondrial Genome-Encoded Long Noncoding RNA Cytochrome B and Mitochondrial Dysfunction in Diabetic Retinopathy.
Mohammad G, Kumar J, Kowluru RA., | 11/16/2023 |
| Association between the single nucleotide variants of the mitochondrial cytochrome B gene (MT-CYB) and the male infertility. | Association between the single nucleotide variants of the mitochondrial cytochrome B gene (MT-CYB) and the male infertility.
Saleh Jaweesh M, Hammadeh ME, Dahadhah FW, Al Zoubi MS, Amor H., Free PMC Article | 06/18/2022 |
| Liver mitochondrial DNA damage and genetic variability of Cytochrome b - a key component of the respirasome - drive the severity of fatty liver disease. | Liver mitochondrial DNA damage and genetic variability of Cytochrome b - a key component of the respirasome - drive the severity of fatty liver disease.
Pirola CJ, Garaycoechea M, Flichman D, Castaño GO, Sookoian S. | 08/21/2021 |
| The heteroplasmy level of some mutations in gene MT-CYB among women with asymptomatic atherosclerosis | [The heteroplasmy level of some mutations in gene MT-CYB among women with asymptomatic atherosclerosis].
Sinyov VV, Chicheva MM, Barinova VA, Ryzhkova AI, Zilinyi RI, Karagodin VP, Postnov AY, Sobenin IA, Orekhov AN, Sazonova MA. | 02/10/2018 |
| The effects of mutation in mitochondrially encoded cytochrome b are reviewed. | [Molecular effects of mitochondrial mutations in cytochrome b of complex III and their impact on the levels of free radical production].
Borek A, Ekiert R, Osyczka A. | 12/23/2017 |
| Mitochondrial mutation m.15804T>C in the mtCYB gene in a family with fibromyalgia is associated with NLRP3-inflammasome activation. | Mutation in cytochrome b gene of mitochondrial DNA in a family with fibromyalgia is associated with NLRP3-inflammasome activation.
Cordero MD, Alcocer-Gómez E, Marín-Aguilar F, Rybkina T, Cotán D, Pérez-Pulido A, Alvarez-Suarez JM, Battino M, Sánchez-Alcazar JA, Carrión AM, Culic O, Navarro-Pando JM, Bullón P. | 11/5/2016 |
| These results indicate that miR-151a-5p may participate in the regulation of cellular respiration and ATP production through targeting Cytb. | Mitochondria-related miR-151a-5p reduces cellular ATP production by targeting CYTB in asthenozoospermia.
Zhou R, Wang R, Qin Y, Ji J, Xu M, Wu W, Chen M, Wu D, Song L, Shen H, Sha J, Miao D, Hu Z, Xia Y, Lu C, Wang X., Free PMC Article | 10/1/2016 |
| This study suggests that, in part, polymorphisms in the MT-ATP6 and MT-CYB genes may contribute to the unexpected fertilization failure. | Polymorphisms in the MT-ATP6 and MT-CYB genes in in vitro fertilization failure.
Mao GH, Wang YN, Xu M, Wang WL, Tan L, Tao SB. | 12/19/2015 |
| The polymorphisms of CYTB as a very useful DNA marker were significantly different between different geographical Uyghur | Genetic diversities of cytochrome B in Xinjiang Uyghur unveiled its origin and migration history.
Ablimit A, Qin W, Shan W, Wu W, Ling F, Ling KH, Zhao C, Zhang F, Ma Z, Zheng X., Free PMC Article | 06/21/2014 |
| Significant elevation of ERalpha and MTCYB transcript levels in premenopausal leiomyomas and its association with ERalpha, -397 CC genotype suggests the mitochondrial-mediated role of estrogen as the promoter of leiomyoma tumorigenesis. | Enhanced transcription of estrogen receptor α and mitochondrial cytochrome b genes in uterine leiomyomas.
Shaik NA, Lone WG, Khan IA, Rao KP, Kodati VL, Hasan Q. | 03/24/2012 |
| Data show that homoplasmic G6709A (MT-CO1) and G14804A (MT-CYB) alterations cause amino acid changes in the highly conserved residues. | Mitochondrial DNA alterations in colorectal cancer cell lines.
Chihara N, Amo T, Tokunaga A, Yuzuriha R, Wolf AM, Asoh S, Suzuki H, Uchida E, Ohta S. | 06/25/2011 |
| mitocryptide-2 (MCT-2) and its human homolog hMCT-2 are cryptides that activate neutrophils | Mitocryptide-2: purification, identification, and characterization of a novel cryptide that activates neutrophils.
Mukai H, Seki T, Nakano H, Hokari Y, Takao T, Kawanami M, Tsukagoshi H, Kimura H, Kiso Y, Shimonishi Y, Nishi Y, Munekata E. | 10/25/2010 |
| cytochrome B gene mutation induces mitochondrial proliferation and prevents apoptosis in human uroepithelial SV-HUC-1 cells. | Forced cytochrome B gene mutation expression induces mitochondrial proliferation and prevents apoptosis in human uroepithelial SV-HUC-1 cells.
Dasgupta S, Hoque MO, Upadhyay S, Sidransky D., Free PMC Article | 01/21/2010 |
| The m.15635T>C transition (S297P) was carried by a newborn who presented with a polyvisceral failure. | A neonatal polyvisceral failure linked to a de novo homoplasmic mutation in the mitochondrially encoded cytochrome b gene.
Fragaki K, Procaccio V, Bannwarth S, Serre V, O'Hearn S, Potluri P, Augé G, Casagrande F, Caruba C, Lambert JC, Paquis-Flucklinger V. | 01/21/2010 |
| CytbI7T has a role in longevity related to caloric restriction | Evolutionary pressure on mitochondrial cytochrome b is consistent with a role of CytbI7T affecting longevity during caloric restriction.
Beckstead WA, Ebbert MT, Rowe MJ, McClellan DA., Free PMC Article | 01/21/2010 |
| Trx2 overexpression modulates the mRNA levels of the COX1 (cytochrome oxidase subunit I) and Cytb (cytochrome b), which are known to be regulated by GR and NF-kappaB. | Interaction of mitochondrial thioredoxin with glucocorticoid receptor and NF-kappaB modulates glucocorticoid receptor and NF-kappaB signalling in HEK-293 cells.
Psarra AM, Hermann S, Panayotou G, Spyrou G. | 01/21/2010 |
| caspase 8-dependent cleavage of mitochondrial Cyt b and translocation of its C-terminal half into the cytoplasm occurred during FAS-induced apoptosis in both chicken and human cells | Functional genetic screening reveals the role of mitochondrial cytochrome b as a mediator of FAS-induced apoptosis.
Komarov AP, Rokhlin OW, Yu CA, Gudkov AV., Free PMC Article | 01/21/2010 |
| Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator) | Mitochondrial DNA variant interactions modify breast cancer risk.
Covarrubias D, Bai RK, Wong LC, Leal SM., Free PMC Article | 09/10/2008 |
| Observational study of gene-disease association. (HuGE Navigator) | See all PubMed (5) articlesMtSNPscore: a combined evidence approach for assessing cumulative impact of mitochondrial variations in disease.
Bhardwaj A, Mukerji M, Sharma S, Paul J, Gokhale CS, Srivastava AK, Tiwari S. Comprehensive analysis of common mitochondrial DNA variants and colorectal cancer risk.
Webb E, Broderick P, Chandler I, Lubbe S, Penegar S, Tomlinson IP, Houlston RS. [Mutation of MTCYB and MTATP6 is associated with asthenospermia].
Feng CQ, Song YB, Zou YG, Mao XM. The mtDNA 15497 G/A polymorphism in cytochrome b in severe obese subjects from Southern Italy.
Liguori R, Mazzaccara C, Pasanisi F, Buono P, Oriani G, Finelli C, Contaldo F, Sacchetti L. Golden mean to longevity: rareness of mitochondrial cytochrome b variants in centenarians but not in patients with Parkinson's disease.
Tanaka M, Fuku N, Takeyasu T, Guo LJ, Hirose R, Kurata M, Borgeld HJ, Yamada Y, Maruyama W, Arai Y, Hirose N, Oshida Y, Sato Y, Hattori N, Mizuno Y, Iwata S, Yagi K. | 03/13/2008 |
| In a mitochondrial myopathy patient, a novel stop-codon mutation (G15761A) was found in the mitochondrial DNA (mtDNA)-encoded cytochrome b gene, resulting in loss of the last 41 amino acids of the protein and complex III deficiency | Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene.
Mancuso M, Filosto M, Stevens JC, Patterson M, Shanske S, Krishna S, DiMauro S. | 01/21/2010 |
| clinical/phenotypic variability of the G15498A mutation in mitochondrial DNA | The deleterious G15498A mutation in mitochondrial DNA-encoded cytochrome b may remain clinically silent in homoplasmic carriers.
Haut S, de Villemeur TB, Brivet M, Guiochon-Mantel A, Boutron A, Rustin P, Legrand A, Slama A. | 01/21/2010 |
| The other proband had a non-synonymous G15221A mutation in the cytochrome b gene. | Atypical muscle pathology and a survey of cis-mutations in deaf patients harboring a 1555 A-to-G point mutation in the mitochondrial ribosomal RNA gene.
Yamasoba T, Goto Yi, Oka Y, Nishino I, Tsukuda K, Nonaka I. | 01/21/2010 |
| biochemical and molecular genetic studies of a patient with both muscle and brain involvement and a severe reduction in the activities of both complexes I and III in skeletal muscle due to a novel mutation in the MTCYB gene | A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeast.
Blakely EL, Mitchell AL, Fisher N, Meunier B, Nijtmans LG, Schaefer AM, Jackson MJ, Turnbull DM, Taylor RW. | 01/21/2010 |