Cargando…

Mitochondrial Polymorphisms, in The D-Loop Area, Are Associated with Brain Tumors

OBJECTIVE: This study was carried out to evaluate the relationship between mtDNA D-loop variations and the pathogenesis of a brain tumor. MATERIALS AND METHODS: In this experimental study, 25 specimens of brain tumor tissue with their adjacent tissues from patients and 454 blood samples from differe...

Descripción completa

Detalles Bibliográficos
Autores principales:	Altafi, Donya, Sadeghi, Soha, Hojatian, Hamed, Torabi Afra, Maryam, Pakizeh Kar, Safoura, Gorji, Mojtaba, Houshmand, Massoud
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Royan Institute 2019
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582428/ https://www.ncbi.nlm.nih.gov/pubmed/31210442 http://dx.doi.org/10.22074/cellj.2019.5947

Ejemplares similares

The mitochondrial C16069T polymorphism, not mitochondrial D310 (D-loop) mononucleotide sequence variations, is associated with bladder cancer
por: Shakhssalim, Nasser, et al.
Publicado: (2013)

Evaluation of FTO rs9939609 and MC4R rs17782313 Polymorphisms as Prognostic Biomarkers of Obesity: A Population-based Cross-sectional Study
por: Mozafarizadeh, Mina, et al.
Publicado: (2019)

Mitochondrial Copy Number and D-Loop Variants in Pompe Patients
por: Bahreini, Fatemeh, et al.
Publicado: (2016)

Association of rs12487066, rs12044852, rs10735781, rs3135388, rs6897932, rs1321172, rs10492972, and rs9657904 Polymorphisms with Multiple Sclerosis in Iranian Population
por: Razavian, Takavar, et al.
Publicado: (2020)

MTHFR polymorphisms and breast cancer risk
por: Hosseini, Mojgan, et al.
Publicado: (2011)

Mitochondrial G8292A and C8794T mutations in patients with Niemann-Pick disease type C
por: Masserrat, Abbas, et al.
Publicado: (2018)

Is 8860 variation a rare polymorphism or associated as a secondary effect in HCM disease?
por: Houshmand, Massoud, et al.
Publicado: (2011)

The mitochondrial DNA mutations associated with cardiac arrhythmia investigated in an LQTS family
por: Khatami, Fatemeh, et al.
Publicado: (2014)

Association of ABCB1 and SLC22A16 Gene Polymorphisms with Incidence of Doxorubicin-Induced Febrile Neutropenia: A Survey of Iranian Breast Cancer Patients
por: Faraji, Abolfazl, et al.
Publicado: (2016)

The mitochondrial ATPase6 gene is more susceptible to mutation than the ATPase8 gene in breast cancer patients
por: Ghaffarpour, Massoud, et al.
Publicado: (2014)

Association of genetic variations in the mitochondrial DNA control region with presbycusis
por: Falah, Masoumeh, et al.
Publicado: (2017)

The potential role for use of mitochondrial DNA copy number as predictive biomarker in presbycusis
por: Falah, Masoumeh, et al.
Publicado: (2016)

Mitochondrial Variants in Pompe Disease: A Comparison between Classic and Non-Classic Forms
por: Bahreini, Fatemeh, et al.
Publicado: (2018)

The prevalence of common CFTR gene mutations and polymorphisms in infertile Iranian men with very severe oligozoospermia
por: Jafari, Leyla, et al.
Publicado: (2022)

Analysis of mitochondrial ND1 gene in human colorectal cancer
por: Akouchekian, Mansoureh, et al.
Publicado: (2011)

Investigation of the Mitochondrial ATPase 6/8 and tRNA(Lys) Genes Mutations in Autism
por: Piryaei, Fahimeh, et al.
Publicado: (2012)

Association of fibroblast growth factor (FGF-21) as a biomarker with primary mitochondrial disorders, but not with secondary mitochondrial disorders (Friedreich Ataxia)
por: Salehi, Mohammad Hossein, et al.
Publicado: (2013)

Mitochondrial A12308G alteration in tRNA(Leu(CUN)) in colorectal cancer samples
por: MA Mohammed, Fawziah, et al.
Publicado: (2015)

BAX pro-apoptotic gene alterations in repeated pregnancy loss
por: Mohammad Seyedhassani, Seyed, et al.
Publicado: (2011)

Liver Mitochondrial DNA Copy Number and Deletion Levels May Contribute to Nonalcoholic Fatty Liver Disease Susceptibility
por: Kamfar, Sharareh, et al.
Publicado: (2016)

New pathogenic variations of mitochondrial DNA in Alzheimer disease!!
por: Nia, Samira Sheibani, et al.
Publicado: (2013)

The effect of CHRNA3 rs1051730 C>T and ABCB1 rs3842 A>G polymorphisms on non-small cell lung cancer and nicotine dependence in Iranian population
por: Veiskarami, Parisa, et al.
Publicado: (2021)

Investigation of FGF21 mRNA levels and relative mitochondrial DNA copy number levels and their relation in nonalcoholic fatty liver disease: a case-control study
por: Houshmand, Massoud, et al.
Publicado: (2023)

Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss
por: Balali, Maryam, et al.
Publicado: (2016)

Gene Expression Profiling of Mitochondrial Oxidative Phosphorylation (OXPHOS) Complex I in Friedreich Ataxia (FRDA) Patients
por: Salehi, Mohammad Hossein, et al.
Publicado: (2014)

Simultaneous Genotyping of the rs4762 and rs699 Polymorphisms in Angiotensinogen Gene and Correlation with Iranian CAD Patients with Novel Hexa-primer ARMS-PCR
por: KHATAMI, Mehri, et al.
Publicado: (2017)

Sequence-Based Polymorphisms in the Mitochondrial D-Loop and Potential SNP Predictors for Chronic Dialysis
por: Chen, Jin-Bor, et al.
Publicado: (2012)

Single nucleotide polymorphisms in the mitochondrial displacement loop and outcome of esophageal squamous cell carcinoma
por: Zhang, Ruixing, et al.
Publicado: (2010)

Single nucleotide polymorphisms in the mitochondrial displacement loop and age at onset of non-Hodgkin lymphoma
por: Fan, Haiyan, et al.
Publicado: (2013)

Single nucleotide polymorphisms in the mitochondrial displacement loop and age-at onset of renal cell carcinoma
por: Xu, Jinsheng, et al.
Publicado: (2013)

The mitochondrial R-loop
por: Holt, Ian J
Publicado: (2019)

ERCC1 intron 1 was associated with breast cancer risk
por: Mojgan, Hosseini, et al.
Publicado: (2012)

The Study of rs693 and rs515135 in APOB in People with Familial Hypercholestrolemia
por: Karami, Fatemeh, et al.
Publicado: (2019)

Different on the abundance of Pampus argenteus in Persian Gulf exceeding in variety comparing to Gulf of Oman
por: Sheibaninia, Atena, et al.
Publicado: (2017)

Optical absorbing origin of chiroptical activity in planar plasmonic metasurfaces
por: Najafabadi, Atefeh Fazel, et al.
Publicado: (2017)

Expression levels of the BAK1 and BCL2 genes highlight the role of apoptosis in age-related hearing impairment
por: Falah, Masoumeh, et al.
Publicado: (2016)

Assessment of Bone Morphogenetic Protein 3 Methylation in Iranian Patients with Colorectal Cancer
por: Houshmand, Massoud, et al.
Publicado: (2017)

Investigation of Mutations in Exon 14 of SH3TC2 Gene and Exon 7 of NDRG1 Gene in Iranian Charcot-Marie-Tooth Disease Type 4 (CMT4D) Patients
por: MOOSAVI, Rahmaneh Sadat, et al.
Publicado: (2020)

Prevalence of the rs7903146C>T polymorphism in TCF7L2 gene for prediction of type 2 diabetes risk among Iranians of different ethnicities
por: Allahdini, Mojgan, et al.
Publicado: (2015)

Identification of a new mutation in an Iranian family with hereditary multiple osteochondromas
por: Akbaroghli, Susan, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_5qssr5ss6cp73rdc26r3lob5vk