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Tissue microarray (TMA) data showed that elevated expression of TFAM was related to the histological grade and TNM (zeige ODZ1 Proteine) stage of NSCLC patients.
The authors did not find statistically significant differences in the genotype frequencies for the TFAM +35G/C polymorphism between women with polycystic ovary syndrome and controls and found that mtDNA copy number is not associated with TFAM+35G/C SNP in polycystic ovary syndrome patients.
Alleles in mitochondrial transcription factor A (TFAM) and AP endonuclease 1 (APE1 (zeige APEX1 Proteine)) are associated with reduced cognitive performance.
In vivo, AICAR (zeige ATIC Proteine) significantly reduced osteosarcoma growth without apparent body weight loss and AICAR (zeige ATIC Proteine) increased both mitochondrial proliferation and apoptotic activity in treated tumor tissues. AICAR (zeige ATIC Proteine) showed anticancer effects in osteosarcoma cells through an AMPK (zeige PRKAA1 Proteine)-dependent peroxisome proliferatoractivated receptor-gamma coactivator-1alpha (PGC-1alpha)/mitochondrial transcription factor A (TFAM)/mitochondrial pathway
the present study identified the interaction of miR (zeige MLXIP Proteine)-590-3p and TFAM in colon cancer. TFAM was identified as a target of miR (zeige MLXIP Proteine)-590-3p, and miR (zeige MLXIP Proteine)-590-3p enhanced the proliferation of SW480 cells.
The results of the present study provided evidence that resistance to cisplatin chemotherapy in ERpositive breast cancer may be through TFAM and indicated that TFAM may be a target for chemoresistance in patients with breast cancer.
miR (zeige MLXIP Proteine)-199a-3p is able to attenuate cisplatin resistance in breast cancer cells through inhibiting TFAM expression.
We conducted a meta-analysis of studies involving CHAT, TFAM, and VR22 (zeige CTNNA3 Proteine) polymorphisms and Alzheimer disease susceptibility. For TFAM and VR22 (zeige CTNNA3 Proteine), no significant association was detected in studied single-nucleotide polymorphisms (SNPs).Rs1937 and rs2306604 of TFAM, are not significantly associated with AD risk.
Results showed that TFAM formed oligomers in mitochondria by in situ chemical cross-linking and suggested the importance of the dimerization of TFAM molecules in the distribution of mtDNA in cells.
Report failed upregulation of TFAM protein and mitochondrial DNA in oxidatively deficient fibers in skeletal muscle of chronic obstructive pulmonary disease patients.
TFAM may exert a critical role in porcine gametogenesis and preimplantation embryo development.
Our results suggest that TFAM plays an important role in lipid metabolism and may be a strong candidate gene for obesity in mammals.
de novo mtTFA expression associated with mitochondrial biogenesis activation & high levels of nuclear respiratory factor-1 (zeige NRF1 Proteine) mRNA from oocyte stage onwards argue for essential function of these factors during the first steps of bovine embryogenesis.
Perturbation of mitochondrial complex function by ablation of the mitochondrial transcription factor A (Tfam) reproduces multiple hallmarks of aging in hippocampal neurogenesis.
During muscle differentiation, Tfam protein levels are regulated by the availability of Tfam mRNA, which is controlled by both transcription and mRNA stability.
TFAM binds to RNA-containing 4-way junctions but does not bind appreciably to RNA hairpins, internal loops, or linear RNA:DNA hybrids.
Data show that mitochondrial transcription factor A (TFAM) packages single mitochondrial DNA (mtDNA) molecules.
There was upregulation of mtDNA and TFAM in 6-wk diabetic mice, suggesting that TFAM activation could be a therapeutic strategy to treat peripheral neuropathy.
This study demonistrated that Tfam gene inactive patkinsin disease cause dopamine loss and circadian rhythm disorder.
Mitochondrial transcription factor A, an endogenous danger signal, promotes TNFalpha (zeige TNF Proteine) release via RAGE (zeige AGER Proteine)- and TLR9 (zeige TLR9 Proteine)-responsive plasmacytoid dendritic cells.
overexpression of TFAM can restore mitochondrial function to normal levels in NYGGF4 (zeige PID1 Proteine)-overexpressing adipocytes
Acute exercise induces tumour suppressor protein p53 (zeige TP53 Proteine) translocation to the mitochondria and promotes a p53 (zeige TP53 Proteine)-Tfam-mitochondrial DNA complex in skeletal muscle.
Data indicate that TFAM-deficient keratinocytes failed to generate mitochondria-derived reactive oxygen species, and prevented the transmission of Notch (zeige NOTCH1 Proteine) and beta-catenin (zeige CTNNB1 Proteine) signals for epidermal differentiation and hair follicle development.
This gene encodes a key mitochondrial transcription factor containing two high mobility group motifs. The encoded protein also functions in mitochondrial DNA replication and repair. Sequence polymorphisms in this gene are associated with Alzheimer's and Parkinson's diseases. There are pseudogenes for this gene on chromosomes 6, 7, and 11. Alternative splicing results in multiple transcript variants.
transcription factor A, mitochondrial
, HMG box mitochondrial transcription factor
, mitochondrial transcription factor 1
, mitochondrial transcription factor A
, transcription factor 6
, transcription factor 6-like 1
, transcription factor 6-like 2 (mitochondrial transcription factor)
, transcription factor 6-like 3
, transcription factor 6-like 2
, testis-specific HMG-box protein m-tsHMG
, testis-specific high mobility group protein