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The protein encoded by MFN1 is a mediator of mitochondrial fusion. Zusätzlich bieten wir Ihnen Mitofusin 1 Antikörper (138) und Mitofusin 1 Kits (5) und viele weitere Produktgruppen zu diesem Protein an.
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The results showed that high level of Mfn1 expression significantly improved the embryo development rates by increasing ATP level and Deltapsim, while reducing H(2)O(2) generation.
Regulation of Mfn1 by MGRN1 (zeige MGRN1 Proteine) and the proteasome modulates mitochondrial fusion.
SLC25A46 (zeige SLC25A46 Proteine) is a new component in mitochondrial dynamics that serves as a regulator for MFN1/2 oligomerization.
MFN1-positive expression could be seen mainly in ganglion cells after 1 week of minus lens intervention, and with time extension, more and more positive cells appeared in the rod-cone cell and bipolar cell layer, and this phenomenon could not be found in the normal control eyes.
crystal structures of engineered human MFN1 containing the GTPase (zeige RACGAP1 Proteine) domain and a helical domain during different stages of GTP (zeige AK3 Proteine) hydrolysis; mechanistic model for MFN1-mediated mitochondrial tethering is proposed; results shed light on the molecular basis of mitochondrial fusion and mitofusin (zeige MFN2 Proteine)-related human neuromuscular disorders
These results suggest that MFN (zeige TLL1 Proteine) tethers apposing membranes, likely through nucleotide-dependent dimerization.
Improper transcriptional (in)activation of mitofusin-1 and dynamin-related protein 1 (zeige DNM1L Proteine) during early in vitro embryo development is associated with a decrease in mitochondrial membrane potential and with embryo fragmentation.
A fine balance of Mfn1 levels is maintained by MARCH5 (zeige MARCH5 Proteine)-mediated quality control on acetylated Mfn1.
miR (zeige MLXIP Proteine)-19b targets 3'UTR sequences of Mfn1 genes inhibit the expression of Mfn1
In a amyotrophic lateral sclerosis transgenic mouse model, Mfn1 is significantly increased in spinal cord.
A novel role for the endoplasmic reticulum-associated Gp78 (zeige AMFR Proteine) ubiquitin ligase and the Mfn1 mitochondrial fusion factor in mitophagy.
These results highlight the crucial role of MFN1 in maintaining the competency of the STING pathway.
Despite apparent mitochondrial dysfunction, hearts deficient in both Mfn1 and Mfn2 (zeige MFN2 Proteine) are protected against acute myocardial infarction due to impaired mitochondria/sarcoplasmic reticulum tethering.
We found that mouse embryonic fibroblasts lacking Mfn2 (zeige MFN2 Proteine) have altered lipid droplet morphology. However, triacylglycerol biosynthesis was not dependent on ER-mitochondrial tethering mediated by mitofusins. Lastly, Mfn2 (zeige MFN2 Proteine) does not have a role in adipocyte differentiation.
MFN1 deficiency leads to defects in mitochondrial activity and male infertility.
Report exposes a novel role for Shh (zeige SHH Proteine) in regulating mitochondrial dynamics and rescue the metabolic profile of tumor cells through regulation of mitofusin 1 and 2.
Ablating Mfn1 eliminates the cardiac-related lethality of Mff (zeige MFF Proteine) knockout mice.
Data suggest that mitochondrial fusion and fission events are regulated by four GTPases: Mfn1, Mfn2 (zeige MFN2 Proteine), OPA1 (optic atrophy 1 (zeige OPA1 Proteine) protein), and Drp1 (dynamin 1-like protein (zeige DNM1L Proteine)). [REVIEW]
Authors present evidence that metabolically challenged mitochondria undergo active fusion to suppress oxidative stress. In response to glucose starvation, mitofusin 1 (MFN1) becomes associated with the protein deacetylase HDAC6 (zeige HDAC6 Proteine).
These findings suggest that mitochondrial impairment is a very early event in Alzheimer disease pathogenesis and abnormal expression of Mfn1 and Mfn2 (zeige MFN2 Proteine) caused by excessive intracellular Abeta (zeige APP Proteine) is the possible molecular mechanism.
Data identify MFN1 as an ERK (zeige EPHB2 Proteine) target to modulate mitochondrial shape and apoptosis.
The protein encoded by this gene is a mediator of mitochondrial fusion. This protein and mitofusin 2 are homologs of the Drosophila protein fuzzy onion (Fzo). They are mitochondrial membrane proteins that interact with each other to facilitate mitochondrial targeting.
, mitofusin 2
, fzo homolog
, mitochondrial transmembrane GTPase FZO-2
, mitochondrial transmembrane GTPase Fzo-1
, putative transmembrane GTPase
, transmembrane GTPase MFN1
, mitochondrial transmembrane GTPase FZO1B