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ANT1 can induce autoimmune myocarditis in A/J mice by generating autoreactive T cells.
miR (zeige MLXIP ELISA Kits)-2861 and ANT1 are regulators of cardiomyocyte necrosis and myocardial infarction.
These results suggest that follicular helper T cells cells and IL-21 (zeige IL21 ELISA Kits) might be involved in the pathogenesis of viral myocarditis and play an important role in anti-ANT autoantibody production.
Data indicate that palmitoyl-carnitine (PC) increases the type 2 ryanodine receptor (RyR2 (zeige RYR2 ELISA Kits)) oxidation and reduces the ATP/ADP translocase (ANT) activity.
Downregulation of adenine nucleotide translocator 1 exacerbates tumor necrosis factor-alpha (zeige TNF ELISA Kits)-mediated cardiac inflammatory responses.
Plasma membrane-localized ANT1 and ANT2 (zeige SLC25A5 ELISA Kits) regulate L1-mediated neurite outgrowth in conjunction with MMP14 (zeige MMP14 ELISA Kits).
Although the molecular mechanism linking ANT1-Cys (zeige DNAJC5 ELISA Kits)(57) nitroalkylation and uncoupling is not yet known, these data suggest that ANT1-mediated uncoupling may be a mechanism for nitroalkene-induced cardioprotection.
The attenuation of ANT-1 in the presence of PGC-1alpha (zeige PPARGC1A ELISA Kits) overexpression preserves the mitochondrial membrane potential in response to hydrogen-peroxide stress.
Data demonstrate that ANT1 protein level (zeige YY1 ELISA Kits)s are upregulated in Mecp2-null mice.
uncoupling protein-3 (zeige UCP3 ELISA Kits) can minimize the induction of the adenine nucleotide translocase (zeige SLC25A5 ELISA Kits)-mediated 'energy-wasting' process during Calorie restriction (CR).
identification by whole-exome sequencing of seven probands harboring dominant, de novo SLC25A4 mutations; all affected individuals presented at birth, were ventilator dependent and, where tested, revealed severe combined mitochondrial respiratory chain deficiencies associated with a marked loss of mitochondrial DNA copy number in skeletal muscle
A directed proteomic approach discovered the novel interaction of BKCa (zeige KCNMA1 ELISA Kits) with Tom22 (zeige TOMM22 ELISA Kits), a component of the mitochondrion outer membrane import system, and the adenine nucleotide translocator (ANT).
Identification of ZNF555 as a putative transcriptional factor that impacts ANT1 promoter activity in facioscapulohumeral dystrophy myoblasts.
elevated ANT1 expression supports EV infection and is associated with EV persistence, a condition with adverse prognosis.
Data suggest acetylation of ANT1 at lysines 10/23/92 has dramatic physiological effects on ADP-ATP exchange; extent of acetylation of lysine 23 decreases following physical activity; this change is highly dependent on insulin (zeige INS ELISA Kits) sensitivity/resistance.
Expression of ANT1 were lower in inclusion body myositis samples versus both polymyositis and controls
Compares and contrasts all the known human SLC25A (zeige SLC25A25 ELISA Kits)* genes and includes functional information.
A 13-generation Mennonite pedigree with autosomal recessive myopathy and cardiomyopathy due to an SLC25A4 frameshift null mutation (c.523delC, p.Q175RfsX38), which codes for the heart-muscle isoform of the adenine nucleotide translocator-1, was studied.
This report expands the clinical spectrum of ANT1-related human diseases, and emphasises the crucial role of the mitochondrial ADP/ATP carriers in muscle function and pathophysiology of human myopathies.
mutant human ANT1 causes dominant mitochondrial defects characterized by decreased ADP-ATP exchange function and abnormal translocator reversal potential
Data show that the binding sites on adenine nucleotide translocator 1 (ANT1) have an affinity for cardiolipin (CL).
This gene is a member of the mitochondrial carrier subfamily of solute carrier protein genes. The product of this gene functions as a gated pore that translocates ADP from the mitochondrial matrix into the cytoplasm. The protein forms a homodimer embedded in the inner mitochondria membrane. Mutations in this gene have been shown to result in autosomal dominant progressive external opthalmoplegia and familial hypertrophic cardiomyopathy.
adenine nucleotide translocator 1
, ADP,ATP carrier protein 1, mitochondrial
, ANT 1
, ADP/ATP translocase 1
, Adenine nucleotide translocator 1
, ADP,ATP carrier protein 1
, ADP,ATP carrier protein, heart/skeletal muscle
, adenine nucleotide translocase-1
, adenine nucleotide translocator 1, skeletal muscle
, solute carrier family 25 member 4
, mitochondrial adenine nucleotide translocator
, solute carrier family 25 (mitochondrial adenine nucleotide translocator) member 4
, adenine nucleotide translocator 1 (skeletal muscle)
, heart/skeletal muscle ATP/ADP translocator
, ADP,ATP carrier protein, heart
, ADP/ATP carrier
, ADP/ATP translocase T1
, 30 kDa CSQ-binding protein
, 30 kDa calsequestrin-binding protein
, CSQ-binding 30 kDa protein
, solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 5