Keywords: Autoimmunity; primary immunodeficiency diseases; BÂ cells; T cells; AID; Activation-induced cytidine deaminase; AIHA; Autoimmune hemolytic anemia; AIRE; Autoimmune regulator; ALPS; Autoimmune lymphoproliferative disease; ANA; Anti-nuclear autoantibody; AP
مقالات ISI (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: ACP5; Acid phosphatase 5; ADAR1; Adenosine deaminase RNA-specific 1; AGS; Aicardi-Goutières syndrome; ALRs; AIM2-like receptors; AIM2; Absent in melanoma 2; ASC; Apoptosis-associated speck-like protein containing a CARD; CANDLE; Chronic atypical neutroph
Keywords: AMPK; AMP-activated protein kinase; ASK1; apoptosis signal-regulating kinase 1; Atg; autophagy-related; ARE; AU-rich element; AUF; ARE RNA binding protein; BRF; butyrate response factor; CaMK; Ca2Â +/calmodulin-dependent protein kinase; CUGBP; CUG-binding
Keywords: AIM2; absent in melanoma 2; AP-1; activating protein-1; APOBEC; apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like; AZT; azidothymidine; CCCR5; C-C chemokine receptor type 5; CDK1; cyclin-dependent kinase 1; CXCR4; C-X-C chemokine receptor t
Systemic activation of NLRP3 inflammasome in patients with severe primary Sjögren's syndrome fueled by inflammagenic DNA accumulations
Keywords: Sjögren's syndrome; Inflammasome; DNase-I; DNase-II; Peripheral blood; Salivary glands; SS-LR; SS patients with low risk for lymphoma development; SS-HR; SS patients with high risk for lymphoma development; SS-Ly; SS patients complicated with mucosa-asso
Mutational game changer: Chromothripsis and its emerging relevance to cancer
Keywords: SAC; spindle assembly checkpoint; APOBEC; apolipoprotein B mRNA-editing catalytic subunit; SNP; single-nucleotide polymorphism; array-CGH; comparative genomic hybridization; CLTP; chromothripsis-like pattern; SKY; spectral karyotyping; FISH; fluorescent i
Type I interferon and HIV: Subtle balance between antiviral activity, immunopathogenesis and the microbiome
Keywords: IFN; interferon; ISGs; IFNstimulated genes; HCV; hepatitis C virus; IL-10; interleukin-10; PDL-1; programmed death-ligand 1; LCMV; lymphocytic choriomeningitis virus; IFNAR; IFNA receptor; IRFs; IFN regulatory factors; pDCs; plasmacytoid dendritic cells;
A homozygote TREX1 mutation in two siblings with different phenotypes: Chilblains and cerebral vasculitis
Keywords: TREX1; Cerebral vasculitis; Chilblain; Autoinflammatory diseases;
SLE redefined on the basis of molecular pathways
Keywords: Interferonopathies; Transcriptome; Epigenome; Genome-wide association studies; Human leukocyte antigens; Aicardi-Goutieres syndrome; C1q deficiency; TREX1; Neuropsychiatric SLE; Omics;
Crosstalk between Mycobacterium tuberculosis and the host cell
Keywords: AC; adenylyl cyclase; AKAP7; A-kinase anchor protein 7 isoform gamma; AM; alveolar macrophage; ATP; adenosine triphosphate; BCG; Bacille Calmette-Guérin; cAMP; cyclic adenosine monophosphate; CD1; cluster of differentiation 1; c-di-AMP; cyclic-di-adeno
Human three prime exonuclease TREX1 is induced by genotoxic stress and involved in protection of glioma and melanoma cells to anticancer drugs
Keywords: TREX1; AP-1; Melanoma; Glioma; Transcriptional regulation; Anticancer drug;
A homozygous NOTCH3 mutation p.R544C and a heterozygous TREX1 variant p.C99MfsX3 in a family with hereditary small vessel disease of the brain
Keywords: CADASIL; homozygous NOTCH3 mutation; NOTCH3; RCVL; TREX1
Innate immune processes in lupus erythematosus
Keywords: Lupus; Cytokines; TREX1; RNase-H2; SAMHD1
Defects in DNA degradation revealed in crystal structures of TREX1 exonuclease mutations linked to autoimmune disease
Keywords: TREX1; Autoimmune disease; Protein structure; Enzyme mechanism; Lupus; Exonuclease;
TREX1 acts in degrading damaged DNA from drug-treated tumor cells
Keywords: Autoimmunity; Camptothecin; DNA degradation; Dying cells; TREX1
TREX1 DNA exonuclease deficiency, accumulation of single stranded DNA and complex human genetic disorders
Keywords: TREX1; Aicardi-Goutieres syndrome; Single stranded DNA; DNA damage response
Do all of the neurologic diseases in patients with DNA repair gene mutations result from the accumulation of DNA damage?
Keywords: Aicardi–Goutières syndrome; Cockayne syndrome; Oligodendrocytes; Myelin; Calcification; Vascular disease; Thyroid hormone; TREX1; RNASEH2; Toll-like receptor; Innate immune system