Pages that link to "Q78556882"
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The following pages link to Mitochondrial DNA mutations in patients with myelodysplastic syndromes (Q78556882):
Displaying 27 items.
- High mitochondrial DNA stability in B-cell chronic lymphocytic leukemia (Q30896674) (← links)
- Mouse models of myelodysplastic syndromes (Q33767319) (← links)
- SOD2 Deficient Erythroid Cells Up-Regulate Transferrin Receptor and Down-Regulate Mitochondrial Biogenesis and Metabolism (Q33822264) (← links)
- NSMAP: a method for spliced isoforms identification and quantification from RNA-Seq. (Q33901532) (← links)
- Mitochondrial DNA copy number and hnRNP A2/B1 protein: biomarkers for direct exposure of benzene (Q34019910) (← links)
- The case for the continuing use of the revised Cambridge Reference Sequence (rCRS) and the standardization of notation in human mitochondrial DNA studies (Q34389694) (← links)
- Mitochondrial DNA aberrations and pathophysiological implications in hematopoietic diseases, chronic inflammatory diseases, and cancers (Q34749561) (← links)
- Autophagy in the pathogenesis of myelodysplastic syndrome and acute myeloid leukemia. (Q35124582) (← links)
- Oxidative stress and the myelodysplastic syndromes (Q35140206) (← links)
- Direct confirmation of quiescence of CD34+CD38- leukemia stem cell populations using single cell culture, their molecular signature and clinicopathological implications (Q35344507) (← links)
- Mitochondrial DNA mutations in the hematopoietic system (Q35582417) (← links)
- Apoptotic mechanisms in the control of erythropoiesis (Q35811887) (← links)
- Mitochondrial DNA spectra of single human CD34+ cells, T cells, B cells, and granulocytes (Q35848412) (← links)
- Impact of growth factors in the regulation of apoptosis in low-risk myelodysplastic syndromes (Q36462759) (← links)
- Mitochondria in hematopoiesis and hematological diseases. (Q36558011) (← links)
- Enhanced growth of myelodysplastic colonies in hypoxic conditions (Q36916269) (← links)
- Purification and characterization of sideroblasts from patients with acquired and hereditary sideroblastic anaemia. (Q37015475) (← links)
- Mitochondrial DNA aberrations of bone marrow cells from patients with aplastic anemia (Q37030177) (← links)
- Erythroid dysplasia, megaloblastic anemia, and impaired lymphopoiesis arising from mitochondrial dysfunction (Q37414694) (← links)
- Zebrafish as a model system for mitochondrial biology and diseases (Q38140444) (← links)
- Role of heteroplasmic mutations in the mitochondrial genome and the ID4 gene promoter methylation region in the pathogenesis of chronic aplastic anemia in patients suffering from Kidney yin deficiency (Q41004047) (← links)
- Erythroid precursors from patients with low-risk myelodysplasia demonstrate ultrastructural features of enhanced autophagy of mitochondria (Q44861594) (← links)
- Marked mitochondrial DNA sequence heterogeneity in single CD34+ cell clones from normal adult bone marrow (Q47612283) (← links)
- Different pathophysiological mechanisms of intramitochondrial iron accumulation in acquired and congenital sideroblastic anemia caused by mitochondrial DNA deletion (Q48466914) (← links)
- Spectrum of mitochondrial genome instability and implication of mitochondrial haplogroups in Korean patients with acute myeloid leukemia (Q57494285) (← links)
- Somatic mitochondrial DNA mutations in adult-onset leukaemia (Q79108457) (← links)
- Profiling of length heteroplasmies in the human mitochondrial DNA control regions from blood cells in the Korean population (Q82665597) (← links)