# عنوان نوع فایل سایز فایل بازدید دانلود امتیاز قیمت (تومان)
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Overexpression of the EZH2, RING1 and BMI1 genes is common in myelodysplastic syndromes: relation to adverse epigenetic alteration and poor prognostic scoring
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Long-term follow-up of patients with chronic myeloid leukemia having received autologous stem cell transplantation
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CYP2B6 gene single nucleotide polymorphisms and leukemia susceptibility
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Sickle-cell disease and malaria: evaluation of seasonal intermittent preventive treatment with Sulfadoxine-pyrimethamine in Senegalese patients—a randomized placebo-controlled trial
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Severe congenital neutropenia in a multigenerational family with a novel neutrophil elastase (ELANE) mutation
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Additional erythrocytic and reticulocytic parameters helpful for diagnosis of hereditary spherocytosis: results of a multicentre study
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Contribution of VKORC1 and CYP2C9 polymorphisms in the interethnic variability of warfarin dose in Malaysian populations
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Impact of cytokine gene polymorphisms on risk and treatment outcomes of aplastic anemia
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The role of zinc protoporphyrin measurement in the differentiation between primary myelofibrosis and essential thrombocythaemia
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Leukemias induced by altered TRK-signaling are sensitive to mTOR inhibitors in preclinical models
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Molecular characterization of a novel 27.6-kb deletion causing α+ thalassemia in a Chinese family
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Cost-effectiveness of adenotonsillectomy in reducing obstructive sleep apnea, cerebrovascular ischemia, vaso-occlusive pain, and ACS episodes in pediatric sickle cell disease
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A prospective study to assess the predictive value for hereditary spherocytosis using five laboratory tests (cryohemolysis test, eosin-5پŒ-maleimide flow cytometry, osmotic fragility test, autohemolysis test, and SDS-PAGE) on 50 hereditary spherocytosis fa
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Oxidative stress contributes to hemolysis in patients with hereditary spherocytosis and can be ameliorated by fermented papaya preparation
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Hydralazine and magnesium valproate as epigenetic treatment for myelodysplastic syndrome. Preliminary results of a phase-II trial
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Myeloid growth factors in acute myeloid leukemia: systematic review of randomized controlled trials
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Dysmetabolic hyperferritinemia is associated with normal transferrin saturation, mild hepatic iron overload, and elevated hepcidin
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Deferasirox effectively decreases iron burden in patients with double heterozygous HbS/â-thalassemia
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Quantitative analysis of Hb Bart’s in cord blood by capillary electrophoresis system
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Expansion of CD4+CD25+ regulatory T cells from cord blood CD4+ cells using the common م-chain cytokines (IL-2 and IL-15) and rapamycin
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Leukemia stem cells
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Iron overload in MDS—pathophysiology, diagnosis, and complications
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Proliferation and differentiation potential of CD133+ and CD34+ populations from the bone marrow and mobilized peripheral blood
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Variant of the extensor pollicis tertius: a case report on a unique extensor muscle to the thumb
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A case of double aortic arch accompanied by sub-aortic and pre-aortic left brachiocephalic veins and anomalous origin and course of left vertebral artery
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Overexpression of the EZH2, RING1 and BMI1 genes is common in myelodysplastic syndromes: relation to adverse epigenetic alteration and poor prognostic scoring

Overexpression of the EZH2, RIN ...

Epigenetics refers to the study of clonally inherited changes in gene expression without accompanying genetic changes. Previous research on the epig ...

348.51 KB
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Long-term follow-up of patients with chronic myeloid leukemia having received autologous stem cell  transplantation

Long-term follow-up of patients ...

Prior to introduction of imatinib mesylate, the median survival of chronic myeloid leukemia (CML) patients was approximately 60 months and the stand ...

208.90 KB
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CYP2B6 gene single nucleotide polymorphisms and leukemia susceptibility

CYP2B6 gene single nucleotide p ...

CYP2B6 is a highly variable and polymorphic cytochrome P450 enzyme which plays a vital role in the degradation of some endogenous metabolites, xenob ...

203.14 KB
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Sickle-cell disease and malaria: evaluation of seasonal intermittent preventive treatment with  Sulfadoxine-pyrimethamine in Senegalese patients—a randomized placebo-controlled trial

Sickle-cell disease and malaria ...

Sickle-cell disease (SCD) patients are at high risk of developing malaria which is a major contributor to morbidity andmortality in this disease. In ...

111.05 KB
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Severe congenital neutropenia in a multigenerational family with a novel neutrophil elastase (ELANE) mutation

Severe congenital neutropenia i ...

We have analysed a family with nine congenital neutropenia patients in four generations, several of which we have studied in a long-term follow-up o ...

217.88 KB
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Additional erythrocytic and reticulocytic parameters helpful for diagnosis of hereditary spherocytosis:  results of a multicentre study

Additional erythrocytic and ret ...

Hereditary spherocytosis (HS) is characterised by weakened vertical linkages between the membrane skeleton and the red blood cell’s lipid bilayer, l ...

341.00 KB
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Contribution of VKORC1 and CYP2C9 polymorphisms in the interethnic variability of warfarin dose in Malaysian populations

Contribution of VKORC1 and CYP2 ...

Within the Asian populations, Indian patients had been reported to require higher warfarin dose compared with the Chinese and Malay patients, and th ...

139.50 KB
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Impact of cytokine gene polymorphisms on risk and treatment outcomes of aplastic anemia

Impact of cytokine gene polymor ...

Autoreactive cytotoxic T cells play a key role in the pathogenesis of aplastic anemia (AA) by myelosuppressive cytokines including interferon-gamma, ...

239.30 KB
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The role of zinc protoporphyrin measurement in the differentiation between primary myelofibrosis  and essential thrombocythaemia

The role of zinc protoporphyrin ...

The differentiation between primary myelofibrosis (PMF) and essential thrombocythaemia (ET) may be difficult especially in early-stage disease. In P ...

185.47 KB
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Leukemias induced by altered TRK-signaling are sensitive to mTOR inhibitors in preclinical models

Leukemias induced by altered TR ...

Rapamycin is a potent allosteric mTORC1 inhibitor with clinical applications as an anticancer agent. However, only a fraction of cancer patients res ...

597.84 KB
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Molecular characterization of a novel 27.6-kb deletion causing α+ thalassemia in a Chinese family

Molecular characterization of a ...

Over 80% of the α-thalassemia cases in southern China are caused by large deletions involving the α-globin gene cluster on chromosome 16p13.3. Here, ...

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Cost-effectiveness of adenotonsillectomy in reducing obstructive sleep apnea, cerebrovascular ischemia, vaso-occlusive pain, and ACS episodes in pediatric sickle cell disease

Cost-effectiveness of adenotons ...

In children with sickle cell disease (SCD), adenotonsillar hypertrophy or recurrent tonsillitis are frequently linked with an increased risk of obst ...

128.78 KB
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A prospective study to assess the predictive value for hereditary spherocytosis using five laboratory tests (cryohemolysis test, eosin-5پŒ-maleimide flow cytometry, osmotic fragility test, autohemolysis test, and SDS-PAGE) on 50 hereditary spherocytosis fa

A prospective study to assess t ...

This prospective study was carried out to assess the usefulness of five laboratory tests in the diagnosis of hereditary spherocytosis (HS), based on ...

450.90 KB
رایگان
Oxidative stress contributes to hemolysis in patients with hereditary spherocytosis and can be ameliorated by fermented papaya preparation

Oxidative stress contributes to ...

In the present study, we questioned the role of oxidative stress in hereditary spherocytosis (HS), where red blood cells (RBC) have a shortened surv ...

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Hydralazine and magnesium valproate as epigenetic treatment for myelodysplastic syndrome.  Preliminary results of a phase-II trial

Hydralazine and magnesium valpr ...

Decitabine and azacitidine, two DNA methyltransferase (DNMT) inhibitors, are the current standard of treatment for myelodysplastic syndrome (MDS). H ...

220.92 KB
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Myeloid growth factors in acute myeloid leukemia: systematic review of randomized controlled trials

Myeloid growth factors in acute ...

Randomized controlled trials (RCT) investigating administration of colony-stimulating factors (CSF) during or after chemotherapy in acute myeloid le ...

404.43 KB
رایگان
Dysmetabolic hyperferritinemia is associated with normal transferrin saturation, mild hepatic iron overload, and elevated hepcidin

Dysmetabolic hyperferritinemia ...

Hyperferritinemia is common in individuals with the metabolic syndrome (dysmetabolic hyperferritinemia), but its pathophysiology and the degree to w ...

99.71 KB
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Deferasirox effectively decreases iron burden in patients with double heterozygous HbS/â-thalassemia

Deferasirox effectively decreas ...

Iron overload is present in several cases of double heterozygous sickle-cell/beta-thalassemia (HbS/β-thal). Deferasirox is an orally administered ir ...

136.38 KB
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Quantitative analysis of Hb Bart’s in cord blood by capillary electrophoresis system

Quantitative analysis of Hb Bar ...

It has long been recognized that the presence of hemoglobin (Hb) Bart’s in newborn’s blood is associated with α-thalassemia. However, the automated ...

311.20 KB
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Expansion of CD4+CD25+ regulatory T cells from cord blood CD4+ cells using the common م-chain cytokines (IL-2 and IL-15) and rapamycin

Expansion of CD4+CD25+ regulato ...

Rapamycin has important roles in the modulation of regulatory T cells. We tried to expand CD4+CD25+ regulatory T cells (Treg cells) from umbilical c ...

269.55 KB
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Leukemia stem cells

Leukemia stem cells

Leukemia-initiating cells (LICs) or leukemia stem cells (LSCs) are defined by their ability to form tumors after xenotransplantation in immunodefici ...

813.02 KB
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Iron overload in MDS—pathophysiology, diagnosis, and complications

Iron overload in MDS—pathophysi ...

Many patients with myelodysplastic syndromes (MDS) become dependent on blood transfusions and develop transfusional iron overload, which is exacerba ...

367.32 KB
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Proliferation and differentiation potential of CD133+ and CD34+ populations from the bone marrow  and mobilized peripheral blood

Proliferation and differentiati ...

CD34 is the most frequently used marker for the selection of cells for bone marrow (BM) transplantation. The use of CD133 as an alternative marker i ...

365.04 KB
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Variant of the extensor pollicis tertius: a case report  on a unique extensor muscle to the thumb

Variant of the extensor pollici ...

Variations on muscular and tendinous connections of the hand occur frequently in the human population and are often discovered during routine surgic ...

246.93 KB
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A case of double aortic arch accompanied by sub-aortic  and pre-aortic left brachiocephalic veins and anomalous origin  and course of left vertebral artery

A case of double aortic arch ac ...

During the elective course of human dissection at the University of Toyama in 2007, we encountered a rare case of double aortic arch accompanied by ...

229.55 KB
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