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Pancytopenia and thrombosis defects in zebrafish mutants of Fanconi anemia genes

期刊: BLOOD CELLS MOLECULES AND DISEASES, 2022; 93 ()

Progressive pancytopenia is a common feature observed in DNA crosslink repair deficiency disorder, Fanconi anemia (FA). However, this phenotype has no......

JIF:2.453

Missense mutation in RPS7 causes Diamond-Blackfan anemia via alteration of erythrocyte metabolism, protein translation and induction of ribosomal stress

期刊: BLOOD CELLS MOLECULES AND DISEASES, 2022; 97 ()

Diamond-Blackfan anemia (DBA) is predominantly underlined by mutations in genes encoding ribosomal proteins (RP); however, its etiology remains unexpl......

JIF:2.453

TMEM16F mediated phosphatidylserine exposure and microparticle release on erythrocyte contribute to hypercoagulable state in hyperuricemia

期刊: BLOOD CELLS MOLECULES AND DISEASES, 2022; 96 ()

The link between hyperuricemia (HUA) and the risk of venous thromboembolism (VTE) has been well established. However, the mechanisms of thrombus gener......

JIF:2.453

VCAM1, HMOX1 and NOS3 differential endothelial expression may impact sickle cell anemia vasculopathy

期刊: BLOOD CELLS MOLECULES AND DISEASES, 2022; 93 ()

Endothelial dysfunction plays a major role in sickle cell anemia (SCA) systemic vasculopathy, with upregulation of adhesion molecules (e.g., VCAM-1), ......

JIF:2.453

Upregulation of cytokine signalling in platelets increases risk of thrombophilia in severe COVID-19 patients

期刊: BLOOD CELLS MOLECULES AND DISEASES, 2022; 94 ()

Abnormal coagulation dynamics, including disseminated intravascular coagulopathy, pulmonary embolism, venous thromboembolism and risk of thrombosis ar......

JIF:2.453

Liver kinase B1 (LKB1) in murine erythroid progenitors modulates erythropoietin setpoint in association with maturation control

期刊: BLOOD CELLS MOLECULES AND DISEASES, 2022; 97 ()

Erythropoiesis is a tightly regulated process. It is stimulated by decreased oxygen in circulation, which leads to the secretion of the hormone erythr......

JIF:2.453

A case of VEXAS syndrome associated with EBV-associated hemophagocytic lymphohistiocytosis

期刊: BLOOD CELLS MOLECULES AND DISEASES, 2022; 93 ()

Vacuoles, E1, X-linked, autoimmunity, somatic (VEXAS) syndrome is characterized by a pathogenic mutation in UBA1, which leads to protean complications......

JIF:2.453

Preclusion of methemoglobinemia caused by nitrate drugs in diabetics and nondiabetics: Possible role of Vitamin C

期刊: BLOOD CELLS MOLECULES AND DISEASES, 2022; 94 ()

The drugs containing nitrates like isosorbide dinitrate, isosorbide mononitrate and glyceryl trinitrate, etc., trigger the oxidation of hemoglobin whi......

JIF:2.453

Anti-TFPI for hemostasis induction in patients with rare bleeding disorders, an ex vivo thrombin generation (TG) guided pilot study

期刊: BLOOD CELLS MOLECULES AND DISEASES, 2022; 95 ()

Background: Rare bleeding disorders (RBD) are inherited coagulopathies, whose hemostatic control is based upon replacement therapy. Marstacimab (PF-06......

JIF:2.453

Indices of iron homeostasis in asymptomatic subjects with HFE mutations and moderate ferritin elevation during iron removal treatment

期刊: BLOOD CELLS MOLECULES AND DISEASES, 2022; 97 ()

We analysed iron biomarkers and their relationships in 30 subjects with HFE mutations and moderate hyperferritinaemia undergoing iron removal at our b......

JIF:2.453

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