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1 Myelofibrosis (MF) is a devastating blood disorder.
2 a mechanosensitive ion channel involved in a blood disorder.
3 r mutations are responsible for a variety of blood disorders.
4 at is used to treat preleukemic and leukemic blood disorders.
5 tributed between malignant and non-malignant blood disorders.
6 mpanion Article to obtain the total costs of blood disorders.
7 from individuals without evidence of clonal blood disorders.
8 ce and for therapeutic strategies in genetic blood disorders.
9 ietic grafts to treat inherited and acquired blood disorders.
10 lymphocytic leukemia (CLL) and other clonal blood disorders.
11 y atherosclerosis, but also septic emboli or blood disorders.
12 velopment and provide new insight into human blood disorders.
13 spectrin tetramer formation, and may lead to blood disorders.
14 o the pathophysiology of cardiopulmonary and blood disorders.
15 ation in cellular immunotherapy of malignant blood disorders.
16 o generate transplantable cells for treating blood disorders.
17 apeutic potential of RNAi for treating these blood disorders.
18 mportant target for the treatment of various blood disorders.
19 ed levels of engraftment for gene therapy of blood disorders.
20 In one form of beta-thalassemia, a genetic blood disorder, a mutation in intron 2 of the beta-globi
21 d to assess the economic burden of malignant blood disorders across the 28 countries in the European
22 assess the economic burden of non-malignant blood disorders across the 28 countries of the European
25 globin gene transfer in treating a fulminant blood disorder and strongly support the efficacy of gene
26 upregulated in a variety of human neoplastic blood disorders and constitutive upregulation of miR-125
28 udied exclusively in patients with inherited blood disorders and hepatitis C virus (HCV) infection.
38 poietic cells from unrelated donors can cure blood disorders but carries a significant risk of acute
39 s, including acute leukaemias and congenital blood disorders, but obtaining suitable numbers of cells
40 genital, disease-associated, or drug-induced blood disorders can cause significant morbidities and mo
42 a (beta-Thal) is a group of life-threatening blood disorders caused by either point mutations or dele
45 ickle cell disease (SCD) is a severe genetic blood disorder characterized by hemolytic anemia, episod
46 CSAs) are a heterogeneous group of inherited blood disorders characterized by pathological mitochondr
53 c cell transplant (HCT) for the treatment of blood disorders, even with optimal donor HLA matching an
54 these costs we added those due to malignant blood disorders (ICD-10 C81-96 and D47) as estimated in
55 ll disease (SCD) is a highly complex genetic blood disorder in which red blood cells (RBC) exhibit he
59 the pathophysiology and treatment of several blood disorders, including the anaemia of renal disease.
61 ain impediments to effective gene therapy of blood disorders is the resistance of human hematopoietic
63 obesity, infectious disease susceptibility, blood disorders, neurosensory disorders, drug addiction
65 ights the economic burden that non-malignant blood disorders place on European health-care systems an
69 ovide a new candidate for the rare inherited blood disorder stomatocytosis with uncompensated anemia.
70 g of the erythrocyte mechanics in hereditary blood disorders such as spherocytosis, elliptocytosis, a
73 turnal hemoglobinuria (PNH) is a rare clonal blood disorder that manifests with hemolytic anemia, bon
76 utations in these genes are commonly seen in blood disorders underscores their critical roles and hig
79 ifying disease-causing variants in Mendelian blood disorders were identified and implemented as AbFab
80 t patients had primary immunodeficiencies or blood disorders, while 4 others had abnormal immune func
81 ll disease (SCD) is a debilitating monogenic blood disorder with a highly variable phenotype characte
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