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1  several RBC disorders, including hereditary spherocytosis.
2 to decreased ANK1 mRNA levels and hereditary spherocytosis.
3 n associated with a hereditary human anemia, spherocytosis.
4  that underlies ankyrin-deficient hereditary spherocytosis.
5 en controls and splenectomized subjects with spherocytosis.
6  affect protein 4.2 and result in hereditary spherocytosis.
7 et formation, thrombocytopenia, and platelet spherocytosis.
8 esembling RBCs from patients with hereditary spherocytosis.
9 ions is a key pathogenic event in hereditary spherocytosis.
10 c hemolytic anemia without family history of spherocytosis.
11 or nondominant spectrin-deficient hereditary spherocytosis.
12    Indication for splenectomy was hereditary spherocytosis (111), immune thrombocytopenic purpura (36
13 s defective in many patients with hereditary spherocytosis, a common hemolytic anemia.
14                  In children with hereditary spherocytosis, a partial splenectomy appears to control
15         Accordingly, the apparently isolated spherocytosis allows investigation of the role of discoi
16 he most common cause in humans of hereditary spherocytosis, an inherited anemia that affects patients
17         For some forms of autism, hereditary spherocytosis and color blindness, the culprits are sing
18 rythrocyte band 3 and its role in hereditary spherocytosis and distal renal tubular acidosis are desc
19 exchanger 1; SLC4A1) causing both hereditary spherocytosis and distal renal tubular acidosis.
20                                  For RBCs in spherocytosis and elliptocytosis, the bilayer-cytoskelet
21 e found in human diseases such as hereditary spherocytosis and elliptocytosis.
22 xt of hereditary hemolytic disorders such as spherocytosis and elliptocytosis.
23 ed blood cells from patients with hereditary spherocytosis and elliptocytosis.
24 of red blood cell shape including hereditary spherocytosis and elliptocytosis.
25 ective RBCs in hereditary disorders, such as spherocytosis and elliptocytosis.
26 consists of a moderate hemolytic anemia with spherocytosis and frequent spiculation of the red cells.
27 rane vesicles and tubules, leading to severe spherocytosis and hemolysis, but the levels of the major
28  gene expression in patients with hereditary spherocytosis and hereditary pyropoikilocytosis.
29 d beta chain, and associated with hereditary spherocytosis and isolated spectrin deficiency.
30 ory responses including increased neutrophil spherocytosis and macrophage production of IL-10.
31 ssential diagnostic component for hereditary spherocytosis and may correlate with hemolytic parameter
32               Using a genetic mouse model of spherocytosis and single-cell RNA sequencing, we found t
33 ably associated with mild autosomal dominant spherocytosis and with the presence of pincered red cell
34  recent studies on band 3-induced hereditary spherocytosis are reviewed and an explanation for the mi
35 ve implications beyond muscle for hereditary spherocytosis, as KCTD6 is also present in erythrocytes,
36                 Fragments with the -108/-153 spherocytosis-associated mutations failed to function as
37 c thrombocytopenic purpura (ITP), hereditary spherocytosis, autoimmune hemolytic anemia, thrombotic t
38 own to be associated with diseases including spherocytosis, cardiac arrhythmia, and bipolar disorder
39                                              Spherocytosis-causing coding mutations in these genes ar
40 as in both the hereditary stomatocytosis and spherocytosis classes.
41 (180 mumol/g) in one patient with hereditary spherocytosis discovered after LT.
42 oform in platelet structure and suggest that spherocytosis does not impair many aspects of platelet f
43 hanics in hereditary blood disorders such as spherocytosis, elliptocytosis, and especially, sickle ce
44 n and regulatory variation at two hereditary spherocytosis genes, ANK1 and SPTA1.
45 the erythrocyte membrane, such as hereditary spherocytosis, hereditary elliptocytosis, and hereditary
46  well-known red cell pathologies (hereditary spherocytosis, hereditary elliptocytosis, hereditary hyd
47 m of RBC removal in diseases like hereditary spherocytosis (HS) and autoimmune hemolytic anemia, but
48                                In hereditary spherocytosis (HS) and hereditary elliptocytosis (HE), d
49 keleton; sph/sph mice have severe hereditary spherocytosis (HS) because of a mutation in the murine e
50  Several subsets of patients with hereditary spherocytosis (HS) have been defined based on the specif
51                                   Hereditary spherocytosis (HS) is a common hemolytic anemia of varia
52                                   Hereditary spherocytosis (HS) is the most common inherited haemolyt
53 eta-spectrin can result in severe hereditary spherocytosis (HS) or hereditary elliptocytosis (HE) in
54 mans lead to the hemolytic anemia Hereditary Spherocytosis (HS) which includes a subpopulation with n
55              Sixteen children had hereditary spherocytosis (HS), and nine children had other erythroc
56 eatures characteristic of RBCs in hereditary spherocytosis (HS), including spherocytes with significa
57 ses the disease ankyrin-deficient Hereditary Spherocytosis (HS).
58 common cause of typical, dominant hereditary spherocytosis (HS).
59 ary pyropoikilocytosis (HPP), and hereditary spherocytosis (HS).
60 ects are the most common cause of hereditary spherocytosis (HS).
61 embrane skeleton components cause hereditary spherocytosis (HS).
62 lpha- or beta-spectrin results in hereditary spherocytosis (HS).
63 .2-null (4.2(-/-)) mice have mild hereditary spherocytosis (HS).
64 ood cells (RBCs) in patients with hereditary spherocytosis (HS).
65 ied a French kindred with typical hereditary spherocytosis (HS).
66 ength and reduced tortuosity) and hereditary spherocytosis (HS; expanded pathlength).
67 or nondominant spectrin-deficient hereditary spherocytosis in approximately 50% of studied families.
68  revealed evidence of compensated anemia and spherocytosis in the dematin headpiece null mice.
69 le cell disease, thalassemia, and hereditary spherocytosis, in which dehydration contributes to disea
70 he mild phenotype of heterozygous hereditary spherocytosis is discussed.
71 Rs and suggest that the origin of hereditary spherocytosis may be related to mechanical failure of AR
72 t quantitative trait locus, Hsm1 (hereditary spherocytosis modifier 1), localizes to mouse Chromosome
73                                              Spherocytosis mutant (Spna1(sph)/Spna1(sph); for simplic
74 vo establishing it as a causative hereditary spherocytosis mutation.
75 = 0.01) but the same levels as subjects with spherocytosis (p = 0.15.) There was no correlation betwe
76 ankyrin gene in ankyrin-deficient hereditary spherocytosis patients and to provide additional insight
77 mbly, and that possible thrombotic events in spherocytosis patients are not likely associated with al
78 ls for further genetic studies of hereditary spherocytosis patients, we cloned the human ANK-1 chromo
79 distinct subsets of patients with hereditary spherocytosis: Patients with isolated spectrin deficienc
80 fiers, these common alleles may explain mild spherocytosis phenotypes that have been observed clinica
81 icient (sph/sph) mice with severe hereditary spherocytosis, providing a model for events preceding th
82 a in most patients with recessive hereditary spherocytosis (rHS) and the related disorder hereditary
83 n gene, Spna1, have been identified in mice (spherocytosis [sph], sph(1J), sph(2J), sph(2BC), sph(Dem
84                                          The spherocytosis syndromes, with a few rare exceptions, are
85 tive markers for diseases such as hereditary spherocytosis, thalassemia, and malaria.
86 gnificantly older age than participants with spherocytosis, these data suggest that an age-related lo
87  membrane such as morphological alterations (spherocytosis), translocation of aminophospholipids to t
88 ne protein, protein 4.2, leads to hereditary spherocytosis type 5.
89           Study of a novel band 3 hereditary spherocytosis variant suggests that expression of mutant
90 , thalassemia, hemoglobin CC, and hereditary spherocytosis, where cellular dehydration may be a signi
91 ant form of HS associated with a conspicuous spherocytosis with frequent spiculated cells (8% to 15%
92 was noted in 92% of patients with hereditary spherocytosis, without relapse for the duration of the o