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1 1) promoter that underlies ankyrin-deficient hereditary spherocytosis.
2 e mutations affect protein 4.2 and result in hereditary spherocytosis.
3 ild type, resembling RBCs from patients with hereditary spherocytosis.
4 ogenesis of several RBC disorders, including hereditary spherocytosis.
5 se interactions is a key pathogenic event in hereditary spherocytosis.
6 recessive or nondominant spectrin-deficient hereditary spherocytosis.
7 egion lead to decreased ANK1 mRNA levels and hereditary spherocytosis.
11 gene are the most common cause in humans of hereditary spherocytosis, an inherited anemia that affec
13 d 3 (anion exchanger 1; SLC4A1) causing both hereditary spherocytosis and distal renal tubular acidos
14 ucture of erythrocyte band 3 and its role in hereditary spherocytosis and distal renal tubular acidos
18 ha-spectrin gene expression in patients with hereditary spherocytosis and hereditary pyropoikilocytos
19 a truncated beta chain, and associated with hereditary spherocytosis and isolated spectrin deficienc
20 ls are an essential diagnostic component for hereditary spherocytosis and may correlate with hemolyti
21 The most recent studies on band 3-induced hereditary spherocytosis are reviewed and an explanation
22 in-1 may have implications beyond muscle for hereditary spherocytosis, as KCTD6 is also present in er
23 e idiopathic thrombocytopenic purpura (ITP), hereditary spherocytosis, autoimmune hemolytic anemia, t
25 sorders of the erythrocyte membrane, such as hereditary spherocytosis, hereditary elliptocytosis, and
26 leading to well-known red cell pathologies (hereditary spherocytosis, hereditary elliptocytosis, her
27 he mechanism of RBC removal in diseases like hereditary spherocytosis (HS) and autoimmune hemolytic a
29 hroid cytoskeleton; sph/sph mice have severe hereditary spherocytosis (HS) because of a mutation in t
33 alpha- or beta-spectrin can result in severe hereditary spherocytosis (HS) or hereditary elliptocytos
34 teins in humans lead to the hemolytic anemia Hereditary Spherocytosis (HS) which includes a subpopula
36 emia with features characteristic of RBCs in hereditary spherocytosis (HS), including spherocytes wit
47 recessive or nondominant spectrin-deficient hereditary spherocytosis in approximately 50% of studied
48 nclude sickle cell disease, thalassemia, and hereditary spherocytosis, in which dehydration contribut
50 erties of ARs and suggest that the origin of hereditary spherocytosis may be related to mechanical fa
51 significant quantitative trait locus, Hsm1 (hereditary spherocytosis modifier 1), localizes to mouse
53 DNA of the ankyrin gene in ankyrin-deficient hereditary spherocytosis patients and to provide additio
54 cessary tools for further genetic studies of hereditary spherocytosis patients, we cloned the human A
55 fines four distinct subsets of patients with hereditary spherocytosis: Patients with isolated spectri
56 pectrin-deficient (sph/sph) mice with severe hereditary spherocytosis, providing a model for events p
59 ell disease, thalassemia, hemoglobin CC, and hereditary spherocytosis, where cellular dehydration may
60 e response was noted in 92% of patients with hereditary spherocytosis, without relapse for the durati
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