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1 mineralization phenotypes of pseudoxanthoma elasticum.
2 an Abcc6(-/-) mouse model of pseudoxanthoma elasticum.
3 act ectopic mineralization in pseudoxanthoma elasticum.
4 a novel model system to study pseudoxanthoma elasticum.
5 an Abcc6(-/-) mouse model of pseudoxanthoma elasticum.
6 the ectopic mineralization in pseudoxanthoma elasticum.
7 s identified in patients with pseudoxanthoma elasticum.
8 ansporter are associated with pseudoxanthoma elasticum, a disease of altered elastic properties in mu
9 mps, are the genetic basis of Pseudoxanthoma elasticum, a disease that affects elastin fibers in the
12 Mutations in ABCC6 result in pseudoxanthoma elasticum, a multi-system heritable connective tissue di
15 t Eye Institute patients with pseudoxanthoma elasticum and at least 1 set of color fundus photographs
16 mising prevention therapy for pseudoxanthoma elasticum and generalized arterial calcification of infa
17 rt summarizes the progress in pseudoxanthoma elasticum and other ectopic mineralization disorders, as
18 in the calcification disorder pseudoxanthoma elasticum and some cases of generalized arterial calcifi
19 urable calcification disorder pseudoxanthoma elasticum and some cases of generalized arterial calcifi
20 tions in the ABCC6 gene cause pseudoxanthoma elasticum and type 2 generalized arterial calcification
21 ototype of such conditions is pseudoxanthoma elasticum, and related conditions with overlapping clini
23 Abcc6(-/-) rats as models of pseudoxanthoma elasticum depicting ectopic mineralization in the skin,
24 familial tumoral calcinosis, pseudoxanthoma elasticum, generalized arterial calcification of infancy
25 of pathologic calcification: pseudoxanthoma elasticum, generalized arterial calcification of infancy
26 ences of patients may explain pseudoxanthoma elasticum heterogeneous manifestations, and that animal
29 n, recent studies showed that pseudoxanthoma elasticum is a metabolic disorder caused by reduced circ
36 prevented the development of pseudoxanthoma elasticum-like spontaneous calcification, but failed to
38 tions have been identified in pseudoxanthoma elasticum patients, the underlying structural defects as
40 soft-tissue calcification in pseudoxanthoma elasticum (PXE) and, in some patients, generalized arter
41 he calcification phenotype of pseudoxanthoma elasticum (PXE) as well as some cases of generalized art
57 The pathologic hallmark of pseudoxanthoma elasticum (PXE) is ectopic mineralization of soft connec
60 analysis on 21 families with pseudoxanthoma elasticum (PXE) using 10 polymorphic markers located on
61 normalities characteristic of pseudoxanthoma elasticum (PXE) were detected by cSLO in 70 of 255 patie
62 tively frequent inborn error, pseudoxanthoma elasticum (PXE), a disorder resulting in aberrant calcif
63 d pathomechanistic details in pseudoxanthoma elasticum (PXE), a heritable multisystem ectopic mineral
64 rototype of such disorders is pseudoxanthoma elasticum (PXE), a late-onset, slowly progressing disord
72 acteristic feature of classic pseudoxanthoma elasticum (PXE), an autosomal recessive disorder caused
74 oid streaks (AS) secondary to pseudoxanthoma elasticum (PXE), and to introduce a clinical classificat
75 isease (STGD1), Best disease, pseudoxanthoma elasticum (PXE), central areolar choroidal dystrophy (CA
77 normalities characteristic of pseudoxanthoma elasticum (PXE), including peau d'orange, angioid streak
78 CC6 gene, which is mutated in pseudoxanthoma elasticum (PXE), resided within a small region of homozy
79 Although clinical similar to pseudoxanthoma elasticum (PXE), the skin changes were found to be due t
80 derstand the pathogenetics of pseudoxanthoma elasticum (PXE), we performed a mutational analysis of A
82 calcification progression in pseudoxanthoma elasticum, that dietary preferences of patients may expl
83 ndidate genes associated with pseudoxanthoma elasticum, the prototype of ectopic mineralization disor
84 The phenotypic spectrum of pseudoxanthoma elasticum varies, and the correlation between genotype a
85 In a humanized mouse model of pseudoxanthoma elasticum, we investigated whether 4-PBA treatments coul
86 l question on pathogenesis of pseudoxanthoma elasticum, whether lack of ABCC6 expression in liver or