戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 ariable ectopic mineralization phenotypes of pseudoxanthoma elasticum.
2 neralization in an Abcc6(-/-) mouse model of pseudoxanthoma elasticum.
3 tion to counteract ectopic mineralization in pseudoxanthoma elasticum.
4 efore provides a novel model system to study pseudoxanthoma elasticum.
5 ssion system in an Abcc6(-/-) mouse model of pseudoxanthoma elasticum.
6 evels underlie the ectopic mineralization in pseudoxanthoma elasticum.
7 issense variants identified in patients with pseudoxanthoma elasticum.
8 rter C6) ABC transporter are associated with pseudoxanthoma elasticum, a disease of altered elastic p
9  drug efflux pumps, are the genetic basis of Pseudoxanthoma elasticum, a disease that affects elastin
10                                              Pseudoxanthoma elasticum, a heritable ectopic mineraliza
11                                              Pseudoxanthoma elasticum, a heritable multisystem ectopi
12                 Mutations in ABCC6 result in pseudoxanthoma elasticum, a multi-system heritable conne
13                                              Pseudoxanthoma elasticum, a prototype of heritable multi
14 eye (3%) had neovascularization secondary to pseudoxanthoma elasticum, all showing similar ORT format
15 f all Vanderbilt Eye Institute patients with pseudoxanthoma elasticum and at least 1 set of color fun
16 early, is a promising prevention therapy for pseudoxanthoma elasticum and generalized arterial calcif
17       This report summarizes the progress in pseudoxanthoma elasticum and other ectopic mineralizatio
18 els, resulting in the calcification disorder pseudoxanthoma elasticum and some cases of generalized a
19 nderlie the incurable calcification disorder pseudoxanthoma elasticum and some cases of generalized a
20 f-function mutations in the ABCC6 gene cause pseudoxanthoma elasticum and type 2 generalized arterial
21          The prototype of such conditions is pseudoxanthoma elasticum, and related conditions with ov
22 ic atrophy independent of CNV can develop in pseudoxanthoma elasticum, causing significant vision los
23 ted a series of Abcc6(-/-) rats as models of pseudoxanthoma elasticum depicting ectopic mineralizatio
24  exemplified by familial tumoral calcinosis, pseudoxanthoma elasticum, generalized arterial calcifica
25 genic disorders of pathologic calcification: pseudoxanthoma elasticum, generalized arterial calcifica
26  dietary preferences of patients may explain pseudoxanthoma elasticum heterogeneous manifestations, a
27                                              Pseudoxanthoma elasticum in humans and dystrophic cardia
28                                              Pseudoxanthoma elasticum is a heritable disease caused b
29  remains unknown, recent studies showed that pseudoxanthoma elasticum is a metabolic disorder caused
30                                              Pseudoxanthoma elasticum is a multisystem ectopic minera
31                                              Pseudoxanthoma elasticum is a prototype of heritable ect
32                                              Pseudoxanthoma elasticum is currently incurable, althoug
33                                              Pseudoxanthoma elasticum like fundus changes are a frequ
34                                              Pseudoxanthoma elasticum-like changes were more frequent
35                                              Pseudoxanthoma elasticum-like fundus changes are a frequ
36  several months prevented the development of pseudoxanthoma elasticum-like spontaneous calcification,
37                                              Pseudoxanthoma elasticum patients and Abcc6(-/-) mice di
38 mately 200 mutations have been identified in pseudoxanthoma elasticum patients, the underlying struct
39                       Phenylketonuria (PKU), pseudoxanthoma elasticum (PXE) and hereditary tyrosinemi
40 BCC6 gene cause soft-tissue calcification in pseudoxanthoma elasticum (PXE) and, in some patients, ge
41 iations cause the calcification phenotype of pseudoxanthoma elasticum (PXE) as well as some cases of
42                                              Pseudoxanthoma elasticum (PXE) is a classic inherited di
43                                              Pseudoxanthoma elasticum (PXE) is a genetic multisystem
44                                              Pseudoxanthoma elasticum (PXE) is a heritable disorder c
45                                              Pseudoxanthoma elasticum (PXE) is a heritable disorder m
46                                              Pseudoxanthoma elasticum (PXE) is a heritable ectopic ca
47                                              Pseudoxanthoma elasticum (PXE) is a multisystem disorder
48                                              Pseudoxanthoma elasticum (PXE) is a multisystem ectopic
49                                              Pseudoxanthoma elasticum (PXE) is a pleiotropic multisys
50                                              Pseudoxanthoma elasticum (PXE) is a systemic heritable d
51                                              Pseudoxanthoma elasticum (PXE) is an autosomal recessive
52                                              Pseudoxanthoma elasticum (PXE) is an autosomal recessive
53                                              Pseudoxanthoma elasticum (PXE) is an autosomal recessive
54                                              Pseudoxanthoma elasticum (PXE) is caused by mutations in
55                                              Pseudoxanthoma elasticum (PXE) is caused by mutations in
56                                              Pseudoxanthoma elasticum (PXE) is caused by mutations in
57                   The pathologic hallmark of pseudoxanthoma elasticum (PXE) is ectopic mineralization
58  in atherosclerosis using Ldlr(-/-) mice and pseudoxanthoma elasticum (PXE) patients.
59                                  The classic pseudoxanthoma elasticum (PXE) phenotype derives from mu
60 rformed linkage analysis on 21 families with pseudoxanthoma elasticum (PXE) using 10 polymorphic mark
61 cular fundus abnormalities characteristic of pseudoxanthoma elasticum (PXE) were detected by cSLO in
62 cause of a relatively frequent inborn error, pseudoxanthoma elasticum (PXE), a disorder resulting in
63 ecular basis and pathomechanistic details in pseudoxanthoma elasticum (PXE), a heritable multisystem
64           The prototype of such disorders is pseudoxanthoma elasticum (PXE), a late-onset, slowly pro
65                                              Pseudoxanthoma elasticum (PXE), a multisystem disorder c
66                                              Pseudoxanthoma elasticum (PXE), a pleiotropic heritable
67                                              Pseudoxanthoma elasticum (PXE), a pleiotropic multisyste
68                                              Pseudoxanthoma elasticum (PXE), a prototype of heritable
69                                              Pseudoxanthoma elasticum (PXE), a prototype of heritable
70                                              Pseudoxanthoma elasticum (PXE), a prototypic heritable d
71                                              Pseudoxanthoma elasticum (PXE), a rare genetic disease c
72                                              Pseudoxanthoma elasticum (PXE), an autosomal recessive d
73          A characteristic feature of classic pseudoxanthoma elasticum (PXE), an autosomal recessive d
74 ients with angioid streaks (AS) secondary to pseudoxanthoma elasticum (PXE), and to introduce a clini
75 A), Stargardt disease (STGD1), Best disease, pseudoxanthoma elasticum (PXE), central areolar choroida
76                                              Pseudoxanthoma elasticum (PXE), characterized by connect
77 cular fundus abnormalities characteristic of pseudoxanthoma elasticum (PXE), including peau d'orange,
78          The ABCC6 gene, which is mutated in pseudoxanthoma elasticum (PXE), resided within a small r
79                 Although clinical similar to pseudoxanthoma elasticum (PXE), the skin changes were fo
80    To better understand the pathogenetics of pseudoxanthoma elasticum (PXE), we performed a mutationa
81 system have been identified in families with pseudoxanthoma elasticum (PXE).
82 ion to mitigate calcification progression in pseudoxanthoma elasticum, that dietary preferences of pa
83 ions in four candidate genes associated with pseudoxanthoma elasticum, the prototype of ectopic miner
84                   The phenotypic spectrum of pseudoxanthoma elasticum varies, and the correlation bet
85                In a humanized mouse model of pseudoxanthoma elasticum, we investigated whether 4-PBA
86  The fundamental question on pathogenesis of pseudoxanthoma elasticum, whether lack of ABCC6 expressi