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1 ly impact protein function and cause a novel autoinflammatory disorder.
2 nderstood, but PG is generally considered an autoinflammatory disorder.
3 ar connection between two seemingly distinct autoinflammatory disorders.
4  disrupt nucleic acid metabolism can lead to autoinflammatory disorders.
5  infections, malignancies, or autoimmune and autoinflammatory disorders.
6 erleukin-1 receptor antagonist used to treat autoinflammatory disorders.
7 implicated in the pathogenesis of hereditary autoinflammatory disorders.
8 ts of systemic inflammation in patients with autoinflammatory disorders.
9 ction and predispose individuals to specific autoinflammatory disorders.
10 rial rash, such as urticarial vasculitis and autoinflammatory disorders.
11 que IFN signaling signature, unlike in other autoinflammatory disorders.
12 ich places these entities in the category of autoinflammatory disorders.
13 ng of caspase-1 inhibitors such as VX-765 in autoinflammatory disorders.
14 e have been recently linked to three chronic autoinflammatory disorders.
15 a pathogenic role in numerous autoimmune and autoinflammatory disorders.
16 ition defects, and (4) Hyperinflammatory and autoinflammatory disorders.
17             It has been associated with rare autoinflammatory disorders.
18 ion through inherited NLRP3 mutations causes autoinflammatory disorders.
19 me, 6 (6.4%) a phagocyte defect, 7 (7.4%) an autoinflammatory disorder, 14 (15%) a combined immunodef
20 n and features prominently in autoimmune and autoinflammatory disorders, allergy, acute and chronic i
21 LCG2)-mutations in which are associated with autoinflammatory disorders and Alzheimer's disease-serve
22 availability can affect infectious diseases, autoinflammatory disorders and antitumour immunity.
23 nsor of double-stranded DNA, is activated in autoinflammatory disorders and by DNA damage.
24 s cause an array of human diseases including autoinflammatory disorders and cancer.
25 nition of self RNAs by RLRs is implicated in autoinflammatory disorders and cancer.
26 in patients with underlying rheumatologic or autoinflammatory disorders and is usually designated mac
27  a broad spectrum of diseases from cancer to autoinflammatory disorders and neurological conditions.
28 g the distinguishing features of the classic autoinflammatory disorders, and appreciating the treatme
29               CARD9 has been associated with autoinflammatory disorders, and loss-of-function mutatio
30 s well as the pathogenesis of autoimmune and autoinflammatory disorders, and serves to link adaptive
31                                      Several autoinflammatory disorders are associated with missense
32  the boundaries of what are considered to be autoinflammatory disorders are constantly evolving and c
33 immunological reclassification of SJIA as an autoinflammatory disorder as well as detailing the drama
34                                   Gout is an autoinflammatory disorder associated with deposition of
35 e, and many features of FMF overlap with the autoinflammatory disorder associated with TNF receptor s
36 ase 1 (ERAP1), Hap10, is associated with the autoinflammatory disorder Behcet's disease (BD) in epist
37          We sought to report a new monogenic autoinflammatory disorder caused by a de novo activating
38 d, autoinflammatory, somatic) syndrome is an autoinflammatory disorder caused by acquired somatic ubi
39 tor-associated periodic syndrome (TRAPS), an autoinflammatory disorder caused by missense mutations i
40  involvement is a defining characteristic of autoinflammatory disorders caused by abnormal IL-1 signa
41 Blau syndrome is a rare, autosomal-dominant, autoinflammatory disorder characterized by granulomatous
42 TRAPS, OMIM 142680) is an autosomal dominant autoinflammatory disorder characterized by prolonged att
43 al Mediterranean Fever (FMF) is an inherited autoinflammatory disorder characterized by unprovoked ep
44  the gene encoding NLRP3 are associated with autoinflammatory disorders characterized with excessive
45  the gene encoding pyrin are associated with autoinflammatory disorder Familial Mediterranean Fever (
46 ing pyrin in humans, are associated with the autoinflammatory disorder familial Mediterranean fever.
47 ense mutations in the CIAS1 gene cause three autoinflammatory disorders: familial cold autoinflammato
48 ed to cause familial Mediterranean fever, an autoinflammatory disorder highly prevalent in Armenians.
49                                   SJIA is an autoinflammatory disorder in which defects of innate imm
50 cal clues and tips that can help to identify autoinflammatory disorders in patients presenting with c
51 opoietic stem cell transplantation (HSCT) in autoinflammatory disorders, including PAMI syndrome, has
52 that compromise TREX1 function are linked to autoinflammatory disorders, including systemic lupus ery
53 ulated, disruption of which triggers various autoinflammatory disorders, including TNF receptor-assoc
54 ment of precise therapeutic targets to treat autoinflammatory disorders, infectious diseases, and can
55       Familial Mediterranean fever (FMF), an autoinflammatory disorder, is associated with mutations
56 , somatic) syndrome is a recently discovered autoinflammatory disorder linked to somatic mutations in
57 th FMF mutation (MefvV726A/V726A) exhibit an autoinflammatory disorder mediated by autoactivation of
58 sum, and acne (PAPA), a dominantly inherited autoinflammatory disorder mediated predominantly by gran
59 inflammatory syndrome (FCAS) and the related autoinflammatory disorders, Muckle-Wells syndrome and ne
60 LP3/CIAS1/cryopyrin gene are linked to three autoinflammatory disorders: Muckle-Wells syndrome, famil
61                                          The autoinflammatory disorder, Neonatal-onset Multisystem In
62 ed, inflammation may result in autoimmune or autoinflammatory disorders, neurodegenerative disease, o
63 function are the most frequent cause of this autoinflammatory disorder of childhood and are also asso
64 ulmonary and cutaneous vasculitis as a novel autoinflammatory disorder of inborn errors of immunity.
65 s and treatment of rare, genetically defined autoinflammatory disorders, physicians are challenged by
66 ns are associated with proteasome-associated autoinflammatory disorders (PRAAS).
67  and introduce major categories of monogenic autoinflammatory disorders recognized to date, including
68                                         Many autoinflammatory disorders result from disruption of com
69              This pathway is dysregulated in autoinflammatory disorders such as hyper-IgD syndrome, i
70 ations in the MEFV gene encoding Pyrin cause autoinflammatory disorders, such as familial Mediterrane
71 ted in the pathogenesis of interferon-driven autoinflammatory disorders, such as SLE.
72                   This mouse strain shows an autoinflammatory disorder that is prevented by genetic d
73 t multifocal osteomyelitis (CRMO) is a human autoinflammatory disorder that primarily affects bone.
74    The cryopyrinopathies are a group of rare autoinflammatory disorders that are caused by mutations
75 s (PFSs) comprise a subset of the hereditary autoinflammatory disorders that are defined by recurrent
76                      Though a complex set of autoinflammatory disorders that can be precipitated by d
77 ells syndrome (MWS) are dominantly inherited autoinflammatory disorders that cause rashes, fever, art
78 urther underscored by their association with autoinflammatory disorders, wherein localized inflammati
79 l Mediterranean fever (FMF) is an archetypal autoinflammatory disorder, which is autosomal recessive
80 utrophilic dermatosis (PAAND) is a monogenic autoinflammatory disorder with autosomal dominant inheri
81 , caused by somatic mutations in UBA1, is an autoinflammatory disorder with diverse systemic manifest
82 anean fever (FMF) is a recessively inherited autoinflammatory disorder with high carrier frequencies
83 thogenesis of pustular psoriasis, a model of autoinflammatory disorders with predominant cutaneous ma