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1 was initially neutrophilic, and later became granulomatous.
2 oni is an opportunistic pathogen that causes granulomatous amoebic encephalitis (GAE), a chronic and
3  of the eye and the almost universally fatal granulomatous amoebic encephalitis.
4  occur in lymphomas, whereas others, such as granulomatous angiitis, are only described in HL.
5               The presence of VZV antigen in granulomatous aortitis was highly significant (P = .0001
6 rizes the pathology of giant cell arteritis, granulomatous aortitis, and intracerebral varicella zost
7 y produces stroke, giant cell arteritis, and granulomatous aortitis, and it develops after virus reac
8 tes with the significant detection of VZV in granulomatous aortitis.
9         Inflammatory infiltrates, often with granulomatous arrangements, are distributed as a panarte
10                                              Granulomatous arteritis characterizes the pathology of g
11 11 of 11 aortas with pathologically verified granulomatous arteritis, in 1 of 1 cases of nongranuloma
12                                    Pediatric granulomatous arthritis (PGA) has been associated with 1
13 ing from mutations in the NOD2 gene, wherein granulomatous arthritis, uveitis, and dermatitis develop
14 , autoinflammatory disorder characterized by granulomatous arthritis, uveitis, and dermatitis.
15 delayed-onset combined immune deficiency and granulomatous/autoimmune manifestations (CID-G/AI), prod
16                                          The granulomatous character of Blau syndrome provides an opp
17 f an infant with severe IBD characterized by granulomatous colitis and severe perianal disease, we id
18 to identify genetic factors that might cause granulomatous colitis and severe perianal disease, with
19 patients develop other complications such as granulomatous colitis and/or fatal pulmonary fibrosis.
20 and in some patients, pulmonary fibrosis and granulomatous colitis.
21 hic epilepsy, lymphoma, mast cell tumour and granulomatous colitis; for morphological traits, we repo
22 us disease, causing recurrent infections and granulomatous complications.
23  thymectomy subsequently developed extensive granulomatous destruction of midface structures, palate,
24 unocompromising condition, including chronic granulomatous disease (CGD) (n=4), diabetes mellitus (DM
25       The rarer PID patients without chronic granulomatous disease (CGD) achieved an OS at 3 years of
26 s involved in the pathophysiology of chronic granulomatous disease (CGD) and sepsis.
27 circulating B cells in patients with chronic granulomatous disease (CGD) and those with HIV infection
28                   Liver abscesses in chronic granulomatous disease (CGD) are typically difficult to t
29                                      Chronic granulomatous disease (CGD) can be cured by allogeneic h
30 fective neutrophils in patients with chronic granulomatous disease (CGD) cause susceptibility to extr
31                        Patients with chronic granulomatous disease (CGD) experience immunodeficiency
32  leukocytes (PMN) from patients with chronic granulomatous disease (CGD) fail to produce microbicidal
33 educed in the blood of patients with chronic granulomatous disease (CGD) for reasons and consequences
34                Although prognosis of Chronic Granulomatous Disease (CGD) has greatly improved, few st
35                        Patients with chronic granulomatous disease (CGD) have a mutated NADPH complex
36 t described the clinical features of chronic granulomatous disease (CGD) in 1959.
37 ears of age) often resembles that of chronic granulomatous disease (CGD) in extent and features of co
38                                      Chronic granulomatous disease (CGD) is a primary immune deficien
39                                      Chronic granulomatous disease (CGD) is a primary immunodeficienc
40                                      Chronic granulomatous disease (CGD) is a primary immunodeficienc
41                                      Chronic granulomatous disease (CGD) is a rare phagocytic disorde
42                                      Chronic granulomatous disease (CGD) is a rare primary immunodefi
43                                      Chronic granulomatous disease (CGD) is an inherited disorder cha
44  aspergillosis (IA) in patients with chronic granulomatous disease (CGD) is Aspergillus fumigatus fol
45                                      Chronic granulomatous disease (CGD) is associated with significa
46                                      Chronic granulomatous disease (CGD) is characterized by recurren
47                                      Chronic granulomatous disease (CGD) is due to defective nicotina
48                  Immunodeficiency in chronic granulomatous disease (CGD) is well characterized.
49     NADPH oxidase 2 (Nox2)-deficient chronic granulomatous disease (CGD) mice that lack the gp91(phox
50  inhibited oxidase, or isolated from chronic granulomatous disease (CGD) patients and mice, formed mo
51                                      Chronic granulomatous disease (CGD) patients are susceptible to
52                                      Chronic granulomatous disease (CGD) patients have recurrent life
53 hosphate (NADPH) oxidase predisposes chronic granulomatous disease (CGD) patients to infection, and a
54 ide (NADPH) oxidase in patients with chronic granulomatous disease (CGD) results in susceptibility to
55 m-negative pathogen in patients with chronic granulomatous disease (CGD), a deficiency in the phagocy
56 r threat for patients suffering from chronic granulomatous disease (CGD), a primary immunodeficiency
57 bacterium that infects patients with chronic granulomatous disease (CGD), a primary immunodeficiency
58 hate oxidase 2 (NOX2) function cause chronic granulomatous disease (CGD), a primary immunodeficiency
59 stem cell transplants, patients with chronic granulomatous disease (CGD), and others.
60 ing mutations in this enzyme lead to chronic granulomatous disease (CGD), associated with increased s
61 (HSCT) is a successful treatment for chronic granulomatous disease (CGD), but the safety and efficacy
62                                   In chronic granulomatous disease (CGD), defective phagocytic nicoti
63 ) and lungs of A. fumigatus-infected chronic granulomatous disease (CGD), hydrocortisone-treated, and
64 s is a major threat to patients with chronic granulomatous disease (CGD).
65 has been isolated from patients with chronic granulomatous disease (CGD).
66 n emerging pathogen in patients with chronic granulomatous disease (CGD).
67 people with cystic fibrosis (CF) and chronic granulomatous disease (CGD).
68 ls with the primary immunodeficiency chronic granulomatous disease (CGD).
69 basis for the human immunodeficiency chronic granulomatous disease (CGD).
70  Wiskott-Aldrich syndrome (WAS), and chronic granulomatous disease (CGD).
71 nditioning of wild-type and X-linked chronic granulomatous disease (X-CGD) mice.
72 model, because in mice with X-linked chronic granulomatous disease (X-CGD) that lack oxidase subunits
73 (iPSCs) from a patient with X-linked chronic granulomatous disease (X-CGD), a defect of neutrophil mi
74 In HSPCs from patients with X-linked chronic granulomatous disease (X-CGD), caused by mutations in th
75 t in patients and mice with X-linked chronic granulomatous disease (X-CGD).
76    Genetic defects in NADPH oxidase (chronic granulomatous disease [CGD]) and corticosteroid-induced
77                                   In chronic granulomatous disease allogeneic haemopoietic stem-cell
78 this complex have been implicated in chronic granulomatous disease and Crohn's disease, highlighting
79 idity and mortality in patients with chronic granulomatous disease and cystic fibrosis.
80 articularly beneficial in areas with endemic granulomatous disease and may improve clinical managemen
81                        Patients with chronic granulomatous disease and modest residual production of
82  abscess formation in a patient with chronic granulomatous disease and review the literature on Phaeo
83 ted for other forms of PID including chronic granulomatous disease and Wiskott-Aldrich syndrome.
84 acoronavirus, resulting in a lethal systemic granulomatous disease called feline infectious peritonit
85 ways of host immune cells in tuberculosis, a granulomatous disease caused by the intracellular pathog
86                          Destructive midline granulomatous disease characterized by necrotizing granu
87               A 28-year-old man with chronic granulomatous disease developed worsening respiratory st
88 G mutations associated with autoimmunity and granulomatous disease did not have altered overall diver
89                     Sarcoidosis is a chronic granulomatous disease for which there are limited therap
90 ss and death among 287 patients with chronic granulomatous disease from 244 kindreds.
91            Chest imaging was consistent with granulomatous disease in 46.7%.
92 virus (FIPV), which leads to lethal systemic granulomatous disease in cats.
93 ximately 30 degrees C, so we sought to model granulomatous disease in the ectothermic zebrafish.
94                                      Chronic granulomatous disease is caused by missense, nonsense, f
95               Sarcoidosis is a multisystemic granulomatous disease of unknown etiology that predomina
96                 Sarcoidosis is a multisystem granulomatous disease of unknown etiology that primarily
97                    Sarcoidosis is a systemic granulomatous disease of unknown etiology.
98 romised patients as well as in patients with granulomatous disease or cystic fibrosis.
99 h compromise p40(phox) function in a chronic granulomatous disease patient, also perturbed class II A
100 fect on endothelial function in NOX2-chronic granulomatous disease patients (-0.9; 95% confidence int
101 d dilatation was not observed in p47-chronic granulomatous disease patients (-1.5%; 95% confidence in
102 ed Mo-DC differentiation observed in chronic granulomatous disease patients lacking p22phox.
103                The response to IR in chronic granulomatous disease patients was compared with that in
104       Additionally, neutrophils from chronic granulomatous disease patients, carrying mutations in th
105 promise antifungal immune control in chronic granulomatous disease patients.
106               While sarcoidosis is a chronic granulomatous disease presumably reflecting an exaggerat
107                             Sarcoidosis is a granulomatous disease that primarily affects the lungs a
108                            Mice with chronic granulomatous disease that were infected with B. multivo
109 SCID), Wiskott-Aldrich syndrome, and chronic granulomatous disease through retrospective, prospective
110 nd the susceptibility of humans with chronic granulomatous disease to mycobacterial infection.
111            Survival of patients with chronic granulomatous disease was strongly associated with resid
112        Patients aged 0-40 years with chronic granulomatous disease were assessed and enrolled at the
113 n age 12.7 years; IQR 6.8-17.3) with chronic granulomatous disease were enrolled from June 15, 2003,
114 age quiescence and prevents mTORC1-dependent granulomatous disease with clinical implications for sar
115 efects in oxidase function result in chronic granulomatous disease with hallmark recurrent microbial
116 6PD deficiency can be a phenocopy of chronic granulomatous disease with regard to the cellular and cl
117 ox), p47(phox), p67(phox) (autosomal chronic granulomatous disease), or gp91(phox) (X-linked chronic
118 the phagocyte NADPH oxidase complex (chronic granulomatous disease), severe congenital neutropenia (S
119 us disease), or gp91(phox) (X-linked chronic granulomatous disease), which result in variable product
120 mmatory disease, 15.4%; malabsorption, 5.9%; granulomatous disease, 9.7%; liver diseases and hepatiti
121                                      Chronic granulomatous disease, an inherited disorder of the NADP
122 ed severe combined immunodeficiency, chronic granulomatous disease, and other diseases.
123 diates (ROIs) is the major defect in chronic granulomatous disease, causing recurrent infections and
124 ncies in the oxidative burst seen in chronic granulomatous disease, could lead to pathologic inflamma
125 such as Wiskott-Aldrich syndrome and chronic granulomatous disease, offering curative engraftment wit
126 bronchiectasis, autoimmunity, other cancers, granulomatous disease, or previous splenectomy.
127         Treatment of tuberculosis, a complex granulomatous disease, requires long-term multidrug ther
128 gene therapy for immunodeficiencies, chronic granulomatous disease, suicide gene therapy for graft-ve
129 ranswells and cells of patients with chronic granulomatous disease, we show that this downregulation
130 OS) because cells from patients with chronic granulomatous disease, which are defective in ROS produc
131 as also observed in individuals with chronic granulomatous disease, who lack NADPH oxidase activity b
132 ts with the NADPH oxidase deficiency chronic granulomatous disease, who require antibiotic and antimy
133 ive ROS production machinery develop chronic granulomatous disease.
134 sed by a Phellinus sp. in a boy with chronic granulomatous disease.
135 ficacious in high-risk patients with chronic granulomatous disease.
136 n-1 deficiency, CARD9 deficiency, or chronic granulomatous disease.
137 ctions, such as the genetic disorder chronic granulomatous disease.
138 es, including splenomegaly, hepatomegaly, or granulomatous disease.
139 olunteers with that in patients with chronic granulomatous disease.
140 edictor of survival in patients with chronic granulomatous disease.
141  linked to survival in patients with chronic granulomatous disease.
142 h X-linked (NOX2) or autosomal (p47) chronic granulomatous disease.
143 ity, lymphoid proliferation, malignancy, and granulomatous disease.
144 the oxidative burst in patients with chronic granulomatous disease.
145 iency, Wiskott-Aldrich syndrome, and chronic granulomatous disease.
146 hagocyte functional defects, such as chronic granulomatous disease.
147  arthritis and uveitis in general as well as granulomatous diseases in particular.
148 hic macrophages constitutes the basis of all granulomatous diseases, such as tuberculosis or sarcoido
149 th other lung diseases, including infectious granulomatous diseases.
150  and questions about macrophage function and granulomatous diseases.
151               Sarcoidosis is an inflammatory granulomatous disorder characterized by accumulation of
152         Chronic beryllium disease (CBD) is a granulomatous disorder characterized by an influx of ber
153            Sarcoidosis is a complex systemic granulomatous disorder of unknown etiology.
154                 Sarcoidosis is a multisystem granulomatous disorder that most often affects the lungs
155    Similar abnormalities may extend to other granulomatous disorders, but not diseases such as ulcera
156 f PBC even in the absence of characteristic, granulomatous, duct destructive lesions.
157 reatening infection of the cornea, and fatal granulomatous encephalitis in humans.
158 erculosis (MAP), occurs worldwide as chronic granulomatous enteritis of domestic and wild ruminants.
159 murafenib treatment, the patient developed a granulomatous eruption, which resolved 3 weeks after ces
160 o patients with melanoma developed cutaneous granulomatous eruptions during targeted BRAF inhibitor t
161                                              Granulomatous eruptions have not been previously reporte
162               We report 2 cases of cutaneous granulomatous eruptions on treatment with targeted BRAF
163       In our previous studies, resolution of granulomatous experimental autoimmune thyroiditis (G-EAT
164                in 30 nongranulomatous and 12 granulomatous eyes, the OCT cell counts correlated well
165 nongranulomatous eyes and 2.0 cells/grade in granulomatous eyes.
166 se includes indolent chronic rhinosinusitis, granulomatous fungal sinusitis, and acute fulminant fung
167 Herein, a case of severe vemurafenib-induced granulomatous hepatitis leading to chronic cholestasis i
168 e characterized by immune dysregulation with granulomatous hyperinflammation and autoimmunity, with r
169 Treg cells to modulate the beryllium-induced granulomatous immune response.
170 elopment of the egg-induced T-helper 2 (Th2) granulomatous immune response.
171  that PTHrP expression is part of the normal granulomatous immune response.
172  correlates, high lung bacterial burden, and granulomatous immunopathology.
173         Ocular rhinosporidiosis is a chronic granulomatous infection caused by a newly classified org
174                  By using a model of chronic granulomatous infection, we also show that lymphatic rem
175  is an uncommon complication of disseminated granulomatous infections.
176 on of PTHrP is the cause of hypercalcemia in granulomatous infections.
177 small vessel disease and other inflammatory, granulomatous, infective, metabolic, and genetic causes
178 ) T cells and macrophages to form prototypic granulomatous infiltrates.
179 the predominant finding (42.2%), followed by granulomatous inflammation (29%), steatosis/steatohepati
180 i develop severe CD4 T cell-mediated hepatic granulomatous inflammation against parasite eggs associa
181 nonhematopoietic cells may partly facilitate granulomatous inflammation and bacterial dissemination.
182 a from the tissues, leading to local chronic granulomatous inflammation and compensatory adaptive imm
183 humans is attributed to parasite egg-induced granulomatous inflammation and fibrosis in the host live
184 thermore, a significant reduction of hepatic granulomatous inflammation and IL-17 production in inter
185 Crohn disease (CD) are both characterized by granulomatous inflammation and related to nucleotide oli
186 yllium (Be) exposure and is characterized by granulomatous inflammation and the accumulation of Be-re
187  occupational lung disorder characterized by granulomatous inflammation and the accumulation of beryl
188 crotizing vasculitis that is associated with granulomatous inflammation and the presence of anti-neut
189 at while a reduction in IL-4/IL-13-dependent granulomatous inflammation and tissue eosinophilia was o
190 nsure that any further complications such as granulomatous inflammation are managed and documented.
191      CBA/J (CBA) mice develop severe hepatic granulomatous inflammation associated with prominent Th1
192 Exserohilum provokes robust neutrophilic and granulomatous inflammation capable of thwarting fungal g
193 understanding of the pathways underlying the granulomatous inflammation characteristic of sarcoidosis
194 ysis of all 3 cases revealed elastolysis and granulomatous inflammation characterized by multinucleat
195 -->TLR2KO) exhibited a marked attenuation in granulomatous inflammation compared with WT mice.
196                                              Granulomatous inflammation consistent with Crohn's disea
197 racterized by pronounced hepatic egg-induced granulomatous inflammation in a proinflammatory cytokine
198                                          The granulomatous inflammation in the bowel of patients with
199 itical for protecting mice from a Th1-driven granulomatous inflammation in the ileum.
200 ritical for the development of Th17-mediated granulomatous inflammation in the lung in response to S.
201 dritic cell-mediated development of a type 1 granulomatous inflammation in the lung in response to SC
202 responses are required for the generation of granulomatous inflammation induced by inhaled S. chartar
203 responses are required for the generation of granulomatous inflammation induced by inhaled SC.
204                                              Granulomatous inflammation is characteristic of many aut
205  such as periprosthetic osteolysis, in which granulomatous inflammation is initiated by particle phag
206                                Extravascular granulomatous inflammation may be initiated by ANCA-indu
207 lated mainly to the egg stage, which induces granulomatous inflammation of affected tissues.
208 pportunistic pathogenic bacterium, developed granulomatous inflammation of the ileum, characterized b
209 se resulting from lymphocytic and frequently granulomatous inflammation of the peripheral airways, al
210 is (GPA; or Wegener's granulomatosis) is the granulomatous inflammation of the upper respiratory trac
211 is syndrome had chronic active colitis, with granulomatous inflammation present in 7 of 11 patients (
212                                  SC-mediated granulomatous inflammation required IFN-gamma and was TL
213                        S. chartarum-mediated granulomatous inflammation required intact IL-23 or IL-1
214  in 2 patients and demonstrated noncaseating granulomatous inflammation surrounding tattoo ink in the
215 ith schistosome helminths is associated with granulomatous inflammation that forms around parasite eg
216 nge with 10(6) S. chartarum spores developed granulomatous inflammation with multinucleate giant cell
217  and challenged with 10(6) SC spores develop granulomatous inflammation with multinucleate giant cell
218                                         With granulomatous inflammation, 52% met the criteria for tub
219  exclude infectious and autoimmune causes of granulomatous inflammation, followed by dermatologic wor
220  Since both responses usually correlate with granulomatous inflammation, we tested six prominently ex
221  intravenously into eight mice bearing local granulomatous inflammation.
222 nocytes, and macrophages and produce typical granulomatous inflammation.
223  necrotizing vasculitis, and eosinophil-rich granulomatous inflammation.
224 attenuated P. acnes-induced ear swelling and granulomatous inflammation.
225  relieving P. acnes-induced ear swelling and granulomatous inflammation.
226 but these may include carcinogenic change or granulomatous inflammation.
227 of HPS and CD, 2 entities characterized by a granulomatous inflammatory reaction pattern but with uni
228                                       During granulomatous inflammatory reactions, myeloid cells can
229                       BeS with evidence of a granulomatous inflammatory response in the lung is diagn
230  two models, with CFA causing a nonresolving granulomatous inflammatory response whereas tissue incis
231 amination revealed the presence of bilateral granulomatous keratic precipitates, anterior chamber cel
232 activated endothelium into the valve to form granulomatous lesions and Aschoff bodies.
233 ve to conditions likely to be present within granulomatous lesions and mediate aspects of M. tubercul
234 lammatory myeloid neoplasia characterized by granulomatous lesions containing pathological CD207(+) d
235  there are no good models that replicate the granulomatous lesions found in granulomatosis with polya
236 f Crohn disease (CD); however, mucocutaneous granulomatous lesions have not been considered among the
237               This bacterium persists within granulomatous lesions in a poorly characterized, nonrepl
238 his study, we show that Wnt6 is expressed in granulomatous lesions in the lung of Mycobacterium tuber
239 hich were observed in close proximity within granulomatous lesions in the lungs of GPA patients.
240 D4(+) T cells and macrophages form organized granulomatous lesions in the walls of affected arteries,
241 induced in the lungs and particularly in the granulomatous lesions of macaques experimentally infecte
242 ammoma body calcifications indicative of the granulomatous lesions that occur during Leishmania infec
243 olytic enzymes in macrophages and T cells in granulomatous lesions.
244 r accumulating only in peripheral regions of granulomatous lesions.
245             We present a case of symptomatic granulomatous liver disease secondary to sarcoidosis, mi
246         Chronic beryllium disease (CBD) is a granulomatous lung disease characterized by the accumula
247         Chronic beryllium disease (CBD) is a granulomatous lung disorder caused by a hypersensitivity
248                             Sarcoidosis is a granulomatous lung disorder of unknown cause.
249          Chronic beryllium (Be) disease is a granulomatous lung disorder that results from Be exposur
250 n exposure, these mice developed more robust granulomatous lung fibrosis than wild-type counterparts.
251 -4Ralpha were associated with development of granulomatous lung inflammation triggered by silica.
252 -negative bacillus initially isolated from a granulomatous lung lesion.
253                 Patient 2 developed inguinal granulomatous lymphadenitis about 40 days after onset of
254  necrotizing vasculitis, glomerulonephritis, granulomatous lymphadenitis, and bronchointerstitial pne
255 , HP is characterized by a bronchiolocentric granulomatous lymphocytic alveolitis, which evolves to f
256 d manifestations (notably the development of granulomatous-lymphocytic interstitial lung disease in C
257 sy of 2 eyes of 1 patient revealed prominent granulomatous lymphohistiocytic choroiditis with giant c
258 anent vision loss, 30 (94%) had a subretinal granulomatous mass/scar, peripheral granuloma with tract
259                                   Subretinal granulomatous mass/scar, vitritis, and scotoma were the
260          Fatal cases had necrosuppurative to granulomatous meningitis and vasculitis, with thrombi an
261 emarkably, one celiac patient presented with granulomatous nodulae in the ileum, thus reflecting an i
262 t, metastatic disease, where ulcerations and granulomatous nodules can affect multiple secondary site
263 hils were detected, GPTD does not resemble a granulomatous or eosinophilic condition.
264 ing complaint for systemic disorders such as granulomatous or eosinophilic polyangiitis, and sarcoido
265 e remaining 2 patients had bilateral chronic granulomatous panuveitis.
266 antly diminished clinical manifestations and granulomatous pathology and characterized by the presenc
267 that a subset of severe "asthma" manifests a granulomatous pathology, which we term "asthmatic granul
268 NOD2) and is phenotypically characterized by granulomatous polyarthritis and uveitis.
269                                      It is a granulomatous process with the possibility of palisading
270 her, variable manifestations included atopy, granulomatous rash, autoimmune thyroiditis, the presence
271 ines from these CAR T cells in vivo drives a granulomatous reaction resulting in chronic toxicity.
272 ells in the mediastinal lymph nodes and lung granulomatous regions while concomitantly accelerating t
273 57BL6/J lacking SK1), to investigate how the granulomatous response and SK1-S1P pathway are interrela
274 y showed that B cells can modulate the local granulomatous response in M. tuberculosis-infected macaq
275 perienced a maturation defect of the ex vivo granulomatous response involving monocytes as well as na
276 apped eggs induce a distinct immune-mediated granulomatous response that causes local and systemic pa
277 ant cells is a distinguishing feature of the granulomatous response to inflammation, infection, and f
278 rain injury patients to develop an effective granulomatous response to mycobacteria.
279 rine proteases for antibacterial protection, granulomatous response, and survival.
280 en- (Ag-) Ag-coated beads to elicit a recall granulomatous response, CCR4(-/-) mice displayed abrogat
281 ormation was not affected during a secondary granulomatous response, even though IL-5 and IL-13 were
282 esponse, phenotype of recruited T cells, and granulomatous response.
283 ity to M. tuberculosis in the context of the granulomatous response.
284 ular killing by phagocytes, and generating a granulomatous response.
285 the phenotypes of recruited T cells, and the granulomatous responses were also similar between WT and
286 y pulmonary infections, chronic invasive and granulomatous rhinosinusitis, and aspergillus bronchitis
287              Inflammation from injections is granulomatous, seen only with intravitreal injections, a
288 -FDG PET/CT for detection of inflammation in granulomatous sites and management of patients with chro
289                      Using an ovine model of granulomatous skin inflammation, we demonstrate that B c
290                                              Granulomatous skin lesions sparing warm regions (eg, fle
291 are found within the mycobacterially induced granulomatous structure in the livers of infected Rag2(-
292 rotective cellular immunity and formation of granulomatous structures in the lung.
293 eficient macrophages formed mTORC1-dependent granulomatous structures in vitro and showed constitutiv
294 e from long-term persistent infection within granulomatous structures.
295              The large B-cell infiltrates in granulomatous tissue and increased molecular signs of an
296  These data demonstrate that surveillance of granulomatous tissue by CD11c+ cells is continuous and t
297 phage differentiation program that regulates granulomatous tissue remodeling.
298 el sprouting and increased lymphatic area in granulomatous tissue.
299                    Giant cell arteritis is a granulomatous vasculitis of the aorta and its branches t
300                                Vitreitis and granulomatous vasculitis were noted in 7 of 30 intravitr

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