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1 n a subpopulation of human memory B cells of mucosa-associated lymphoid tissue.
2 d has been implicated in B cell lymphomas of mucosa-associated lymphoid tissue.
3 /memory lymphocytes to the intestine and the mucosa-associated lymphoid tissue.
4 f gastric adenocarcinoma and lymphoma of the mucosa-associated lymphoid tissue.
5 the spectrum of low-grade B-cell lymphoma of mucosa-associated lymphoid tissue.
6 ts with extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue.
7 controlling dendritic cell (DC) functions in mucosa-associated lymphoid tissue.
8 s of mammalian mucosal surfaces exhibiting a mucosa-associated lymphoid tissue.
9 ulate the risk of lymphomagenesis in gastric mucosa-associated lymphoid tissue.
10 nfection, most likely through M cells of the mucosa-associated lymphoid tissue.
11 ow trout and that it resembles other teleost mucosa-associated lymphoid tissues.
12 is known about the B cell response to RSV in mucosa-associated lymphoid tissues.
13 eir interaction directs lymphocyte homing to mucosa-associated lymphoid tissues.
14 reased IgD CSR exclusively within B cells of mucosa-associated lymphoid tissues.
15 uded caspase recruitment domain 11 (CARD11), mucosa-associated lymphoid tissue 1 (MALT1) for combined
17 hoid tissue (LDALT), a first known report of mucosa-associated lymphoid tissue activation at the port
18 ly 50% of patients with gastric lymphomas of mucosa-associated lymphoid tissue, although long-term fo
19 The probable source of persistent virus is mucosa-associated lymphoid tissue, although the molecula
22 he specialized regions where antigens access mucosa-associated lymphoid tissue, are sites where HIV-1
24 ll lymphomas (DLBCLs), including DLBCLs with mucosa-associated lymphoid tissue (DLBCL[MALT]) and with
25 tered to mimic those normally present within mucosa-associated lymphoid tissues (e.g., Peyer's patche
27 , five extranodal marginal zone lymphomas of mucosa-associated lymphoid tissue, five anaplastic large
28 of apoptotic cells was also observed in the mucosa-associated lymphoid tissue lining the trachea and
29 uces remission in most patients with gastric mucosa-associated lymphoid tissue lymphoma (GML) that is
32 ptake), including 4 patients with coexisting mucosa-associated lymphoid tissue lymphoma (maximal stan
33 lymphoma (n = 6), plasmacytoma (n = 5), and mucosa-associated lymphoid tissue lymphoma (n = 3) were
34 iduals also had an increased risk of stomach mucosa-associated lymphoid tissue lymphoma (SIR, 5.99; 9
35 h the development of both gastric cancer and mucosa-associated lymphoid tissue lymphoma in humans is
36 heilmannii" is associated with gastritis and mucosa-associated lymphoid tissue lymphoma in people.
37 h studies on the diagnosis and management of mucosa-associated lymphoid tissue lymphoma published ear
38 tations of TNFAIP3 have been observed in the mucosa-associated lymphoid tissue lymphoma subtype frequ
39 Brd4, phosphoinositide-3-kinase, annexin A1, mucosa-associated lymphoid tissue lymphoma translocation
41 , as well as B-cell lymphoma/leukemia 10 and mucosa-associated lymphoid tissue lymphoma translocation
42 tant protein-1-induced protein (MCPIP)-1 and mucosa-associated lymphoid tissue lymphoma translocation
43 part of the CARD-B-cell lymphoma/leukemia 10-mucosa-associated lymphoid tissue lymphoma translocation
44 rotein 3]-BCL-10 [B-cell lymphoma 10]-MALT1 [mucosa-associated lymphoid tissue lymphoma translocation
45 c proteins associated with B-cell lymphomas, mucosa-associated lymphoid tissue lymphoma translocation
46 ablish an important T cell-intrinsic role of mucosa-associated lymphoid tissue lymphoma translocation
47 plex with B-cell CLL/lymphoma 10 (BCL10) and mucosa-associated lymphoid tissue lymphoma translocation
48 ated with B-cell CLL/lymphoma 10 (BCL10) and mucosa-associated lymphoid tissue lymphoma translocation
49 nic lymphocytic leukemia/lymphoma 10 (BCL10)-mucosa-associated lymphoid tissue lymphoma translocation
50 composed of B cell CLL/lymphoma 10 (BCL10), mucosa-associated lymphoid tissue lymphoma translocation
52 ase (MAGUK) protein 1/B-cell CLL-lymphoma 10/mucosa-associated lymphoid tissue lymphoma translocation
54 pregnancy or nursing, malignancy or gastric mucosa-associated lymphoid tissue lymphoma, allergy or c
55 ical factor in peptic ulcer disease, gastric mucosa-associated lymphoid tissue lymphoma, and gastric
56 , including gastric and duodenal ulceration, mucosa-associated lymphoid tissue lymphoma, and gastric
57 bserved in diffuse large B-cell lymphoma and mucosa-associated lymphoid tissue lymphoma, being associ
58 ts of distinct chromosomal translocations in mucosa-associated lymphoid tissue lymphoma, cooperate in
59 able outcome; and in patients with low grade mucosa-associated lymphoid tissue lymphoma, eradication
61 of diffuse large B-cell lymphoma (DLBCL) and mucosa-associated lymphoid tissue lymphoma, lymphomas re
62 ymphoma (MCL), marginal zone lymphoma (MZL), mucosa-associated lymphoid tissue lymphoma, lymphoplasma
63 ents with newly diagnosed, untreated stage I mucosa-associated lymphoid tissue lymphoma, the 2-year l
65 tudied, gastrointestinal lymphoma is gastric mucosa-associated lymphoid tissue lymphoma, which is a p
66 can cause the development of gastric B cell mucosa-associated lymphoid tissue lymphoma, yet little i
67 otrimers with B-cell lymphoma 10 (BCL10) and mucosa-associated lymphoid tissue lymphoma-translocation
68 ion studies were performed with T cells from mucosa-associated lymphoid tissue lymphoma-translocation
83 onship to gastric adenocarcinoma and gastric mucosa-associated lymphoid tissue lymphoma.(2) In the la
84 lorambucil demonstrated superior efficacy in mucosa-associated lymphoid tissue lymphoma; however, imp
87 This is important as early-stage gastric mucosa-associated lymphoid tissue lymphomas can be manag
88 Further, the development of ocular adnexal mucosa-associated lymphoid tissue lymphomas has been ass
89 trasound, in the diagnosis and management of mucosa-associated lymphoid tissue lymphomas of the stoma
90 understanding of the genetic alterations in mucosa-associated lymphoid tissue lymphomas, including v
93 esized that direct intranodal vaccination of mucosa associated lymphoid tissue (MALT) such as the rea
96 l marginal zone (MZ) B-cell lymphomas of the mucosa-associated lymphoid tissue (MALT) arise from lymp
98 ow-grade, small lymphocytic lymphomas of the mucosa-associated lymphoid tissue (MALT) have recently b
99 yphlocolitis, associated epithelial defects, mucosa-associated lymphoid tissue (MALT) hyperplasia, an
101 59 = 42%) (germinal center cell origin) and mucosa-associated lymphoid tissue (MALT) lymphoma (19 of
102 ice has been described as a model of gastric mucosa-associated lymphoid tissue (MALT) lymphoma (GML).
103 ression profiling (GEP) of primary pulmonary mucosa-associated lymphoid tissue (MALT) lymphoma (n = 3
105 ulture who previously received rituximab for mucosa-associated lymphoid tissue (MALT) lymphoma and st
109 jogren's syndrome (SS) developed a low-grade mucosa-associated lymphoid tissue (MALT) lymphoma in the
110 reated by the recurrent t(11;18)(q21;q21) in mucosa-associated lymphoid tissue (MALT) lymphoma induce
117 stopathology and immunohistochemistry showed mucosa-associated lymphoid tissue (MALT) lymphoma with i
118 as chronic gastritis, peptic ulcer disease, mucosa-associated lymphoid tissue (MALT) lymphoma, and g
119 ude active or inactive peptic ulcer disease, mucosa-associated lymphoid tissue (MALT) lymphoma, as we
120 he standard of care in patients with gastric mucosa-associated lymphoid tissue (MALT) lymphoma, much
121 avourable prognosis of patients with gastric mucosa-associated lymphoid tissue (MALT) lymphoma, treat
127 ion resulted in the best OS in patients with mucosa-associated lymphoid tissue (MALT) lymphomas (HR =
130 phoma specimens, as follows: 8 of 120 (6.7%) mucosa-associated lymphoid tissue (MALT) lymphomas, 4 of
131 ning protein involved in the etiology of the mucosa-associated lymphoid tissue (MALT) lymphomas, has
132 idy are recurrent chromosomal aberrations in mucosa-associated lymphoid tissue (MALT) lymphomas.
133 munoglobulin heavy chain (IgH) locus in some mucosa-associated lymphoid tissue (MALT) lymphomas.
135 developments concerning gastric lymphomas of mucosa-associated lymphoid tissue (MALT) origin, ranging
136 Low-grade lesions nearly always arise from mucosa-associated lymphoid tissue (MALT) secondary to ch
137 central player in immune surveillance in the mucosa-associated lymphoid tissue (MALT) such as those i
138 utes can allow antigens to interact with the mucosa-associated lymphoid tissue (MALT) to induce both
139 nodal marginal zone B-cell lymphoma (MZL) of mucosa-associated lymphoid tissue (MALT) type is listed
142 a case of primary gastric B-cell lymphoma of mucosa-associated lymphoid tissue (MALT) with a secondar
143 ncurrent gastric and intestinal lymphomas of mucosa-associated lymphoid tissue (MALT), the clonal rel
144 -cell lymphomas (DLBCLs) without features of mucosa-associated lymphoid tissue (MALT), the pure (de n
145 vestigation revealed that she had an orbital mucosa-associated lymphoid tissue (MALT)-type B cell lym
151 eligible patients (339 with WM, 37 with non-mucosa-associated lymphoid tissue marginal zone lymphoma
152 spores, phagocytosis of spores in the nasal mucosa-associated lymphoid tissue (NALT) and lungs by ma
153 the cervical lymph nodes (CLN) and the nasal mucosa-associated lymphoid tissue (NALT) and tested for
154 ections have two portals of entry, the nasal mucosa-associated lymphoid tissue (NALT) and the lumen o
155 eported that GAS preferentially target nasal mucosa-associated lymphoid tissue (NALT) in mice, a tiss
158 lar lymphoma, diffuse large B-cell lymphoma, mucosa-associated lymphoid tissue non-Hodgkin lymphoma,
159 calization, the chief immunoglobulins of all mucosa-associated lymphoid tissue operate under the guid
160 l lymphoma, angiotropic large cell lymphoma, mucosa-associated lymphoid tissue, primary pulmonary T-c
161 omains of c-IAP2 with the paracaspase/MALT1 (mucosa-associated lymphoid tissue) protein, a critical m
162 nversion (RT-QuIC) assay by using recto-anal mucosa-associated lymphoid tissue (RAMALT) biopsy specim
163 ced conversion (RT-QuIC) assay of recto-anal mucosa-associated lymphoid tissue (RAMALT) biopsy specim
165 Functional analysis of the gastrointestinal mucosa-associated lymphoid tissue revealed increased sig
166 ization of a human NK cell subset located in mucosa-associated lymphoid tissues, such as tonsils and
167 icular-associated epithelium (FAE) overlying mucosa-associated lymphoid tissues, their density increa
169 hocyte responses, is aberrantly expressed in mucosa-associated lymphoid tissue-type marginal zone (MZ