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Gene Information

Gene symbol: CD300C

Gene name: CD300c molecule

HGNC ID: 19320

Synonyms: CMRF35, LIR, CMRF-35A, CMRF35A, IGSF16

Related Genes

# Gene Symbol Number of hits
1 CD300A 1 hits
2 CD4 1 hits
3 CD8A 1 hits
4 IFNG 1 hits

Related Sentences

# PMID Sentence
1 17702825 Novel human CD4+ T lymphocyte subpopulations defined by CD300a/c molecule expression.
2 17702825 The CD300c (CMRF-35A) and CD300a (CMRF-35H) molecules are leukocyte surface proteins that are part of a larger family of immunoregulatory molecules encoded by a gene complex on human chromosome 17.
3 17702825 The CMRF-35 monoclonal antibody binds to an epitope common to both molecules, expressed on most human leukocyte populations, apart from B lymphocytes and a subpopulation of CD4(+) and CD8(+) T lymphocytes.
4 17702825 We describe the CMRF-35(pos) and CMRF-35(-) fractions of CD4(+) T lymphocytes.
5 17702825 The CMRF-35(pos) fraction can further be divided into CMRF-35(++) and CMRF-35(+)CD4(+) T lymphocyte subpopulations.
6 17702825 Resting peripheral CD4(+) T lymphocytes express CD300a mRNA and very low amounts of CD300c.
7 17702825 Activation results in an initial decrease in CD300a gene expression before an increase in both CD300a and CD300c gene expression.
8 17702825 The CMRF-35(-) fraction of CD4(+) T lymphocytes proliferated to a greater extent than the CMRF-35(pos) fraction, in response to mitogens or allogeneic antigen.
9 17702825 The poor proliferation of the CMRF-35(pos) CD4(+) in response to mitogens was explained by increased apoptosis within this subpopulation.
10 17702825 The recall antigen, tetanus toxoid, stimulated the CMRF-35(++)CD4(+)CD45RO(+) but not the CMRF-35(-)CD4(+)CD45RO(+) subpopulation.
11 17702825 Resting CMRF-35(++) CD4(+) lymphocytes express low levels of IFN-gamma mRNA.
12 17702825 Within 18 h following in vitro activation, CMRF-35(++) CD4(+) lymphocytes express more IFN-gamma mRNA and protein compared with the CMRF-35(-)CD4(+) lymphocytes, however, after 24 h, both the CMRF-35(+) and CMRF-35(-)CD4(+) T lymphocytes were able to produce IFN-gamma.
13 17702825 The CMRF-35(++)CD4(+) T lymphocyte population contains the Th(1) memory effector cells.
14 17702825 Novel human CD4+ T lymphocyte subpopulations defined by CD300a/c molecule expression.
15 17702825 The CD300c (CMRF-35A) and CD300a (CMRF-35H) molecules are leukocyte surface proteins that are part of a larger family of immunoregulatory molecules encoded by a gene complex on human chromosome 17.
16 17702825 The CMRF-35 monoclonal antibody binds to an epitope common to both molecules, expressed on most human leukocyte populations, apart from B lymphocytes and a subpopulation of CD4(+) and CD8(+) T lymphocytes.
17 17702825 We describe the CMRF-35(pos) and CMRF-35(-) fractions of CD4(+) T lymphocytes.
18 17702825 The CMRF-35(pos) fraction can further be divided into CMRF-35(++) and CMRF-35(+)CD4(+) T lymphocyte subpopulations.
19 17702825 Resting peripheral CD4(+) T lymphocytes express CD300a mRNA and very low amounts of CD300c.
20 17702825 Activation results in an initial decrease in CD300a gene expression before an increase in both CD300a and CD300c gene expression.
21 17702825 The CMRF-35(-) fraction of CD4(+) T lymphocytes proliferated to a greater extent than the CMRF-35(pos) fraction, in response to mitogens or allogeneic antigen.
22 17702825 The poor proliferation of the CMRF-35(pos) CD4(+) in response to mitogens was explained by increased apoptosis within this subpopulation.
23 17702825 The recall antigen, tetanus toxoid, stimulated the CMRF-35(++)CD4(+)CD45RO(+) but not the CMRF-35(-)CD4(+)CD45RO(+) subpopulation.
24 17702825 Resting CMRF-35(++) CD4(+) lymphocytes express low levels of IFN-gamma mRNA.
25 17702825 Within 18 h following in vitro activation, CMRF-35(++) CD4(+) lymphocytes express more IFN-gamma mRNA and protein compared with the CMRF-35(-)CD4(+) lymphocytes, however, after 24 h, both the CMRF-35(+) and CMRF-35(-)CD4(+) T lymphocytes were able to produce IFN-gamma.
26 17702825 The CMRF-35(++)CD4(+) T lymphocyte population contains the Th(1) memory effector cells.
27 17702825 Novel human CD4+ T lymphocyte subpopulations defined by CD300a/c molecule expression.
28 17702825 The CD300c (CMRF-35A) and CD300a (CMRF-35H) molecules are leukocyte surface proteins that are part of a larger family of immunoregulatory molecules encoded by a gene complex on human chromosome 17.
29 17702825 The CMRF-35 monoclonal antibody binds to an epitope common to both molecules, expressed on most human leukocyte populations, apart from B lymphocytes and a subpopulation of CD4(+) and CD8(+) T lymphocytes.
30 17702825 We describe the CMRF-35(pos) and CMRF-35(-) fractions of CD4(+) T lymphocytes.
31 17702825 The CMRF-35(pos) fraction can further be divided into CMRF-35(++) and CMRF-35(+)CD4(+) T lymphocyte subpopulations.
32 17702825 Resting peripheral CD4(+) T lymphocytes express CD300a mRNA and very low amounts of CD300c.
33 17702825 Activation results in an initial decrease in CD300a gene expression before an increase in both CD300a and CD300c gene expression.
34 17702825 The CMRF-35(-) fraction of CD4(+) T lymphocytes proliferated to a greater extent than the CMRF-35(pos) fraction, in response to mitogens or allogeneic antigen.
35 17702825 The poor proliferation of the CMRF-35(pos) CD4(+) in response to mitogens was explained by increased apoptosis within this subpopulation.
36 17702825 The recall antigen, tetanus toxoid, stimulated the CMRF-35(++)CD4(+)CD45RO(+) but not the CMRF-35(-)CD4(+)CD45RO(+) subpopulation.
37 17702825 Resting CMRF-35(++) CD4(+) lymphocytes express low levels of IFN-gamma mRNA.
38 17702825 Within 18 h following in vitro activation, CMRF-35(++) CD4(+) lymphocytes express more IFN-gamma mRNA and protein compared with the CMRF-35(-)CD4(+) lymphocytes, however, after 24 h, both the CMRF-35(+) and CMRF-35(-)CD4(+) T lymphocytes were able to produce IFN-gamma.
39 17702825 The CMRF-35(++)CD4(+) T lymphocyte population contains the Th(1) memory effector cells.
40 17702825 Novel human CD4+ T lymphocyte subpopulations defined by CD300a/c molecule expression.
41 17702825 The CD300c (CMRF-35A) and CD300a (CMRF-35H) molecules are leukocyte surface proteins that are part of a larger family of immunoregulatory molecules encoded by a gene complex on human chromosome 17.
42 17702825 The CMRF-35 monoclonal antibody binds to an epitope common to both molecules, expressed on most human leukocyte populations, apart from B lymphocytes and a subpopulation of CD4(+) and CD8(+) T lymphocytes.
43 17702825 We describe the CMRF-35(pos) and CMRF-35(-) fractions of CD4(+) T lymphocytes.
44 17702825 The CMRF-35(pos) fraction can further be divided into CMRF-35(++) and CMRF-35(+)CD4(+) T lymphocyte subpopulations.
45 17702825 Resting peripheral CD4(+) T lymphocytes express CD300a mRNA and very low amounts of CD300c.
46 17702825 Activation results in an initial decrease in CD300a gene expression before an increase in both CD300a and CD300c gene expression.
47 17702825 The CMRF-35(-) fraction of CD4(+) T lymphocytes proliferated to a greater extent than the CMRF-35(pos) fraction, in response to mitogens or allogeneic antigen.
48 17702825 The poor proliferation of the CMRF-35(pos) CD4(+) in response to mitogens was explained by increased apoptosis within this subpopulation.
49 17702825 The recall antigen, tetanus toxoid, stimulated the CMRF-35(++)CD4(+)CD45RO(+) but not the CMRF-35(-)CD4(+)CD45RO(+) subpopulation.
50 17702825 Resting CMRF-35(++) CD4(+) lymphocytes express low levels of IFN-gamma mRNA.
51 17702825 Within 18 h following in vitro activation, CMRF-35(++) CD4(+) lymphocytes express more IFN-gamma mRNA and protein compared with the CMRF-35(-)CD4(+) lymphocytes, however, after 24 h, both the CMRF-35(+) and CMRF-35(-)CD4(+) T lymphocytes were able to produce IFN-gamma.
52 17702825 The CMRF-35(++)CD4(+) T lymphocyte population contains the Th(1) memory effector cells.
53 17702825 Novel human CD4+ T lymphocyte subpopulations defined by CD300a/c molecule expression.
54 17702825 The CD300c (CMRF-35A) and CD300a (CMRF-35H) molecules are leukocyte surface proteins that are part of a larger family of immunoregulatory molecules encoded by a gene complex on human chromosome 17.
55 17702825 The CMRF-35 monoclonal antibody binds to an epitope common to both molecules, expressed on most human leukocyte populations, apart from B lymphocytes and a subpopulation of CD4(+) and CD8(+) T lymphocytes.
56 17702825 We describe the CMRF-35(pos) and CMRF-35(-) fractions of CD4(+) T lymphocytes.
57 17702825 The CMRF-35(pos) fraction can further be divided into CMRF-35(++) and CMRF-35(+)CD4(+) T lymphocyte subpopulations.
58 17702825 Resting peripheral CD4(+) T lymphocytes express CD300a mRNA and very low amounts of CD300c.
59 17702825 Activation results in an initial decrease in CD300a gene expression before an increase in both CD300a and CD300c gene expression.
60 17702825 The CMRF-35(-) fraction of CD4(+) T lymphocytes proliferated to a greater extent than the CMRF-35(pos) fraction, in response to mitogens or allogeneic antigen.
61 17702825 The poor proliferation of the CMRF-35(pos) CD4(+) in response to mitogens was explained by increased apoptosis within this subpopulation.
62 17702825 The recall antigen, tetanus toxoid, stimulated the CMRF-35(++)CD4(+)CD45RO(+) but not the CMRF-35(-)CD4(+)CD45RO(+) subpopulation.
63 17702825 Resting CMRF-35(++) CD4(+) lymphocytes express low levels of IFN-gamma mRNA.
64 17702825 Within 18 h following in vitro activation, CMRF-35(++) CD4(+) lymphocytes express more IFN-gamma mRNA and protein compared with the CMRF-35(-)CD4(+) lymphocytes, however, after 24 h, both the CMRF-35(+) and CMRF-35(-)CD4(+) T lymphocytes were able to produce IFN-gamma.
65 17702825 The CMRF-35(++)CD4(+) T lymphocyte population contains the Th(1) memory effector cells.
66 17702825 Novel human CD4+ T lymphocyte subpopulations defined by CD300a/c molecule expression.
67 17702825 The CD300c (CMRF-35A) and CD300a (CMRF-35H) molecules are leukocyte surface proteins that are part of a larger family of immunoregulatory molecules encoded by a gene complex on human chromosome 17.
68 17702825 The CMRF-35 monoclonal antibody binds to an epitope common to both molecules, expressed on most human leukocyte populations, apart from B lymphocytes and a subpopulation of CD4(+) and CD8(+) T lymphocytes.
69 17702825 We describe the CMRF-35(pos) and CMRF-35(-) fractions of CD4(+) T lymphocytes.
70 17702825 The CMRF-35(pos) fraction can further be divided into CMRF-35(++) and CMRF-35(+)CD4(+) T lymphocyte subpopulations.
71 17702825 Resting peripheral CD4(+) T lymphocytes express CD300a mRNA and very low amounts of CD300c.
72 17702825 Activation results in an initial decrease in CD300a gene expression before an increase in both CD300a and CD300c gene expression.
73 17702825 The CMRF-35(-) fraction of CD4(+) T lymphocytes proliferated to a greater extent than the CMRF-35(pos) fraction, in response to mitogens or allogeneic antigen.
74 17702825 The poor proliferation of the CMRF-35(pos) CD4(+) in response to mitogens was explained by increased apoptosis within this subpopulation.
75 17702825 The recall antigen, tetanus toxoid, stimulated the CMRF-35(++)CD4(+)CD45RO(+) but not the CMRF-35(-)CD4(+)CD45RO(+) subpopulation.
76 17702825 Resting CMRF-35(++) CD4(+) lymphocytes express low levels of IFN-gamma mRNA.
77 17702825 Within 18 h following in vitro activation, CMRF-35(++) CD4(+) lymphocytes express more IFN-gamma mRNA and protein compared with the CMRF-35(-)CD4(+) lymphocytes, however, after 24 h, both the CMRF-35(+) and CMRF-35(-)CD4(+) T lymphocytes were able to produce IFN-gamma.
78 17702825 The CMRF-35(++)CD4(+) T lymphocyte population contains the Th(1) memory effector cells.
79 17702825 Novel human CD4+ T lymphocyte subpopulations defined by CD300a/c molecule expression.
80 17702825 The CD300c (CMRF-35A) and CD300a (CMRF-35H) molecules are leukocyte surface proteins that are part of a larger family of immunoregulatory molecules encoded by a gene complex on human chromosome 17.
81 17702825 The CMRF-35 monoclonal antibody binds to an epitope common to both molecules, expressed on most human leukocyte populations, apart from B lymphocytes and a subpopulation of CD4(+) and CD8(+) T lymphocytes.
82 17702825 We describe the CMRF-35(pos) and CMRF-35(-) fractions of CD4(+) T lymphocytes.
83 17702825 The CMRF-35(pos) fraction can further be divided into CMRF-35(++) and CMRF-35(+)CD4(+) T lymphocyte subpopulations.
84 17702825 Resting peripheral CD4(+) T lymphocytes express CD300a mRNA and very low amounts of CD300c.
85 17702825 Activation results in an initial decrease in CD300a gene expression before an increase in both CD300a and CD300c gene expression.
86 17702825 The CMRF-35(-) fraction of CD4(+) T lymphocytes proliferated to a greater extent than the CMRF-35(pos) fraction, in response to mitogens or allogeneic antigen.
87 17702825 The poor proliferation of the CMRF-35(pos) CD4(+) in response to mitogens was explained by increased apoptosis within this subpopulation.
88 17702825 The recall antigen, tetanus toxoid, stimulated the CMRF-35(++)CD4(+)CD45RO(+) but not the CMRF-35(-)CD4(+)CD45RO(+) subpopulation.
89 17702825 Resting CMRF-35(++) CD4(+) lymphocytes express low levels of IFN-gamma mRNA.
90 17702825 Within 18 h following in vitro activation, CMRF-35(++) CD4(+) lymphocytes express more IFN-gamma mRNA and protein compared with the CMRF-35(-)CD4(+) lymphocytes, however, after 24 h, both the CMRF-35(+) and CMRF-35(-)CD4(+) T lymphocytes were able to produce IFN-gamma.
91 17702825 The CMRF-35(++)CD4(+) T lymphocyte population contains the Th(1) memory effector cells.
92 17702825 Novel human CD4+ T lymphocyte subpopulations defined by CD300a/c molecule expression.
93 17702825 The CD300c (CMRF-35A) and CD300a (CMRF-35H) molecules are leukocyte surface proteins that are part of a larger family of immunoregulatory molecules encoded by a gene complex on human chromosome 17.
94 17702825 The CMRF-35 monoclonal antibody binds to an epitope common to both molecules, expressed on most human leukocyte populations, apart from B lymphocytes and a subpopulation of CD4(+) and CD8(+) T lymphocytes.
95 17702825 We describe the CMRF-35(pos) and CMRF-35(-) fractions of CD4(+) T lymphocytes.
96 17702825 The CMRF-35(pos) fraction can further be divided into CMRF-35(++) and CMRF-35(+)CD4(+) T lymphocyte subpopulations.
97 17702825 Resting peripheral CD4(+) T lymphocytes express CD300a mRNA and very low amounts of CD300c.
98 17702825 Activation results in an initial decrease in CD300a gene expression before an increase in both CD300a and CD300c gene expression.
99 17702825 The CMRF-35(-) fraction of CD4(+) T lymphocytes proliferated to a greater extent than the CMRF-35(pos) fraction, in response to mitogens or allogeneic antigen.
100 17702825 The poor proliferation of the CMRF-35(pos) CD4(+) in response to mitogens was explained by increased apoptosis within this subpopulation.
101 17702825 The recall antigen, tetanus toxoid, stimulated the CMRF-35(++)CD4(+)CD45RO(+) but not the CMRF-35(-)CD4(+)CD45RO(+) subpopulation.
102 17702825 Resting CMRF-35(++) CD4(+) lymphocytes express low levels of IFN-gamma mRNA.
103 17702825 Within 18 h following in vitro activation, CMRF-35(++) CD4(+) lymphocytes express more IFN-gamma mRNA and protein compared with the CMRF-35(-)CD4(+) lymphocytes, however, after 24 h, both the CMRF-35(+) and CMRF-35(-)CD4(+) T lymphocytes were able to produce IFN-gamma.
104 17702825 The CMRF-35(++)CD4(+) T lymphocyte population contains the Th(1) memory effector cells.
105 17702825 Novel human CD4+ T lymphocyte subpopulations defined by CD300a/c molecule expression.
106 17702825 The CD300c (CMRF-35A) and CD300a (CMRF-35H) molecules are leukocyte surface proteins that are part of a larger family of immunoregulatory molecules encoded by a gene complex on human chromosome 17.
107 17702825 The CMRF-35 monoclonal antibody binds to an epitope common to both molecules, expressed on most human leukocyte populations, apart from B lymphocytes and a subpopulation of CD4(+) and CD8(+) T lymphocytes.
108 17702825 We describe the CMRF-35(pos) and CMRF-35(-) fractions of CD4(+) T lymphocytes.
109 17702825 The CMRF-35(pos) fraction can further be divided into CMRF-35(++) and CMRF-35(+)CD4(+) T lymphocyte subpopulations.
110 17702825 Resting peripheral CD4(+) T lymphocytes express CD300a mRNA and very low amounts of CD300c.
111 17702825 Activation results in an initial decrease in CD300a gene expression before an increase in both CD300a and CD300c gene expression.
112 17702825 The CMRF-35(-) fraction of CD4(+) T lymphocytes proliferated to a greater extent than the CMRF-35(pos) fraction, in response to mitogens or allogeneic antigen.
113 17702825 The poor proliferation of the CMRF-35(pos) CD4(+) in response to mitogens was explained by increased apoptosis within this subpopulation.
114 17702825 The recall antigen, tetanus toxoid, stimulated the CMRF-35(++)CD4(+)CD45RO(+) but not the CMRF-35(-)CD4(+)CD45RO(+) subpopulation.
115 17702825 Resting CMRF-35(++) CD4(+) lymphocytes express low levels of IFN-gamma mRNA.
116 17702825 Within 18 h following in vitro activation, CMRF-35(++) CD4(+) lymphocytes express more IFN-gamma mRNA and protein compared with the CMRF-35(-)CD4(+) lymphocytes, however, after 24 h, both the CMRF-35(+) and CMRF-35(-)CD4(+) T lymphocytes were able to produce IFN-gamma.
117 17702825 The CMRF-35(++)CD4(+) T lymphocyte population contains the Th(1) memory effector cells.
118 17702825 Novel human CD4+ T lymphocyte subpopulations defined by CD300a/c molecule expression.
119 17702825 The CD300c (CMRF-35A) and CD300a (CMRF-35H) molecules are leukocyte surface proteins that are part of a larger family of immunoregulatory molecules encoded by a gene complex on human chromosome 17.
120 17702825 The CMRF-35 monoclonal antibody binds to an epitope common to both molecules, expressed on most human leukocyte populations, apart from B lymphocytes and a subpopulation of CD4(+) and CD8(+) T lymphocytes.
121 17702825 We describe the CMRF-35(pos) and CMRF-35(-) fractions of CD4(+) T lymphocytes.
122 17702825 The CMRF-35(pos) fraction can further be divided into CMRF-35(++) and CMRF-35(+)CD4(+) T lymphocyte subpopulations.
123 17702825 Resting peripheral CD4(+) T lymphocytes express CD300a mRNA and very low amounts of CD300c.
124 17702825 Activation results in an initial decrease in CD300a gene expression before an increase in both CD300a and CD300c gene expression.
125 17702825 The CMRF-35(-) fraction of CD4(+) T lymphocytes proliferated to a greater extent than the CMRF-35(pos) fraction, in response to mitogens or allogeneic antigen.
126 17702825 The poor proliferation of the CMRF-35(pos) CD4(+) in response to mitogens was explained by increased apoptosis within this subpopulation.
127 17702825 The recall antigen, tetanus toxoid, stimulated the CMRF-35(++)CD4(+)CD45RO(+) but not the CMRF-35(-)CD4(+)CD45RO(+) subpopulation.
128 17702825 Resting CMRF-35(++) CD4(+) lymphocytes express low levels of IFN-gamma mRNA.
129 17702825 Within 18 h following in vitro activation, CMRF-35(++) CD4(+) lymphocytes express more IFN-gamma mRNA and protein compared with the CMRF-35(-)CD4(+) lymphocytes, however, after 24 h, both the CMRF-35(+) and CMRF-35(-)CD4(+) T lymphocytes were able to produce IFN-gamma.
130 17702825 The CMRF-35(++)CD4(+) T lymphocyte population contains the Th(1) memory effector cells.
131 17702825 Novel human CD4+ T lymphocyte subpopulations defined by CD300a/c molecule expression.
132 17702825 The CD300c (CMRF-35A) and CD300a (CMRF-35H) molecules are leukocyte surface proteins that are part of a larger family of immunoregulatory molecules encoded by a gene complex on human chromosome 17.
133 17702825 The CMRF-35 monoclonal antibody binds to an epitope common to both molecules, expressed on most human leukocyte populations, apart from B lymphocytes and a subpopulation of CD4(+) and CD8(+) T lymphocytes.
134 17702825 We describe the CMRF-35(pos) and CMRF-35(-) fractions of CD4(+) T lymphocytes.
135 17702825 The CMRF-35(pos) fraction can further be divided into CMRF-35(++) and CMRF-35(+)CD4(+) T lymphocyte subpopulations.
136 17702825 Resting peripheral CD4(+) T lymphocytes express CD300a mRNA and very low amounts of CD300c.
137 17702825 Activation results in an initial decrease in CD300a gene expression before an increase in both CD300a and CD300c gene expression.
138 17702825 The CMRF-35(-) fraction of CD4(+) T lymphocytes proliferated to a greater extent than the CMRF-35(pos) fraction, in response to mitogens or allogeneic antigen.
139 17702825 The poor proliferation of the CMRF-35(pos) CD4(+) in response to mitogens was explained by increased apoptosis within this subpopulation.
140 17702825 The recall antigen, tetanus toxoid, stimulated the CMRF-35(++)CD4(+)CD45RO(+) but not the CMRF-35(-)CD4(+)CD45RO(+) subpopulation.
141 17702825 Resting CMRF-35(++) CD4(+) lymphocytes express low levels of IFN-gamma mRNA.
142 17702825 Within 18 h following in vitro activation, CMRF-35(++) CD4(+) lymphocytes express more IFN-gamma mRNA and protein compared with the CMRF-35(-)CD4(+) lymphocytes, however, after 24 h, both the CMRF-35(+) and CMRF-35(-)CD4(+) T lymphocytes were able to produce IFN-gamma.
143 17702825 The CMRF-35(++)CD4(+) T lymphocyte population contains the Th(1) memory effector cells.
144 17702825 Novel human CD4+ T lymphocyte subpopulations defined by CD300a/c molecule expression.
145 17702825 The CD300c (CMRF-35A) and CD300a (CMRF-35H) molecules are leukocyte surface proteins that are part of a larger family of immunoregulatory molecules encoded by a gene complex on human chromosome 17.
146 17702825 The CMRF-35 monoclonal antibody binds to an epitope common to both molecules, expressed on most human leukocyte populations, apart from B lymphocytes and a subpopulation of CD4(+) and CD8(+) T lymphocytes.
147 17702825 We describe the CMRF-35(pos) and CMRF-35(-) fractions of CD4(+) T lymphocytes.
148 17702825 The CMRF-35(pos) fraction can further be divided into CMRF-35(++) and CMRF-35(+)CD4(+) T lymphocyte subpopulations.
149 17702825 Resting peripheral CD4(+) T lymphocytes express CD300a mRNA and very low amounts of CD300c.
150 17702825 Activation results in an initial decrease in CD300a gene expression before an increase in both CD300a and CD300c gene expression.
151 17702825 The CMRF-35(-) fraction of CD4(+) T lymphocytes proliferated to a greater extent than the CMRF-35(pos) fraction, in response to mitogens or allogeneic antigen.
152 17702825 The poor proliferation of the CMRF-35(pos) CD4(+) in response to mitogens was explained by increased apoptosis within this subpopulation.
153 17702825 The recall antigen, tetanus toxoid, stimulated the CMRF-35(++)CD4(+)CD45RO(+) but not the CMRF-35(-)CD4(+)CD45RO(+) subpopulation.
154 17702825 Resting CMRF-35(++) CD4(+) lymphocytes express low levels of IFN-gamma mRNA.
155 17702825 Within 18 h following in vitro activation, CMRF-35(++) CD4(+) lymphocytes express more IFN-gamma mRNA and protein compared with the CMRF-35(-)CD4(+) lymphocytes, however, after 24 h, both the CMRF-35(+) and CMRF-35(-)CD4(+) T lymphocytes were able to produce IFN-gamma.
156 17702825 The CMRF-35(++)CD4(+) T lymphocyte population contains the Th(1) memory effector cells.