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1 portion of the receptor tyrosine kinase ALK (anaplastic lymphoma kinase).
2 es the fusion protein NPM-ALK (nucleophosmin-anaplastic lymphoma kinase).
3  molecular target for the kinase activity of anaplastic lymphoma kinase.
4  expression was not related to expression of anaplastic lymphoma kinase-1.
5               The proto-oncogene ALK encodes anaplastic lymphoma kinase, a receptor tyrosine kinase t
6 he presence of a translocation involving the anaplastic lymphoma kinase ALK gene.
7 ide 1 was identified as a novel inhibitor of anaplastic lymphoma kinase (ALK enzyme assay IC(50) = 0.
8                                              Anaplastic lymphoma kinase (ALK) -positive anaplastic la
9                    Concomitant inhibition of anaplastic lymphoma kinase (ALK) and bromodomain-4 (BRD4
10                 The tyrosine kinase receptor anaplastic lymphoma kinase (ALK) and its ligand, the gro
11                                              Anaplastic lymphoma kinase (Alk) and leucocyte tyrosine
12                                Activation of Anaplastic lymphoma kinase (ALK) and leukocyte tyrosine
13 belly (Jeb) and its receptor tyrosine kinase Anaplastic lymphoma kinase (Alk) are localized to develo
14 ncogenic fusion genes consisting of EML4 and anaplastic lymphoma kinase (ALK) are present in a subgro
15                                We discovered anaplastic lymphoma kinase (ALK) as a candidate thinness
16                  We have recently identified anaplastic lymphoma kinase (ALK) as a tyrosine kinase re
17  recently identified nucleophosmin (NPM) and anaplastic lymphoma kinase (ALK) as the genes on chromos
18 t inhibitors of the receptor tyrosine kinase anaplastic lymphoma kinase (ALK) blocked D2R desensitiza
19   The phylogenetic proximity of the ROS1 and anaplastic lymphoma kinase (ALK) catalytic domains led t
20 Abnormal expression of constitutively active anaplastic lymphoma kinase (ALK) chimeric proteins in th
21 essed CD30, epithelial membrane antigen, and anaplastic lymphoma kinase (ALK) consistent with a null
22                                              Anaplastic lymphoma kinase (ALK) constitutes a part of t
23  epidermal growth factor receptor (EGFR) and anaplastic lymphoma kinase (ALK) define two unique subty
24                          We demonstrate that anaplastic lymphoma kinase (Alk) efficiently protects ne
25  lymphoma (ALCL) is a T-cell lymphoma, whose anaplastic lymphoma kinase (ALK) expression varies accor
26  distinguished by the presence or absence of anaplastic lymphoma kinase (ALK) expression.
27  This review describes the identification of anaplastic lymphoma kinase (ALK) fusion genes in approxi
28 microtubule-associated protein-like 4 (EML4)-anaplastic lymphoma kinase (ALK) fusion oncogene represe
29 ag in this study and was used to degrade the anaplastic lymphoma kinase (ALK) fusion protein by linki
30 microtubule-associated protein-like 4 (EML4)-anaplastic lymphoma kinase (ALK) fusion protein, presume
31                                    Oncogenic anaplastic lymphoma kinase (ALK) fusion proteins (nucleo
32                                              Anaplastic lymphoma kinase (ALK) fusion variants in Non-
33                 Rearrangements involving the anaplastic lymphoma kinase (ALK) gene are defining event
34 d here to detection of rearrangements in the anaplastic lymphoma kinase (ALK) gene associated with AL
35 ssed nucleophosmin (NPM) gene at 5q35 to the anaplastic lymphoma kinase (ALK) gene at 2p23, which is
36  Here we show that germline mutations in the anaplastic lymphoma kinase (ALK) gene explain most hered
37                                          The anaplastic lymphoma kinase (ALK) gene fuses to the nucle
38 he discovery of rearrangements involving the anaplastic lymphoma kinase (ALK) gene in thyroid cancer.
39                                          The Anaplastic Lymphoma Kinase (ALK) gene is a receptor tyro
40                                          The anaplastic lymphoma kinase (ALK) gene is characteristica
41 as (ALCLs) carry translocations in which the anaplastic lymphoma kinase (ALK) gene is juxtaposed to v
42 normalities of 2p23 and rearrangement of the anaplastic lymphoma kinase (ALK) gene locus.
43         Molecular testing is positive for an anaplastic lymphoma kinase (ALK) gene rearrangement usin
44                                              Anaplastic lymphoma kinase (ALK) gene rearrangements are
45          In 2007, scientists discovered that anaplastic lymphoma kinase (ALK) gene rearrangements are
46 dermal growth factor receptor (EGFR) gene or anaplastic lymphoma kinase (ALK) gene rearrangements.
47                    Patients positive for the anaplastic lymphoma kinase (ALK) gene showed elevated sI
48 (2;5)(p23;q35) translocation which fuses the Anaplastic Lymphoma Kinase (ALK) gene with the Nucleopho
49 uently carry oncogenic fusions involving the anaplastic lymphoma kinase (ALK) gene.
50                       Aberrant activation of anaplastic lymphoma kinase (ALK) has been described in a
51                                              Anaplastic lymphoma kinase (Alk) has been proposed to re
52                        Aberrant forms of the anaplastic lymphoma kinase (ALK) have been implicated in
53                Activating point mutations in Anaplastic Lymphoma Kinase (ALK) have positioned ALK as
54 2 gene, which, we show, encodes the nematode anaplastic lymphoma kinase (ALK) homolog, a proto-oncoge
55 usly shown both humoral and CTL responses to anaplastic lymphoma kinase (ALK) in patients with ALK-po
56            Analogues structurally related to anaplastic lymphoma kinase (ALK) inhibitor 1 were optimi
57                         Here we investigated anaplastic lymphoma kinase (ALK) inhibitor resistance in
58               Ceritinib is a next-generation anaplastic lymphoma kinase (ALK) inhibitor, which has sh
59                                         Most anaplastic lymphoma kinase (ALK) inhibitors adopt a type
60                                    find that anaplastic lymphoma kinase (ALK) inhibitors can enhance
61  that may rationalize clinical evaluation of anaplastic lymphoma kinase (ALK) inhibitors in this sett
62  lending impetus to the development of novel anaplastic lymphoma kinase (ALK) inhibitors with differe
63 naene macrocycles were prepared as potential anaplastic lymphoma kinase (ALK) inhibitors, designed to
64                                              Anaplastic lymphoma kinase (ALK) is a promising new targ
65                                    Targeting Anaplastic lymphoma kinase (ALK) is a promising therapeu
66                                              Anaplastic lymphoma kinase (ALK) is a promising therapeu
67                                              Anaplastic lymphoma kinase (ALK) is a receptor tyrosine
68                                              Anaplastic lymphoma kinase (ALK) is a receptor tyrosine
69                                              Anaplastic lymphoma kinase (ALK) is a receptor tyrosine
70                                              Anaplastic lymphoma kinase (ALK) is a receptor tyrosine
71                                              Anaplastic lymphoma kinase (Alk) is a receptor tyrosine
72                                          The anaplastic lymphoma kinase (ALK) is a receptor tyrosine
73                                              Anaplastic lymphoma kinase (ALK) is a receptor tyrosine
74                                              Anaplastic lymphoma kinase (ALK) is a receptor tyrosine
75                                              Anaplastic lymphoma kinase (ALK) is a receptor tyrosine
76                                              Anaplastic lymphoma kinase (ALK) is a transmembrane rece
77                        Here we show that the anaplastic lymphoma kinase (ALK) is aberrantly activated
78                                          The anaplastic lymphoma kinase (ALK) is chromosomally rearra
79                          The orphan receptor anaplastic lymphoma kinase (ALK) is one of very few RTKs
80           Here we show that transcription of anaplastic lymphoma kinase (Alk) is repressed by LMO4 in
81  MYCN overexpression combined with activated anaplastic lymphoma kinase (ALK) is sufficient to induce
82                Genetic rearrangements of the anaplastic lymphoma kinase (ALK) kinase occur in 3% to 1
83 ely half of IMTs carry rearrangements of the anaplastic lymphoma kinase (ALK) locus on chromosome 2p2
84                                   Activating anaplastic lymphoma kinase (ALK) mutations are frequentl
85                                              Anaplastic lymphoma kinase (ALK) mutations occur in 3% t
86 malignant transformation of T cells that are anaplastic lymphoma kinase (ALK) negative and CD30 posit
87                                          The anaplastic lymphoma kinase (ALK) on 2p23 is a tyrosine k
88 microtubule-associated protein-like 4 (EML4)-anaplastic lymphoma kinase (ALK) oncogenic fusion protei
89                                              Anaplastic lymphoma kinase (ALK) oncogenic fusions are a
90  The metabolic shift is mediated through the anaplastic lymphoma kinase (ALK) phosphorylation of the
91 , we found that a selective inhibitor of the anaplastic lymphoma kinase (ALK) potently suppressed gro
92  developed a folate-caged pomalidomide-based anaplastic lymphoma kinase (ALK) PROTAC, FA-S2-MS4048, w
93      The aim of this study is to investigate anaplastic lymphoma kinase (ALK) protein expression and
94 hromosomal translocations that juxtapose the anaplastic lymphoma kinase (ALK) proto-oncogene to a dim
95  growth factor receptor (EGFR) mutations and anaplastic lymphoma kinase (ALK) rearrangements have dem
96                                          The anaplastic lymphoma kinase (ALK) receptor is expressed b
97 l fusion gene that incorporates parts of the anaplastic lymphoma kinase (ALK) receptor tyrosine kinas
98                           Crizotinib (1), an anaplastic lymphoma kinase (ALK) receptor tyrosine kinas
99 ent work identified ALKAL2, a ligand for the Anaplastic Lymphoma Kinase (ALK) receptor, as a key medi
100  the oncogenic, chimeric nucleophosmin (NPM)/anaplastic lymphoma kinase (ALK) remain only partially u
101 romoting phenotype through activation of the anaplastic lymphoma kinase (ALK) signaling pathway.
102        Here we report a novel isoform of the anaplastic lymphoma kinase (ALK) that is expressed in ap
103  and rhabdomyosarcoma, harbour activation of anaplastic lymphoma kinase (ALK) through different mecha
104 aim of the present review is to describe the anaplastic lymphoma kinase (ALK) translocation as a prom
105 sets of lung cancers with EGFR mutations and anaplastic lymphoma kinase (ALK) translocations.
106 ormation mediated by the nucleophosmin (NPM)/anaplastic lymphoma kinase (ALK) tyrosine kinase are onl
107                                              Anaplastic lymphoma kinase (ALK) tyrosine kinase inhibit
108  a potent, brain-penetrant, third-generation anaplastic lymphoma kinase (ALK) tyrosine kinase inhibit
109 h epidermal growth factor receptor (EGFR) or anaplastic lymphoma kinase (ALK) tyrosine kinase inhibit
110  epidermal growth factor receptor (EGFR) and anaplastic lymphoma kinase (ALK) tyrosine kinase inhibit
111  epidermal growth factor receptor (EGFR) and anaplastic lymphoma kinase (ALK) tyrosine kinase inhibit
112                                              Anaplastic lymphoma kinase (ALK) tyrosine kinase inhibit
113 ell transformation mediated by the oncogenic anaplastic lymphoma kinase (ALK) tyrosine kinase remain
114 n protein containing the catalytic domain of anaplastic lymphoma kinase (ALK) under the control of th
115                                              Anaplastic Lymphoma Kinase (ALK) was originally identifi
116 protein (p80) derived from the fusion of the anaplastic lymphoma kinase (ALK) with nucleophosmin (NPM
117 ;5)(p23;q35) results in the juxtaposition of anaplastic lymphoma kinase (ALK) with nucleophosmin (NPM
118 t down-regulation of TIMP1 expression in two anaplastic lymphoma kinase (ALK)(+) ALCL cell lines, Kar
119 vered in many T-cell malignancies, including anaplastic lymphoma kinase (ALK)(-) anaplastic large cel
120                                              Anaplastic lymphoma kinase (ALK)(1) and the related leuk
121             Genetic studies have established anaplastic lymphoma kinase (ALK), a cell surface recepto
122 ntained chromosomal translocations involving anaplastic lymphoma kinase (ALK), a novel receptor tyros
123  Jeb receptor is the Drosophila homologue of anaplastic lymphoma kinase (Alk), a receptor tyrosine ki
124                                              Anaplastic lymphoma kinase (ALK), a receptor tyrosine ki
125 a distinct role for one of the DMGs encoding anaplastic lymphoma kinase (ALK), an important regulator
126 se domain that is physiologically related to anaplastic lymphoma kinase (ALK), and is undergoing Phas
127 EGFR), rearranged during transfection (RET), anaplastic lymphoma kinase (ALK), and MAPK1/3 and other
128 ts in nonsmall cell lung cancer fuse EML4 to anaplastic lymphoma kinase (ALK), causing expression of
129                                              Anaplastic lymphoma kinase (ALK), EGF receptor (EGFR), a
130 otubule-associated protein like 4 (EML4) and anaplastic lymphoma kinase (ALK), generated by an invers
131                  Crizotinib, an inhibitor of anaplastic lymphoma kinase (ALK), has also recently show
132 ecently identified receptor tyrosine kinase, anaplastic lymphoma kinase (ALK), in embryonic chick by
133  of epidermal growth factor receptor (EGFR), anaplastic lymphoma kinase (ALK), KRAS, and BRAF, induce
134  by R1-R6 axons interacts with its receptor, anaplastic lymphoma kinase (Alk), on budding dendrites t
135 omosome 5q35 to a novel protein kinase gene, Anaplastic Lymphoma Kinase (ALK), on chromosome 2p23.
136                                              Anaplastic lymphoma kinase (ALK), physiologically expres
137                                              Anaplastic lymphoma kinase (ALK), physiologically expres
138 e phosphatase receptor zeta (PTPRZ1) and the anaplastic lymphoma kinase (ALK), respectively.
139 genes encoding the receptor tyrosine kinases anaplastic lymphoma kinase (ALK), ROS proto-oncogene 1 (
140 r (TKI) with specificity for gene rearranged anaplastic lymphoma kinase (ALK), such as the EML4-ALK,
141                                  MK binds to anaplastic lymphoma kinase (ALK), the receptor for PTN,
142 lating evidence indicates that expression of anaplastic lymphoma kinase (ALK), typically due to t(2;5
143 ), human epidermal growth factor receptor 2, anaplastic lymphoma kinase (ALK), v-Raf murine sarcoma v
144           A gene residing in this locus, the anaplastic lymphoma kinase (Alk), was expressed at signi
145                                     MYCN and Anaplastic Lymphoma Kinase (ALK), which are often involv
146  SCD-2, the C. elegans ortholog of mammalian anaplastic lymphoma kinase (ALK), which has been implica
147 YCN cooperates with mutational activation of anaplastic lymphoma kinase (ALK), which promotes progres
148  absence of translocations that activate the anaplastic lymphoma kinase (ALK), with nucleophosmin-ALK
149                     For comparison, CNAs for anaplastic lymphoma kinase (ALK)- nodal anaplastic large
150 ied, angioimmunoblastic T-cell lymphoma, and anaplastic lymphoma kinase (ALK)-negative anaplastic lar
151                                              Anaplastic lymphoma kinase (ALK)-negative anaplastic lar
152 d) and active (underphosphorylated), in four anaplastic lymphoma kinase (ALK)-positive ALCL cell line
153                                              Anaplastic lymphoma kinase (ALK)-positive anaplastic lar
154 e SHH/GLI1 signaling pathway is activated in anaplastic lymphoma kinase (ALK)-positive anaplastic lar
155                                              Anaplastic lymphoma kinase (ALK)-positive anaplastic lar
156 ssion was seen in only 1 of 15 patients with anaplastic lymphoma kinase (ALK)-positive anaplastic lar
157 orrelates with relapse risk in children with anaplastic lymphoma kinase (ALK)-positive anaplastic lar
158  a small subset of cells purified from human anaplastic lymphoma kinase (ALK)-positive and -negative,
159 ngioimmunoblastic T-cell lymphoma (AITL), 31 anaplastic lymphoma kinase (ALK)-positive and 48 ALK-neg
160 heterogeneous disease that includes systemic anaplastic lymphoma kinase (ALK)-positive and ALK-negati
161                                   While most anaplastic lymphoma kinase (ALK)-positive non-Hodgkin ly
162 h crizotinib demonstrates robust efficacy in anaplastic lymphoma kinase (ALK)-positive non-small-cell
163 positive T-cell lymphoma, comprises systemic anaplastic lymphoma kinase (ALK)-positive, and ALK-negat
164 ere, we perform a phosphoproteomic screen in anaplastic lymphoma kinase (ALK)-rearranged ("ALK+") pat
165 oma, small molecule inhibitor crizotinib for anaplastic lymphoma kinase (ALK)-rearranged inflammatory
166              In a patient who had metastatic anaplastic lymphoma kinase (ALK)-rearranged lung cancer,
167 cacy of ceritinib in patients with untreated anaplastic lymphoma kinase (ALK)-rearranged non-small-ce
168                           Most patients with anaplastic lymphoma kinase (ALK)-rearranged or ROS proto
169                                Resistance to anaplastic lymphoma kinase (ALK)-targeted therapy in ALK
170 scaffold will be described for inhibitors of anaplastic lymphoma kinase (ALK).
171 somatic aberrations in the gene encoding for anaplastic lymphoma kinase (ALK).
172 he dimerization domain of nucleophosmin with anaplastic lymphoma kinase (ALK).
173 express the receptor for this growth factor, anaplastic lymphoma kinase (ALK).
174 (ECD) of the orphan receptor tyrosine kinase anaplastic lymphoma kinase (ALK).
175 smic portion of the receptor tyrosine kinase anaplastic lymphoma kinase (ALK).
176 2;5)(p23;q35) resulting in overexpression of anaplastic lymphoma kinase (ALK).
177 smic portion of the receptor tyrosine kinase anaplastic lymphoma kinase (ALK).
178 pression of CD30 and a lack of expression of anaplastic lymphoma kinase (ALK).
179 eloped as potent and selective inhibitors of anaplastic lymphoma kinase (ALK).
180 lymphomas characterized by the expression of anaplastic lymphoma kinase (ALK+ TCL) fail to express th
181 leophosmin/B23 (NPM) gene (5q35) and a novel anaplastic lymphoma kinase (ALK; 2p23) are the fused gen
182 chimeric tyrosine kinase nucleophosmin (NPM)-anaplastic lymphoma kinase [ALK; ALK(+) T-cell lymphoma
183 h epidermal growth factor receptor [EGFR] or anaplastic lymphoma kinase [ALK] genetic alterations wer
184 or survivin expression in 62 ALCL tumors (30 anaplastic lymphoma kinase [ALK]-positive and 32 ALK-neg
185 r inhibitors, 2.46% (range, 1.75%-4.66%) for anaplastic lymphoma kinase and ROS1 inhibitors, and 3.06
186 to be independent of nuclear localization of anaplastic lymphoma kinase; and phospholipase C-gamma wa
187 2;5) were mapped; constitutive activation of anaplastic lymphoma kinase by a chromosomal inversion wa
188       During the last year the expression of anaplastic lymphoma kinase clarified presentation and pr
189      PF-2341066 was selective for c-Met (and anaplastic lymphoma kinase) compared with a panel of >12
190 noderm microtubule-associated protein-like 4-anaplastic lymphoma kinase (EML4-ALK) fusion protein is
191 noderm microtubule-associated protein-like 4-anaplastic lymphoma kinase fusion protein.
192 idermal growth factor receptor mutations and anaplastic lymphoma kinase fusions, but significantly re
193 timal first-line treatment for patients with anaplastic lymphoma kinase fusions.
194 p studies, chromosomal rearrangements of the anaplastic lymphoma kinase gene (ALK) have been associat
195  xenograft models of the novel and selective anaplastic lymphoma kinase inhibitor 15b (LDK378) are de
196 ells that are sensitive and resistant to the anaplastic lymphoma kinase inhibitor alectinib.
197 r inhibitors, 0.999 (range, 0.982-0.999) for anaplastic lymphoma kinase inhibitors, and 0.999 for BRA
198 epidermal growth factor receptor inhibitors, anaplastic lymphoma kinase inhibitors, ROS1 inhibitors,
199 , we determined that the Midkine-a receptor, anaplastic lymphoma kinase, is upstream of the HLH regul
200 cell lymphoma (BIA-ALCL) is a CD30-positive, anaplastic lymphoma kinase-negative T-cell lymphoma.
201 CD30(+) T cell lymphoproliferative disorder (anaplastic lymphoma kinase-negative) 3 years after recei
202 d the resulting fusion protein nucleophosmin-anaplastic lymphoma kinase (NPM-ALK) are detected in 50%
203 utively active tyrosine kinase nucleophosmin-anaplastic lymphoma kinase (NPM-ALK) expressing anaplast
204 Constitutive overexpression of nucleophosmin-anaplastic lymphoma kinase (NPM-ALK) is a key oncogenic
205                                Nucleophosmin-anaplastic lymphoma kinase (NPM-ALK) is an aberrant fusi
206 ction of the nucleolar protein nucleophosmin-anaplastic lymphoma kinase (NPM-ALK) protein.
207 mation of the chimeric protein nucleophosmin-anaplastic lymphoma kinase (NPM-ALK), which possesses si
208 ting in aberrant expression of nucleophosmin-anaplastic lymphoma kinase (NPM-ALK).
209 neration of the fusion protein nucleophosmin-anaplastic lymphoma kinase (NPM-ALK).
210 ;q35) and aberrantly expresses nucleophosmin-anaplastic lymphoma kinase (NPM-ALK).
211  oncogenic fusion protein: the nucleophosmin-anaplastic lymphoma kinase (NPM-ALK).
212 neration of the fusion protein nucleophosmin-anaplastic lymphoma kinase (NPM-ALK).
213                            The nucleophosmin-anaplastic lymphoma kinase (NPM-ALK)/phospholipase C-gam
214 ted by the oncogenic, chimeric nucleophosmin/anaplastic lymphoma kinase (NPM/ALK) tyrosine kinase rem
215 plying these design principles, we developed anaplastic lymphoma kinase oncoprotein-targeting PROTACs
216 microtubule-associated protein-like 4 (EML4)-anaplastic lymphoma kinase positive (ALK+) non-small-cel
217 t this receptor is expressed on T cells from anaplastic lymphoma kinase-positive (ALK(+)) anaplastic
218 r angioimmunoblastic T-cell lymphoma (AITL), anaplastic lymphoma kinase-positive (ALK(+)) anaplastic
219       Using conditional transgenic models of anaplastic lymphoma kinase-positive (ALK(+)) lymphomas a
220                                              Anaplastic lymphoma kinase-positive (ALK+) ALCL is assoc
221                                           In anaplastic lymphoma kinase-positive (ALK+) ALCL, WASP an
222                                              Anaplastic lymphoma kinase-positive (ALK-positive) disea
223                          Using nucleophosmin-anaplastic lymphoma kinase-positive (NPM-ALK(+)) anaplas
224 sociated T-cell lymphoma patients (excluding anaplastic lymphoma kinase-positive anaplastic large cel
225                                              Anaplastic lymphoma kinase-positive anaplastic large-cel
226 d in a caspase-dependent manner in apoptotic anaplastic lymphoma kinase-positive, anaplastic large ce
227                         For patients with an anaplastic lymphoma kinase rearrangement, a performance
228                         For patients with an anaplastic lymphoma kinase rearrangement, a PS of 0-2, a
229 accompanied by mutational activation of ALK (anaplastic lymphoma kinase), suggesting their pathogenic
230 clude the possibility of an EGFR mutation or anaplastic lymphoma kinase translocation or to identify
231 assively parallel sequencing instrument, and anaplastic lymphoma kinase translocation was evaluated b
232 vity to epidermal growth factor receptor and anaplastic lymphoma kinase tyrosine kinase inhibitors ha

 
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