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1 , in which homologous chromosomes are paired somatically.
2 codes a single transcript which is expressed somatically.
3 these cases, competency stages are inherited somatically.
4 bridge cycles generate dicentric chromosomes somatically.
5 xcept for most cancer mutations, which arise somatically.
6 and other hypoproliferative anemias may have somatically acquired 5q deletions with RPS14 haploinsuff
8 tle imbalances were detected that are likely somatically acquired alterations and include genes invol
11 hey also represent the first human report of somatically acquired altered stromal TGF-beta signaling
12 dissected tissues, we show that TGFBR1*6A is somatically acquired by stromal and epithelial cells adj
14 easurement and single-molecule sequencing of somatically acquired carcinogenic translocations at extr
15 roximately 220 kb in length and represents a somatically acquired change in the primary breast cancer
18 lymphoma, and leukemia are characterized by somatically acquired chromosome translocations that resu
20 Human neuroblastomas are characterized by somatically acquired copy number changes, including loss
21 of myelodysplastic syndrome, is caused by a somatically acquired deletion of chromosome 5q, which le
23 ated a system whereby PML-RARA expression is somatically acquired from the mouse Pml locus in the con
24 ic loss of 18q markers and in one of these a somatically acquired G-->T missense mutation was found i
27 biology of neuroblastoma is characterized by somatically acquired genetic events that lead to gene ov
31 We have previously shown that TGFBR1*6A is somatically acquired in head and neck and colon cancer (
34 espite these physical barriers, we show that somatically acquired mitochondrial-nuclear genome fusion
35 lorectal cancer, and the firstmouse model of somatically acquired MMR-deficient colorectal cancer.
38 aternally inherited diseases; maternally and somatically acquired mutations also accumulate over time
39 cent cancer sequencing studies also revealed somatically acquired mutations and deletions in ribosoma
40 e largest public resource for information on somatically acquired mutations in human cancer and is av
41 performed whole-exome sequencing to identify somatically acquired mutations in six patients who had p
42 n 194 high-risk neuroblastoma samples showed somatically acquired mutations in the tyrosine kinase do
43 we report that ASC tumors frequently harbor somatically acquired mutations in the UPF1 gene, which e
45 other cancers, is characterized by multiple somatically acquired mutations that affect genes of diff
55 uch studies lies in correctly distinguishing somatically acquired, cancer-specific lesions from patie
56 a remodeled replication origin, inherited or somatically acquired, provides a survival advantage and
59 Copy number abnormalities (CNAs) such as somatically-acquired chromosomal deletions and duplicati
60 ganization of c-Myc but many had one or more somatically-acquired MuLV proviral integrations that wer
65 odulated excitatory and inhibitory inputs to somatically aligned, morphologically realistic pyramidal
66 ve identified many genes that are frequently somatically altered across multiple tumour types, sugges
70 ddition, the PTPRJ gene has been shown to be somatically altered in several human cancer types such a
72 F-V600E kinase-activating mutation, which is somatically and clonally present in almost all patients
74 lease of several key factors, which act both somatically as hormones and within the brain as neuromod
79 repeats and that the duplication is mediated somatically by homologous recombination between the flan
80 that the Ph1 locus acts both meiotically and somatically by reducing non-homologous centromere associ
81 DNA (RAPD) markers, conclusively showed that somatically compatible isolates are not necessarily gene
83 e studies demonstrate that it is feasible to somatically delete a large chromosomal segment implicate
84 eted validation studies further confirm that somatically deleted genes function both in adult (meioti
87 uclear protein present in the germ cells and somatically derived follicle cells throughout oogenesis
88 t prospective isolation of a wide variety of somatically derived stem cells has affirmed the notion t
89 cificity for dsDNA is generated but also how somatically derived structures generated during V-D-J re
90 (SE), primitive zygotic (EC), embryonal-like somatically differentiated (TE), and extra-embryonally d
91 of jawed vertebrates, that clonally express somatically diversified antigen receptors termed variabl
92 invertebrate defense molecules because it is somatically diversified by gene conversion and point mut
93 ly of V structures resembling those that are somatically diversified in adaptive immunological respon
94 ess adaptive immune systems based on a vast, somatically diversified repertoire of lymphocyte-bound a
99 adaptive immune system in which lymphocytes somatically diversify their variable lymphocyte receptor
100 bit establishes its primary Ab repertoire by somatically diversifying an initial repertoire that is l
101 ased adaptive immune system that is based on somatically diversifying leucine-rich repeat (LRR)-based
103 Asexual animals maintain telomere length somatically during reproduction by fission or when regen
106 oviruses with different insertion sites that somatically emerged during malignant transformation or p
110 o eliminated striatal mutant huntingtin with somatically expanded glutamine tracts and caused an appr
112 We isolated the D. virilis orthologs of the somatically expressed gene, alpha4_dm, and the testes-sp
113 eport, we demonstrate that the function of a somatically expressed gene, cut, is critical for maintai
114 their ability to transduce the activity of a somatically expressed TGF-beta ligand, the BMP5/8 orthol
116 the ability of granule cell axons to convey somatically generated action potentials to distant synap
120 e prenegative selection TCR repertoire, many somatically generated complementary-determining region (
123 s are not germline encoded; rather, they are somatically generated in each developing lymphocyte by a
124 ved RFs, we previously demonstrated that the somatically generated light chain complementarity-determ
125 neural cells throughout the neuraxis showing somatically generated mosaic aneuploidy indicates that t
126 residues as well as the enhanced presence of somatically generated proline residues that preclude hyd
127 In principle, either germline-encoded or somatically generated sequences could function as target
128 of the CDR3 loop in the axolotl consisted of somatically generated sequences, compared with 44% in ta
129 y points to the critical contribution of the somatically generated VJ junction to RF autoantibody spe
130 eural cell survival, providing evidence that somatically generated, cell-autonomous genomic alteratio
133 lity of their nontransformed counterparts to somatically hypermutate Ig V genes by nucleotide substit
134 that both Pms2- and Mlh1-deficient mice can somatically hypermutate the Ig test gene at approximatel
135 -cell receptor repertoire is oligoclonal and somatically hypermutated and shares similar clonal group
136 ity, neutralizing antibodies by selection of somatically hypermutated B cell antigen receptors (BCR)
137 lts from the selection of B cells expressing somatically hypermutated B cell receptors (BCRs) with in
138 ines was introduced based on the analysis of somatically hypermutated donor-derived repertoires.
139 pecific MBCs consisted of three populations: somatically hypermutated immunoglobulin M(+) (IgM(+)) an
141 nge experiments revealed that high affinity, somatically hypermutated Plasmodium-specific IgM(+) MBCs
144 ction is essential for the generation of the somatically hypermutated, high-affinity antibodies that
146 me FGFR3 mutations have also been identified somatically in human cancers, including multiple myeloma
147 me FGFR3 mutations have also been identified somatically in human cancers, including multiple myeloma
157 first showed that KLF6 is a tumor suppressor somatically inactivated in prostate cancer and since the
159 rthermore, using tetracycline regulation, we somatically induced human GAA in the knockout mice, and
162 rent conditions that might occur in vivo, we somatically injected aperiodic current waveforms into co
163 Furthermore, mutant genes are introduced somatically into animals, as occurs in the majority of n
166 LEOPARD syndrome frequently carry a second, somatically introduced subset of missense mutations in S
168 f the two genomic loci encoding miR-101 were somatically lost in 37.5% of clinically localized prosta
169 at autosomal testis-biased miRNAs tend to be somatically male-biased, whereas autosomal ovary-biased
171 ng regions (CDRs) 1 and 3, both germline and somatically matured V regions displayed significant stru
172 structurally characterized the germline and somatically matured versions of a type II variable (V) r
173 eurofibromatosis type 1 (NF1) patient who is somatically mosaic for a large maternally derived deleti
174 d sources of microDNA in the adult brain are somatically mosaic for microdeletions that appear to ari
176 etogenesis result in a greater proportion of somatically mosaic transmitting mothers who are thus at
177 at B cells of the putative fetal lineage can somatically mutate and diversify an initially limited re
178 c PAHA created a B cell population primed to somatically mutate and Ig class switch when subjected to
179 tem that lethally mutate viral pathogens and somatically mutate immunoglobulins, and contribute to th
181 u) sequences were identified and found to be somatically mutated (range, 1.4% to 6.5%), with a low le
183 from CD138(+) cells in MS CeSF has revealed somatically mutated and expanded IgG clonotypes consiste
185 and IgG3 antibodies in the mice were highly somatically mutated and used distinct repertoires of VH
186 tent with the x-ray crystal structure of the somatically mutated anti-Ars Ab 36-71, while Sulf bindin
187 knock-in mouse that expresses V regions of a somatically mutated anti-Id mAb with intermediate affini
190 , we identified 68 genes that appeared to be somatically mutated at elevated frequency, many of which
192 on competitive selection of B cells carrying somatically mutated B-cell receptors by follicular helpe
193 We have recently demonstrated that a novel somatically mutated B220(-) memory B cell subset rapidly
195 ing (bn) Abs and that identification of less somatically mutated bn Abs may help in the design of eff
197 p between the genes involved in OGID and 260 somatically mutated cancer driver genes (p = 1.75 x 10(-
200 in heavy and light chains in 6 patients with somatically mutated CLL-cell immunoglobulin genes and id
203 ns in this autoimmune disease are encoded by somatically mutated genes in the patients' incipient can
207 ration of B cells and plasma cells producing somatically mutated gut antigen-specific IgA antibodies
208 ia (PNH) lack GPI proteins on the surface of somatically mutated hematopoietic stem cell and its prog
209 entarity-determining region 2 (HCDR2) of the somatically mutated high-affinity anti-p-azophenylarsona
213 ells, considered to be memory cells based on somatically mutated Ig genes, we found that the reductio
214 that have frequently acquired rearranged and somatically mutated Ig genes.1,2 Despite their B-cell or
215 tion to the marginal zone, the expression of somatically mutated Ig V region genes, and the preferent
216 cells have been shown in some cases to have somatically mutated Ig variable region genes, indicating
217 ice and demonstrate that after re-infection, somatically mutated IgM(+) memory B cells function as fi
218 (PB) IgM(+)IgD(+)CD27(+) B lymphocytes with somatically mutated IgV genes are controversially discus
220 ization to mucosal epithelium, expression of somatically mutated immunoglobulin (Ig) variable (V) reg
221 indicated that a fraction of B-CLL displays somatically mutated immunoglobulin variable heavy chain
222 istinguished as carrying either unmutated or somatically mutated immunoglobulins (Igs), which are ass
225 ies that broadly neutralize HIV-1 are highly somatically mutated in antibody clonal lineages that per
227 arbor germline mutations; the same genes are somatically mutated in CMM, or their encoded proteins ar
229 are germ-line variants at FLT3 (a gene often somatically mutated in leukemia) associated with monocyt
230 APC(AS9) and the wild-type APC alleles were somatically mutated in most colorectal tumors from these
232 osophila gene capicua) on chromosome 19q was somatically mutated in six cases and that the FUBP1 gene
235 ived beta-gal+ B cells exclusively contained somatically mutated lambda1 V regions and were capable o
239 pha exposure creates an environment in which somatically mutated preleukemic stem cell clones are sel
240 cans were recognized by germline-encoded and somatically mutated residues on the Ab heavy chain.
246 nd VH1 (1 of 5) families and were all highly somatically mutated with strong evidence for antigen sel
250 ined in overrepresented populations and were somatically mutated, consistent with an antigen-targeted
251 The cloned anti-talin-H IgGs were highly somatically mutated, indicative of an antigen-driven, af
252 Multiple myeloma (MM), a malignant tumor of somatically mutated, isotype-switched plasma cells (PC),
255 ce analysis revealed that the Abs are highly somatically mutated, with high replacement to silent rat
261 ll as 1,586 non-germline DNMs arising either somatically or in the cell lines from which the DNA was
262 nation ensures genomic integrity while cells somatically rearrange their antigen receptor genes [in a
265 , is a more recent development that utilizes somatically recombined antigen receptor genes to recogni
267 t T22 recognition correlates strongly with a somatically recombined TCRdelta complementarity-determin
269 (TCRmu) that has V, D, and J that are either somatically recombined, as in conventional TCRs, or are
270 though we observed minimal alteration of the somatically recorded action potential waveform, action p
273 g spontaneous slow oscillatory activity that somatically recorded delta (1-4 Hz) and slow (<1 Hz) osc
274 KChIP proteins supports the hypothesis that somatically recorded native Kv4 channels in neurons incl
276 variable electrotonic distances that distort somatically recorded synaptic currents, it is not known
283 We use the rodent malaria P. yoelii, and somatically transinfected An. stephensi as a model syste
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