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1 that this segment of chromosomal DNA was not transcribed.
2 show that the active ES-adjacent telomere is transcribed.
3 ated with the chromosome from which they are transcribed.
4 nging of these nutrients were being actively transcribed.
5 orded, with the participants' permission,and transcribed.
6 ch cell type only a subset of genes is being transcribed.
7 sequences which, in some cases, are actively transcribed.
8 D59 and show that this segment of DNA is not transcribed.
9          The noncoding genome is pervasively transcribed.
10 istal regulatory elements, we adapt the self-transcribing active regulatory region sequencing (STARR-
11                             By adapting self-transcribing active regulatory region sequencing, we eva
12 ncluding retrotransposons, some of which are transcribed after fertilization.
13    In eukaryotes, RNA polymerase II (pol II) transcribes all protein-coding genes and many noncoding
14 e yeast RNA polymerase II (Pol II) molecules transcribing along a DNA template with two nucleosomes.
15 in HMPV RNA and proteins to more efficiently transcribe and replicate the viral genome.
16  in the ambient temperature range and FLM is transcribed and alternatively spliced in a temperature-d
17 edly, in wild-type (WT) TSCs these genes are transcribed and are enriched for active chromatin hallma
18                                       Highly transcribed and highly inducible genes display strong tr
19 everal of the TP53 retrogenes (TP53RTGs) are transcribed and likely translated.
20           Eukaryotic genomes are pervasively transcribed and only a small portion of the transcribed
21                        These are also highly transcribed and peak according to the diel lifestyle of
22  to study how native genes resided there are transcribed and regulated.
23 omprises eight RNA segments (vRNA) which are transcribed and replicated by the heterotrimeric IAV RNA
24     The RNA genome of influenza A viruses is transcribed and replicated by the viral RNA-dependent RN
25 uggested that the replicating pool of DNA is transcribed and that few if any additional viral protein
26 encoding the core complex of the T9SS are co-transcribed and that the gene products are distributed i
27 essary resistance marker NeoR to be a highly transcribed and translated gene.
28 osome of Escherichia coli can form a defined transcribing and translating "expressome" complex.
29 aracterizing the bacterial extracts used for transcribing and translating gene sequences into protein
30 ter the coaching session was audio recorded, transcribed, and analyzed by using linear regression mod
31                 Conversations were recorded, transcribed, and analyzed.
32 urgical coaching program were audiorecorded, transcribed, and coded on the basis of 3 relationship-bu
33 rt sites of HSV-1-induced and constitutively transcribed antisense transcripts are highly similar, in
34 RACE mapping revealed that lpiA/acvB were co-transcribed as an operon from an RpoN promoter.
35 oximately 98% of the human genomic output is transcribed as non-protein coding RNA, <2% of the protei
36 tional program; all protein-coding genes are transcribed as part of a polygenic precursor mRNA (pre-m
37 ted endings of these sensory neurons, and is transcribed at different levels in distinct olfactory ne
38            We showed that the DP148R gene is transcribed at early times postinfection.
39 a found abundant enhancer RNAs (eRNAs) being transcribed at ESEs.
40 tly enriched with H3K9me3 or H3K27me3 and is transcribed at higher levels than the rest of NL genes.
41                All var genes are silenced or transcribed at low levels in blood stages (gametocyte/ri
42 nes, compared with their receptor genes, are transcribed at much greater absolute levels, which sugge
43 NA for the major heat shock protein Hsp70 is transcribed at robust levels in both H2Av and JIL-1 null
44                       Whereas rRNA genes are transcribed at similar rates throughout the day, some ne
45                During development, genes are transcribed at specific times, locations and levels.
46 ed, whereas MHC-C alleles, when present, are transcribed at very low levels.
47 Prognostic discussion was assessed by coding transcribed audio-recorded visits using the Prognostic a
48 d multiple such loci that are differentially transcribed between healthy and diseased tissues in colo
49 ion revealed that two of seven G84E carriers transcribed both the variant and wild-type allele, while
50                                         Loci transcribing both lineage-specific annotated and novel l
51 stochastically expressed protocadherins were transcribed by increased numbers of cortical neurons, in
52  and localization of a set of mRNAs that are transcribed by NDT80 but not translated until the end of
53                   Human mitochondrial DNA is transcribed by POLRMT with the help of two initiation fa
54 6 is commonly associated with genes actively transcribed by RNA polymerase II (RNAPII) and is catalyz
55  exists a subset of PRC-bound genes actively transcribed by RNA polymerase II (RNAPII).
56 e of downstream regulatory element for genes transcribed by RNA polymerase II.
57 y contributes to the expression of all genes transcribed by RNA polymerase II.
58                                    BocaSR is transcribed by RNA polymerase III (Pol III) from an intr
59           SINE is a class of retrotransposon transcribed by RNA polymerase III (Pol III).
60 Transfer RNA (tRNA) genes (tDNAs), which are transcribed by RNA polymerase III (RNAPIII) and encode R
61 on of the viral positive-sense genome and is transcribed by RNA polymerase III into a noncoding RNA o
62  abundant class of retrotransposons that are transcribed by RNA polymerase III, thus generating exclu
63                  Influenza A virus mRNAs are transcribed by the viral RNA-dependent RNA polymerase in
64  that are typically associated with actively transcribed chromatin are detrimental to ATXR5 activity.
65                We conclude that proximity of transcribed chromatin to the nuclear pore helps restrain
66 moters and enhancers, and CTCF-occupied, non-transcribed chromatin.
67 ns, and with spatial distributions of highly-transcribed chromosomal regions matching recent experime
68 aches to demonstrate that two differentially transcribed, co-diverging genes in the eukaryotic associ
69 or every base pair of the genome that may be transcribed: coding, noncoding, and intergenic regions,
70 tart from TFIIS-induced cleavage in a pol II transcribing complex.
71 st that basic building blocks of divergently transcribed core promoter pairs, in combination with the
72 PML NBs are closely associated with actively transcribed DDIT4 loci, implicating these bodies in regu
73               Three distinct RNA polymerases transcribe different classes of genes in the eukaryotic
74 s), which are enveloped viruses with reverse-transcribed DNA genomes, constitute the family Hepadnavi
75    Escherichia coli replisome movement along transcribed DNA is promoted by Rep and UvrD accessory he
76 n-induced (cytosine) deaminase access to the transcribed DNA strand.
77 transcription and facilitating the repair of transcribed DNA.
78 nd breaks and must function even on actively transcribed DNA.
79  sense and antisense strand DNA mutations on transcribed duplex DNA contributes to the development of
80                                 This gene is transcribed during infection and when expressed in yeast
81 nd Hoxd9, two genes of the HoxD complex, are transcribed during mammary bud (MB) development.
82 or the specific set of transcription factors transcribed during tertiary cell wall formation were rev
83 jected into the host along with phage DNA to transcribe early phage genes, and a non-virion RNAP (nvR
84  We have shown that one of these, DP148R, is transcribed early during virus replication in cells and
85 ce in situ hybridization identified actively transcribing, EdU-labeled HIV-1 genomes in productively
86 pression pattern, where the offspring stably transcribed either the maternal or paternal allele.
87 e fidelity of nascent RNAs from all actively transcribing elongation complexes (ECs) in Escherichia c
88 east cancer subtype-specific TFs that act at transcribed enhancers to dictate gene expression pattern
89                                           Do transcribed enzymes operate to obtain N from SOM?
90 his demonstrates the essentiality of a Pol I-transcribed ES, as well as conserved VSG 3'UTR 16-mer se
91                                        Newly transcribed eukaryotic precursor messenger RNAs (pre-mRN
92  circRNAs (f-circRNA) that are produced from transcribed exons of distinct genes affected by the tran
93 e found that not all episomes were uniformly transcribed following reactivation stimuli.
94 lope genes, its encoding gene is found to be transcribed from a unique CpG-rich promoter not related
95                                  Linc-RAM is transcribed from an intergenic region of myogenic cells
96 vity of HBV enhancer and the amount of pgRNA transcribed from cccDNA) were significantly higher in ce
97 Tubular and toroid shapes, among others, are transcribed from DNA cages to liposomes with high fideli
98       Lineage-specific novel lncRNA loci are transcribed from lineage-specific typical- and supertran
99      Our findings suggested that LTR lncRNAs transcribed from many of the 4000 copies of ERV-9 LTR re
100 ng intergenic non-coding RNAs (lincRNAs) are transcribed from non-coding DNA sequences.
101 ght better explain how low-abundance lncRNAs transcribed from noncoding DNA function in organisms.
102 gate the intracellular localization of sRNAs transcribed from plasmids in Escherichia coli using RNA
103 sites of initiation and found that many were transcribed from promoters containing a new consensus se
104                      Ribosomal RNA (rRNA) is transcribed from rDNA by RNA polymerase I (Pol I) to pro
105 RNA (TERRA), the long noncoding RNA (lncRNA) transcribed from telomeres, have eluded researchers.
106            Novel enhancer-associated lncRNAs transcribed from the IFNG locus bind the transcription f
107 ns-acting sRNAs, are the most abundant sRNAs transcribed from the intergenic regions (IGRs) of the ba
108 that in primary human erythroblasts, lncRNAs transcribed from the LTR retrotransposons of ERV-9 human
109 NA produced by alternative processing of RNA transcribed from the same gene that promotes recovery fr
110                          Long noncoding RNAs transcribed from ultraconserved regions (T-UCRs) control
111 n cells can help to silence the DNA they are transcribed from.
112       Each PPI-mediated RNAPN-RNAPC assembly transcribes from a separate promoter on a supplied DNA s
113 xyR2 is required to activate its divergently transcribed gene ahpC, encoding an alkylhydroperoxide re
114             In endothelial cells, ETS1 binds transcribed gene promoters and stimulates their expressi
115 direct association with an RNA polymerase II-transcribed gene.
116                                     Actively transcribed genes adopt a unique chromatin environment w
117                               Constitutively transcribed genes also loop and crumple yet fail to coal
118 lex contribute to Chd1 recruitment to highly transcribed genes and identified Spt4 as a factor that a
119 uently found at promoter regions of actively transcribed genes and is therefore generally considered
120 cterial chromosomes, explaining why actively transcribed genes are always co-oriented with replicatio
121 high-throughput study of the complete set of transcribed genes at increasingly fine resolution to the
122 ts in cell-free human DNA data as a relic of transcribed genes from apoptosing cells.
123 on signal in the downstream region of highly transcribed genes in a temperature-sensitive mutant of C
124                                     The most transcribed genes in all seasons were associated with ph
125  Importantly, DNA-RNA hybrids accumulated at transcribed genes in mlp1/2 mutants, indicating that Mlp
126 PRC2 acts as a brake to prevent induction of transcribed genes on the inactive X chromosome, a mode o
127 27ac and H3K9ac on the promoters of actively transcribed genes that are essential for leukaemia.
128  frequent templated inserts originating from transcribed genes that, in rare cases, comprised exons w
129                                              Transcribed genes were approximately two-fold more likel
130 litate assembly of the elongation complex on transcribed genes when RNA emerges from Pol II, and that
131 ell RNAseq and ChIPseq to find that actively transcribed genes with Polycomb marks have greater cell-
132 tistical distribution of all isoforms of all transcribed genes, and reveals that previously unexplain
133 y associated with RNA polymerase II (Pol II)-transcribed genes, but is not an unambiguous mark for ac
134                           Even for the least transcribed genes, Mfd played a role in preferential rep
135 plication fork stalling in RNAPI- and RNAPII-transcribed genes, suggesting that RECQ5 exerts its geno
136  networks, each containing just a few Pol II transcribed genes, that generate specific signal-process
137 including G4 DNA are located within actively transcribed genes, the reshaping of DNA topology necessa
138 bromodomain proteins at the loci of actively transcribed genes, whereas PRC2 is excluded from these r
139  shapes intragenic CpG-methylation of highly-transcribed genes.
140 oncert with 5hmC elevation in differentially transcribed genes.
141 ation (H3K27ac) on the promoters of actively transcribed genes.
142 th strong preference for promoters of highly transcribed genes.
143 ely to be differentially methylated than non-transcribed genes.
144 ons and similarly extended H3K4me3 on highly transcribed genes.
145 or of about 2 on average for the most highly transcribed genes.
146 restricted to intragenic regions of actively transcribing genes by EHMT2.
147 r THSC) facilitates localization of actively transcribing genes such as GAL1 to the nuclear periphery
148 d3S histone deacetylase complex recruited to transcribing genes, operate in a combinatorial manner in
149  these sites to splice cellular pre-mRNAs at transcribing genes, we reveal a functional subversion of
150                 A substantial portion of the transcribed genome (18%) was differentially expressed co
151                                          Our transcribed genome array (TGA) assayed both rare and abu
152 ach provides new insights into the nature of transcribing HIV-1 genomes and allows us to track the en
153 , RNA polymerase III is highly conserved and transcribes housekeeping genes such as ribosomal 5S rRNA
154 -pass filtering circuit; repeated Erk pulses transcribe IEGs more efficiently than sustained Erk inpu
155      A substantial fraction of the genome is transcribed in a cell-type-specific manner, producing lo
156               The expression levels of genes transcribed in antennae were compared between 5(th) inst
157 ression of the isoform BAX-beta, exclusively transcribed in apoptotic cells, was negatively correlate
158 ification pipeline and reveal that enhancers transcribed in breast cancer cells direct critical gene
159 iguingly, the G84E variant allele was rarely transcribed in carriers, suggesting that HOXB13 expressi
160  same RNA binding proteins (RBPs) or (2) are transcribed in corresponding tissues.
161                                              Transcribed in gametocytes, LIMP is translated in the oo
162 tions as a long-distance mRNA signal that is transcribed in leaves and moves into roots and stolons t
163  immune cell subsets, we found that BCMA was transcribed in plasmacytoid dendritic cells (pDCs) in bo
164  identified a retrotransposon that is highly transcribed in roots and whose spliced transcript consti
165 ication requires that some of the viral RNAs transcribed in the cell nucleus be exported to the cytop
166 sent regions of the genome that are actively transcribed in the human heart.
167 dization (smRNA FISH), we show that egl-1 is transcribed in the mother of a cell programmed to die an
168                   Divergent lncRNAs that are transcribed in the opposite direction to nearby protein-
169  infection, despite the gene being primarily transcribed in the vector with a transient expression in
170  promoter regions are frequently divergently transcribed in vivo, but it is unknown whether the resul
171 arch has revealed that most of the genome is transcribed into a broad array of noncoding RNAs, rangin
172 e same strand of a bacterial genome that are transcribed into a single mRNA molecule under certain co
173 meres that all alpha-satellite sequences are transcribed into chromatin-bound RNAs and are required f
174 re and lysed, and the mRNA was extracted and transcribed into DNA.
175 losed inside a capsid shell, must be reverse transcribed into double-stranded DNA and released from t
176 ll entry, the RNA genome of HIV-1 is reverse transcribed into double-stranded DNA that ultimately int
177 tron retention (IR) occurs when an intron is transcribed into pre-mRNA and remains in the final mRNA.
178                                         Once transcribed into pre-mRNA, these introns must be removed
179 es, we show that defective proviruses can be transcribed into RNAs that are spliced and translated.
180       These sequences, known as spacers, are transcribed into short CRISPR RNA guides that specify th
181                                  DNA data is transcribed into single-stranded RNA, which folds into s
182 ter known to execute nuclear export of newly transcribed intron-containing pre-tRNAs.
183          Audio recordings of interviews were transcribed, iteratively analyzed, and emergent themes i
184 f the SPbeta bacteriophage that specifically transcribes its late genes, and thus represents a novel
185 hich is synthesized during the infection and transcribes late phage genes.
186 eading to increased mutation rates at highly transcribed loci.
187  recombination in the context of an actively transcribed locus in Saccharomyces cerevisiae, we tested
188 cial tethering to the nuclear periphery of a transcribed locus suppressed R loops in mlp1 cells.
189 alian genomes contain thousands of loci that transcribe long noncoding RNAs (lncRNAs), some of which
190                 RNA polymerase III (Pol III) transcribes medium-sized non-coding RNAs (collectively t
191  determine if stress affects mitochondrially transcribed mRNA (mtRNA) expression, we exposed adult ma
192 stability and low immunogenicity to in vitro transcribed mRNAs, thereby facilitating expression of th
193 ermination complex in which TEFM is bound to transcribing mtRNAP.
194 resence of "defective" proviruses capable of transcribing novel unspliced HIV-RNA (usHIV-RNA) species
195  and edits the 3UTR of nuclear-retained Cat2 transcribed nuclear RNA (Ctn RNA).
196 , especially between regions that are highly transcribed or contain super-enhancers, providing a leve
197                                        Cells transcribing P2rx7 in hippocampal slices from epileptic
198            VAR2CSA protein levels in var2csa-transcribing parasites are dependent on the expression l
199 ming catalyst region can be removed from the transcribed peptide by peptidases, artificial and biomac
200 east tumorigenesis, the fraction of actively transcribed Pol III genes increases reaching a plateau d
201 that many EFs crosslink to RNA emerging from transcribing Pol II in the yeast Saccharomyces cerevisia
202 nascent RNA contributes to EF recruitment to transcribing Pol II.
203        Furthermore, the density of antisense transcribing polymerase upstream of the promoter region
204 es transcription by increasing the number of transcribing polymerases and thus the amount of mRNA syn
205 ana The intron increased expression from all transcribed positions but had no effect when upstream of
206 allenge, genes governed by these domains are transcribed rapidly.
207 evels of VSG117 were obtained from the Pol I-transcribed rDNA.
208 b recruitment and histone acetylation on the transcribed region of the Adipoq gene.
209 iting P-TEFb onto acetylated histones in the transcribed region of the gene and regulates adipocyte d
210 genetic memory histone H3 acetylation on the transcribed region of the gene.
211  exchanged discriminators, all with the same transcribed region.
212 otein bromodomain containing 4 (BRD4) on the transcribed region.
213  polymerase II results in H3K4me2 throughout transcribed regions and similarly extended H3K4me3 on hi
214 MT3A occupancy and mCA deposition within the transcribed regions of genes is negatively regulated by
215 inely considered for all variants within the transcribed regions of genes.
216 ltransferase DNMT3A transiently binds across transcribed regions of lowly expressed genes, and its bi
217 ed 635 novel protein-coding genes, 508 novel transcribed regions, 5178 non-coding RNAs, and 35 846 sm
218  if present at replication forks or actively transcribed regions, may interfere with DNA replication
219   Since disease-causing CAG repeats occur in transcribed regions, our results suggest that R-loop-med
220 P5CS1, containing 1.2-kB promoter and 0.8-kb transcribed regions.
221 a, and that Poleta is enriched over actively transcribed regions.
222 t enhancers in untranscribed regions than in transcribed regions.
223 romatin, to induce nucleosome disassembly at transcribing regions during RNAPII transcription.
224  that the three PANS are present in actively transcribing regions in a substantial amount.
225 s a chromatin remodeller, which localizes at transcribing regions to promote RNAPII transcription.
226 of mRNA-encoding genes, including the highly transcribed ribosomal protein- and glycolytic enzyme-enc
227  is used to transfect cells, and barcodes in transcribed RNA are quantified by high-throughput sequen
228          We now show that SFM4-3 efficiently transcribes RNA or 2'-F-modified RNA and that it also ef
229 down resulted in reduced binding of actively transcribing RNA polymerase II to the endogenous Asc gen
230 en co-transcriptional RNA processing and the transcribing RNAPII.
231 RTANCE In higher eukaryotes, the majority of transcribed RNAs do not encode proteins.
232                                 That is, the transcribed RNAs participate the biological process as r
233 f T7 RNAP, to assess the quality of in vitro transcribed RNAs.
234 identify the specific loci that are actively transcribed separate from the excess of L1-related seque
235  basis of the gene encoding nuclear internal transcribed sequence (ITS) and mitochondrial cox1 Restri
236  transcribed and only a small portion of the transcribed sequences belongs to protein coding genes.
237              These mutations were located in transcribed sequences encoding enhancer RNAs (eRNAs) and
238 ings indicate that the majority of genes are transcribed simultaneously during the trophozoite stage
239 xaptation into gene regulatory elements, how transcribed SINE RNA impacts transcriptional and post-tr
240 entified an additional HBoV1 gene, bocavirus-transcribed small noncoding RNA (BocaSR), within the 3'
241                               This bocavirus-transcribed small RNA (BocaSR) diverges from both adenov
242 ce that any of the nonnative rDNA units were transcribed; some showed indications of having been sile
243                                 The internal transcribed spacer (ITS) as one part of nuclear ribosoma
244 n based on pyrosequencing of fungal internal transcribed spacer (ITS) barcode markers.
245  bacterial 16S rRNA gene and fungal internal transcribed spacer (ITS) copy numbers and extracellular
246  DNA barcoding of nuclear ribosomal internal transcribed spacer (ITS) of the rRNA gene with fungal sp
247                               Using internal transcribed spacer (ITS) region as the phylogenetic mark
248                                 The internal transcribed spacer (ITS) region of the ribosomal DNA is
249   The genetic markers used were the internal transcribed spacer (ITS) region, and fragments of the be
250 heir origin was traceable via their internal transcribed spacer (ITS) sequence to five distinct Panic
251 ping was performed using 3'hsp65and internal transcribed spacer (ITS) sequencing.
252 arkers used for sequencing were the internal transcribed spacer (ITS), a portion of the nuclear large
253 PCR amplification and sequencing of internal transcribed spacer 1 (ITS1), was employed.
254                             We used internal transcribed spacer 1-based metabarcoding to compare feca
255 nventional PCR amplification of the internal transcribed spacer 2 (ITS2) region (ITS2-PCR) followed b
256  exit, and the domain including the internal transcribed spacer 2 (ITS2) that separates 5.8S and 25S
257              PCR amplicons from the internal transcribed spacer 2 and the D2 region of 28S ribosomal
258 g amplicon sequencing of the fungal internal transcribed spacer 2, we studied the root and rhizospher
259  biogenesis complexes assist the 5' external transcribed spacer and U3 small nucleolar RNA in providi
260       After bronchoscopy, ribosomal internal transcribed spacer region 1 DNA was amplified and sequen
261 PCR amplification and sequencing of internal transcribed spacer region 1.
262 h mitochondrial (cox1) and nuclear (internal transcribed spacer) DNA data from the Schistosoma eggs o
263 to the rDNA promoter and to the 5'- external transcribed spacer.
264  NTS and transcription-coupled repair of the transcribed strand (TS).
265 ermutation was increased specifically on the transcribed strand from mu-gamma joins, indicating that
266 events arise when the enzyme cleaves the non-transcribed strand of DNA.
267  played a role in preferential repair of the transcribed strand.
268 ulated by transcription, specifically in the transcribed strand.
269                  Genome-wide analysis of the transcribed strand/nontranscribed strand (TS/NTS) repair
270 3 chromatin binding and expression of highly transcribed target genes like MYC, PIM1, MCL1, CD30, IL2
271            The active VSG gene is in a Pol I-transcribed telomeric expression site (ES).
272 ckdown of the H3K27 demethylase ubiquitously transcribed tetratricopeptide repeat X chromosome suppre
273 s is a strategy to efficiently replicate and transcribe the viral genome.
274  aggressive in the two variant carriers that transcribed the variant allele compared to the five that
275 nt and wild-type allele, while five carriers transcribed the wild-type allele.
276 I is decorated with elongation factors as it transcribes the genome.
277  that the genetic loci are already poised to transcribe these novel RNAs.
278                                         Once transcribed, these elements form 5'-RNA aptamers that bi
279   While this implies that the intron must be transcribed to increase expression, the TSS changed when
280  with a large fraction of RNA polymerase III-transcribed tRNA genes, independent of hormone treatment
281                                 We find that transcribed uc.339 is upregulated in archival NSCLC samp
282                                          The transcribed ultraconserved regions (T-UCRs) encode long
283                              Our findings of transcribed uncharacterized regulatory regions that cont
284 roject (NIH HMP) stool samples, and they are transcribed under conditions of host colonization.
285 line bearing a complete deletion of the PEAT-transcribed unit.
286  mammalian adaptive immunity through reverse-transcribed vDNA circles and the systemic dissemination
287 ructured interviews were digitally recorded, transcribed verbatim and analysed using a qualitative da
288                          All interviews were transcribed verbatim and analyzed thematically using int
289              Interviews were audio-recorded, transcribed verbatim, and coded by two reviewers.
290                 Interviews were audio taped, transcribed verbatim, and translated into English.
291                 Interviews were recorded and transcribed verbatim.
292 was trapped in these factories and served to transcribe viral genomes, which coincided with an overal
293 f its life cycle upon integration of reverse-transcribed viral DNA into host chromatin.
294 etroviruses via deamination of newly reverse-transcribed viral DNA.
295             To release the contained reverse-transcribing viral genome, the capsid must disassemble i
296  the gene dunk, which we show is transiently transcribed when cellularization starts and functions to
297 es demonstrate that MHC-A alleles are highly transcribed, whereas MHC-C alleles, when present, are tr
298 t in a transcriptionally repressed state was transcribed with 12 pure proteins (80 polypeptides): RNA
299                             The lprI gene co-transcribes with the glbN gene (encoding hemoglobin (HbN
300 e excess of L1-related sequences that are co-transcribed within genes.
301      However, those episomes that were being transcribed would spontaneously aggregate to form transc

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