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1 tion of aromatic amino acid side chains into genomic DNA.
2 removal of incorporated ddC from replicating genomic DNA.
3 e condensin, cohesin and SMC5/6) to organize genomic DNA.
4 r aldehyde functionalities known to exist in genomic DNA.
5  all other biological processes occurring on genomic DNA.
6  an accumulation of cytoplasmic fragments of genomic DNA.
7 ancient organisms that lack large amounts of genomic DNA.
8  reposition and reorganize nucleosomes along genomic DNA.
9 p dsDNA analytes, including both plasmid and genomic DNA.
10 judged from binding competition against bulk genomic DNA.
11 to identify the sequence of cut sites within genomic DNA.
12 ure of target DNA from a pool of interfering genomic DNA.
13  stranded breaks (DSBs) in murine macrophage genomic DNA.
14 moval of UV-induced direct photolesions from genomic DNA.
15 ctivity by controlling its ability to access genomic DNA.
16 nely evaluated with a PCR-based method using genomic DNA.
17 etion and reduced the L1-mediated nicking of genomic DNA.
18 pecific amplification by directly sequencing genomic DNA.
19 es and sequences the 4.8-Mbp MHC region from genomic DNA.
20 med Cas9 locates the target site by scanning genomic DNA.
21 ive cell birth dating measuring carbon-14 in genomic DNA.
22 that mediate the conversion of A*T to G*C in genomic DNA.
23 reventing the hyper-negative supercoiling of genomic DNA.
24 of protein-DNA interactions on synthetic and genomic DNA.
25 en the expanded repeat RNA and complementary genomic DNA.
26 the incorporation of high levels of rNMPs in genomic DNA.
27 s) enable targeted C*G-to-T*A conversions in genomic DNA.
28 TP-powered molecular motors to package their genomic DNA.
29 ir (RER) efficiently removes single rNMPs in genomic DNA.
30 mbers of spacers originating from the entire genomic DNA.
31 ere sequences at chromosomal ends to protect genomic DNA.
32 ine the structures of nucleosomes containing genomic DNA.
33 structures known as i-motif are prevalent in genomic DNA.
34 ntification of RNA, short linearized DNA, or genomic DNA.
35 elf-sufficient HACs that showed no uptake of genomic DNA.
36 ed DNAs, including circular plasmid DNAs and genomic DNAs.
37 l factories localized with replicating viral genomic DNAs.
38  of Cory's Shearwater (Calonectris borealis) genomic DNA, a model species for the study of olfaction-
39 stinguishable behaviors from random-sequence genomic DNA, AA-TT condenses in all alkaline earth metal
40 ty was achieved, with as low as 71-188 pg of genomic DNA able to be detected using mixtures of contro
41 ents (TRFs), along with MinION sequencing of genomic DNA allowed us to document the precise molecular
42          Furthermore, the injection of mouse genomic DNA alone is sufficient to recapitulate many fea
43                                  Whole heart genomic DNA analysis revealed iterative oxidative cytosi
44     The limits of detection were 0.5ng/ml of genomic DNA and 10 colony-forming units (CFU)/ml of bact
45 was 97.3% at 240 attograms (ag) of T. solium genomic DNA and 100% analytic specificity.
46 es into the PCR products of Escherichia coli genomic DNA and accurately reconstruct the encoded data
47 xes in eukaryotes that provide compaction of genomic DNA and are implicated in regulation of transcri
48 1LG2 cis-regulatory regions were cloned from genomic DNA and assessed in full or by mutating and/or d
49 The nCATS sequencing requires only ~3 mug of genomic DNA and can target a large number of loci in a s
50  ability due to off-target interactions with genomic DNA and cellular metabolites.
51 d to induce unguided cytosine deamination in genomic DNA and cellular RNA.
52 ct the rpoB gene in PCR-amplified samples of genomic DNA and could also discriminate between the wild
53 ified 1,741 unique AAV integration events in genomic DNA and expanded cell clones in five dogs, with
54  that noncanonical structures are present in genomic DNA and have biological functions.
55 lyses of tough decoy abundance in hepatocyte genomic DNA and input plasmid pools identified several t
56 e analyzed for the presence of S epidermidis genomic DNA and mRNA.
57 nsuming and often requires a large amount of genomic DNA and radioactively labeled probes.
58  important cytosolic sensor of P. falciparum genomic DNA and reveal the role of the cGAS/STING pathwa
59  SCCIS and the adjacent epidermis to isolate genomic DNA and RNA for next-generation sequencing.
60 ISH allows for simultaneous visualization of genomic DNA and RNA transcripts in living cells.
61 systems allows simultaneous visualization of genomic DNA and RNA transcripts in living cells.
62 pplications to identify this modification in genomic DNA and RNA.
63 l to insert the 7-deazaguanine base in phage genomic DNA and that 2'-deoxy-7-deazaguanine modificatio
64 cluding the removal of UV photoproducts from genomic DNA and the activation of ATR/ATM DNA damage kin
65 % and cassette function can be traced at the genomic DNA and the mRNA level.
66  to "write" programmed sequence changes into genomic DNA and thus promises significant technical adva
67 ndependent off-target adenine deamination in genomic DNA and very low levels of adenine deamination i
68 mation about how gyrase is distributed along genomic DNA and whether its distribution is affected by
69 of protein production, (ii) the digestion of genomic DNA, and (iii) the disruption of the cell membra
70  PCR analysis revealed presence of bacterial genomic DNA, and infection elicited significant immunogl
71 -reporter mice, polymerase chain reaction of genomic DNA, and quantitation of Bmp6 messenger RNA expr
72  pipelines designed to map rNMPs embedded in genomic DNA are customized for data generated using only
73                            Here we used EHEC genomic DNA as a template to amplify and assemble an art
74 and hydroxyl radicals in vivo, and protected genomic DNA as well as sensitive enzymes from intracellu
75 have probed the interplay between chromatin (genomic DNA associated with proteins and RNAs) and trans
76                     The HpSGN system cleaved genomic DNA at an efficiency of ~40% and ~20% in bacteri
77  on restriction enzymes capable of digesting genomic DNA at defined sequence motifs.
78 rated from 108 replicates, we found that one genomic DNA-based method and two non-unique molecular id
79 ed in the circulation by both mRNA-based and genomic DNA-based sequencing.
80 d with various concentrations of Aspergillus genomic DNA before extraction following international re
81 re anucleate cytoplasmic fragments that lack genomic DNA, but continue to synthesize protein using a
82 c principles of how the replisome duplicates genomic DNA, but little is known about its dynamics duri
83 ls for detection of gRNA-driven digestion of genomic DNA by Cas9 in vitro.
84 geal specimens were tested for HBoV mRNA and genomic DNA by quantitative polymerase chain reaction.
85                           Precise editing of genomic DNA can be achieved upon repair of CRISPR-induce
86               Structural variations (SVs) in genomic DNA can have profound effects on the evolution o
87                                              Genomic DNA capture and sequencing of a modifier haploty
88 le blood proves that the large mass of human genomic DNA captured from the lysed cells does not inhib
89                We screened 2.45 Mbp of human genomic DNA containing 12 strongly AF-associated loci fo
90                           In the presence of genomic DNA containing the target gene, CRISPR-Chip gene
91 library constructed from randomly fragmented genomic DNA coupled with affinity selection for antibody
92  of the DNA repair protein XRCC1 to sites of genomic DNA damage and impacted the amount of accumulate
93 breast CSCs, penetrates the nucleus, induces genomic DNA damage, and prompts caspase-dependent apopto
94 g telomerase and promoting radiation-induced genomic DNA damage.
95 to nick the inosine-containing DNA strand of genomic DNA deaminated by ABE in vitro.
96 e, we demonstrate that Plasmodium falciparum genomic DNA delivered to the cytosol of human monocytes
97                                              Genomic DNA did not differ between groups, with donor DN
98  properties of different functional units on genomic DNA differ in their signatures.
99                                        Thus, genomic DNA DSBs act as signaling intermediates in murin
100 les, in response to pathogens can also cause genomic DNA DSBs.
101    The ability to rewrite large stretches of genomic DNA enables the creation of new organisms with c
102               Additionally, in one donor the genomic DNA encoding the VH and CH1 domains was deleted,
103 mosome (BAC) reporters using human and mouse genomic DNAs encompassing the TERT genes and neighboring
104 the detection of 5 copies of M. tuberculosis genomic DNA (equaling 0.3 cell) in real biofluids using
105 ratio method to determine telomere length in genomic DNA extracted from buccal smears from 63 patient
106      It can detect <10 copies of the gene in genomic DNA extracted from E. coli or K. pneumoniae clin
107 sensor cam distinguish multiple genes of the genomic DNA extracted from Escherichia coli and Campylob
108 ed and validated in samples of non-amplified genomic DNA extracted from genetically modified (GM)-Soy
109                            Here, we screened genomic DNA extracted from spinal cord specimens of spor
110 y in just 100 ng of non-fragmented denatured genomic DNA extracted from tomato seeds.
111                Fluorescence titrations using genomic DNA extracted from various cell lines demonstrat
112                              We improved the genomic DNA extraction method, and reduced extraction ti
113 cation for the HIV env gene was performed on genomic DNA extracts from different CD4(+) T cell subset
114 n amplification and sizing of fragments from genomic DNA extracts.
115 G level using sodium bisulfite conversion of genomic DNA followed by sequencing or array hybridizatio
116 d from sequencing M. perstans and M. ozzardi genomic DNA for new repeat biomarker candidates which we
117 ir targets by scanning and interrogating the genomic DNA for sequences complementary to the gRNA.
118 ucleoside monophosphates (rNMPs) embedded in genomic DNA for sequencing.
119 studies suggest noncoding RNAs interact with genomic DNA, forming an RNA*DNA-DNA triple helix that re
120 pproaches, microfluidic partitioning of long genomic DNA fragments and barcoding of shorter fragments
121 rcoding of more than 8 million 20- to 300-kb genomic DNA fragments.
122                           We sequenced whole genomic DNA from 1,250 ash trees in 31 DNA pools, each p
123 entify a G > C transversion present in human genomic DNA from a ductal carcinoma cell line, a mutatio
124 onal signatures are indeed present in tumour genomic DNA from a variety of cancer types.
125                                              Genomic DNA from all 1007 NYBCS probands was sequenced f
126   DNA libraries are constructed using native genomic DNA from any source of interest, preserving cell
127 eloped a method for the rapid preparation of genomic DNA from bacteria based on hydrophilic ionic liq
128                                              Genomic DNA from clinical cases of spontaneous miscarria
129                                        Total genomic DNA from grain, old leaf and young leaf tissues
130 e absence of nonspecific amplification using genomic DNA from human or DNA from other closely-related
131 lective amplification of Wolbachia pipientis genomic DNA from infected Drosophila melanogaster and My
132      Samples contained equimolar mixtures of genomic DNA from lambda bacteriophage, Escherichia coli
133 sent in normal cells, similar to findings in genomic DNA from normal tissues of GI tumor patients.
134                                  Analysis of genomic DNA from older cells by qPCR indicates that tran
135 oned from the patient as well as in cDNA and genomic DNA from other individuals, suggesting that gene
136                     In addition, we purified genomic DNA from paraffin-embedded tissue and performed
137                                  Analysis of genomic DNA from pathogenic strains of Burkholderia ceno
138    The concept was proved on analysis of the genomic DNA from PC-3 cells and DNA isolated from melano
139                                  We analyzed genomic DNA from skin fibroblasts using whole-exome sequ
140 elanoma and detection in serum of methylated genomic DNA from the AGTR1 CpG island in metastatic mela
141                               The folding of genomic DNA from the beads-on-a-string-like structure of
142                                Sequencing of genomic DNA from the infant's saliva yielded 1.44 Gbp of
143             AcanR3990 qPCR failed to amplify genomic DNA from the other related Angiostrongylus speci
144 icate population periodically, and sequenced genomic DNA from the populations at generation 20.
145 t AID is transiently in spatial contact with genomic DNA from the time the nuclear membrane breaks do
146 by deep whole-genome bisulfite sequencing of genomic DNA from tissues representing the three germ lay
147            We also describe the isolation of genomic DNA (gDNA) and bisulfite treatment for the asses
148 er used 16S rRNA gene amplicon sequencing of genomic DNA (gDNA) and complementary DNA (cDNA) and meta
149 frequency of insertions was compared between genomic DNA (gDNA) collected from cells in the biofilm a
150 uNPs), we have developed a novel unamplified genomic DNA (gDNA) nanosensor, exploiting dispersion and
151                                              Genomic DNA (gDNA) of Ac were used to determine the anal
152      We utilized 25 gSSRs on a collection of genomic DNA (gDNA) samples from germplasm bank, and two
153                              We obtained 866 genomic DNA (gDNA) sequences from thirteen individuals a
154 xist and play regulatory roles in eukaryotic genomic DNA (gDNA).
155 evel (MGMT promoter region) in just 10 ng of genomic DNA (gDNA, ~2700 genomes) extracted from cancer
156 is cut and recombined within a single cell's genomic DNA, generally independent of DNA replication an
157  cloned from Cellulophaga algicola DSM 14237 genomic DNA, heterologously expressed, and characterized
158 Papa-B exon 2 and 3 were determined from the genomic DNA in 255 fecal samples, minimally representing
159  76.92, 769.2 and 7692 copies of RRS soybean genomic DNA in a non-GMO background.
160  is the region of the cell that contains the genomic DNA in a rather compact form.
161    The presence of billions of base pairs of genomic DNA in all nucleated cells raises the question o
162 lian CD59 genes to identify the only span of genomic DNA in C. porcellus that is homologous to a port
163                              Over 85% of all genomic DNA in eukaryotes is organized in arrays of nucl
164                                              Genomic DNA in eukaryotes is organized into chromatin th
165                                              Genomic DNA in eukaryotes is organized into chromatin th
166 hibitor also prevented the cleavage of viral genomic DNA in infected cells.
167 was successfully applied to the detection of genomic DNA in real seawater samples.
168                     However, massive loss of genomic DNA in these lineages often occurred in the dist
169 ortantly, despite high copy number of vector genomic DNA in transplanted heart tissue, there was no e
170                         Finally, analysis of genomic DNA in WT mice revealed cisplatin-induced hypome
171                       MCL-1 association with genomic DNA increased postirradiation, and the protein c
172   The assay requires just picogram levels of genomic DNA input, is sensitive and specific enough to d
173                       RAG1/2 can also induce genomic DNA insertions by transposition and trans-V(D)J
174                          Nucleosomes package genomic DNA into chromatin.
175                  Eukaryotic cells pack their genomic DNA into euchromatin and heterochromatin.
176      We confirmed that RAG1/2 also mobilizes genomic DNA into independent physiological breaks by ide
177 oiling and conversion of multiple regions of genomic DNA into left-handed Z-form.
178                             The packaging of genomic DNA into nucleosomes creates a barrier to transc
179                                  Wrapping of genomic DNA into nucleosomes poses thermodynamic and kin
180                          The organization of genomic DNA into nucleosomes profoundly affects all DNA-
181 ation begins with regulated transcription of genomic DNA into RNA.
182 ting) must occur before integration of viral genomic DNA into the host chromosomes, yet remarkably, t
183 virus terminase complex cleaves concatemeric genomic DNA into unit lengths during genome packaging an
184 transcription factor (TF) binding signals in genomic DNA is a fundamental problem.
185              The double-helical structure of genomic DNA is both elegant and functional in that it se
186  enrichment of high-quality mtDNA from total genomic DNA is critical to obtain entire mtDNA sequences
187             During mitosis, transcription of genomic DNA is dramatically reduced, before it is reacti
188                                        Bound genomic DNA is eluted from the TF and sequenced using ne
189                                              Genomic DNA is folded into a higher-order structure that
190                                         HBoV genomic DNA is frequently detected in both ill and healt
191  damage occurs during cell-cycle phases when genomic DNA is packaged into nucleosomes.
192                              This is because genomic DNA is physically associated with an astonishing
193 or the understanding of how accessibility to genomic DNA is regulated in cells.
194                                              Genomic DNA is replicated every cell cycle by the progra
195                                Chromatinized genomic DNA is resistant to MjAgo degradation, and recom
196                                              Genomic DNA is susceptible to endogenous and environment
197                         In eukaryotic cells, genomic DNA is wrapped around histone octamers (an H3-H4
198 rough a vast excess of competing, unmodified genomic DNA, is a mechanistic challenge that may limit t
199 osome inactivation ratios were determined in genomic DNA isolated from blood (n = 42) and saliva (n =
200     We performed bisulfite sequencing PCR of genomic DNA isolated from HBV-related HCCs and HBV repli
201  marks 5-methyl-dC and 5-hydroxymethyl-dC in genomic DNA isolated from lungs of A/J mice exposed whol
202 lation with average CAG repeat length at the genomic DNA level determined by PCR method in striatal t
203 alable single-step approach performed at the genomic DNA level in solution that combines with most do
204                               We constructed genomic DNA libraries for AFGP-bearing and AFGP-lacking
205 ied TFs with next-generation sequencing of a genomic DNA library.
206   Our results suggest coincidence of massive genomic DNA losses and increased power of genetic drift,
207 ous generation of interstrand cross-links in genomic DNA may contribute to aging, neurodegeneration,
208                 This study demonstrates that genomic DNA methylation analysis can facilitate the mole
209 which genetics, sex, and pregnancy influence genomic DNA methylation by intercrossing 2 inbred mouse
210 NA demethylation is critical for shaping the genomic DNA methylation landscape in Arabidopsis.
211 del is sensitive enough to detect changes in genomic DNA methylation levels as a function of growth p
212                                              Genomic DNA methylation maps (methylomes) encode genetic
213 tic syndromes have been shown to have unique genomic DNA methylation patterns (called "episignatures"
214                                  We compared genomic DNA methylation patterns and gene expression in
215                     To gain insight into how genomic DNA methylation patterns are regulated during iA
216 -(+)-fipronil dysregulated a higher level of genomic DNA methylation than R-(-)-fipronil.
217 emonstrate in this study that IL-26 binds to genomic DNA, mitochondrial DNA, and neutrophil extracell
218 olism, mitochondrial mass, and mitochondrial genomic DNA (mtDNA) homeostasis.
219 ect MSV in as little as 10 fg/ul of purified genomic DNA obtained from a MSV-infected maize plant, a
220 uences were obtained by direct sequencing of genomic DNA obtained from shark fin tissue.
221 , we performed whole exome sequencing on the genomic DNA of 13 transgender males and 17 transgender f
222            We used cheek swabs to obtain the genomic DNA of 200 ADHD male probands (mean age: 8.7 yea
223  formation of O(4)-POBdT in naked DNA and in genomic DNA of cultured mammalian cells exposed with NNK
224  in archaeal tRNAs, was recently detected in genomic DNA of Enterobacteria phage 9g and was proposed
225   Deep sequencing of amplicon libraries from genomic DNA of gene-edited parasites revealed Cas9-catal
226 ymethylcytosine, and 5-formylcytosine in the genomic DNA of human CMSCs isolated from diabetic donors
227 o quantitatively detect a 563 bp fragment of genomic DNA of Mycobacterium avium subspecies paratuberc
228                        In this cohort study, genomic DNA of women from 12 major cancer centers with a
229 strated by the simultaneous detection of the genomic DNAs of three microorganisms: E. coli, B. cereus
230 es encoding candidate acid phosphatases from genomic DNA or recovered from metagenomic libraries or g
231 provirus gene-editing were confirmed by cell genomic DNA PCR and fluorescent marker expression analys
232 g a limit of detection of 40 copies of human genomic DNA per reaction volume.
233 ruct a Dub-seq library with Escherichia coli genomic DNA, performed 155 genome-wide fitness assays in
234     The association of nucleosomes with most genomic DNA prevents initiation from cryptic promoters.
235 psis is a primary mechanism that accelerates genomic DNA rearrangement and amplification into ecDNA a
236  DNA sequences, linear or circular DNA, bulk genomic DNA, recombinant or native Drosophila core histo
237  efficiently locate sequence homology across genomic DNA remains unclear.
238 s ribonucleoside monophosphates (rNMPs) from genomic DNA, replacing the error with the appropriate de
239 ion increases G4 accumulation and slows bulk genomic DNA replication.
240  a human FXN-GAA-Luciferase repeat expansion genomic DNA reporter model of FRDA, we screened the Stru
241             Replication and transcription of genomic DNA requires partial disassembly of nucleosomes
242 f rs9315202 in a human kidney cell line HK-2 genomic DNA resulted in a change in KL transcriptional a
243 sufficiently abundant to completely wrap all genomic DNA, resulting in a consistent protein barrier t
244 equence specifically designed not to bind to genomic DNA, resulting in a duplex flanked by single str
245 ed to three different gRNAs targeting HEK293 genomic DNA, resulting in a set of 55 high-confidence gR
246 alysis of mutated target sequences and human genomic DNA reveal that Cascade recognizes an extended p
247 he high-throughput purification of plasmids, genomic DNA, RNA and total nucleic acid (TNA) from a ran
248                           New approaches for genomic DNA/RNA detection are in high demand in order to
249 response enhancement for direct detection of genomic DNA samples at the level of interest without pre
250                   Using Sanger sequencing on genomic DNA samples from 472 SB and 565 control samples,
251                                    Screening genomic DNA samples from exudative vitreoretinopathy pat
252       Prior to analysis, dsDNA fragments and genomic DNA samples were first denatured and then anneal
253 inder model without fitting parameters, with genomic DNA sequence being the only input, we further va
254 iple generations in the presence of the same genomic DNA sequence.
255  PCR method in diagnostics, we amplify human genomic DNA sequences from a approximately 1 muL droplet
256 fficient program to predict SINE elements in genomic DNA sequences.
257 eterozygous mutation at codon 526 (L526S) in genomic DNA sequencing but a homozygous L526S mutation i
258                            Here, we employed genomic DNA sequencing of multiple variable (V) regions
259 ies with inherited hearing loss, panel-based genomic DNA sequencing, followed by segregation analysis
260          Overall, our findings indicate that genomic DNA serves as a reservoir to initiate a pro-infl
261 iments using this method to sequence E. coli genomic DNA showed that the TGIRT enzyme has surprisingl
262 ant nucleoid-associated proteins at numerous genomic DNA sites and stabilization of distinct long-ran
263 he LAMP assay were evaluated using bacterial genomic DNA-spiked cerebrospinal fluid (CSF) and blood s
264 tant TDP-43, which correlated with increased genomic DNA strand breaks, activation of the DNA damage
265     DNA replication requires that the duplex genomic DNA strands be separated; a function that is imp
266              Persistent protein obstacles on genomic DNA, such as DNA-protein crosslinks (DPCs) and t
267                            BROCA analysis of genomic DNA suggested 120 rare mutations from 150 famili
268 scriptional factories with replicating viral genomic DNA suggests that KSHV assembles an "all-in-one"
269 etitive primer extension assays for specific genomic DNA targets such as gene exons.
270 ght induce the formation of photoproducts in genomic DNA that are potentially mutagenic and detriment
271                       Here, we show that the genomic DNA that is excised during recombination, the ex
272      Abasic (Ap) sites are common lesions in genomic DNA that readily undergo spontaneous and amine-c
273 ine dimers (the major UV-induced lesions) in genomic DNA; the quantum yield of these dimers in TEL21/
274 emoves mis-incorporated ribonucleotides from genomic DNA through ribonucleotide excision repair.
275       However, transcription also sensitises genomic DNA to damage from a number of endogenous source
276  and single molecule real-time sequencing on genomic DNA to determine these target sequences and thei
277             We amplified switch regions from genomic DNA to investigate the quality of the double-str
278                         Instead of apoptotic genomic DNA, tumor-derived mitochondrial DNA triggers in
279  machinery, shows dynamic binding across the genomic DNA under different growth conditions.
280 te whole-genome amplification of single-cell genomic DNA using linear nucleic acid amplification.
281 expansion number in the Huntington's gene of genomic DNA using quantitative PCR.
282 horylation state in complete (containing the genomic DNA) versus empty (genome-free) HBV virions.
283 ues were collected 14 months after delivery; genomic DNA was analyzed by PCR to detect the Dnajb1-Prk
284                                              Genomic DNA was analyzed by Sanger sequencing or high-th
285                         Patients and Methods Genomic DNA was analyzed for TP53, CTNNB1, CDKN1C, ATRX,
286                                              Genomic DNA was extracted from blood of participants and
287                                              Genomic DNA was extracted from brain tissue in all cases
288                                              Genomic DNA was extracted from leaf, must and wine of th
289                   In addition, the bacterium genomic DNA was quantified with a detection limit of 7.1
290                                              Genomic DNA was tested for the KRAS-variant in a CLIA-ce
291                       WGS from blood-derived genomic DNA was used for homozygosity mapping and a rare
292 y measuring nuclear bomb test-derived 14C in genomic DNA, we determined the turnover rates of CD4+ an
293 for the coiling and contraction in length of genomic DNA, we suggest that it serves primarily in the
294                                      RNA and genomic DNA were isolated from peripheral blood mononucl
295 he method was further validated by detecting genomic DNA with high specificity.
296 g" RoundUp Ready (RRS)" and MON89788 soybean genomic DNA with P35S and lectin primer sets.
297                                    Yields of genomic DNA with PCR-identifiable 18S rRNA gene sequence
298 allows stable labeling and monitoring of HIV genomic DNA within infected cells during cytoplasmic tra
299 gans cuticle makes it challenging to extract genomic DNA without harsh procedures that can artifactua
300 action and analysis of non-amplified soybean genomic DNA without sample treatment was developed and v

 
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