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1 sembled using a meta-assembly strategy after sequencing of 10 lines derived from a maize-teosinte cro
2                    We performed whole-genome sequencing of 102 primary PanNETs and defined the genomi
3                           Using whole-genome sequencing of 11 262 Icelanders, we found 1403 cases of
4      Forty-six PMMs underwent targeted exome sequencing of 111 cancer-associated genes.
5 enome variation map generated through genome sequencing of 117 diverse accessions.
6                                Transcriptome sequencing of 120 cultivated and wild spinach accessions
7                     Whole-exome and targeted sequencing of 13 individuals from 10 unrelated families
8                                       RT-PCR sequencing of 16 childhood ependymoma samples identified
9              Using single-molecule long-read sequencing of 16 diverse fungal genomes, we observed tha
10 onhuman primates, we performed transcriptome sequencing of 16 regions of adult human, chimpanzee, and
11                                  Marker gene sequencing of 16S ribosomal genes revealed that the gut
12 . heliophila, using next-generation Illumina sequencing of 16S rRNA gene sequences to characterize sy
13                              High-throughput sequencing of 16SrRNA genes demonstrated that plants in
14 de variants (SNVs) by conducting whole exome sequencing of 18 trios consisting of Japanese patients w
15 oss of methicillin resistance through genome sequencing of 180 isolates from 2016.
16 ecurrently mutated in 36 genes, and targeted sequencing of 20 sites in 17,688 patients with NDD ident
17 lelic clusters, identified from whole-genome sequencing of 228 DO mice.
18    Through comprehensive whole-transcriptome sequencing of 231 children with acute lymphoblastic leuk
19                      Here, we report the RNA sequencing of 240 lettuce accessions sampled from the ma
20  Phylogenetic analysis based on whole-genome sequencing of 250 isolates revealed two major M chimaera
21  this issue, we carried out 60x whole-genome sequencing of 26 metastases from four patients with panc
22  new disease genes, we performed whole-exome sequencing of 26 unrelated CG patients.
23                                     Targeted sequencing of 283 genes was performed in 240 women with
24                                        Exome sequencing of 291 parent-offspring trios with midline NS
25                                 Through deep sequencing of 3' ends, we provide evidence that PARN can
26 erval) using high-depth (579x+/-315) nextgen sequencing of 30 lung cancer and 89 control samples, res
27                    We used molecular barcode sequencing of 32 genes on the pretreatment peripheral bl
28                                  Whole-exome sequencing of 33 unrelated patients with EoE revealed 39
29           Here, we report the targeted exome sequencing of 330 genes, including genes known to be inv
30 an additional 182 families, and whole-genome sequencing of 4 of the remaining 242 families revealed 2
31                                              Sequencing of 40 people with arhinia revealed that 84% o
32 2 SNPs derived from DNA resequencing and RNA-sequencing of 41 groundnut accessions and wild diploid a
33                     We performed whole-exome sequencing of 43 unrelated probands affected by severe s
34 ng, targeted amplicon sequencing, and/or RNA-sequencing of 46 pediatric primary MDS patients.
35                                        Exome sequencing of 5 affected members identified a single nov
36                               Here we report sequencing of 5,205 samples from families with ASD, acco
37 re we perform whole-exome and -transcriptome sequencing of 500 adult patients with metastatic solid t
38                      Here we report targeted sequencing of 59 DISC1 Interactome genes and 154 Regulom
39           Here we conducted a targeted exome-sequencing of 63 trios of Chinese epilepsy families usin
40 on in 117 Wilms tumors, followed by targeted sequencing of 651 Wilms tumors.
41 l dynamics using whole-exome and/or targeted sequencing of 699 patients, of whom 122 were analyzed lo
42 tuary by rRNA and rDNA-based high throughput sequencing of 97 samples collected along the entire sali
43                       Whole exome and genome sequencing of a 19-year-old girl (P7), initially diagnos
44                                  Whole-exome sequencing of a breast cancer from a c.104T>C carrier re
45 on with selected advanced cancers, universal sequencing of a broad panel of cancer-related genes in p
46                                              Sequencing of a cDNA encoding ArPPLNP2 revealed that it
47 ain-containing 2 (MAGI2) through whole-exome sequencing of a deeply phenotyped cohort of patients wit
48                                              Sequencing of a distal IL1RL1 promoter region demonstrat
49                          Through whole exome sequencing of a family of three affected siblings with i
50 , Dudek et al. show that shotgun metagenomic sequencing of a less-well-studied environment - dolphin
51       Here, we performed high-throughput RNA sequencing of a Mabuya placenta transcriptome and screen
52                                              Sequencing of a P. malariae relative that infects chimpa
53               Here, we performed whole-exome sequencing of a patient with disseminated Mycobacterium
54                                  Here, exome sequencing of a single cohort of 2,871 CHD probands, inc
55 ring postnatal maturation by performing deep sequencing of accessible chromatin regions by using the
56 r results show that timing and probabilistic sequencing of actions can share the same neural circuits
57                                 Whole-genome sequencing of all patients allowed exclusion of promiscu
58                                  We used RNA sequencing of allelic six-rowed spike3 (vrs3) mutants wi
59                 Here we describe the shotgun-sequencing of ancient DNA from five specimens of Neander
60 ordances were clarified upon high-throughput sequencing of antigen-receptor rearrangements and blind
61                       Whole-genome bisulfite sequencing of antigen-specific murine CD8 T cells at the
62 elative to the reference method (culture and sequencing of any carbapenem-nonsusceptible isolate).
63                                              Sequencing of ARL15 in 375 severely insulin resistant pa
64 mporal cerebellar expression profiles by RNA sequencing of ATXN2Q127 mice versus wild-type (WT) litte
65                           As high-throughput sequencing of B cells becomes more common, the need for
66  we focused on incorporating next-generation sequencing of B-cell transcripts to determine the origin
67                              High-throughput sequencing of barcoded Kras (HDR) alleles from bulk lung
68  approach to this question by performing RNA sequencing of brain tissue from mice chronically treated
69  been characterized across cancers by genome sequencing of bulk tumors, including chronic lymphocytic
70                                Moreover, RNA sequencing of c-Kit(+) cells showed that CHD7 functions
71                   The recent high-throughput sequencing of cancer genomes and transcriptomes has prod
72 equencing (NGS) technology, such as targeted sequencing of candidate cancer genes and whole-exome and
73                                  Single-cell sequencing of cardiac CD45(-)c-kit(+) cells showed innat
74                                          RNA sequencing of CD138(+) tumor cells from t(4;14)-positive
75 t of the transactivation domain of YAP1, and sequencing of cDNA from the patient shows it does not re
76           Analysis of 16S ribosomal RNA gene sequencing of cervicovaginal lavage clustered each parti
77                                 Whole genome sequencing of CFW-passaged strains showed no specific ch
78             We used comparative whole-genome sequencing of chemically mutagenized and natural Pgt iso
79                                     Finally, sequencing of chromatin immunoprecipitates containing sp
80 those with advanced metastatic disease, deep sequencing of circulating cell free DNA (cfDNA) obtained
81                      Through massive shotgun sequencing of circulating cell-free DNA from the blood,
82 ts with MM and healthy controls by small RNA sequencing of circulating exosomes.
83 ing targeted clinical-grade, next-generation sequencing of circulating tumor DNA (ctDNA).
84 at technological advances in next-generation sequencing of circulating, tumor-derived nucleic acids h
85  laboratory conditions; and (4) whole-genome sequencing of clinical and environmental isolates.
86 E, allowing proximity-dependent ligation and sequencing of cognate sRNA-mRNA pairs as chimeric reads.
87                                          RNA sequencing of cultured astrocytes derived from trkB.T1(+
88 l network, successful development involves a sequencing of developmental events.
89                                    Small RNA sequencing of dissected regions of immature seed coats d
90 ning systemic dsx knockdown, high-throughput sequencing of diverse tissues and a genome-wide analysis
91         Short- and long-read high-throughput sequencing of DNA and RNA demonstrated that the chloropl
92                   Here, we show whole-genome sequencing of DNA and RNA in 94 Chinese individuals with
93                  Methods for next-generation sequencing of DNA are producing a wealth of information
94                            Metagenomics, the sequencing of DNA extracted directly from natural microb
95                      Multiplexed tag-encoded sequencing of DNA from the samples was performed, and th
96  chromosome pairs allows for the independent sequencing of each of the complementary and homologous s
97                                              Sequencing of ELF3 in ICCV 96029 revealed an 11-bp delet
98                                        m(6)A sequencing of embryonic mouse cortex reveals enrichment
99  demonstration of tandem ME-SIMS for de novo sequencing of endogenous neuropeptides from tissue in si
100           This method combines de novo MS/MS sequencing of enriched antibodies and co-extracted prote
101                     High-throughput amplicon sequencing of environmental DNA (eDNA metabarcoding) rep
102                                  Large-scale sequencing of environmental microbiomes has the potentia
103                              Single-cell RNA sequencing of epidermal progenitors revealed the emergen
104                                          RNA sequencing of Erdr1-overexpressing cells identified the
105                                    Bisulfite sequencing of exposed and control animals highlighted di
106               We are performing whole-genome sequencing of families with autism spectrum disorder (AS
107  de novo mutations discovered by large-scale sequencing of family samples, 215 genes spanning rare an
108                             V4 16S rRNA gene sequencing of fecal DNA demonstrated minimal shifts in t
109                                              Sequencing of fern mitogenomes could shed light on the m
110 cteristics were observed for next-generation sequencing of FFPET, whole blood, and dried blood spot i
111                                              Sequencing of FGFR1 identified a previously unreported d
112 ed NO and N2 O to varying degrees and genome sequencing of four indicated that two isolates held gene
113 ed and analyzed, enables fast and affordable sequencing of full human genomes.
114                           Further, small RNA sequencing of GBM patients identified significant miRNA
115                               Targeted exome sequencing of genes encoding the mitochondrial proteome
116  Precision Oncology relies on indiscriminate sequencing of genomes in biopsies that barely represent
117                                              Sequencing of genomic DNA from the infant's saliva yield
118         We demonstrate ultra-high-throughput sequencing of >50,000 cells per run in a synthetic commu
119                  Metagenomic next generation sequencing of his cerebrospinal fluid and brain biopsy t
120                                         Deep sequencing of HIV reverse transcriptase (RT) was perform
121                                  Whole exome sequencing of HLHS fibroblasts identified deleterious va
122 this methodology particularly useful for the sequencing of HS saccharides, because the lack of contam
123                   We perform single-cell RNA-sequencing of human gliomas and identify phenotypic diff
124 ecovered using UV-crosslinking, ligation and sequencing of hybrids (CLASH).
125 althy controls, we performed high-throughput sequencing of immunoglobulin heavy chain VDJ rearrangeme
126                              Large-scale DNA sequencing of immunological repertoires offers an opport
127                                  Metagenomic sequencing of incubation samples revealed that LREE-cont
128                                              Sequencing of independent clonal isolates of replication
129   Autozygosity mapping in families and exome sequencing of index patients were performed in 152 consa
130                                     Dual RNA sequencing of individual host cell populations and C. al
131                              Moreover, exome sequencing of individuals with idiopathic SZ identified
132                           By next-generation sequencing of infected tissue homogenates, we assembled
133 formally identified by PCR amplification and sequencing of internal transcribed spacer 1 (ITS1), was
134 -type mice and performed high throughput RNA-Sequencing of kidney tissue in aged mice.
135                              Next generation sequencing of Kupffer cell miRNA identified miRNA 181b-3
136                                     Targeted sequencing of LAMB4 in 148 non-familial and unrelated sp
137                                              Sequencing of LanFTc1 revealed a 1.4-kb deletion in the
138  primers enable massively parallel, targeted sequencing of large STR sets.
139 c leukemia (T-ALL), but detailed genome-wide sequencing of large T-ALL cohorts has not been carried o
140  vertebrate species, we used single-cell RNA sequencing of lck:GFP cells in zebrafish and obtained th
141                      In conclusion, 454-deep sequencing of liver and plasma compartments in treatment
142                               Similarly, RNA sequencing of lupus patient blood revealed similar expre
143                             We performed RNA sequencing of lupus patient whole blood to determine com
144                                         Deep sequencing of lymphocyte receptor repertoires has made i
145                      An important feature in sequencing of mAbs is the discrimination of isobaric res
146 Here we use highly parallel, single-cell RNA sequencing of malaria cultures undergoing sexual commitm
147  combination of community fingerprinting and sequencing of marker genes to identify community changes
148                 Here, we analyze whole exome sequencing of matched pre- and post-neoadjuvant cisplati
149 nt and convenient method for high-throughput sequencing of mature tRNAs.
150 tro microbiology approaches and whole-genome sequencing of Methanomicrobium mobile, a key species wit
151                                              Sequencing of methylomes, transcriptomes, and genomes of
152 study of the human microbiome through direct sequencing of microbial DNA, resulting in an enormous am
153                          High-throughput DNA sequencing of microbiota from a diverse collection of fe
154                 Here we used Next Generation Sequencing of microRNAs to identify negative regulators
155                                miR-seq (deep sequencing of miRNAs) data reveal that the degradation o
156                Isolation and next-generation sequencing of MIWI2-positive multiciliated cells reveale
157          Here, Patel et al. use targeted DNA sequencing of MODY patients and large-scale publically a
158                            A high-throughput sequencing of mRNAs was performed to investigate the eff
159                Here, we employed genomic DNA sequencing of multiple variable (V) regions of the bacte
160 ely 10,000 cells) whole-genome shotgun (WGS) sequencing of Mycobacterium tuberculosis and soil micro-
161                                         Deep sequencing of nasopharyngeal samples produced partial se
162                        Here we conduct exome sequencing of nine non-serous epithelial ovarian tumors
163                                          RNA sequencing of NOD.Abd3 common bile duct early in disease
164            We further performed whole-genome sequencing of nosocomial MDRPa strains to evaluate genot
165     Population-based sequencing and 454 deep sequencing of NS5B gene were performed on plasma and liv
166 ed for comparative chromatin biology because sequencing of numerous genomes from many clades is coupl
167                                              Sequencing of OG paves the way to address chemical and b
168                                              Sequencing of one molecular type (RNA, methylated DNA or
169 herefore ideal for fast and massive parallel sequencing of parasite transcriptomes directly from host
170 se mutations can be best identified by exome sequencing of parent-offspring trios.
171                                Targeted deep sequencing of parental fibroblasts revealed that most va
172  characterized by next-generation (Illumina) sequencing of partial (V4) 16S rRNA gene sequences.
173                             Fast, affordable sequencing of pathogen genomes - now a staple of the pub
174 study highlights the power of data from deep sequencing of pathogens as a component of outbreak inves
175                                 Whole-genome sequencing of pathogens from host samples becomes more a
176 tation of the human genome and transition to sequencing of patient genomes instead of exomes will be
177                  Using information from deep sequencing of patients with neurological or psychiatric
178                           In this study, the sequencing of PCR amplicons generated using primers targ
179                          Conventional Sanger sequencing of PCR products is the gold standard for spec
180 the performance of pY-MIP for enrichment and sequencing of phosphopeptides obtained by tryptic digest
181                                    Using RNA-sequencing of platelets followed by validation via RT-PC
182 enomes of single cells, followed by Illumina sequencing of pooled DNA.
183                         We conclude that DNA sequencing of pooled samples of large numbers of bacteri
184                                    Using RNA sequencing of Populus trichocarpa roots in mutualistic s
185                               However, exome sequencing of PP;Trp53 KO melanomas failed to reveal any
186 ripotent cells in vivo, obtained by the deep sequencing of pre-implantation embryos.
187          Ultra-deep targeted next generation sequencing of pretreatment plasma cfDNA from DLBCL patie
188                                  Plasmid DNA sequencing of previously uncharacterized clinical extend
189                       Whole-genome bisulfite sequencing of primary human naive, short-lived effector
190 genesis, we performed whole-genome bisulfite sequencing of primary leukemic and non-leukemic cells in
191 o-HCT was profiled by means of 16S ribosomal sequencing of prospectively collected stool samples.
192  to oligosaccharide standards and to de novo sequencing of purified plant metabolite glycoconjugates,
193                                          RNA sequencing of resident CD45(-) joint cells from advanced
194                                   Ultra-deep sequencing of resistant parasites identifies the sarco/e
195  analysis, an unbiased approach based on RNA sequencing of resistant subclones, to discover the molec
196 ration chromatin immunoprecipitation and RNA sequencing of reward brain regions indicates that the re
197                                    Using RNA sequencing of ribosome-bound mRNA from hippocampal CA3 n
198 se and can be measured using next-generation sequencing of RNA (RNA-seq).
199                        Using high-throughput sequencing of RNA isolated by crosslinking immunoprecipi
200                              High-throughput sequencing of RNA prepared using RPAD from human cervica
201 ions were identified through next-generation sequencing of saliva or blood samples, and RNA was extra
202                  In conclusion, whole-genome sequencing of samples obtained following neoadjuvant che
203 tivity of HALE estimates was assessed to the sequencing of select comorbidities for the dependent com
204 P calls closely concordant with whole-genome sequencing of selected lines.
205                                     Amplicon sequencing of selected samples revealed the prevalence o
206                                     Amplicon sequencing of several independent saddle pattern mutants
207                      We used high-throughput sequencing of short, cyclobutane pyrimidine dimer-contai
208 encing technologies such as exome and genome sequencing of similar patient cohorts will reveal additi
209 n this study, we demonstrate that sparse DNA sequencing of single-cell nuclei from prostate core biop
210                                         Deep sequencing of size-selected DNase I-treated chromatin (D
211      In the present study, we performed deep sequencing of small RNA molecules in the embryonic fibro
212      Here, using high-throughput marker gene sequencing of soils collected from 18 sites throughout N
213 l abnormalities that suggest a syndrome, and sequencing of specific genes or next-generation sequenci
214                                         Deep sequencing of Spo11 oligonucleotides demonstrates that T
215 ion of these compounds based on whole genome sequencing of spontaneous resistant mutants, which ident
216 nd spp3 revealed they were allelic, and deep sequencing of spp3 identified an independent disruptive
217                                 Finally, RNA sequencing of ST18-depleted tumors before involution rev
218 were determined using metatranscriptomic RNA sequencing of stomach biopsy specimens from individuals
219 rmed gene expression profile analysis by RNA sequencing of subsets of interferon gamma (IFNG)-produci
220 ssessed by both 16S rDNA and metagenomic DNA sequencing, of TB cases during antimycobacterial treatme
221                              High-throughput sequencing of TEM-1 populations shows that this advantag
222                                        Exome sequencing of Tet2(-/-) tumours reveals accumulation of
223          Each participant underwent targeted sequencing of TGM1.
224 ion of flow cytometric cell sorting and deep sequencing of the 16S rDNA gene was used to characterize
225 y, bacterial composition was identified with sequencing of the 16S ribosomal RNA gene in breast milk,
226 east milk, areolar skin, and infant stool by sequencing of the 16S ribosomal RNA gene.
227                    Using next-generation DNA sequencing of the 16S rRNA gene, we analyzed the composi
228                                              Sequencing of the 16S-rRNA components of this aerosol re
229                                              Sequencing of the 3'UTR of common HLA-A alleles indicate
230                                       Sanger sequencing of the AH cfDNA and tumor DNA with polymerase
231 e isolated and characterized using RAPDs and sequencing of the almost complete 16S rRNA gene.
232                                          DNA sequencing of the APOC2 gene in the patient and one of h
233 tes in combination with improvements in deep sequencing of the autologous cancer have provided new in
234                                          RNA sequencing of the basolateral amygdala revealed transcri
235 ctivation by Fos immunofluorescence, and RNA sequencing of the basolateral amygdala.
236 opose that the information generated by deep sequencing of the BBCE cell lines coupled with phenotypi
237  To address this question, we performed deep sequencing of the BCR repertoire of AChR-MG, MuSK-MG, an
238            We performed high-throughput deep sequencing of the beta-TCR repertoire in 29 lesional and
239  cross-linked to RNA in vivo High-throughput sequencing of the bound RNAs revealed strong Set1 enrich
240 quencing in an IO IBD patient and subsequent sequencing of the candidate gene in 12 additional IO IBD
241                                              Sequencing of the coding regions of all linked genes fai
242       Nevertheless, during our isolation and sequencing of the complete genome of faustovirus, follow
243                                              Sequencing of the deletions caused by CRISPR-Cas self ta
244 ficance, informational content, and temporal sequencing of the different types of movement in dance.
245 evidence for trait association from complete sequencing of the DISC1 locus.
246                                              Sequencing of the dynemicin biosynthetic gene cluster in
247                                       Recent sequencing of the fiber-degrading Ruminococcus flavefaci
248                               Using amplicon sequencing of the fungal internal transcribed spacer 2,
249                                              Sequencing of the HAstV-2 capsid genes reveals mutations
250                 More than a decade after the sequencing of the human genome, a deluge of genome-wide
251                            Quantitative deep sequencing of the Ig heavy chain locus from B220(+)CD43(
252                                       Genome sequencing of the immigrant identified it as a G. coniro
253                                       Sanger sequencing of the LAT gene showed a mutation that result
254  To study this, we performed next generation sequencing of the livers of Sprague-Dawley rats treated
255                                          DNA sequencing of the lysozyme gene in the patient and his m
256 ne strains, and field isolates, whole-genome sequencing of the M. gallisepticum vaccine strain ts-11
257 oreover, whole exome sequencing and targeted sequencing of the major pancreatic cysts has identified
258                                         ChIP sequencing of the major players NUT, ZNF532, BRD4, EP300
259  make it possible to analyse high-throughput sequencing of the methylome of any given organism under
260                             We performed DNA sequencing of the ORAI1 gene, modeling of mutations on O
261 We believe we report the first transcriptome sequencing of the postmortem human dorsal striatum compa
262                    Here we used whole-genome sequencing of the proposed serovar 16 reference strain A
263                                       Direct sequencing of the purified DNA segments can have >100-fo
264                                              Sequencing of the recovered ssODNs provided quantitative
265                                  Whole-exome sequencing of the remaining 424 families revealed mutati
266                                We report the sequencing of the Stentor coeruleus macronuclear genome
267                                              Sequencing of the switch regions of memory B cells from
268                                              Sequencing of the syncytial variants revealed mutations
269 herited variants detected using simultaneous sequencing of the tumor and normal tissue ("tumor-normal
270                                         Deep sequencing of the tumor genome showed a highly heterogen
271 to compare bacterial load and Illumina MiSeq sequencing of the V1-V3 regions of the 16S rRNA gene use
272 s were collected and analyzed using 16S rRNA sequencing of the V3-V4 hypervariable region.
273                                        MiSeq sequencing of the V4 region of both bacterial and archae
274 mposition was assessed via amplification and sequencing of the V4 region of the 16S ribosomal RNA gen
275                                 Sanger-based sequencing of the viral protein 1 (VP1) capsid region is
276                Pyrosequencing genotyping and sequencing of the voltage gated sodium channel (VGSC) ge
277                                       Sanger sequencing of this candidate gene in independent allelic
278                                 Whole-genome sequencing of three mangrove species further shows the d
279                               We perform RNA sequencing of tissues from American alligator embryos to
280                   We assessed if metagenomic sequencing of total DNA extracts obtained direct from so
281 tive and quantitative method for single-cell sequencing of total RNA.
282                                          RNA sequencing of TPB-resistant tumors revealed that extrace
283 additives to feedlot cattle using metagenome sequencing of treated and control animals.
284                              Next-generation sequencing of tumors and matched normal DNA.
285                              Next-generation sequencing of tumors as part of clinical care included h
286 ways that would not be as apparent from bulk sequencing of tumors, and can potentially establish whet
287 cted genome-wide mRNA profiling and DNA exon sequencing of two cell lines (TMD and BMD) derived from
288                           We also report the sequencing of two diploids from the ancestral gene pools
289                                        Exome sequencing of two Finnish sisters with non-syndromic POI
290                                   Ultra-deep sequencing of two healthy-looking skin biopsies identifi
291 a major mitochondrial DNA (mtDNA) survey and sequencing of two nuclear markers (AME and RAG-1) from P
292 is remarkable property is applied to de novo sequencing of underivatized oligosaccharides.Establishin
293                                 Whole genome sequencing of UNG/SMUG1-deficient tumours revealed that
294 anscriptional dynamics using single-cell RNA sequencing of unstimulated and stimulated naive and effe
295 nature, we performed whole-transcriptome RNA sequencing of untreated, apoptotic, and recovering HeLa
296                                              Sequencing of viral nucleic acids from the stool of vacc
297 ore relatively recently, coinciding with the sequencing of whole genomes.
298 vercomes this drawback by untargeted shotgun sequencing of whole metagenomes at affordable cost.
299 ve structural diversity arises, we used deep sequencing of wild populations to reveal genetic variati
300 lecular basis for abnormal KSC function, RNA sequencing of wild-type (WT) and VDR(-/-) KSCs was perfo

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