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1                                              Mb (100 ug/mL) reduced the vascular contractility induce
2 affold N50 of 8.7 Mb and the longest of 19.0 Mb.
3 ) in early prophase and extending to 1.5-2.0 Mb in late prophase as chromosomes compact and homologs
4  ways; some (chromosome 19; position 3.0-4.0 Mb) are associated with closely related taxa (Prevotella
5 RF16), some (chromosome 27; position 3.0-4.0 Mb) are associated with distantly related taxa (Prevotel
6 ning a total of 55 848 composite parts (71.0 Mb).
7 Among them, 273 QTLs were delimited to <=1.0-Mb intervals and 7 of them are either known genes (Rht-D
8 ong-read assembly, compared to those of 1.04 Mb for B73 and 1.48 Mb for Mo17.
9 tes were identified within a conserved 40.09 Mb linkage-disequilibrium (LD) block on the X chromosome
10 his method to efficiently deliver large (1.1 Mb) synthetic yeast centromeric plasmids (YCps) to cultu
11 DB1-dependent loop formations bypassed 0.2-1 Mb of linear genome and radiated from the TAD(cPcdh) fri
12  genome, coldspots have a median size of 2.1 Mb and are spatially clustered.
13 d TdDof to within a physical interval of 2.1 Mb inside the SSt1 locus.
14 iant, including four with a heterozygous 3.1 Mb 16p13 deletion encompassing XYLT1 and two with a hete
15 we sequenced and assembled approximately 3.1 Mb of the S(2) -haplotype of the S-locus in Petunia infl
16 meric satellite DNA array (approximately 3.1 Mb) and closed the 29 remaining gaps in the current refe
17 tosomes with sizes ranging from 12.4 to 33.1 Mb and a total size, in chromosomes, of 726 Mb, which ha
18 ne-mapped the classical MHC (chr6: 29.6-33.1 Mb), imputing 216 human leukocyte antigen (HLA) alleles
19 gies produced a draft nuclear genome of 36.1 Mb, organized into 321 scaffolds with L50 of 31 and N50
20 OH classes with different sizes (Small 0.5-1 Mb, Medium 1-5 Mb and Large >5 Mb), the numbers and tota
21 ssembly of C. salicifolius, comprising 820.1 Mb of genomic sequence with a contig N50 of 2.3 Mb and c
22 he gyrA and parC loci are positioned about 1 Mb away from each other.
23 ed to a 35-kb region and was approximately 1 Mb away from Pl(17), flanked by SNP markers C4_6676629 a
24  one of the two genes in the approximately 1 Mb interval and the only gene disruption shared between
25 uencing to fine map it to an approximately 1 Mb interval.
26 oidies and copy-number variants (CNVs) at ~1 Mb resolution.
27  associations, and that long-range eQTMs (>1 Mb) are reduced when controlling for tissue/muscle fiber
28 expression quantitative trait loci (eQTL; <1 Mb from TSS, FDR < 1%).
29                   All have small genomes (<1 Mb) characteristic of parasitic species and dramatically
30 ct with smoking were in close vicinity (</=1 Mb) to SNPs previously associated with IBD; many were lo
31     We identified 32 rare CNVs larger than 1 Mb in 31 patients.
32  gains and losses of 17p11.2, occur up to ~1 Mb away from the breakpoint junctions, and favor C > G t
33 antly associated genes were located within 1 Mb of known GWAS-identified loci and were not significan
34 dy weight, and residual feed intake within 1 Mb of significant SNPs.
35 r kg fat (n = 47) that were located within 1 Mb of significant SNPs.
36 and 59 NMP-linked indels within a single 1.1-Mb nonrecombining region on chromosome I.
37 e - a single recessive gene located in a 1.1-Mb region on chromosome 2.
38 t of genetic variance accounted for by any 1-Mb window indicated that viral neutralization antibody l
39                      The top associations (1-Mb windows) were located on 7 chromosomes.
40                             A total of six 1-Mb windows were associated with greater than 1% of the g
41                               Although six 1-Mb windows were identified as associated with 1% or grea
42                              Twenty unique 1-Mb genomic windows were associated with BW1, BW35 or BW4
43 ssociated with methylations of as much as 10 Mb from the promoters or more, and the long-range methyl
44        M. glaziovii alleles on the distal 10 Mb of chr. 1 increased dry matter and root number.
45      We found 160 individuals that carry >10 Mb copy number changes, including 56 with whole chromoso
46 highly concordant with large-scale (order 10 Mb) features of previously reported genetic maps for mou
47 his genetic map enabled the anchoring of 100 Mb of WGS and 420 Mb of BAC sequences, an exploration of
48 s occupying 74 Mb of the A subgenome and 104 Mb of the D subgenome, and identified 19 candidate loci
49 ded to cover 50% of the genome [N50] = 18.11 Mb mainly on 8 pseudomolecules) and Trigoniulus corallin
50  chromosome (SSC) 2 (154-157 Mb), 7 (107-110 Mb), 8 (4-6 Mb), and 10 (8-19 Mb).
51                   These CG-DMRs comprise ~12 Mb of the genome that is highly enriched for genomic reg
52 ome assemblies, of which sizes vary from 120 Mb to 3.5 Gb.
53 e for S. baicalensis where 93% of the 408.14-Mb genome has been assembled into nine pseudochromosomes
54 er than 2.5 Mb, and scaffolds longer than 15 Mb.
55  species with haploid genome assemblies ~150 Mb are among the largest in Agaricales, and we found tha
56 ts on Sus scrofa chromosome (SSC) 2 (154-157 Mb), 7 (107-110 Mb), 8 (4-6 Mb), and 10 (8-19 Mb).
57    Like many draft genomes, however, the 158-Mb Spirodela genome sequence has not been resolved to ch
58  chromosome 3 (236 Mb) and chromosome 9 (162 Mb), and 53 Mb of the Ab10 meiotic drive haplotype.
59 mposed of 63 contigs and a contig N50 of 162 Mb.
60             The study demonstrated that a 17-Mb long 129P1 genomic region on mouse chromosome 7 confe
61 kage analysis identified an approximately 18 Mb disease-associated locus on chromosome 4 (maximal log
62 elicorthomorpha holstii (assembly size = 182 Mb; shortest scaffold/contig length needed to cover 50%
63 b), 7 (107-110 Mb), 8 (4-6 Mb), and 10 (8-19 Mb).
64                 One selects specific 0.1-0.2 Mb high molecular weight DNA targets with custom-designe
65 with a final assembled genome size of 1013.2 Mb and a contig N50 of 3.3 Mb.
66 usly mapped to a gene cluster spanning a 3.2 Mb region at the upper end of sunflower chromosome 4.
67 e pseudochromosomes with a super-N50 of 33.2 Mb.
68 is the identification of an inversion of 4.2 Mb among landraces and cultivars, which includes a gene
69                                    The 761.2 Mb sequences (45 scaffolds with an N50 of 29.8 Mb) are a
70 pseudochromosomes with a total size of 843.2 Mb.
71 panded the C. elegans reference genome by >2 Mb due to a more accurate determination of repetitive se
72 y of large clonal autosomal mosaic events >2 Mb in size in the aging population.
73 ed for the study of mid-range (e.g., 20 kb-2 Mb for human genome) intra-chromosomal contacts; however
74 re positioning because many of its large ( 2 Mb) centromeres are not dominated by satellite DNA.
75 ormatics analysis, from a window frame of ~2 Mb containing 314 SNPs, we obtain imputation accuracy (r
76      In addition to TBX4, the overlapping ~2 Mb recurrent and nonrecurrent deletions at 17q23.1q23.2
77 cluding a large topologically associated 1.2-Mb domain conserved in humans and mice that encompasses
78 e 4727 deposited genomic trajectories of a 2-Mb-long chromatin interval from human chromosome 21.
79              We used it to interrogate the 2-Mb POU5F1 locus in human embryonic stem cells, and ident
80            On chr. 4, introgressions in a 20 Mb region improved harvest index and brown streak diseas
81 that this cancer phenotype is linked to a 20 Mb region of 129P2 chromosome 15 harboring the Wnt7b gen
82 the presence and absence variants of over 20 Mb, one of which is a circum-basmati-specific deletion o
83 le allowed a unique shared haplotype of 1.22 Mb to be defined around this locus.
84 0.5 to 66 Mb, with an average length of 1.22 Mb.
85 udes gapless assemblies of chromosome 3 (236 Mb) and chromosome 9 (162 Mb), and 53 Mb of the Ab10 mei
86 b of the estimated almond genome size of 238 Mb, of which 91% is anchored to eight pseudomolecules co
87 over 50% of the known genome (NG50) up to 25 Mb and phased ~99.5% of heterozygous sites at 98-99% acc
88 ng effect on maintenance of H3K27me3 in a 26 Mb region around the locus, demonstrating cell type-spec
89 s single fly genome assembly has a N50 of 26 Mb, a length that encompasses entire chromosome arms, co
90 alysis and homozygosity mapping defined a 26-Mb candidate region in canine chromosome 20.
91 udicots with a relatively small genome ( 260 Mb).
92 e merged into 978 CNV regions, spanning ~262 Mb of total length and corresponding to ~8.96% of the go
93 e-scale A. paniculata genome sequence of 269 Mb that was assembled by Illumina short reads, PacBio lo
94 Despite possessing the smallest genome (0.27 Mb) of any organism not subsisting within a host cell, t
95  genomic regions on SSC 1 (87-91 and 282-287 Mb) and 5 (67 Mb) were identified.
96 ciation study (GWAS), which identified a 1.3 Mb disease-associated region on canine chromosome 33, fo
97 -throughput STARR-seq to test the entire 1.3 Mb human and mouse TBX3 locus, including two cardiac con
98 d in Amaranthus palmeri is approximately 1.3 Mb with 121 predicted gene models.
99 of genomic sequence with a contig N50 of 2.3 Mb and containing 36 651 annotated protein-coding genes.
100 me size of 1013.2 Mb and a contig N50 of 3.3 Mb.
101  a mouse model of autism that duplicates 6.3 Mb region of chromosome 7 (Dp/+) corresponding to a regi
102 me assembly for P. dactylifera that is 772.3 Mb in length, with contig N50 of 897.2 Kb, and use this
103 g data from a single MinION flowcell, a 90.3 Mb nuclear genome was assembled into 202 contigs with an
104 rate that parents transmitting the de novo 3 Mb LCR22A-D 22q11.2 deletion, the reciprocal duplication
105 ctivity of cis-regulatory elements in over 3 Mb of genome sequence.
106  deletions, relative to those with typical 3 Mb deletions.
107 whether any of the other 29 genes in the 1.3-Mb M-locus are also needed for complete sex-conversion.
108 egans, piRNA loci are clustered within two 3-Mb regions on chromosome IV.
109     The assemblies show a contig N50 of 6.32 Mb and 10.53 Mb for Basmati 334 and Dom Sufid, respectiv
110                     Here, we present its 326 Mb genome, assembled to high contiguity (N50: 9.88 Mb) w
111 nd assembled the pomegranate genome with 328 Mb anchored into nine pseudo-chromosomes and annotated 2
112 e also identified coldspots encompassing 329 Mb, or [Formula: see text] of observable genome, in whic
113 dreae has a drastically smaller genome (1.34 Mb) than the symbiont's free-living relatives (4.29-4.97
114 calling and phase block lengths up to N50 34 Mb.
115 tate, while the distal enhancer located 1.35 Mb from the promoter induces CCL5 expression in activate
116    Our assembly has a scaffold N50 of 223.35 Mb, with 19 scaffolds containing 95% of the genome.
117                                      The 353 Mb genome contains 35 597 predicted protein-coding genes
118 the smallest genome size in the genus at 357 Mb and has a reduced set of predicted protein-coding gen
119 me of T. wilfordii with a contig N50 of 4.36 Mb.
120  genome assembly with a total size of 695.36 Mb and a draft genome assembly of Calycanthus chinensis.
121 osome 11 modifier but instead harbors an ~37 Mb region containing non-B6-derived segments on chromoso
122       We identify >300,000 eRNA loci in ~377 Mb super-enhancer regions that are regulated by evolutio
123             Linked-Reads allow mapping to 38 Mb of sequence not accessible to short reads, adding seq
124 ach revealed 634 novel regions covering ~398 Mb of the human genome and harbouring ~9000 genes.
125 enetic Schwann-cell disorder featuring a 1.4 Mb chromosomal duplication.
126                     The duplication of a 1.4 Mb segment surrounding this gene in chromosome 17p12 (c1
127 ological insights that emerge from this 17.4 Mb genome, we find an unexpected diploid structure for m
128  sweeps covering, respectively, 11.0 and 2.4 Mb of the P. avium genome.
129 ssembled into 202 contigs with an N50 of 2.4 Mb.
130                                           4) Mb heme insertion was significantly increased in cells t
131                             Except for a 2.4-Mb unequal chromosome translocation in watercress, both
132 n this study, we report a high-quality 313.4-Mb genome sequence of a bottle gourd inbred line, USVL1V
133                            Trkin lies in a 4-Mb region of Ab10 that is not syntenic with any other re
134 says, targeting the BRCA1 gene, the entire 4-Mb major histocompatibility complex locus and 18 well-ch
135 eles and are furthermore embedded within ~40 Mb of minimally recombining repetitive DNA.
136 The scaffold N50 for this assembly was 43.41 Mb and the annotation yielded 56,469 genes.
137 abled the anchoring of 100 Mb of WGS and 420 Mb of BAC sequences, an exploration of genetic diversity
138              Among them, approximately 71.43 Mb of novel CNVRs were detected in the Chinese cattle po
139 ore frequently and are undergone by 14% (430 Mb) of the human genome.
140 ientation (TDDOs) ranging from 60 kb to 1.44 Mb.
141             Its rapid life cycle, small (440-Mb) genome, and advanced germplasm resources make birch
142 e assembled a total length of 1.536 Gbp, 444 Mb and 527 Mb of which were assigned to the canephora an
143  Trigoniulus corallinus (assembly size = 449 Mb, N50 = 26.78 Mb mainly on 17 pseudomolecules).
144                    Enhancers within the 1.45 Mb cluster exhibit highly synergistic activity that is d
145 ogenitor development at distances up to 1.45 Mb.
146 vated accession of white lupin (2n = 50, 451 Mb), as well as de novo assemblies of a landrace and a w
147 ome sequencing and analysis suggested a 9.47 Mb genome size with 42 predicted biosynthetic gene clust
148 ompared to those of 1.04 Mb for B73 and 1.48 Mb for Mo17.
149  different sizes (Small 0.5-1 Mb, Medium 1-5 Mb and Large >5 Mb), the numbers and total lengths of RO
150 ly greater in 22q11DS cases with smaller 1.5 Mb deletions, relative to those with typical 3 Mb deleti
151  reciprocal duplication, and the smaller 1.5 Mb LCR22A-B 22q11.2 deletion carry inversions of LCR22B-
152 ng these previous findings, we sequenced 1.5 Mb of the PDE4D genomic locus in 20 families (consisting
153 hed both at short (<500 kb) and longer (>1.5 Mb) genomic distances.
154 ic distance range ( approximately 700 kb-1.5 Mb), while interactions involving actively marked DNase
155 een the X and the Y spans approximately 17.5 Mb on the X chromosome.
156 14) and female (n = 938) carriers of 0.8-2.5 Mb duplications spanning STS, and non-carrier male (n =
157 er than 100 kb, phase blocks longer than 2.5 Mb, and scaffolds longer than 15 Mb.
158                           We designed a 20.5 Mb array targeting coding and regulatory regions of gene
159 embled Han Chinese genomes and detected 29.5 Mb novel genomic sequences and at least 188 novel protei
160   The interacting loci cover a total of ~3.5 Mb of the human genome.
161                                 At only 32.5 Mb, the genome is the smallest yet reported for any arth
162 enced the genomes of T. cruzi Y strain (35.5 Mb) and three benznidazole-resistant clones derived from
163 rs the ability to visualize up to thirty 4.5 Mb DNA sequences simultaneously using one of five suppor
164 rom which an algorithm-guided 192-member 4.5 Mb library is built.
165  (Small 0.5-1 Mb, Medium 1-5 Mb and Large >5 Mb), the numbers and total lengths of ROH per individual
166 iated multi-megabase deletions of the Slx (5 Mb) and Slxl1 (2.3Mb) ampliconic regions result in post-
167 ing RNA (mencRNA) genes transcribed from 1.5-Mb intervals surrounding 139 breast cancer GWAS signals
168 oma, we find that T is associated with a 1.5-Mb region containing 'super-enhancers' and is the most h
169  Of these DMCs, 52% were located in one 15.5-Mb locus on chromosome 13, which encompassed the Bhmt ge
170 ns separated by large genomic distances (>50 Mb) have yet to be characterized.
171 localize to large genomic regions (e.g., >50 Mb), mapped regions are well defined for RV-NPL.
172  reorganization including the removal of ~50 Mb from thousands of loci called internal eliminated seq
173 ing the Agilent SureSelect Human all Exon 51 Mb version 5 capture kit.
174 omosus var. bracteatus CB5 and assembled 513 Mb into 25 chromosomes with 29,412 genes.
175                               A total of 519 Mb is included in the assembled sequences.
176  of S. tora at the chromosome level with 526 Mb (96%) assembled into 13 chromosomes.
177  a total length of 1.536 Gbp, 444 Mb and 527 Mb of which were assigned to the canephora and eugenioid
178 blies show a contig N50 of 6.32 Mb and 10.53 Mb for Basmati 334 and Dom Sufid, respectively.
179 3 (236 Mb) and chromosome 9 (162 Mb), and 53 Mb of the Ab10 meiotic drive haplotype.
180 mbled a high-quality genome sequence of ~542 Mb and found that retrotransposon proliferation contribu
181                   GALNT6 resides at least 55 Mb away from any previously identified glioma risk varia
182  (Oncorhynchus mykiss) and characterize a 55-Mb double-inversion supergene that mediates sex-specific
183                    The genome size was 32.57 Mb, and 14 contigs ranging from 0.35 to 4.58 Mb with an
184 Mb, and 14 contigs ranging from 0.35 to 4.58 Mb with an N50 of 2.86 Mb were assembled, including 4 co
185  210 kb region on chromosome 11 (50.37-50.58 Mb, mm10) containing two protein-coding genes (Hnrnph1,
186 riants, which overall account for nearly 580 Mb of DNA sequence not included in the reference genome
187 sorder caused by hemizygous deletion of ~1.6 Mb affecting 26 genes on chromosome 7 (7q11.23) and is c
188 inantly inverted and separated by up to ~1.6 Mb, an extraordinary distance for homology-based DNA rep
189 We obtained a genome assembly totaling 227.6 Mb of the estimated almond genome size of 238 Mb, of whi
190 (SSC) 2 (154-157 Mb), 7 (107-110 Mb), 8 (4-6 Mb), and 10 (8-19 Mb).
191 several contigs, with combined length of 4.6 Mb and with 147 gene models, were identified as belongin
192 e constructed directed assemblies of the 4.6 Mb E. coli genome, 48.5 kb lambda genome, and a represen
193 rols from a research colony determined a 4.6 Mb locus on canine chromosome 32.
194 ents involving up to 65 breakpoints and 60.6 Mb across four chromosomes, further defining rare catego
195                 In addition, we discover ~60 Mb of non-redundant genome content missing in the refere
196 curvula have been obtained by sequencing 602 Mb of a diploid genotype using a strategy that combined
197      However, a novel region on BTA20 (55-63 Mb) for SCK2 was also identified, which was not reported
198  map was also successfully extended from 658 Mb to 969 Mb by assigning unplaced scaffolds to the pseu
199 s varied considerably ranging from 0.5 to 66 Mb, with an average length of 1.22 Mb.
200                          In addition, a 1.67 Mb inversion is highly associated with fruit shape, and
201 ns on SSC 1 (87-91 and 282-287 Mb) and 5 (67 Mb) were identified.
202     Two combinatorial libraries totaling 0.7 Mb were constructed: An expression library of 6 partial
203             Correspondingly, carriers of 1.7 Mb BP1-BP5 rearrangements that encompass both the BP2-BP
204 EMISH to human lymphoblastoid cells at a 1.7 Mb segment of the genome and visualize a large number of
205 line, USVL1VR-Ls, with a scaffold N50 of 8.7 Mb and the longest of 19.0 Mb.
206 to haplotype contigs with N50 greater than 7 Mb.
207 s cohesin-driven RAG scanning across the 2.7-Mb Igh locus.
208  Mb and a total size, in chromosomes, of 726 Mb, which has been corroborated by a high-resolution lin
209 scanned 93 domestication sweeps occupying 74 Mb of the A subgenome and 104 Mb of the D subgenome, and
210 plex gene family, the DNA sequence of a 1.75-Mb genomic region spanning the Gli-2 locus was analyzed
211 sis showed that these children shared a 4.76 Mb region of homozygosity on chromosome 1, with an ident
212  was achieved for 99.5% of the targeted 1.77-Mb region.
213 allinus (assembly size = 449 Mb, N50 = 26.78 Mb mainly on 17 pseudomolecules).
214 nd its distal enhancer cluster residing ~1.8 Mb downstream.
215 8% identity to N2 but with an additional 1.8 Mb including tandem repeat expansions and genome duplica
216 ssembly is 1.71 Gb long, with an N50 of 16.8 Mb and L50 of 24.
217 omes containing 76 contigs (N50 contig = 2.8 Mb).
218   Recombination hotspots occur once per 23.8 Mb on average and account for ~9% of the physical map le
219  sequences (45 scaffolds with an N50 of 29.8 Mb) are assembled into 26 pseudochromosomes.
220 core genome is estimated to converge at 39.8 Mb (8.67% of the genome).
221 16), which depends on contraction of the 2.8-Mb-long immunoglobulin heavy chain (Igh) locus by Pax5(1
222 llowing, for example, the detection of a 7.8-Mb inversion on Chromosome 12 underlying ecological adap
223 ing from 0.35 to 4.58 Mb with an N50 of 2.86 Mb were assembled, including 4 contigs with telomeric se
224                                      The 865-Mb gypsy moth genome is the largest Lepidoptera genome s
225 roximity guided assembly to generate a 15.87 Mb assembly of the Y chromosome.
226 oximately 1.2-Gb genome (scaffold N50 = 1.88 Mb) with at least 26 723 predicted genes for E. ulmoides
227 ome, assembled to high contiguity (N50: 9.88 Mb) with 23 chromosomes on 24 scaffolds.
228  insertions, in aggregate accounting for 1.9 Mb of sequence absent from the GRCh38 reference.
229 hogenic or likely pathogenic CNVs (0.08-18.9 Mb).
230 sed genomic coverage across the 670 cM/352.9 Mb cherry whole genome sequence.
231  the region of high-confidence calls by 68.9 Mb.
232  with 392 traits and diseases, covering 73.9 Mb (2.2%) of the human genome.
233 onsensus sequencing reads, an additional 8.9 Mb of DNA sequence was mappable, variant calling achieve
234                                    The 264.9-Mb assembly contains nine chromosomal pseudomolecules wi
235 ng-by-sequencing analyses and identify a 3.9-Mb genomic interval where the lavender variant resides.
236                                      The 926-Mb Oncopeltus genome is well represented by the current
237 lso successfully extended from 658 Mb to 969 Mb by assigning unplaced scaffolds to the pseudo-chromos
238  symbiont's free-living relatives (4.29-4.97 Mb) but retains a versatile and energy-efficient metabol
239 le a high-quality genome (contig N50 of 6.99 Mb) of the apple anther-derived homozygous line HFTH1, i
240                                We identify a Mb-scale genomic region present in weedy rice but not cu
241 g of alpha,beta-unsaturated aldehydes affect Mb oxidation and the onset of lipid oxidation are discus
242                               alphaLA-RL and Mb-RL form surfactant-saturated complexes above 5.6 and
243  to promote heme insertion into immature apo-Mb, and thus generate functional Mb during muscle myotub
244 on of C2C12 myoblasts into myotubes, the apo-Mb-hsp90 complex associates with 5 cell cochaperons, Hsp
245  Hsp90 drives heme insertion into apoprotein-Mb in an ATP-dependent process.
246 es being separated by tens of million bases (Mb) along genomic sequence show a significantly higher t
247 ve a N50 contig length of 7.7 million bases (Mb) directly from long-read assembly, compared to those
248  highest recombination rates of 0.26-0.27 cM/Mb.
249                               In conclusion, Mb significantly decreased blood pressure in hypertensiv
250 gG and its small-molecular-weight derivative Mb.
251 and increase in BMI by 0.14 kg/m(2) for each Mb of total deletion burden (P = 2.5 x 10(-10), 6.0 x 10
252 ttern that is consistent with their enabling Mb maturation.
253 NE and HHE (4-hydroxy-2-hexenal) facilitated Mb-mediated lipid oxidation similarly.
254                                          For Mb-RL, the analysis gives complexes of two connected mic
255 ctly interacts preferentially with heme-free Mb both in purified form and in cells.
256 mmature apo-Mb, and thus generate functional Mb during muscle myotube formation.
257                           Results using H97A Mb suggested that the combination of HNE and low hemin a
258 ed a role for heat shock protein (hsp) 90 in Mb maturation in C2C12 skeletal muscle myoblasts and cel
259 ius prefactors associated with CO binding in Mb and Hb.
260              These SNP loci were detected in Mb-scale haplotype blocks and may be close to the functi
261                   Melicoccus bijugatus Jacq (Mb) has been reported to have cardiovascular modulatory
262 rmation-based contacts at high (Kb) and low (Mb) genomic resolutions.
263  of individuals with the typical 3 megabase (Mb) deletion from LCR22A-D have congenital heart disease
264 d sequencing method for generating megabase (Mb)-scale haplotypes with short reads.
265 e genome with a contig N50 of >15 megabases (Mb) and concordance of 99.997%, substantially outperform
266 ed QTL, ranging from 47.4 to 64.4 megabases (Mb) on chromosome 7.
267 anchor loci that may be dozens of megabases (Mb) apart, as well as inter-chromosomal links.
268  more mut/Mb versus TMB of fewer than 10 mut/Mb (median, 7.1 v 2.6 months).
269 , < 1%, 47%) versus TMB of fewer than 10 mut/Mb (n = 50: PD-L1, >= 1%, 18%; PD-L1, < 1%, 5%), and pro
270 eauing at 10 or more mutations/megabase (mut/Mb).
271 al burden (TMB) >=10 mutations/megabase (mut/Mb)] and larotrectinib/entrectinib (NTRK fusions).
272 igher in patients with TMB of 10 or more mut/Mb (n = 48: PD-L1, >= 1%, 48%; PD-L1, < 1%, 47%) versus
273 onger in patients with TMB of 10 or more mut/Mb versus TMB of fewer than 10 mut/Mb (median, 7.1 v 2.6
274                        TMB of 10 or more mut/Mb was associated with improved response and prolonged p
275 ations/Mb), intermediate (5.5-19.5 mutations/Mb), and high (>= 19.5 mutations/Mb).
276 ups based on TMB level: low (< 5.5 mutations/Mb), intermediate (5.5-19.5 mutations/Mb), and high (>=
277 5 mutations/Mb), and high (>= 19.5 mutations/Mb).
278                            TMB (in mutations/Mb) was significantly higher among smokers vs nonsmokers
279                                   Myoglobin (Mb) maturation involves heme incorporation as a final st
280 ing in other heme systems such as myoglobin (Mb) and hemoglobin (Hb).
281         Peptides originating from myoglobin (Mb) and myosin (My) were analyzed using multiple reactio
282                Electroanalysis of myoglobin (Mb) in 10 plasma samples of healthy donors (HDs) and 14
283  structure or redox properties of myoglobin (Mb).
284 ertensive effects and mechanism of action of Mb on N(G)-Nitro-L-arginine Methyl Ester (L-NAME) and De
285                     More uniform contents of Mb markers were found in raw beef cuts, and for My marke
286                           Aqueous extract of Mb fruit (100 mg/kg) was administered for 6 weeks to rat
287 idation more readily than oxidative forms of Mb that retain their protoporphyrin moiety.
288                   The MS signal intensity of Mb marker peptides in raw pork depended significantly on
289 rs of magnitude larger than the prefactor of Mb and Hb ( approximately 10(9) s(-1)).
290                               A 3:1 ratio of Mb:Hb promoted lipid oxidation similarly compared to add
291  similarly compared to adding a 1:1 ratio of Mb:Hb to washed muscle.
292 despite sometimes being separated by tens of Mb along the genomic sequence than those belonging to di
293 nfer loops averaging 0.8-1.0 megabase pairs (Mb) in early prophase and extending to 1.5-2.0 Mb in lat
294 an genomes and recover 33-79 megabase pairs (Mb) of duplications in which approximately half of the l
295 proliferative fitness ( approximately 3% per Mb), slowed tumor growth, and reduced metastatic progres
296 64)Cu-NODAGA-PSMA-IgG and (64)Cu-NODAGA-PSMA-Mb retained the ability to bind cell surface PSMA, and b
297 ansverse sections of the ventricles from the Mb group did not show abnormalities.
298 ains or losses of greater than or equal to10 Mb.
299 hanced lipid oxidation compared to wild-type Mb exposed to HNE.
300            The potential mechanisms by which Mb binding of alpha,beta-unsaturated aldehydes affect Mb

 
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