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1 aturation is controlled by a separate QTL on chromosome 2.
2 ome 1 of V. anguillarum 775(pJM1) and two in chromosome 2.
3 1 and found some evidence for another QTL on chromosome 2.
4 s) is linked to an inversion polymorphism on chromosome 2.
5 ed by ref(2)P and is caused by other loci on chromosome 2.
6 syndrome (DRS) linked to the DURS2 locus on chromosome 2.
7 of five SCPL genes arranged in a cluster on chromosome 2.
8 us was minimally affected by the presence of chromosome 2.
9 major QTL on chromosome 3 and a minor QTL on chromosome 2.
10 ty 6 [MOB6]) and 84-180 Mb (MOB5) from mouse chromosome 2.
11 due to the presence of the SLC11A1 locus on chromosome 2.
12 linkage, for both CAD and MI, to a region on chromosome 2.
13 AML) is characterized by loss of one copy of chromosome 2.
14 e carriers to map ADANE to a 6.5Mb region on chromosome 2.
15 s spanning more than 55 kb of genomic DNA on Chromosome 2.
16 nt of DiGeorge syndrome, was mapped to mouse chromosome 2.
17 converted to the corresponding sequences of chromosome 2.
18 genes are contiguous and localized on mouse chromosome 2.
19 26 intergenes in a 68-kb region of S. pombe chromosome 2.
20 luster of putative Eppin-like genes on mouse chromosome 2.
21 tion of AAGAG repeats near the distal tip of chromosome 2.
22 c contribution to variance in life span from chromosome 2.
23 nd resulted in a maximum LOD score of 3.4 on chromosome 2.
24 oughout chromosome 1 and one binding site in chromosome 2.
25 gulated principally by the Hc locus on mouse chromosome 2.
26 4% of the predicted genes and pseudogenes on chromosome 2.
27 the nine IL-1 family genes that lie on human chromosome 2.
28 h occupy an approximately 400-kb interval on chromosome 2.
29 and sheath blight disease resistance on rice chromosome 2.
30 f the causal mutations to a narrow region in chromosome 2.
31 ocated in one of the runs of homozygosity on chromosome 2.
32 lex rearrangement involving the short arm of chromosome 2.
33 etic analyses assigned the bs locus to mouse chromosome 2.
34 ) for rs9679290 in the EPAS1 (HIF2A) gene on chromosome 2.
35 s a mutant allele of the Gata3 gene on mouse Chromosome 2.
36 ta = -0.23) at the integrin, alpha 4 gene on chromosome 2.
37 of five microsatellite markers from proximal Chromosome 2.
38 around the site of ancestral fusion in human chromosome 2.
39 rg) within a shared haplotype of 2.93 Mbp on chromosome 2.
40 and mapping localized the critical region to Chromosome 2.
41 Snn2, which mapped to the short arm of wheat chromosome 2D.
42 ops tauschii contains W2 and Iw2 paralogs on chromosome 2D.
43 and three of these were designated as marker chromosomes 2.
44 speciation, and additional candidate loci on chromosomes 2 (079 and 175) and 3 (088) are discovered t
47 or nine) IBK scores showed that locations on chromosomes 2, 12, 13 and 21 were associated with IBK di
51 the tip with the centric heterochromatin of chromosome 2 (2h), which contains megabases of AAGAG rep
52 conducted for trisomics for the left arm of chromosome 2 (2L) and compared with the normal genotype.
53 of the Rf alleles mapped to the long arm of chromosome 2 (2L), and 5 of these were further mapped to
55 /= 3) were detected at 33-42 centimorgans of chromosome 2 (2p24.3-2p24.1), with a maximum LOD score o
57 solution deletion mapping of the long arm of chromosome 2 (2q) in invasive cervical carcinoma (CC).
61 al new significant or suggestive QTLs on rat chromosomes 2, 3, 7, 10, and 19 that control susceptibil
64 data suggest that quantitative trait loci on chromosomes 2, 3, 9, and 10 may influence circulating ad
65 he SR region spans more than half of the mat chromosome (>2.3 Mbp) and that it is of very recent orig
68 n new prostate cancer susceptibility loci on chromosomes 2, 4, 8, 11 and 22 (with P = 1.6 x 10(-8) to
70 ur findings provide evidence that regions of chromosomes 2, 4, and 12 influence the development and p
71 tified four quantitative trait loci (QTL) on chromosomes 2, 4, and 8, with the QTL on chromosome 8 sh
72 o isolate large centromeric regions of human chromosomes 2, 5, 8, 11, 15, 19, 21 and 22 from human ce
73 trate the approach using root-growth QTLs on chromosomes 2, 5, and 9 of the Bala x Azucena rice mappi
75 me 1 (93% of the tumor cell lines analyzed), chromosome 2 (53%), chromosome 6 (73%), chromosome 7 (80
76 25-family data set, including two regions on chromosome 2 (57 Mb, NPL = 2.98; 145 Mb, NPL = 3.09), as
80 . C. thermophilum genome was composed of two chromosomes (2,683,362 bp and 1,012,010 bp), and both en
81 i for influenza virus resistance) located on chromosomes 2, 7, 11, 15, and 17 associated with resista
83 We find that all four HOX gene clusters on chromosomes 2, 7, 12, and 17 are preferential targets fo
84 ogous POTE family genes are found on 8 human chromosomes (2, 8, 13, 14, 15, 18, 21 and 22), which can
85 e been found dispersed among eight different chromosomes (2, 8, 13, 14, 15, 18, 21, and 22) with pres
88 ) and two QTLs (qSNAX.2 A.1, qSNAX.2 A.2) on chromosome 2 A coincided with a reported major NAX QTL (
91 , all CAI-4 strains tested were trisomic for chromosome 2 although this trisomy appears to be unstabl
93 llion base pairs of the Adh-cactus region of chromosome 2 and 85,000 base pairs of the 82F region of
94 A significant, protective modifier locus on chromosome 2 and a suggestive locus on chromosome 13 tha
95 (Mcs1), is located on the centromeric end of chromosome 2 and appears to act in a semidominant fashio
97 lines, we mapped Moo1 to an 8-Mb segment of chromosome 2 and demonstrated that Moo1 exerts its effec
98 ferase 1 (UGT1) locus spans nearly 200 kb on chromosome 2 and encodes nine UGT1A proteins that play a
101 i (top SNPs: rs76114856 in the CENPO gene on chromosome 2 and rs6669072 near LOC105378853 on chromoso
103 t percent of these ESTs were present on rice chromosome 2 and the remaining were on other rice chromo
105 y conserved flanking Npdc1 and Abca2 loci on chromosome 2 and which contains the complete transcripti
106 he frequency of polymorphisms across the two chromosomes (2 and 3) examined most extensively, with an
109 ) with chromosome 12 (LOD 5.03 at 35 cM) and chromosomes 2 and 12 for FEF(25-75%)/FVC (LOD 4.12 at 22
111 OXO1, resulting from a translocation between chromosomes 2 and 13, is the most common genetic aberrat
112 ant (P < .01) polymorphic loci were found on chromosomes 2 and 16 for liver and on chromosomes 8 and
114 al mapping identified new angiogenic QTLs on chromosomes 2 and 19, in addition to confirming our prev
116 el' for the evolution of rice (Oryza sativa) chromosomes 2 and 3, implying that the grass common ance
117 identified 18 A. gambiae SRPN genes, all on chromosomes 2 and 3, through searches of genomic DNA and
121 tenic with duplicated regions of Arabidopsis chromosomes 2 and 4, none of which harbor CLV1 or any ot
123 ave identified two modifying loci on C57BL/6 chromosomes 2 and 5, which affect the penetrance of embr
126 emonstrate consistent evidence of linkage to chromosomes 2 and X and also support the hypothesis that
129 HOSPHO1, SYNGAP1 and an intergenic region in chromosome 2) and triglycerides (MYLIP, TXNIP and SLC7A1
130 re linked to the X chromosome, 16 markers to chromosome 2, and 10 and 11 markers to chromosomal arms
131 ately 237 million base pairs of sequence for chromosome 2, and 186 million base pairs for chromosome
132 rotein-coding genes and 1,239 pseudogenes on chromosome 2, and 796 protein-coding genes and 778 pseud
133 onary TNF-alpha production was identified on chromosome 2, and a region affecting both polymorphonucl
135 nking radiation-sensitive fragile domains on chromosome 2, and subsequent R235 conversion are highly
136 ave suggested that polymorphisms in CASP8 on chromosome 2 are associated with breast cancer risk.
137 wo ancestral chromosomes fused to form human chromosome 2 are duplicated elsewhere in the human genom
138 dicate at least 50% of hypothetical genes on chromosome 2 are expressed in the cDNA populations with
140 e-long region of the Drosophila melanogaster chromosome 2 as a model, we observed that the six gene-p
141 reased gene amplication in the distal arm of chromosome 2, as shown by comparative genomic hybridizat
143 study (GWAS) detected a significant peak on chromosome 2 associated with the polygenic component of
146 ral regions of suggestive linkage for CFPWV: chromosome 2 at 94 cM (LOD=2.46), chromosome 7 at 29 cM
147 subjects (logarithm of odds [LOD] = 3.4) on chromosome 2 at 95 cM (between GATA69E12 and GATA71G04)
148 l GWS association (1.17 x 10(-10)) mapped to chromosome 2 at rs1437396, between MTIF2 and CCDC88A, ac
149 sociations with homoarginine serum levels on chromosome 2 at the carbamoyl phosphate synthetase I loc
150 cting oocyst density were identified: one on chromosome 2 between markers AG2H135 and AG2H603 and the
151 nt in NCAM1 (chromosome 11) and a variant on chromosome 2 (between TEX41 and PABPC1P2) that has a tra
152 een recombination map positions 54 and 81 on chromosome 2, between 0 and 30 on chromosome 3, and near
153 initiator of replication of Vibrio cholerae chromosome 2 (chr2), binds to the origin of replication
155 QTL) regulating Scg5 expression in two mouse chromosome 2 congenic strains and three additional F2 in
156 iterpenoid phytoalexins, with the cluster on chromosome 2 containing four closely related/homologous
157 to possess crop haplotypes in the portion of chromosome 2 containing the ACETOLACTATE SYNTHASE gene,
161 y QTL in the 36E;38B cytogenetic interval on chromosome 2 contains multiple closely linked QTLs, incl
162 These data support evidence for a gene on chromosome 2 contributing to risk of AutD, and they sugg
163 aps near a quantitative trait locus (QTL) on chromosome 2 controlling ear rank differences between ma
164 ven its strong effect, the linkage region on chromosome 2 could harbor a potentially important determ
169 t for the phytocassanes, is not found in the chromosome 2 diterpenoid biosynthetic gene cluster.
171 because we could define a critical region in chromosome 2 encoding eight genes including BMP10 that c
174 Only markers from the centromeric tip of Chromosome 2 failed to segregate independently from jal,
176 sis, two marker chromosomes 1 and two marker chromosomes 2 formed bivalents, whereas the others were
177 nzee pericentric inversion and the ancestral chromosome 2 fusion both predisposed and protected the c
179 g place Bhlhb4 at the telomeric end of mouse chromosome 2 (H3-H4), syntenic to human chromosome 20q13
181 sequences totalling approximately 2 Mb from chromosome 2 have been duplicated and inserted into chro
182 ells were previously stably transferred with chromosome 2 (HCT116+chr2), restoring a single regulated
183 linkage for the ratio FEV1/FVC was found on chromosome 2 (heterogeneity lod = 2.36, dominant model)
185 d TMEM18 and regions downstream of TMEM18 on chromosome 2 in 3976 individuals of European ancestry fr
186 locus (QTL), Tmc1m1, for DPOAE amplitude on chromosome 2 in [(C/B)F1xC]N2-Tmc1Bth/+ backcross progen
187 he GRD3 family was acquired more recently on chromosome 2 in a lineage of N. tomentosiformis, the pat
190 of Iw1 has >94% identity to an IR region on chromosome 2 in Ae. tauschii that also produces miRW1 an
191 by alternative splicing of a gene located on chromosome 2 in humans, and orthologs of CRIP1a occur th
194 carry a nonreciprocal translocation on human chromosome 2, in which synchronized double stranded brea
195 ain 2 quantitative trait loci: the region on chromosome 2 included the C5 fraction of complement know
196 us work has shown that the presence of human chromosome 2 increases HIV-1 production in mouse cells.
199 gene trees supports genetic introgression of chromosome 2 inversions between An. gambiae and An. arab
201 as been observed that a major QTL, se2.1, on chromosome 2 is responsible for a large portion of pheno
203 ncreased capsid production in the absence of chromosome 2, it did not result in a corresponding incre
205 led disruption of a single noncoding gene on chromosome 2, LINC00299, whose RNA product is expressed
206 yotyping shows gross abnormalities involving chromosome 2 (location of the FRZB gene) in five of twel
207 eterozygosity (LOH) was detected only at the chromosome 2 locus in all tumors from this family, consi
211 or linkage also was robust for FEV(1)/FVC on chromosome 2 (LOD 4.13 at 229 cM) and FEV(1) on chromoso
212 in addition to strong evidence of linkage to chromosome 2 (LOD=4.9), also produced a LOD of 2.4 on ch
214 tative evidence of linkage was also found on chromosomes 2 (LOD = 1.7 at 89 cM), 3 (LOD = 1.9 at 124
217 construction for (1) genome-wide or multiple chromosomes, (2) multi-allelic and (3) extremely sparse
220 ariants all map to a novel genetic region on chromosome 2 near the ASB3 gene, a region associated wit
221 CN and carrier FRE) mapped to the region of chromosome 2 near the candidate gene fruitless, identify
222 aches link VEGF responsiveness to regions on chromosomes 2 (near D2Mit6) and 10 (near D10Mit20).
224 velopment were recently mapped to the NOR on chromosome 2, NOR2, whereas active rRNA genes map to NOR
225 ease 2-like 1; P=5.7x10(-15)) and a locus on chromosome 2 (not near known genes) were associated with
227 as well as 163 other genes from one copy of chromosome 2 occurred in a hematopoietic stem cell (HSC)
228 howed that body weight (BW) loci on proximal chromosome 2 occurred in the same region as body length,
229 e cryptic (fla2) flagellar system encoded on chromosome 2 of B. thailandensis supported rapid intrace
232 mpact imprinted Gnas cluster on distal mouse chromosome 2, one at exon 1A upstream of Gnas itself and
233 25% of the tumors displayed either a gain of chromosome 2 or loss of Y, the majority (75%) showed no
234 lso identified mouse (chromosome 3) and rat (chromosome 2) orthologues, as well as two human paralogu
236 5-5.02]) and rs9309464 in the EXOC6B gene on chromosome 2 (p = 6.01 x 10(-5); G allele OR 0.66 [95% C
238 arker D10S189) and the centromeric region of chromosome 2 (peak lod score of 2.99 at marker D2S139).
239 ith highly significant linkage were found on chromosomes 2 (Pgis2) and 18 (Pgis1) accounting for 40%
242 (positive) or chromosome 7 (negative); this chromosome 2 region has been implicated elsewhere in stu
243 ingle-nucleotide polymorphisms (SNPs) in the chromosome 2 region that included the Frizzled-related p
244 of 62 pheochromocytomas with LOH within the chromosome 2 region, which further narrowed down the loc
245 nstrated definitively that a locus on murine chromosome 2 regulates hematopoietic stem cell aging.
246 his system the presence of Sd on one copy of chromosome 2 results in dysfunction of the non-Sd-bearin
251 are referred to as "hypothetical genes." On chromosome 2, sequenced by The Institute for Genomic Res
254 condensin subunit, structural maintenance of chromosomes 2 (SMC2), in unextracted metaphase chromosom
255 The admixture mapping signal identified on chromosome 2, spanning q11.2-14.1 and not previously rep
257 polar spindle structures around unreplicated chromosomes; 2) sperm nuclei added to extracts that cycl
259 ngs of nonrandom distribution of SNPs across chromosome 2, suggest that the Plasmodium falciparum gen
260 scriptional hotspot of vir genes observed on chromosome 2 suggests a potential active site modulating
261 ne integrations into the same locus on mouse chromosome 2 targeting a gene that is expressed in the n
262 genes in the 45A region on the right arm of chromosome 2 that are involved in oogenesis in Drosophil
264 ficant quantitative trait locus was found on chromosome 2 that could not be confirmed in congenic mic
266 gs strongly suggest that there is a locus on chromosome 2 that influences coronary atherosclerosis ri
267 F in the rat is influenced by a locus on rat chromosome 2 that is also associated with cardiac capill
268 dominant suppressors, in the cases tested on chromosome 2 the suppressor mapped to the 2L telomere, r
269 uding (1) the folding patterns of individual chromosomes; (2) the highly enriched interactions betwee
271 antly reduced fork arrest at the Ter site on chromosome 2, thereby revealing a cooperative mechanism
272 rected by one or more genes present on human chromosome 2 to allow production of infectious HIV from
273 in by introgression of a segment of C57BL/6J chromosome 2 to the BALB/c background to confirm the gen
274 veying the panel of strains with substituted chromosomes; (2) to rapidly develop congenic strains ove
275 t linkage to AMD was found for one marker on chromosome 2, two adjacent markers on chromosome 3, two
276 d 2005 revealed that the V. parahaemolyticus chromosome 2 type III secretion system is not specifical
277 QTL) for fruit firmness was mapped to tomato chromosome 2 using the Zamir Solanum pennellii interspec
279 single-nucleotide polymorphism (SNP) loci on chromosome 2 was common to all affected sheep and it was
283 low frequency of an interstitial deletion of chromosome 2) was similar to that of the previous transg
284 3), which is 20 kb upstream of CXCR7 gene on chromosome 2, was associated with the total mean FA valu
285 rs from all of the 797 hypothetical genes on chromosome 2 were designed, and, through 5' and 3' RACE,
286 lymorphisms (SNPs) across STAT1 and STAT4 on chromosome 2 were genotyped using the Illumina platform,
289 t (IL-1RN), are present at a single locus on chromosome 2, whereas IL-18 and IL-33 lie on chromosomes
291 region exhibiting conserved synteny to human chromosome 2, which included one of the three dilute can
292 icrosatellite loci within the j inversion on chromosome 2, which is fixed in the Bamako form but abse
293 o the UBCS pattern found in all autosomes is chromosome 2, which shows a UBCS peak midchromosome, map
294 ed many associations with genomic regions in chromosome 2 with also the highest explained variation c
295 asis for association of the PARK11 region of chromosome 2 with familial Parkinson disease (PD) is unk
296 with a maximum model-free LOD score of 2.2; chromosome 2, with a LOD score of 2.1; chromosome 6, wit
298 ss a 40Kb region of Drosophila pseudoobscura chromosome 2, with one 20kb interval assayed every 5Kb a
299 ithm of odds [LOD] 4.53) was a broad peak on chromosome 2, with weaker linkage to age of type 2 diabe
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