戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1  as a cluster spanning a region of 619 kb on chromosome 22.
2  the most proximal pericentromeric region of chromosome 22.
3 duplications (> or = 1 kb and > or = 90%) on chromosome 22.
4 ene were identified from a cosmid library of chromosome 22.
5 hinery, and recombination hot spots on human chromosome 22.
6 ave constructed a map of 2,730 SNPs on human chromosome 22.
7 lymorphism markers on both chromosome 11 and chromosome 22.
8 he sequence of the euchromatic part of human chromosome 22.
9 11;22) breakpoints on both chromosome 11 and chromosome 22.
10 didates for other diseases that map to human chromosome 22.
11 reading frame in genomic sequence from human chromosome 22.
12 from adult brain library, that was mapped to chromosome 22.
13 ociated with the loss of genetic material on chromosome 22.
14 cardiac defects have hemizygous deletions of chromosome 22.
15  heterozygosity of the surrounding region of chromosome 22.
16  developed to localize loci subregionally on chromosome 22.
17 n studies and transcription mapping of human chromosome 22.
18 DGS patients are hemizygous for a portion of chromosome 22.
19 n mapped to this deleted (22q11.2) region of chromosome 22.
20 positional cloning of disease loci mapped to chromosome 22.
21 ce panel, and spanning the entirety of human chromosome 22.
22 4882, P = 2.73 x 10-7), intronic to SEZ6L on chromosome 22.
23  entire rDNA array end-to-end from a copy of chromosome 22.
24 a collection of pre-computed gRNAs for human chromosome 22.
25  hemizygous deletion of a 1.5-3 Mb region of chromosome 22.
26 ss of the whole, or part of the long arm, of chromosome 22.
27 cytidine deaminase genes is present on human chromosome 22.
28 ived sample, using SNP markers spaced across chromosome 22.
29 ee with established gene annotation on human chromosome 22.
30 scriptional activity of pseudogenes on human chromosome 22.
31 esponding to the intergenic regions of human chromosome 22.
32 tion/deletion polymorphism, located on human chromosome 22.
33 with the poor drug-metabolizing phenotype on chromosome 22.
34 and ABL, to form an aberrant BCR-ABL gene on chromosome 22.
35  analyses did not support the observation on chromosome 22.
36 a second-generation gene annotation of human chromosome 22.
37 ying a difference in the meiotic behavior of chromosome 22.
38 hromosomal microdeletions in the q11 band of chromosome 22.
39 h the loci of the DiGeorge syndrome on human chromosome 22.
40 t of LD along the complete sequence of human chromosome 22.
41 in smokers only, the maximum LOD was 2.08 at chromosome 22.
42 ed APOBEC3A to 3G), are arrayed in tandem on chromosome 22.
43 ed evolutionary segments) with 157 copies on chromosome 22.
44 athogenic variants affecting the long arm of chromosome 22 (22q) result in meningiomas in neural-cres
45 ) mice, which model a microdeletion on human chromosome 22 (22q11.2) that constitutes one of the larg
46 ial syndrome results from a microdeletion on chromosome 22 (22q11.2).
47 fort to localize a novel tumor suppressor on chromosome 22, a psv2neo tagged human chromosome 22 was
48  provide evidence, using alignments of human chromosome 22 against a five-species alignment from the
49 t of the complete human genomic sequences of chromosome 22 allowed us to select 29 genes for this ana
50  chromosomal translocation occurring between chromosome 22 and (in most cases) chromosome 11, which g
51 hylation at 52 CpG sites, with 48 located on chromosome 22 and 18 in the vicinity of APOL1-4 and MYH9
52 ch, we accurately mapped >400 breakpoints on chromosome 22 and a region of chromosome 11, refining th
53 the assembly of physical maps and contigs of chromosome 22 and assist in positional cloning of diseas
54 nally significant association between UPD of chromosome 22 and autism risk, we do not find significan
55 alleles, for markers above the breakpoint on chromosome 22 and below the breakpoint on chromosome 11,
56 nalyze the complete sequence data from human chromosome 22 and compare microsatellite repeat distribu
57 ons and deletions (3 Mb to 18 kb) located on chromosome 22 and even a homozygous deletion smaller tha
58 at the conserved intergenic regions in human chromosome 22 and mouse appear to have evolved from thei
59                     Genes on the long arm of chromosome 22 and near the neurofibromatosis type 2 (NF2
60 myosin heavy chain 9 gene (MYH9) variants on chromosome 22 and nondiabetic nephropathy in African Ame
61 ressed sequence tag (EST) contigs with human chromosome 22 and with a non-redundant set of mRNA seque
62       We identified areas of homozygosity on chromosome 22 and, subsequently, PLA2G6 mutations.
63 a balanced chromosomal translocation between chromosomes 22 and 12, is considered the definitional fe
64 ly sequenced rDNAs to reference sequence for chromosomes 22 and 21 revealed variants that are shared
65 en, IL-1beta and IL-18, which are encoded on chromosomes 22 and 24, respectively.
66 chromosome 21 is more homogeneous than human chromosome 22, and bacterial genomes may not be homogene
67 s, the breakpoints on both chromosome 11 and chromosome 22 are clustered in multiple unrelated famili
68 lipoprotein L1 (APOL1 [OMIM 603743]) gene on chromosome 22 are common in individuals of West African
69 sis I in the proximal region of the affected chromosome 22 as the likely etiology for the deletion.
70 are genes on chromosome 13q, and possibly on chromosome 22 as well, that influence the susceptibility
71 tergenic, transcriptionally active region of chromosome 22, as the recipient site, to provide robust,
72           Suggestive linkage was detected on chromosome 22 at 27-29 cM in each sample, with a LOD sco
73 E1 (rs7099485, p(meta) = 1.48 x 10(-8)), and chromosome 22 at CHEK2 = 1.47 x 10(-9)).
74 ized by a hemizygous deletion of 1.5-3 Mb on chromosome 22 at locus 11.2, is the most common microdel
75  hybrid mapping, the MCT3 gene was mapped to chromosome 22 between markers WI11639 and SGC30687.
76 ip), we have identified the regions of human chromosome 22 bound by STAT1 and STAT2 in interferon-tre
77                                          The chromosome 22 breakpoint disrupts the 3' coding region o
78 genomic breakpoint junctions showed that the chromosome 22 breakpoints fell in BCR introns whereas th
79 coding gene has five exons and is located on chromosome 22 but has not been correctly identified by e
80  22; this translocation leads to a shortened chromosome 22, called the Philadelphia chromosome.
81 s deletion of a 1.5- to 3-megabase region on chromosome 22 causes 22q11.2 deletion syndrome (22q11DS)
82          A clathrin homolog encoded on human chromosome 22 (CHC22) displays distinct biochemistry, di
83 date genes that lie within the q11 region of chromosome 22 commonly deleted in DGS patients have been
84               We have created a resource for chromosome 22 consisting of 96 unique, well-characterize
85 d an ADCC gene in this family to a region of chromosome 22 containing three beta-crystallin genes.
86                             We observed that chromosome 22 contains regions of early- and late-replic
87 h imputed SNPs, the authors then apply it to chromosome 22 data from the Mexico City Childhood Asthma
88 pendent tests by the permutation analysis on chromosome 22 data.
89 sis revealed that 1p LOH was associated with chromosome 22 deletions and with abnormalities of the NF
90 nship between psychiatric illness, VCFS, and chromosome 22 deletions, we evaluated 26 VCFS patients b
91 d other small insertions/deletions) of human chromosome 22, discovered in the overlaps of 460 clones
92 cipitation and a genomic microarray of human chromosome 22 DNA.
93 eport the generation of a dense map of horse chromosome 22 (ECA22) comprising 83 markers, of which 52
94 formed in the entire published 34.9-Mb human chromosome 22 euchromatic sequence.
95 ndent sequence variants in the APOL1 gene on chromosome 22 {FSGS odds ratio = 10.5 [95% confidence in
96 ated the function of Gas2-related protein on chromosome 22 (GAR22beta), a poorly characterized protei
97 mily (SLC5) that was first identified by the chromosome 22 genome project.
98                     An analysis of the human chromosome 22 genomic sequence shows that both Z-DNA for
99 h both the molecular and clinical aspects of chromosome 22 genomic variations.
100 arge percentage exhibit heterozygous loss of chromosome 22 (harboring the NF2 gene) and functional in
101 e evolutionary origin of the duplications on chromosome 22 has been assessed by FISH analysis of non-
102 inhibitor of metalloproteinases-3 (TIMP3) on chromosome 22 has been identified as a gene that is muta
103                  Likewise, the breakpoint on chromosome 22 has been localized within an ATRR that is
104                     NF2 gene inactivation on chromosome 22 has been shown as an early event in tumori
105                 Since the entire sequence of chromosome 22 has now been identified, the study of VCFS
106 sults provide additional evidence that human chromosome 22 has undergone multiple small-scale and lar
107 s cryptic deletions of the q11 band of human chromosome 22 have been associated with a number of psyc
108 10 (MMU10) show conserved synteny with human chromosome 22 (HSA22) and the telomeric region of HSA21.
109              We performed a linkage study of chromosome 22 in 200 families with AS affected sibling-p
110 LH1 foci, localize to the distal long arm of chromosome 22 in 75% of human spermatocytes tested, also
111            To conclude, we uncovered loss of chromosome 22 in almost half of all cases with hybrid ne
112 lity was recently linked to polymorphisms on chromosome 22 in individuals of African descent.
113 human iPLA2 gene has been found to reside on chromosome 22 in region q13.1 and to contain 16 exons re
114                        The top result was on chromosome 22 in SYN3 at rs2710383 (p-value = 4.6 x 10(-
115                                  A search of chromosome 22 in the Sanger Centre database confirmed th
116  used to examine the two separated copies of chromosome 22 in the somatic hybrid cell lines.
117                          Instead, the normal chromosome 22 in these probands showed interchromosomal
118 resolution along an entire human chromosome (chromosome 22) in two different cell types.
119    22qDS is caused by a microdeletion in one chromosome 22, including DGCR8, an essential gene for mi
120 aracterized by a number of gene deletions in chromosome 22, including the chicken tumor virus number
121              Overall, 10.8% (3.7/33.8 Mb) of chromosome 22 is duplicated, with an average sequence id
122             Evidence that a gene or genes on chromosome 22 is involved in susceptibility to schizophr
123 condition caused by a hemizygous deletion on chromosome 22-is associated with an elevated risk of psy
124 ecombination between the low copy repeats on Chromosome 22 (LCR22s).
125                                          The Chromosome 22 LCRs (LCR22s) mediate nonallelic homologou
126 st year have focused on genomic disorders of chromosome 22, little progress has been made in the impl
127 atterns linked to an area on the long arm of chromosome 22, localizing the gene encoding this minor H
128 contrast, meningiomas with mutant NF2 and/or chromosome 22 loss were more likely to be atypical, show
129 tic methods, we found significant linkage on chromosome 22 (maximum heterogeneity logarithm of odds s
130  cleft palate, hypocalcemia, associated with chromosome 22 microdeletion) syndrome, exhibit craniofac
131               The location of CLTCL on human chromosome 22 near the region commonly deleted in DiGeor
132                                           On chromosome 22, newly acquired and recurrent deletions of
133 1-CHUK on chromosome 10 and PNPLA3-SAMM50 on chromosome 22), one locus influencing gamma-glutamyl tra
134                       The trisomic region on chromosome 22 overlaps the region hemizygously deleted i
135 ntrols and identified an associated locus on chromosome 22 (p = 1.2 x 10(-6), passing Bonferroni corr
136                                              Chromosome 22, particularly band 22q11.2, is predisposed
137                  The sequence of the larger, chromosome 22 PATRR deduced from junction fragments has
138 ublication of the complete sequence of human chromosome 22 provides a platform from which to investig
139                        Finally, we find that chromosome 22 pseudogene population is dominated by immu
140 sequenced: the BAC DNA aligns with the human chromosome 22 reference sequence except for a 75-kb regi
141                              We identified a chromosome 22 region with a genome-wide logarithm of the
142   The method has been tested on 98 BACs from chromosome 22 regions where large-scale sequencing is un
143 a patient with BSS who has a deletion on one chromosome 22, resulting in velocardiofacial syndrome.
144 - to 3-megabase hemizygous deletion on human chromosome 22, results in dramatically increased suscept
145 aining all of the nonrepetitive DNA of human chromosome 22 revealed 215 binding sites corresponding t
146                                          The Chromosome 22 Sequencing Consortium estimated a minimum
147  We have found that Fosmid clones from human chromosome 22 show remarkable stability and are useful f
148                     In adults, three SNPs on chromosome 22 showed associations with histological para
149                      The map consists of 613 chromosome 22-specific BAC clones that have been localiz
150                        The identification of chromosome 22-specific duplicated sequences or low copy
151 s of the q arm of the chromosome by means of chromosome 22-specific yeast artificial chromosome clone
152 can be observed in patients with deletion of chromosome 22 syndrome, the immune pathogenesis of this
153                      Inspection of the human chromosome 22 syntenic region identified the proapoptoti
154                                 The genes on chromosome 22 that exhibited interferon-induced up- or d
155  a novel tumor suppressor locus (or loci) on chromosome 22 that is important in ovarian cancer tumori
156 as also tested for predicting genes of human Chromosome 22 (the last variant of Fgenesh can analyze t
157                                          For chromosome 22, the authors had data on 7,293 SNPs that w
158                           PURPOSE OF REVIEW: Chromosome 22, the first human chromosome to be complete
159 utside the typically deleted region of human chromosome 22 to fully recapitulate the deletion 22q11 p
160 es of all potential NF-kappaB sites on human chromosome 22, together with the effects of known single
161                    Two hundred nine (21%) of chromosome 22 transcripts participated in 77 cis-antisen
162              First, we analyzed 61 loci from chromosome 22, using the complete sequence of this chrom
163  nearly all of the unique sequences of human Chromosome 22 was constructed and used to measure global
164                            While the loss of chromosome 22 was seen in approximately half of all thes
165 sor on chromosome 22, a psv2neo tagged human chromosome 22 was transferred into the malignant epithel
166  that the 88% of manually annotated exons in Chromosome 22 were among the ab initio predicted exons.
167 diation hybrid, and integrated maps of human chromosome 22 were compared with their corresponding pos
168 novo calls, while highly concordant calls on chromosome 22 were validated by quantitative PCR.
169             The gene for human EPI64 lies on chromosome 22 where nine exons specify a protein of 508
170 ene has been mapped to the 22q11.2 region of chromosome 22 which was deleted from one chromosome of t
171 abetes variance (logarithm of odds = 3.4) on chromosome 22, which overlaps a positive type 2 diabetes
172 , we are following up our linkage results on chromosome 22 with a dense map of >1,500 single-nucleoti
173  the first step toward identifying a gene on chromosome 22 with an influence on common myopia.
174   A construct with an alphoid DNA array from chromosome 22 with no detectable CENP-B motifs formed mi

 
Page Top