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1 the most proximal pericentromeric region of chromosome 22.
2 duplications (> or = 1 kb and > or = 90%) on chromosome 22.
3 ene were identified from a cosmid library of chromosome 22.
4 hinery, and recombination hot spots on human chromosome 22.
5 ave constructed a map of 2,730 SNPs on human chromosome 22.
6 lymorphism markers on both chromosome 11 and chromosome 22.
7 he sequence of the euchromatic part of human chromosome 22.
8 11;22) breakpoints on both chromosome 11 and chromosome 22.
9 didates for other diseases that map to human chromosome 22.
10 reading frame in genomic sequence from human chromosome 22.
11 hemizygous deletion of a 1.5-3 Mb region of 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 ss of the whole, or part of the long arm, of chromosome 22.
22 cytidine deaminase genes is present on human chromosome 22.
23 ived sample, using SNP markers spaced across chromosome 22.
24 ee with established gene annotation on human chromosome 22.
25 scriptional activity of pseudogenes on human chromosome 22.
26 esponding to the intergenic regions of human chromosome 22.
27 tion/deletion polymorphism, located on human chromosome 22.
28 with the poor drug-metabolizing phenotype on chromosome 22.
29 and ABL, to form an aberrant BCR-ABL gene on chromosome 22.
30 analyses did not support the observation on chromosome 22.
31 a second-generation gene annotation of human chromosome 22.
32 ying a difference in the meiotic behavior of chromosome 22.
33 hromosomal microdeletions in the q11 band of chromosome 22.
34 h the loci of the DiGeorge syndrome on human chromosome 22.
35 t of LD along the complete sequence of human chromosome 22.
36 in smokers only, the maximum LOD was 2.08 at chromosome 22.
37 ed APOBEC3A to 3G), are arrayed in tandem on chromosome 22.
38 ed evolutionary segments) with 157 copies on chromosome 22.
39 as a cluster spanning a region of 619 kb on chromosome 22.
40 ) mice, which model a microdeletion on human chromosome 22 (22q11.2) that constitutes one of the larg
42 fort to localize a novel tumor suppressor on chromosome 22, a psv2neo tagged human chromosome 22 was
43 provide evidence, using alignments of human chromosome 22 against a five-species alignment from the
44 t of the complete human genomic sequences of chromosome 22 allowed us to select 29 genes for this ana
45 chromosomal translocation occurring between chromosome 22 and (in most cases) chromosome 11, which g
46 ch, we accurately mapped >400 breakpoints on chromosome 22 and a region of chromosome 11, refining th
47 the assembly of physical maps and contigs of chromosome 22 and assist in positional cloning of diseas
48 alleles, for markers above the breakpoint on chromosome 22 and below the breakpoint on chromosome 11,
49 nalyze the complete sequence data from human chromosome 22 and compare microsatellite repeat distribu
50 ons and deletions (3 Mb to 18 kb) located on chromosome 22 and even a homozygous deletion smaller tha
51 at the conserved intergenic regions in human chromosome 22 and mouse appear to have evolved from thei
53 myosin heavy chain 9 gene (MYH9) variants on chromosome 22 and nondiabetic nephropathy in African Ame
54 ressed sequence tag (EST) contigs with human chromosome 22 and with a non-redundant set of mRNA seque
56 a balanced chromosomal translocation between chromosomes 22 and 12, is considered the definitional fe
58 chromosome 21 is more homogeneous than human chromosome 22, and bacterial genomes may not be homogene
59 s, the breakpoints on both chromosome 11 and chromosome 22 are clustered in multiple unrelated famili
60 sis I in the proximal region of the affected chromosome 22 as the likely etiology for the deletion.
61 are genes on chromosome 13q, and possibly on chromosome 22 as well, that influence the susceptibility
62 tergenic, transcriptionally active region of chromosome 22, as the recipient site, to provide robust,
65 ized by a hemizygous deletion of 1.5-3 Mb on chromosome 22 at locus 11.2, is the most common microdel
67 ip), we have identified the regions of human chromosome 22 bound by STAT1 and STAT2 in interferon-tre
69 genomic breakpoint junctions showed that the chromosome 22 breakpoints fell in BCR introns whereas th
70 coding gene has five exons and is located on chromosome 22 but has not been correctly identified by e
72 s deletion of a 1.5- to 3-megabase region on chromosome 22 causes 22q11.2 deletion syndrome (22q11DS)
74 date genes that lie within the q11 region of chromosome 22 commonly deleted in DGS patients have been
76 d an ADCC gene in this family to a region of chromosome 22 containing three beta-crystallin genes.
78 h imputed SNPs, the authors then apply it to chromosome 22 data from the Mexico City Childhood Asthma
80 sis revealed that 1p LOH was associated with chromosome 22 deletions and with abnormalities of the NF
81 nship between psychiatric illness, VCFS, and chromosome 22 deletions, we evaluated 26 VCFS patients b
82 d other small insertions/deletions) of human chromosome 22, discovered in the overlaps of 460 clones
84 eport the generation of a dense map of horse chromosome 22 (ECA22) comprising 83 markers, of which 52
86 ndent sequence variants in the APOL1 gene on chromosome 22 {FSGS odds ratio = 10.5 [95% confidence in
87 ated the function of Gas2-related protein on chromosome 22 (GAR22beta), a poorly characterized protei
91 e evolutionary origin of the duplications on chromosome 22 has been assessed by FISH analysis of non-
92 inhibitor of metalloproteinases-3 (TIMP3) on chromosome 22 has been identified as a gene that is muta
96 sults provide additional evidence that human chromosome 22 has undergone multiple small-scale and lar
97 s cryptic deletions of the q11 band of human chromosome 22 have been associated with a number of psyc
98 10 (MMU10) show conserved synteny with human chromosome 22 (HSA22) and the telomeric region of HSA21.
100 LH1 foci, localize to the distal long arm of chromosome 22 in 75% of human spermatocytes tested, also
103 human iPLA2 gene has been found to reside on chromosome 22 in region q13.1 and to contain 16 exons re
108 aracterized by a number of gene deletions in chromosome 22, including the chicken tumor virus number
111 st year have focused on genomic disorders of chromosome 22, little progress has been made in the impl
112 atterns linked to an area on the long arm of chromosome 22, localizing the gene encoding this minor H
113 contrast, meningiomas with mutant NF2 and/or chromosome 22 loss were more likely to be atypical, show
114 tic methods, we found significant linkage on chromosome 22 (maximum heterogeneity logarithm of odds s
115 cleft palate, hypocalcemia, associated with chromosome 22 microdeletion) syndrome, exhibit craniofac
118 1-CHUK on chromosome 10 and PNPLA3-SAMM50 on chromosome 22), one locus influencing gamma-glutamyl tra
122 ublication of the complete sequence of human chromosome 22 provides a platform from which to investig
124 sequenced: the BAC DNA aligns with the human chromosome 22 reference sequence except for a 75-kb regi
126 The method has been tested on 98 BACs from chromosome 22 regions where large-scale sequencing is un
127 a patient with BSS who has a deletion on one chromosome 22, resulting in velocardiofacial syndrome.
128 - to 3-megabase hemizygous deletion on human chromosome 22, results in dramatically increased suscept
129 aining all of the nonrepetitive DNA of human chromosome 22 revealed 215 binding sites corresponding t
131 We have found that Fosmid clones from human chromosome 22 show remarkable stability and are useful f
135 s of the q arm of the chromosome by means of chromosome 22-specific yeast artificial chromosome clone
136 can be observed in patients with deletion of chromosome 22 syndrome, the immune pathogenesis of this
139 a novel tumor suppressor locus (or loci) on chromosome 22 that is important in ovarian cancer tumori
140 as also tested for predicting genes of human Chromosome 22 (the last variant of Fgenesh can analyze t
143 utside the typically deleted region of human chromosome 22 to fully recapitulate the deletion 22q11 p
144 es of all potential NF-kappaB sites on human chromosome 22, together with the effects of known single
147 nearly all of the unique sequences of human Chromosome 22 was constructed and used to measure global
149 sor on chromosome 22, a psv2neo tagged human chromosome 22 was transferred into the malignant epithel
150 that the 88% of manually annotated exons in Chromosome 22 were among the ab initio predicted exons.
151 diation hybrid, and integrated maps of human chromosome 22 were compared with their corresponding pos
154 ene has been mapped to the 22q11.2 region of chromosome 22 which was deleted from one chromosome of t
155 abetes variance (logarithm of odds = 3.4) on chromosome 22, which overlaps a positive type 2 diabetes
156 , we are following up our linkage results on chromosome 22 with a dense map of >1,500 single-nucleoti
158 A construct with an alphoid DNA array from chromosome 22 with no detectable CENP-B motifs formed mi
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