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1 he Dlk1 gene as a new imprinted gene that is paternally expressed.
2 IGF2, a fetal-specific growth factor that is paternally expressed.
3 e evidence suggesting that this locus may be paternally expressed.
4 signed to 7q32 and shown to be imprinted and paternally expressed.
5 15 ancient imprinted genes, of which 10 were paternally expressed.
6 ing antisense transcript, Kcnq1ot1, which is paternally expressed.
7 ns and a common promoter, and both genes are paternally expressed.
8 PEG3 gene, including a novel transcript, are paternally expressed.
9 e sequencing of cDNA libraries to identify 9 paternally expressed and 34 maternally expressed imprint
10 ur results demonstrate that Pref-1 is indeed paternally expressed and is important for normal develop
11 insulin-like growth factor II (IGF2) gene is paternally expressed and is surrounded by maternally exp
14 ow that the region contains a promoter for a paternally expressed anti-sense transcript, Kcnq1ot1, an
16 alleles in normal tissues, where the IGF2 is paternally expressed, as well as in normal liver where g
20 PN maps to human chromosome 15q11-q13 and is paternally expressed, each cistron is a candidate for a
21 oduction; extralarge G(s)alpha (XLalphas), a paternally expressed G(s)alpha isoform; and neuroendocri
22 olute carrier family 38 member 4), and Peg1 (paternally expressed gene 1)--both MBD1 and H3K9me3 bind
23 actor receptor-bound protein 10), Peg1/Mest (paternally expressed gene 1/mesoderm-specific transcript
24 -/- cells showed aberrant methylation of the paternally expressed gene 3 (Peg3) tumor suppressor gene
26 tment of breast carcinoma xenografts induces paternally expressed gene 3 (Peg3), an imprinted gene en
28 hin 3 maternally methylated imprinted genes: paternally expressed gene 3 (PEG3), insulin-like growth
30 ICR (Imprinting Control Region) of the Peg3 (Paternally Expressed Gene 3) domain contains an unusual
31 ation status of the CpG islands of the PEG3 (Paternally expressed gene 3) imprinted domain in the mou
34 (H19 fetal liver mRNA), p57(Kip2), Peg3/Pw1 (paternally expressed gene 3), and Zac1 (zinc finger-bind
38 e previously identified Peg1/Mest as a novel paternally expressed gene in the developing mouse embryo
40 determined that Pw1 is identical to Peg3, a paternally expressed gene of unknown function (and will
41 osome 6q, believed to contain an exclusively paternally expressed gene or genes that cause transient
42 d the expression and methylation status of a paternally expressed gene Peg3, in germ cells from sex-r
43 LK1 (delta, Drosophila, homolog-like 1) is a paternally expressed gene that encodes for a transmembra
44 mprinting disorder caused by a deficiency of paternally expressed gene(s) in the 15q11-q13 chromosoma
45 stigate the role of the maternally imprinted/paternally expressed gene, Peg3, in several aspects of b
49 ernally expressed genes (Igf2r, H19) and two paternally expressed genes (Igf2, U2af1-rs1) in ES cells
50 ressed genes (MEGs) and approximately 29% of paternally expressed genes (PEGs) in C. rubella were com
51 the mechanism by which PWS-IC activates the paternally expressed genes (PEGs) using transgenes that
52 ic crosses, whereas approximately 90% of 272 paternally expressed genes (PEGs) were found only in one
53 162 maternally expressed genes (MEGs) and 95 paternally expressed genes (PEGs), which were associated
54 and H3K36me3 peaks mostly co-localized with paternally expressed genes (PEGs), while endosperm-speci
56 ssed genes, activated expression of silenced paternally expressed genes and resulted in methylation o
57 er-Willi syndrome (PWS) is caused by loss of paternally expressed genes at an imprinted locus on chro
58 oter regions and transcriptional termini and paternally expressed genes at promoters and gene bodies,
59 sults from loss of function of 10 clustered, paternally expressed genes in a 1.5-Mb region of chromos
60 -Willi syndrome (PWS) is caused by a loss of paternally expressed genes in an imprinted region of chr
61 y the inactivation or deletion of imprinted, paternally expressed genes in chromosome band 15q11.2.
62 nomic alterations that inactivate imprinted, paternally expressed genes in human chromosome region 15
63 the two parental alleles of SNRPN and other paternally expressed genes in the region by using a chro
67 PWS is caused by the loss of one or more paternally expressed genes on chromosome 15q11-q13, whic
68 located adjacent to a cluster of imprinted, paternally expressed genes that are known to be positive
70 Mash2, Kvlqt1, and p57(Kip2), as well as two paternally expressed genes, Igf2 and Ins2, and assess th
71 e required for the genomic imprinting of two paternally expressed genes, Ins-2 (encodes insulin-2) an
72 mplete abolition of the transcription of two paternally expressed genes, Peg3 and Usp29, causing the
73 ched for coexpressed pairs of maternally and paternally expressed genes, showed accelerated expressio
74 PWS involves loss of function of multiple paternally expressed genes, while mutations in a single
81 nts in which the expression of all the known paternally expressed Gnasxl proteins (XLalphas, XLN1 and
85 o the mouse, the human IGF2-P0 transcript is paternally expressed; however, its expression is not lim
87 played a paternal-specific enrichment at the paternally expressed Igf2 locus, H3K79me3 was paternally
88 ation and has been recently reported to be a paternally expressed imprinted gene at human chromosome
89 ternally methylated region associated with a paternally expressed imprinted gene, Ras protein-specifi
90 ically examine the functional requirement of paternally expressed imprinted genes (PEGs) during seed
92 -regulated expression of both maternally and paternally expressed imprinted genes and microRNAs, incl
94 CI in the trophectoderm, rather than loss of paternally expressed imprinted genes, is the primary cau
96 ess contain different doses of maternally or paternally expressed imprinted loci affecting endosperm
97 rs, certain noncoding RNAs, and generally to paternally expressed imprinted loci, but not paternally
98 associated with overexpression of genes at a paternally expressed imprinted locus on chromosome 6q24.
100 is normally caused by deficiency of several paternally expressed imprinted transcripts within chromo
101 PWS) is caused by deficiency for one or more paternally expressed imprinted transcripts within chromo
110 i syndrome (PWS) is caused by the absence of paternally expressed, maternally silenced genes at 15q11
112 transcript is the candidate for Oed and the paternally expressed mutant Gnasxl transcript is the can
113 y juxtaposed maternally expressed (Nesp) and paternally expressed (Nespas, Gnasxl, Exon 1A) transcrip
114 ron 10 of Kcnq1, contains the promoter for a paternally expressed, noncoding, antisense transcript, K
115 on the frequency of the favored allele: the paternally expressed pattern permits faster genetic chan
117 now been shown to target degradation of the paternally expressed Peg11 mRNA by an RNAi-mediated mech
120 some, is necessary for the repression of the paternally expressed protein-coding genes and for activa
121 ified on distal chromosome 12 contains three paternally expressed protein-coding genes and multiple n
128 hromosome 7 recently identified Inpp5f_v2, a paternally expressed retrogene lying within an intron of
129 dystonic symptoms and caused by mutations in paternally expressed SGCE, which codes for epsilon-sarco
130 r RNAs (snoRNAs) encoded within the complex, paternally expressed SNRPN (small nuclear ribonuclear pr
135 cation in mouse of four brain-specific novel paternally expressed transcripts and an additional three
136 unlike its positive effect on all the other paternally expressed transcripts in the region, the PWS-
137 anonymous transcript, PAR-5, are two of the paternally expressed transcripts mapped to the Prader-Wi
138 associated with Igf2 and Igf2r both contain paternally expressed transcripts that act as enhancers o
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