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1 PTPN1 is located in 20q13, a genomic region linked to ty
2 ein tyrosine phosphatase nonreceptor type 1 (PTPN1) and PTPN2, whose expression is significantly high
4 We replicated the ADO-EGR2, IRF8, and CEBPB-PTPN1 loci by genotyping 969 Iranian cases and 826 contr
5 ee new risk loci, IL1A-IL1B, IRF8, and CEBPB-PTPN1, with genome-wide significance (P < 5 x 10(-8)) by
7 the first intron of the PTP1B encoding gene PTPN1, correlating with an AR-mediated increase in RNA p
8 erase reporter assay revealed that the genes PTPN1, HOXA1, and TP53I11 were miR-210 target genes regu
9 ee single nucleotide polymorphisms (SNPs) in PTPN1 were genotyped and assessed for association with I
12 with SNPs spanning the 3' end of intron 1 of PTPN1 through intron 8 (P values ranging from 0.043 to 0
14 ast, there is no evidence for association of PTPN1 polymorphisms with acute insulin response (a measu
16 hed the AR as a transcriptional regulator of PTPN1 transcription and implicated PTP1B in a tumor-prom
17 ilibrium encompassing the coding sequence of PTPN1 were significantly associated with CorCP (P values
19 effects of miR-210, coordinate silencing of PTPN1, HOXA1, and TP53I11 dramatically decreased tumor c
20 phosphatases, five of which - DUSP6, PPTC7, PTPN1, PTPN13 and PPP3CA - promote differentiation by ne
22 The protein-tyrosine phosphatase 1B (PTP1B; PTPN1) is an important regulator of mammalian metabolism
24 re coamplified in metastatic tumors and that PTPN1 amplification was associated with a subset of high
30 yrosine phosphatase (PTP)-1B, encoded by the PTPN1 gene, catalyzes the dephosphorylation of proteins
31 ms (SNPs) spanning 161 kb and containing the PTPN1 gene were genotyped and tested for association.
32 0.1 in a single haplotype block covering the PTPN1 genomic sequence show significant association with
34 DNA arrays to genotype 6 SNP markers in the PTPN1 gene and 10 mutations in the cystic fibrosis trans
39 response of CML cells to imatinib treatment: PTPN1, NF1, SMARCB1, and SMARCE1, and 5 regulators of th
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