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■ Abbreviation / Long Form : MT / mutant type

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Total Number of Papers: 31
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Abbreviation:   MT  (>> Co-occurring Abbreviation)
Long Form:   mutant type
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No. Year Title Co-occurring Abbreviation
2020 A novel mutation in GPD1‑L associated with early repolarization syndrome via modulation of cardiomyocyte fast sodium currents. ERS, WT
2020 Detection of TERT promotor mutation in serum cell-free DNA using wild-type blocking PCR combined with Sanger sequencing in hepatocellular carcinoma. C228T, cfDNA, HCC, TERT, WT, WTB-PCR
2019 A SNP Mutation of SiCRC Regulates Seed Number Per Capsule and Capsule Length of cs1 Mutant in Sesame. CL, IAA, SNC, WT
2019 Exome Sequencing Reveals a Heterozygous OAS3 Mutation in a Chinese Family With Juvenile-Onset Open-Angle Glaucoma. JOAG, OAS3, POAG, WES, WT
2019 Rapid discrimination of colon cancer cells with single base mutation in KRAS gene segment using laser tweezers Raman spectroscopy. LTRS, PCA-LDA, WT
2018 Comparative study of the effect of disease causing and benign mutations in position Q92 on cholesterol binding by the NPC1 n-terminal domain. CLR, NPC, NPC1, NTD
2018 Monitoring circulating tumor DNA revealed dynamic changes in KRAS status in patients with metastatic colorectal cancer. mCRC, MctDNA, WT
2018 Predicting calvarial growth in normal and craniosynostotic mice using a computational approach. WT
2018 The inhibitory performance of flavonoid cyanidin-3-sambubiocide against H274Y mutation in H1N1 influenza virus. C3S, NA, WT
10  2017 MicroRNA-107 Promotes Proliferation, Migration, and Invasion of Osteosarcoma Cells by Targeting Tropomyosin 1. qRT-PCR, TPM1, WT
11  2017 Mutational Impact on the Interaction Between Human IL27 and gp130: In silico Approach for Defending HIV Infection. MD
12  2017 Two-dimensional salt and temperature DNA denaturation analysis using a magnetoresistive sensor. MNPs, SNP, WT
13  2016 The role of polyamines during exocarp formation in a russet mutant of 'Dangshansuli' pear (Pyrus bretschneideri Rehd.). MGBG, WT
14  2016 [Molecular pathogenesis of Waardenburg syndrome type II resulting from SOX10 gene mutation]. WT
15  2015 Eprobe-mediated screening system for somatic mutations in the KRAS locus. CRC, EGFR, KRAS, NGS, WT
16  2015 MicroRNA-15a induces cell apoptosis and inhibits metastasis by targeting BCL2L2 in non-small cell lung cancer. miRNAs, NSCLC, qRT-PCR, UTR, WT
17  2015 Prospective associations between vitamin D status, vitamin D-related gene polymorphisms, and risk of tobacco-related cancers. HT, RXR, VDR, WT
18  2015 The predictive and prognostic role of phosphatase phosphoinositol-3 (PI3) kinase (PIK3CA) mutation in HER2-positive breast cancer receiving HER2-targeted therapy: a meta-analysis. OR, pCR, PFS, PI-3, WT, WT
19  2014 Molecular simulation investigation on the interaction between barrier-to-autointegration factor or its Gly25Glu mutant and DNA. BAF, MD, WT
20  2013 Substitution rtq267h of hepatitis B virus increases the weight of replication and Lamivudine resistance. ADV, CHB, HBV, LMV, LMVr, NAs, qRT-PCR, RT, WT
21  2013 UNC5H4-induced apoptosis in non-small cell lung cancer is not dependent on p53 status only. NSCLC, UNC5H4
22  2012 Pro-arrhythmogenic effects of the S140G KCNQ1 mutation in human atrial fibrillation - insights from modelling. APD, APs, CV, ERP, LS, WT
23  2011 Effect of intratumoral injection of mutant type p27Kip1 followed by in vivo electroporation on radiotherapy-resistant human oral tongue cancer xenografts. EGFP
24  2010 The role of nucleophosmin/B23 in radiation-induced chromosomal instability in human lymphoblastoid cells of different p53 genotypes. OLO, shRNA, siRNA, WT
25  2009 Salt tolerant mutant of Anabaena doliolum exhibiting efficient ammonium uptake and assimilation. GS, NR, WT
26  2008 Influence of Lys656Asn polymorphism of leptin receptor gene on leptin response secondary to two hypocaloric diets: a randomized clinical trial. WT
27  2006 [Inducement effect of recombinant human TNF-alpha on apoptosis of breast cancer cell line ZR75-1 and Its mechanism]. NF-kappaB, rh, TNF-alpha, WT
28  2004 Hyperthermia induces translocation of apoptosis-inducing factor (AIF) and apoptosis in human glioma cell lines. AIF, WT
29  2002 A novel nonstop mutation in the stop codon and a novel missense mutation in the type II 3beta-hydroxysteroid dehydrogenase (3beta-HSD) gene causing, respectively, nonclassic and classic 3beta-HSD deficiency congenital adrenal hyperplasia. 3beta-HSD, WT
30  1997 Increasing drug resistance in human lung cancer cells by mutant-type p53 gene mediated by retrovirus. FCM, MRP, P-gp, PCR
31  1993 The state of p53 in primary human cervical carcinomas and its effects in human papillomavirus-immortalized human cervical cells. HPV-18, PCR-SSCP, WT