frameshift mutation Search Results


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Illumina Inc frameshift mutation in the nrip1 coding sequence (rip msi)
Biological characterization of the RIP MSI <t>frameshift</t> mutation. ( A ) Intrinsic transrepression assay in HCT116LR cells transiently transfected with increasing doses of the Gal4DBD-fused NRIP1 and RIP MSI expression vectors. ( B ) MSH2 and MSH6 mRNA levels in RIPKO MEFs stably expressing GFP, GFP-RIP140 or GFP-RIP MSI ; n = 3 independent experiments. ( C ) Luciferase assay with the MSH2 gene reporter and increasing doses of NRIP1 or RIP MSI expression vectors (mean ± SD; n = 3 independent experiments). ( D ) MSH2 and MSH6 mRNA levels in HT29 cells transiently transfected with pEGFP, pEGFP-RIP140 or pEGFP-RIP MSI expression vectors. ( E ) MSH2 and MSH6 mRNA levels in stably transfected MEF-WT MSI and MEF-KO MSI . Data were normalized as compared to WT and RIPKO control cells expressing GFP alone and set at 1. ( F ) Cell proliferation of RIPKO MEFs stably expressing GFP, GFP-RIP140 or GFP-RIP MSI at day 4 and 6 after seeding. Results are the fold-change vs. control (GFP) cells after normalization to the cell density at day 1; n = 3 independent experiments. ( G ) Cell proliferation of human RKO CRC cells transiently transfected with pEGFP, pEGFP-RIP140 or pEGFP-RIP MSI expression vectors over 8 days. Results are the fold-change (triplicates) after normalization to the cell density at day 0. For all panels: data are the mean ± SD; ns = not significant, * p < 0.05, ** p < 0.01, *** p < 0.001 (Kruskal–Wallis test).
Frameshift Mutation In The Nrip1 Coding Sequence (Rip Msi), supplied by Illumina Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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SAS institute frameshift mutation c.376_378delinstt, p.leu126serfsx6
Biological characterization of the RIP MSI <t>frameshift</t> mutation. ( A ) Intrinsic transrepression assay in HCT116LR cells transiently transfected with increasing doses of the Gal4DBD-fused NRIP1 and RIP MSI expression vectors. ( B ) MSH2 and MSH6 mRNA levels in RIPKO MEFs stably expressing GFP, GFP-RIP140 or GFP-RIP MSI ; n = 3 independent experiments. ( C ) Luciferase assay with the MSH2 gene reporter and increasing doses of NRIP1 or RIP MSI expression vectors (mean ± SD; n = 3 independent experiments). ( D ) MSH2 and MSH6 mRNA levels in HT29 cells transiently transfected with pEGFP, pEGFP-RIP140 or pEGFP-RIP MSI expression vectors. ( E ) MSH2 and MSH6 mRNA levels in stably transfected MEF-WT MSI and MEF-KO MSI . Data were normalized as compared to WT and RIPKO control cells expressing GFP alone and set at 1. ( F ) Cell proliferation of RIPKO MEFs stably expressing GFP, GFP-RIP140 or GFP-RIP MSI at day 4 and 6 after seeding. Results are the fold-change vs. control (GFP) cells after normalization to the cell density at day 1; n = 3 independent experiments. ( G ) Cell proliferation of human RKO CRC cells transiently transfected with pEGFP, pEGFP-RIP140 or pEGFP-RIP MSI expression vectors over 8 days. Results are the fold-change (triplicates) after normalization to the cell density at day 0. For all panels: data are the mean ± SD; ns = not significant, * p < 0.05, ** p < 0.01, *** p < 0.001 (Kruskal–Wallis test).
Frameshift Mutation C.376 378delinstt, P.Leu126serfsx6, supplied by SAS institute, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Morishita Jintan mbd4/ med1 gene
Biological characterization of the RIP MSI <t>frameshift</t> mutation. ( A ) Intrinsic transrepression assay in HCT116LR cells transiently transfected with increasing doses of the Gal4DBD-fused NRIP1 and RIP MSI expression vectors. ( B ) MSH2 and MSH6 mRNA levels in RIPKO MEFs stably expressing GFP, GFP-RIP140 or GFP-RIP MSI ; n = 3 independent experiments. ( C ) Luciferase assay with the MSH2 gene reporter and increasing doses of NRIP1 or RIP MSI expression vectors (mean ± SD; n = 3 independent experiments). ( D ) MSH2 and MSH6 mRNA levels in HT29 cells transiently transfected with pEGFP, pEGFP-RIP140 or pEGFP-RIP MSI expression vectors. ( E ) MSH2 and MSH6 mRNA levels in stably transfected MEF-WT MSI and MEF-KO MSI . Data were normalized as compared to WT and RIPKO control cells expressing GFP alone and set at 1. ( F ) Cell proliferation of RIPKO MEFs stably expressing GFP, GFP-RIP140 or GFP-RIP MSI at day 4 and 6 after seeding. Results are the fold-change vs. control (GFP) cells after normalization to the cell density at day 1; n = 3 independent experiments. ( G ) Cell proliferation of human RKO CRC cells transiently transfected with pEGFP, pEGFP-RIP140 or pEGFP-RIP MSI expression vectors over 8 days. Results are the fold-change (triplicates) after normalization to the cell density at day 0. For all panels: data are the mean ± SD; ns = not significant, * p < 0.05, ** p < 0.01, *** p < 0.001 (Kruskal–Wallis test).
Mbd4/ Med1 Gene, supplied by Morishita Jintan, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Biological characterization of the RIP MSI frameshift mutation. ( A ) Intrinsic transrepression assay in HCT116LR cells transiently transfected with increasing doses of the Gal4DBD-fused NRIP1 and RIP MSI expression vectors. ( B ) MSH2 and MSH6 mRNA levels in RIPKO MEFs stably expressing GFP, GFP-RIP140 or GFP-RIP MSI ; n = 3 independent experiments. ( C ) Luciferase assay with the MSH2 gene reporter and increasing doses of NRIP1 or RIP MSI expression vectors (mean ± SD; n = 3 independent experiments). ( D ) MSH2 and MSH6 mRNA levels in HT29 cells transiently transfected with pEGFP, pEGFP-RIP140 or pEGFP-RIP MSI expression vectors. ( E ) MSH2 and MSH6 mRNA levels in stably transfected MEF-WT MSI and MEF-KO MSI . Data were normalized as compared to WT and RIPKO control cells expressing GFP alone and set at 1. ( F ) Cell proliferation of RIPKO MEFs stably expressing GFP, GFP-RIP140 or GFP-RIP MSI at day 4 and 6 after seeding. Results are the fold-change vs. control (GFP) cells after normalization to the cell density at day 1; n = 3 independent experiments. ( G ) Cell proliferation of human RKO CRC cells transiently transfected with pEGFP, pEGFP-RIP140 or pEGFP-RIP MSI expression vectors over 8 days. Results are the fold-change (triplicates) after normalization to the cell density at day 0. For all panels: data are the mean ± SD; ns = not significant, * p < 0.05, ** p < 0.01, *** p < 0.001 (Kruskal–Wallis test).

Journal: Cancers

Article Title: A Truncated NRIP1 Mutant Amplifies Microsatellite Instability of Colorectal Cancer by Regulating MSH2/MSH6 Expression, and Is a Prognostic Marker of Stage III Tumors

doi: 10.3390/cancers13174449

Figure Lengend Snippet: Biological characterization of the RIP MSI frameshift mutation. ( A ) Intrinsic transrepression assay in HCT116LR cells transiently transfected with increasing doses of the Gal4DBD-fused NRIP1 and RIP MSI expression vectors. ( B ) MSH2 and MSH6 mRNA levels in RIPKO MEFs stably expressing GFP, GFP-RIP140 or GFP-RIP MSI ; n = 3 independent experiments. ( C ) Luciferase assay with the MSH2 gene reporter and increasing doses of NRIP1 or RIP MSI expression vectors (mean ± SD; n = 3 independent experiments). ( D ) MSH2 and MSH6 mRNA levels in HT29 cells transiently transfected with pEGFP, pEGFP-RIP140 or pEGFP-RIP MSI expression vectors. ( E ) MSH2 and MSH6 mRNA levels in stably transfected MEF-WT MSI and MEF-KO MSI . Data were normalized as compared to WT and RIPKO control cells expressing GFP alone and set at 1. ( F ) Cell proliferation of RIPKO MEFs stably expressing GFP, GFP-RIP140 or GFP-RIP MSI at day 4 and 6 after seeding. Results are the fold-change vs. control (GFP) cells after normalization to the cell density at day 1; n = 3 independent experiments. ( G ) Cell proliferation of human RKO CRC cells transiently transfected with pEGFP, pEGFP-RIP140 or pEGFP-RIP MSI expression vectors over 8 days. Results are the fold-change (triplicates) after normalization to the cell density at day 0. For all panels: data are the mean ± SD; ns = not significant, * p < 0.05, ** p < 0.01, *** p < 0.001 (Kruskal–Wallis test).

Article Snippet: For samples from ICM and CRCT, the frameshift mutation in the NRIP1 coding sequence (RIP MSI ) was detected by Illumina HiSeq4000 deep-sequencing (Integragen genomics, France) using specific primers ( ) and DNA extracted using the QIAamp DNA FFPE kit (Qiagen, Hilden, Germany).

Techniques: Mutagenesis, Transfection, Expressing, Stable Transfection, Luciferase, Control

RIP MSI frameshift mutation and survival of patients with CRC. Kaplan–Meier plots of OS rate in patients with CRC divided according to the presence/absence of the RIP MSI mutation in the tumor DNA. ( A ) Whole cohort ( n = 189); Patients with ( B ) stage I/II CRC ( n = 127); ( C ) stage III CRC ( n = 62); ( D ) stage III CRC with dMLH1 ( n = 40); ( E ) stage III CRC and proficient MLH1 ( n = 20). ( F ) Forest plot of the associations between the indicated variables and OS (Cox univariate analysis; * p < 0.05 and ** p < 0.01) in the whole cohort and in the indicated subgroups. HR, Cox Hazard Ratio; CI, Confidence Interval of HR.

Journal: Cancers

Article Title: A Truncated NRIP1 Mutant Amplifies Microsatellite Instability of Colorectal Cancer by Regulating MSH2/MSH6 Expression, and Is a Prognostic Marker of Stage III Tumors

doi: 10.3390/cancers13174449

Figure Lengend Snippet: RIP MSI frameshift mutation and survival of patients with CRC. Kaplan–Meier plots of OS rate in patients with CRC divided according to the presence/absence of the RIP MSI mutation in the tumor DNA. ( A ) Whole cohort ( n = 189); Patients with ( B ) stage I/II CRC ( n = 127); ( C ) stage III CRC ( n = 62); ( D ) stage III CRC with dMLH1 ( n = 40); ( E ) stage III CRC and proficient MLH1 ( n = 20). ( F ) Forest plot of the associations between the indicated variables and OS (Cox univariate analysis; * p < 0.05 and ** p < 0.01) in the whole cohort and in the indicated subgroups. HR, Cox Hazard Ratio; CI, Confidence Interval of HR.

Article Snippet: For samples from ICM and CRCT, the frameshift mutation in the NRIP1 coding sequence (RIP MSI ) was detected by Illumina HiSeq4000 deep-sequencing (Integragen genomics, France) using specific primers ( ) and DNA extracted using the QIAamp DNA FFPE kit (Qiagen, Hilden, Germany).

Techniques: Mutagenesis