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MessagePosté le: Ven 10 Oct - 10:59 (2014) Sujet du message: Discussion If wing digit identity were 2, three, 4, coincid Répondre en citant

 Information are analyzed when mutant and wildtype controls have a legitimate status. A re port is produced instantly and オーダー ARQ 197 success could be distin guished between mutation detected and mutation not detected. This test is specific for the p. V600E mutation which has a reported sensitivity of 5% mutated alleles inside a background of wildtype alleles. Limit of detection in our preselected cohort was 7% mutant alleles within a back ground of wildtype alleles. 36 of 37 p. V600E mutations were detected with all the cobas BRAF V600 check. One case that has a border line frequency of 5% of mutated alleles utilizing pyrosequencing couldn't be detected. However it really should be taken into consideration that we extracted the DNA with our typical in house process rather than together with the advised kit.

This could influence the check effects. On top of that, the marked place to the HE stained slide contained several lymphocytes diluting the p. V600E alleles. Curry et al. showed an even reduced limit of detection of 4. 4% mutated alleles per one. 25 ng ul on FFPE tissues for purchase AZD0530 that p. V600E mutation. In contrast, Lade Keller et al. carried out a dilution series of p. V600E mutated DNA followed by examination within the cobas 4800 BRAF V600 check. This check was not capable of detect a p. V600E mutation within the dilution stage that theoretically contained 10% mutant alleles. Evaluation have proven cross reactivity with p. V600E2, p. V600K and p. V600D but not with p. V600R mutation. In our cohort, the cobas BRAF V600 check showed cross reactivity 5 instances in p.

V600K mutated samples containing 59, 61, twice 62 and 64% of mutated alleles employing pyrosequencing. One particular p. V600K mutation by using a frequency of 57% that's above the described cross reactivity, was Alvocidib 臨床試験 not detected by the cobas 4800 BRAF V600 check. Moreover, various further circumstances having a mutation frequency under the described limit of detection have been missed in our research, case 9 showed a frequency of six. 6% for p. V600K, case 36 25% to the similar mutation and case 24 an allele frequency of 46% for the p. V600E2 mutation. Situation 3, 33 and 38 showed a mutation frequency of 37, 42 and 39% for p. V600R mutation that may not be detected by this kit. This tends to make an general failure price of 13. 3% in our prese lected cohort in addition to a failure fee of mutation found in codon 600 of sixteen.

3%. Halait et al. even showed the cobas 4800 BRAF V600 test failed to detect 19% of your mutations taking place in codon 600 in the BRAF gene. In the research of Curry et al. 82. 3% of non p. V600E mutations weren't detected obtaining a tumor content material range from five 45% and 14% median mutant alleles. But current studies showed that even individuals with p. V600K, p. V600D and p. V600E2 mu tation constructive melanomas may advantage from treatment with vemurafenib. In addition, patients with un common mutations as p. V600R and double mutations as e. g. p. treated with dabrafenib showed response based mostly on RECIST criteria and regression of metastatic le sions. As anticipated, all other mutations evaluated could not be detected by this technique. three. 8% of all muta tions detected in malignant melanomas are outside of codon 600 of the BRAF gene. To date, you will discover 121 diverse missense mutations described for BRAF.

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MessagePosté le: Ven 10 Oct - 10:59 (2014) Sujet du message: Publicité

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