Sentence examples for identification of kit from inspiring English sources

The advancement of immunohistochemistry, molecular technology and the identification of KIT oncogene mutation in more than 80% of GISTs have accelerated our understanding of GISTs [ 6- 8].

In conclusion, this report describes the clinical responses to KIT kinase inhibitors in melanoma patients harbouring diverse KIT mutations and supports the utility of selecting patients for therapy based on the identification of KIT mutations.

The identification of KIT, a proto-oncogene which encodes the c-Kit receptor, as a target for miR-146b-5p miR-146b-5p miR-146b-5p suggested a direct association between cHenget in miR-146alb-5p expression and the development of cancer.

Our identification of KIT protein, but not c-KIT mRNA, in the HMC-1 exosomes, and the transfer of the protein to lung adenocarcinoma cells, suggests that the presence of KIT in the A549 cells after exosomes depend on transfer of KIT protein, rather than transfer of its mRNA.

Identification of KIT-activating mutations as a key factor in the pathogenesis of GIST has substantially altered the diagnosis and treatment of GIST (Hirota et al, 1998; Corless et al, 2004; Miettinen and Lasota, 2006).

Because the kit tyrosine kinase inhibitor imatinib mesylate (Gleevec, formerly known as STI571, Novartis Pharma AG, Basel, Switzerland) has been shown to produce a promising clinical result in an advanced GIST patient [ 6], identification of GIST by kit immunopositivity has become paramount.

In this study, we compare six commercially available cDNA synthesis kits (Table  1), for the identification of the most suitable kit for use in a CML MRD assay.

Hence, identification of which commercially available kit is more suitable for the synthesis of cDNA is essential, in order to achieve better results at the MMR level.

The expression of KIT and the identification of these activating mutations in c-KIT implicate KIT in the pathogenesis of these tumors.

The objective of this project too was improved service provision through using clean delivery kits, identification of danger signs and making timely referrals for home deliveries.

We show here that, when excluding the small number of samples that could not be amplified with the PCR technique provided in the kit, correct identification of HCV subtypes 1a and 1b was achieved in more than 99% of cases.