Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADα, and MO25α, in Peutz–Jeghers syndrome
Open Access
- 8 March 2005
- journal article
- research article
- Published by Springer Nature in British Journal of Cancer
- Vol. 92 (6) , 1126-1129
- https://doi.org/10.1038/sj.bjc.6602454
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Genetic and Epigenetic screening for gene alterations of the chromatin‐remodeling factor, SMARCA4/BRG1, in lung tumorsGenes, Chromosomes and Cancer, 2004
- Mapping of a translocation breakpoint in a Peutz–Jeghers hamartoma to the putative PJS locus at 19q13.4 and mutation analysis of candidate genes in polyp and STK11‐negative PJS casesGenes, Chromosomes and Cancer, 2004
- MO25 / interact with STRAD / enhancing their ability to bind, activate and localize LKB1 in the cytoplasmThe EMBO Journal, 2003
- Activation of the tumour suppressor kinase LKB1 by the STE20-like pseudokinase STRADThe EMBO Journal, 2003
- Search for the second Peutz-Jeghers syndrome locus: exclusion of the STK13, PRKCG, KLK10, and PSCD2 genes on chromosome 19 and the STK11IP gene on chromosome 2Cytogenetic and Genome Research, 2002
- Vascular Abnormalities and Deregulation of VEGF in Lkb1 -Deficient MiceScience, 2001
- Peutz-Jeghers syndrome is caused by mutations in a novel serine threoninekinaseNature Genetics, 1998
- Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3.Journal of Medical Genetics, 1998
- Peutz-Jeghers syndrome.Journal of Medical Genetics, 1997
- Increased Risk of Cancer in the Peutz–Jeghers SyndromeNew England Journal of Medicine, 1987