LKB1 has been implicated in a wide range of cellular functions and is associated with many potential substrates in in vitro studies, however the in vivo role of LKB1 remains unclear and its precise contribution to the prevention of intestinal tumours in the hereditary Peutz-Jegers syndrome is as yet uncharacterised. Conditional deletion of LKB1 in the murine small intestine resulted in significant disruption of intestinal homeostasis, particularly that of the differentiation process, suggesting LKB1 plays a key role in intestinal differentiation and it is loss of this function that predisposes to tumourigenesisEThOS - Electronic Theses Online ServiceGBUnited Kingdo
We describe in this review increasing evidence that loss of LKB1 kinase in Peutz-Jeghers syndrome (P...
Recent developments have placed the serine/threonine kinase LKB1 on the crossroads linking energy me...
Mutations in the tumor suppressor gene LKB1 are important in hereditary Peutz–Jeghers syndrome, as w...
AbstractThe LKB1 tumor suppressor gene is frequently mutated in sporadic lung adenocarcinomas and ce...
The Lkb1 tumour suppressor is a multitasking kinase participating in a range of physiological proces...
The Lkb1 tumour suppressor is a multitasking kinase participating in a range of physiological proces...
Inactivating mutations of the tumor-suppressor kinase gene LKB1 underlie Peutz-Jeghers syndrome (PJS...
International audienceGermline mutations in the gene encoding tumor suppressor kinase LKB1 lead to g...
AbstractRecent developments have placed the serine/threonine kinase LKB1 on the crossroads linking e...
Peutz-Jeghers syndrome (PJS) is a dominantly inherited human disorder characterized by gastrointesti...
Germline mutations of the LKB1 tumor suppressor gene result in Peutz–Jeghers syndrome (PJS) charac-t...
Inactivating germline mutations of the tumor suppressor kinase LKB1 lead to Peutz-Jeghers Syndrome (...
LKB1 is a serine-threonine protein kinase mutated in patients with an autosomal dominantly inherited...
BACKGROUND & AIMS: In addition to the Notch and Wnt signaling pathways, energy metabolism also regul...
We describe in this review increasing evidence that loss of LKB1 kinase in Peutz-Jeghers syndrome (P...
Recent developments have placed the serine/threonine kinase LKB1 on the crossroads linking energy me...
Mutations in the tumor suppressor gene LKB1 are important in hereditary Peutz–Jeghers syndrome, as w...
AbstractThe LKB1 tumor suppressor gene is frequently mutated in sporadic lung adenocarcinomas and ce...
The Lkb1 tumour suppressor is a multitasking kinase participating in a range of physiological proces...
The Lkb1 tumour suppressor is a multitasking kinase participating in a range of physiological proces...
Inactivating mutations of the tumor-suppressor kinase gene LKB1 underlie Peutz-Jeghers syndrome (PJS...
International audienceGermline mutations in the gene encoding tumor suppressor kinase LKB1 lead to g...
AbstractRecent developments have placed the serine/threonine kinase LKB1 on the crossroads linking e...
Peutz-Jeghers syndrome (PJS) is a dominantly inherited human disorder characterized by gastrointesti...
Germline mutations of the LKB1 tumor suppressor gene result in Peutz–Jeghers syndrome (PJS) charac-t...
Inactivating germline mutations of the tumor suppressor kinase LKB1 lead to Peutz-Jeghers Syndrome (...
LKB1 is a serine-threonine protein kinase mutated in patients with an autosomal dominantly inherited...
BACKGROUND & AIMS: In addition to the Notch and Wnt signaling pathways, energy metabolism also regul...
We describe in this review increasing evidence that loss of LKB1 kinase in Peutz-Jeghers syndrome (P...
Recent developments have placed the serine/threonine kinase LKB1 on the crossroads linking energy me...
Mutations in the tumor suppressor gene LKB1 are important in hereditary Peutz–Jeghers syndrome, as w...