Add to ORKGInactivating germline mutations of the tumor suppressor kinase LKB1 lead to Peutz-Jeghers Syndrome (PJS), which is characterized by gastrointestinal polyposis and an elevated risk for cancer (Hemminki et al., 1998). To investigate the physiological function
SummaryPeutz-Jeghers syndrome (PJS) is an autosomal dominant disease characterized by mucocutaneous ...
Germline mutations of the LKB1 gene are associated with Peutz-Jeghers syndrome (PJS), which is chara...
We describe in this review increasing evidence that loss of LKB1 kinase in Peutz-Jeghers syndrome (P...
Peutz-Jeghers syndrome (PJS) is caused by inactivating mutations of the LKB1 (STK11) serine/threonin...
Peutz-Jeghers syndrome (PJS) is a dominantly inherited human disorder characterized by gastrointesti...
Peutz-Jeghers syndrome (PJS) is a well-described inherited syndrome, characterized by the developmen...
textabstractPeutz-Jeghers syndrome (PJS) is an autosomal dominant inherited disorder, characterized ...
Peutz-Jeghers syndrome (PJS) is an autosomal dominant disease characterized by mucocutaneous pigment...
Peutz-Jeghers Syndrome is a dominantly inherited disorder characterized by mucocutaneous melanin pig...
Peutz-Jeghers syndrome (PJS) is caused by germline mutations in the LKB1 gene, which encodes a serin...
Germline mutations in the LKB1/STK11 tumour suppressor gene cause Peutz-Jeghers syndrome (PJS), a ra...
Peutz-Jeghers syndrome (PJS) is caused by germline mutations in the LKB1 gene, which encodes a serin...
International audienceGermline mutations in the gene encoding tumor suppressor kinase LKB1 lead to g...
Peutz–Jeghers syndrome (PJS, MIM175200) is an autosomal dominant condition defined by the developmen...
Item does not contain fulltextPeutz-Jeghers syndrome (PJS, MIM175200) is an autosomal dominant condi...
SummaryPeutz-Jeghers syndrome (PJS) is an autosomal dominant disease characterized by mucocutaneous ...
Germline mutations of the LKB1 gene are associated with Peutz-Jeghers syndrome (PJS), which is chara...
We describe in this review increasing evidence that loss of LKB1 kinase in Peutz-Jeghers syndrome (P...
Peutz-Jeghers syndrome (PJS) is caused by inactivating mutations of the LKB1 (STK11) serine/threonin...
Peutz-Jeghers syndrome (PJS) is a dominantly inherited human disorder characterized by gastrointesti...
Peutz-Jeghers syndrome (PJS) is a well-described inherited syndrome, characterized by the developmen...
textabstractPeutz-Jeghers syndrome (PJS) is an autosomal dominant inherited disorder, characterized ...
Peutz-Jeghers syndrome (PJS) is an autosomal dominant disease characterized by mucocutaneous pigment...
Peutz-Jeghers Syndrome is a dominantly inherited disorder characterized by mucocutaneous melanin pig...
Peutz-Jeghers syndrome (PJS) is caused by germline mutations in the LKB1 gene, which encodes a serin...
Germline mutations in the LKB1/STK11 tumour suppressor gene cause Peutz-Jeghers syndrome (PJS), a ra...
Peutz-Jeghers syndrome (PJS) is caused by germline mutations in the LKB1 gene, which encodes a serin...
International audienceGermline mutations in the gene encoding tumor suppressor kinase LKB1 lead to g...
Peutz–Jeghers syndrome (PJS, MIM175200) is an autosomal dominant condition defined by the developmen...
Item does not contain fulltextPeutz-Jeghers syndrome (PJS, MIM175200) is an autosomal dominant condi...
SummaryPeutz-Jeghers syndrome (PJS) is an autosomal dominant disease characterized by mucocutaneous ...
Germline mutations of the LKB1 gene are associated with Peutz-Jeghers syndrome (PJS), which is chara...
We describe in this review increasing evidence that loss of LKB1 kinase in Peutz-Jeghers syndrome (P...