Add to ORKGLKB1 is a serine/threonine kinase that is mutated in most cases of Peutz-Jeghers syndrome, which is an autosomal dominant disorder in which patients develop benign hamartomas and a high frequency of malignant tumors (Alessi et al., 2006). Further
Germline mutations of the LKB1 (STK11) tumor suppressor gene lead to Peutz-Jeghers syndrome (PJS) an...
The tumor suppressor LKB1 (STK11) is a cytoplasmic/nuclear serine/threonine kinase, defects in which...
AbstractLKB1 is a serine-threonine protein kinase mutated in patients with an autosomal dominantly i...
Peutz-Jeghers syndrome (PJS) is an autosomal dominant disease characterized by mucocutaneous pigment...
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...
LKB1 is a serine-threonine protein kinase mutated in patients with an autosomal dominantly inherited...
Studies of hereditary cancer syndromes have contributed greatly to our understanding of molecular ev...
Germline mutations of the LKB1 (STK11) serine/threonine kinase gene (chromosome 19p13.3) cause Peutz...
Germline mutations of the LKB1 gene are responsible for the cancer-prone Peutz-Jeghers syndrome (PJS...
International audienceGermline mutations in the gene encoding tumor suppressor kinase LKB1 lead to g...
Inactivating germline mutations of the tumor suppressor kinase LKB1 lead to Peutz-Jeghers Syndrome (...
SummaryPeutz-Jeghers syndrome (PJS) is an autosomal dominant disease characterized by mucocutaneous ...
Germline mutations in the STK11/LKB1 gene cause Peutz-Jeghers syndrome, an autosomal-dominantly inhe...
AbstractThe LKB1 tumor suppressor gene is frequently mutated in sporadic lung adenocarcinomas and ce...
Germline mutations of the LKB1 (STK11) tumor suppressor gene lead to Peutz-Jeghers syndrome (PJS) an...
The tumor suppressor LKB1 (STK11) is a cytoplasmic/nuclear serine/threonine kinase, defects in which...
AbstractLKB1 is a serine-threonine protein kinase mutated in patients with an autosomal dominantly i...
Peutz-Jeghers syndrome (PJS) is an autosomal dominant disease characterized by mucocutaneous pigment...
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...
LKB1 is a serine-threonine protein kinase mutated in patients with an autosomal dominantly inherited...
Studies of hereditary cancer syndromes have contributed greatly to our understanding of molecular ev...
Germline mutations of the LKB1 (STK11) serine/threonine kinase gene (chromosome 19p13.3) cause Peutz...
Germline mutations of the LKB1 gene are responsible for the cancer-prone Peutz-Jeghers syndrome (PJS...
International audienceGermline mutations in the gene encoding tumor suppressor kinase LKB1 lead to g...
Inactivating germline mutations of the tumor suppressor kinase LKB1 lead to Peutz-Jeghers Syndrome (...
SummaryPeutz-Jeghers syndrome (PJS) is an autosomal dominant disease characterized by mucocutaneous ...
Germline mutations in the STK11/LKB1 gene cause Peutz-Jeghers syndrome, an autosomal-dominantly inhe...
AbstractThe LKB1 tumor suppressor gene is frequently mutated in sporadic lung adenocarcinomas and ce...
Germline mutations of the LKB1 (STK11) tumor suppressor gene lead to Peutz-Jeghers syndrome (PJS) an...
The tumor suppressor LKB1 (STK11) is a cytoplasmic/nuclear serine/threonine kinase, defects in which...
AbstractLKB1 is a serine-threonine protein kinase mutated in patients with an autosomal dominantly i...