resembling PHTS of soft tissue in a patient with Cowden syndrome The phosphatase and tensin homologue on chromosome ten (PTEN) is one of the most commonly inactivated tumour sup-pressors in human neoplasia.1 PTEN inactivation can result from somatic muta-tion or can be a consequence of epigenetic events including promoter methylation. Rarely, germline mutations in PTEN occur and these are associated with a spectrum of clinical disorders that include hamarto-matous and neoplastic proliferations in a variety of organs which, collectively, ar
Cowden syndrome (CS), an autosomal dominant disorder, is associated with germline mutations of the P...
Cowden syndrome (CS) is a rare disease that was first described in 1963 and later included in the la...
Cowden disease, also known as multiple hamartoma syndrome, is a rare disease inherited in an autosom...
Germline mutations of PTEN (phosphatase and tensin homolog deleted on chromosome 10) are associated ...
Germline mutations of PTEN (phosphatase and tensin homolog deleted on chromosome 10) are associated ...
Phosphate and tensin homolog on chromosome ten (PTEN) germline mutations are associated with an over...
Phosphatase and tensin homolog deleted on chromosome ten (PTEN)-hamartoma tumor syndrome (PHTS) is a...
Cowden syndrome (CS) or multiple hamartoma syndrome (MIM 158350) is an autosomal dominant disorder w...
Phosphate and tensin homolog on chromosome ten (PTEN) germline mutations are associated with an over...
Cowden syndrome (CS) or multiple hamartoma syndrome (MIM 158350) is an autosomal dominant disorder w...
Cowden syndrome (CS) is a phosphatase and tensin homolog gene (PTEN) -associated condition character...
Cowden syndrome (CS) is an infrequent genodermatosis caused by mutations in the phosphatase and tens...
Germline mutations distributed across the PTEN tumor-suppressor gene have been found to result in a ...
Inactivation of tumor suppressor genes is one way in which cancer cells circumvent normal growth con...
Phosphatase and tensin homolog deleted on chromosome 10 (PTEN) encodes a tumor-suppressor phosphatas...
Cowden syndrome (CS), an autosomal dominant disorder, is associated with germline mutations of the P...
Cowden syndrome (CS) is a rare disease that was first described in 1963 and later included in the la...
Cowden disease, also known as multiple hamartoma syndrome, is a rare disease inherited in an autosom...
Germline mutations of PTEN (phosphatase and tensin homolog deleted on chromosome 10) are associated ...
Germline mutations of PTEN (phosphatase and tensin homolog deleted on chromosome 10) are associated ...
Phosphate and tensin homolog on chromosome ten (PTEN) germline mutations are associated with an over...
Phosphatase and tensin homolog deleted on chromosome ten (PTEN)-hamartoma tumor syndrome (PHTS) is a...
Cowden syndrome (CS) or multiple hamartoma syndrome (MIM 158350) is an autosomal dominant disorder w...
Phosphate and tensin homolog on chromosome ten (PTEN) germline mutations are associated with an over...
Cowden syndrome (CS) or multiple hamartoma syndrome (MIM 158350) is an autosomal dominant disorder w...
Cowden syndrome (CS) is a phosphatase and tensin homolog gene (PTEN) -associated condition character...
Cowden syndrome (CS) is an infrequent genodermatosis caused by mutations in the phosphatase and tens...
Germline mutations distributed across the PTEN tumor-suppressor gene have been found to result in a ...
Inactivation of tumor suppressor genes is one way in which cancer cells circumvent normal growth con...
Phosphatase and tensin homolog deleted on chromosome 10 (PTEN) encodes a tumor-suppressor phosphatas...
Cowden syndrome (CS), an autosomal dominant disorder, is associated with germline mutations of the P...
Cowden syndrome (CS) is a rare disease that was first described in 1963 and later included in the la...
Cowden disease, also known as multiple hamartoma syndrome, is a rare disease inherited in an autosom...
.jpg%3Fwidth%3D300&w=3840&q=75)
Add to ORKG