Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Afolake Arowolo"'
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-7 (2022)
Abstract Background Mutations of the human FAM111B gene are associated with hereditary fibrosing poikiloderma with tendon contracture, myopathy, and pulmonary fibrosis (POIKTMP), a rare and autosomal dominant multi-systemic fibrosing disease. To date
Externí odkaz:
https://doaj.org/article/65b4216de284407a82dc9c8f4354de47
Publikováno v:
Cancer Treatment and Research Communications, Vol 34, Iss , Pp 100679- (2023)
Introduction: Mutations in the uncharacterised human FAM111B gene are associated with POIKTMP, a rare multi-organ fibrosing disease. Recent studies also reported the overexpression of FAM111B in specific cancers. Moreover, FAM111B mutation screening
Externí odkaz:
https://doaj.org/article/a013da94e415405788c9264fd887f95a
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
FAM111B gene mutations are associated with a hereditary fibrosing poikiloderma known to cause poikiloderma, tendon contracture, myopathy, and pulmonary fibrosis (POIKTMP). In addition, the overexpression of FAM111B has been associated with cancer pro
Externí odkaz:
https://doaj.org/article/388a0d4d3e5c4a6d829a6db6a1ed005b
Publikováno v:
Experimental Dermatology. 31:648-654
Mutations in the human FAM111B gene are associated with a rare, hereditary multi-systemic fibrosing disease, POIKTMP. To date, there are ten POIKTMP-associated FAM111B gene mutations reported in thirty-six patients from five families globally. To inv
Publikováno v:
Cancer treatment and research communications. 34
Mutations in the uncharacterised human FAM111B gene are associated with POIKTMP, a rare multi-organ fibrosing disease. Recent studies also reported the overexpression of FAM111B in specific cancers. Moreover, FAM111B mutation screening may prove expe