Zobrazeno 1 - 10
of 18
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee4c9c820acda9cc669f98e623894b4f
https://doi.org/10.1111/exd.14537
https://doi.org/10.1111/exd.14537
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f1fd37f48962822aeb700e271d64060
https://pubmed.ncbi.nlm.nih.gov/36610347
https://pubmed.ncbi.nlm.nih.gov/36610347
Autor:
Naicker, Danielle1 (AUTHOR) nckdan004@myuct.ac.za, Rhoda, Cenza2 (AUTHOR) cenza.rhoda@uct.ac.za, Sunda, Falone2 (AUTHOR) sndfal001@myuct.ac.za, Arowolo, Afolake2,3 (AUTHOR) at.arowolo2@uct.ac.za
Publikováno v:
International Journal of Molecular Sciences. Mar2024, Vol. 25 Issue 5, p2845. 16p.
Autor:
Arowolo, Afolake1,2 (AUTHOR), Rhoda, Cenza1 (AUTHOR), Mbele, Mzwandile1,2 (AUTHOR), Oluwole, Oluwafemi G.3 (AUTHOR) oluwafemi.oluwole@uct.ac.za, Khumalo, Nonhlanhla1,2 (AUTHOR)
Publikováno v:
Egyptian Journal of Medical Human Genetics. 12/25/2022, Vol. 23 Issue 1, p1-7. 7p.
Autor:
Arowolo, Afolake1 (AUTHOR) at.arowolo2@uct.ac.za, Rhoda, Cenza1 (AUTHOR), Khumalo, Nonhlanhla1 (AUTHOR)
Publikováno v:
Experimental Dermatology. May2022, Vol. 31 Issue 5, p648-654. 7p.
Autor:
Musa, Ezekiel, Salazar‐Petres, Esteban, Arowolo, Afolake, Levitt, Naomi, Matjila, Mushi, Sferruzzi‐Perri, Amanda N.
Publikováno v:
Journal of Physiology; Apr2023, Vol. 601 Issue 7, p1287-1306, 20p
Publikováno v:
Frontiers in Oncology; 7/4/2022, Vol. 12, p1-7, 7p