Zobrazeno 1 - 10
of 14
pro vyhledávání: '"J W, Harbour"'
Publikováno v:
Oncogene
The retinoblastoma protein (Rb) inhibits both cell division and apoptosis, but the mechanism by which Rb alternatively regulates these divergent outcomes remains poorly understood. Cyclin dependent kinases (Cdks) promote cell division by phosphorylat
Uveal melanoma (UM) is a genetically and biologically distinct type of melanoma, and once metastatic there is no effective treatment currently available. 80% of UMs harbor mutations in the Gαq family members GNAQ and GNA11. Understanding the effecto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a34e6cd11c8eb0564fbf4fc00870f327
https://europepmc.org/articles/PMC4356624/
https://europepmc.org/articles/PMC4356624/
Aim: To investigate the association between posterior uveal melanoma and iris freckles, iris naevi, and choroidal naevi. Methods: Cross sectional study of 65 patients with posterior uveal melanoma and 218 controls. Iris colour, iris freckles, iris na
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc33d4bbb8fd7aca26799985d5d0257b
https://europepmc.org/articles/PMC1771959/
https://europepmc.org/articles/PMC1771959/
Autor:
J. W. Harbour
Publikováno v:
Pigment Cell & Melanoma Research. 24:1081-1082
Autor:
J. W. Harbour, D. C. Dean
Publikováno v:
Current Topics in Microbiology and Immunology ISBN: 9783642087097
The retinoblastoma protein (Rb) is a ubiquitous transcriptional repressor and a negative regulator of the Gl-to-S phase transition in the eukaryotic cell cycle. Through this inhibitory activity, Rb plays a critical role in suppressing neoplastic tran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ae2e5c1775e882dbecae88037be7215
https://doi.org/10.1007/978-3-662-10595-5_7
https://doi.org/10.1007/978-3-662-10595-5_7
Autor:
M A, Brantley, J W, Harbour
Publikováno v:
Cancer research. 60(16)
Uveal melanoma is the most common malignancy of the eye, but little is known about its underlying genetic defects. Melanomas of uveal origin, unlike those of the skin, are rarely familial and have not been linked consistently to mutations in tumor su
Autor:
J W, Harbour
Publikováno v:
Ophthalmology. 105(8)
This study aimed to determine the distribution of germline mutations in the retinoblastoma (RB) gene in patients with retinoblastoma to design more effective genetic testing.A meta-analysis.192 cases identified from literature.All identifiable report
Autor:
J W, Harbour, T G, Murray, D, Hamasaki, N, Cicciarelli, E, Hernández, B, Smith, J, Windle, J M, O'Brien
Publikováno v:
Investigative ophthalmologyvisual science. 37(9)
To determine the efficacy and toxicity associated with intraocular delivery of carboplatin in the treatment of murine transgenic hereditary retinoblastoma.Forty-eight transgenic BLH-SV40 Tag retinoblastoma mice were administered five intravitreal inj
Publikováno v:
American journal of ophthalmology. 121(4)
Purpose To evaluate the surgical results in a series of patients with diabetic macular edema associated with traction from a thickened and taut posterior hyaloid membrane and to identify features associated with better visual outcome. Methods We revi
Publikováno v:
Ophthalmology. 101(6)
Carcinoid tumor is a low-grade malignancy that usually arises in the gastrointestinal tract or bronchus and rarely metastasizes to the eye. Metastasis of carcinoid tumor to the uvea can be confused clinically with other primary and metastatic uveal t