137 related articles for article (PubMed ID: 38006838)
1. Investigation of the methylation changes in the promoter region of RB1 gene in retinoblastoma: Unraveling the epigenetic puzzle in retinoblastoma.
Erdoğan ÖŞ; Ödemiş DA; Kayım ZY; Gürbüz O; Tunçer ŞB; Kılıç S; Çelik B; Tuncer S; Bay SB; Kebudi R; Yazıcı H
Pathol Res Pract; 2024 Jan; 253():154939. PubMed ID: 38006838
[TBL] [Abstract][Full Text] [Related]
2. "Monoallelic germline methylation and sequence variant in the promoter of the RB1 gene: a possible constitutive epimutation in hereditary retinoblastoma".
Quiñonez-Silva G; Dávalos-Salas M; Recillas-Targa F; Ostrosky-Wegman P; Aranda DA; Benítez-Bribiesca L
Clin Epigenetics; 2016; 8():1. PubMed ID: 26753011
[TBL] [Abstract][Full Text] [Related]
3. Detection and reporting of RB1 promoter hypermethylation in diagnostic screening.
Price EA; Kolkiewicz K; Patel R; Hashim S; Karaa E; Scheimberg I; Sagoo MS; Reddy MA; Onadim Z
Ophthalmic Genet; 2018 Aug; 39(4):526-531. PubMed ID: 29851531
[TBL] [Abstract][Full Text] [Related]
4. Mutational screening of germline
Nguyen HH; Nguyen HTT; Vu NP; Le QT; Pham CM; Huyen TT; Manh H; Pham HLB; Nguyen TD; Le HTT; Van Nong H
Mol Vis; 2018; 24():231-238. PubMed ID: 29568217
[TBL] [Abstract][Full Text] [Related]
5. Spectrum of germline
Rojanaporn D; Boontawon T; Chareonsirisuthigul T; Thanapanpanich O; Attaseth T; Saengwimol D; Anurathapan U; Sujirakul T; Kaewkhaw R; Hongeng S
Mol Vis; 2018; 24():778-788. PubMed ID: 30636860
[TBL] [Abstract][Full Text] [Related]
6. Spectrum of mutations in the
Kiet NC; Khuong LT; Minh DD; ; Quan NHM; Xinh PT; Trang NNC; Luan NT; Khai NM; Vu HA
Mol Vis; 2019; 25():215-221. PubMed ID: 30996590
[TBL] [Abstract][Full Text] [Related]
7. Next-Generation Sequencing of Retinoblastoma Identifies Pathogenic Alterations beyond RB1 Inactivation That Correlate with Aggressive Histopathologic Features.
Afshar AR; Pekmezci M; Bloomer MM; Cadenas NJ; Stevers M; Banerjee A; Roy R; Olshen AB; Van Ziffle J; Onodera C; Devine WP; Grenert JP; Bastian BC; Solomon DA; Damato BE
Ophthalmology; 2020 Jun; 127(6):804-813. PubMed ID: 32139107
[TBL] [Abstract][Full Text] [Related]
8. Evidence of predisposing epimutation in retinoblastoma.
Gelli E; Pinto AM; Somma S; Imperatore V; Cannone MG; Hadjistilianou T; De Francesco S; Galimberti D; Currò A; Bruttini M; Mari F; Renieri A; Ariani F
Hum Mutat; 2019 Feb; 40(2):201-206. PubMed ID: 30427563
[TBL] [Abstract][Full Text] [Related]
9.
Fang X; Chen J; Wang Y; Zhao M; Zhang X; Yang L; Ni X; Zhao J; Gallie BL
Ophthalmic Genet; 2021 Oct; 42(5):593-599. PubMed ID: 34190019
[No Abstract] [Full Text] [Related]
10. Epigenetic regulation of human retinoblastoma.
Singh U; Malik MA; Goswami S; Shukla S; Kaur J
Tumour Biol; 2016 Nov; 37(11):14427-14441. PubMed ID: 27639385
[TBL] [Abstract][Full Text] [Related]
11. IVF and retinoblastoma revisited.
Dommering CJ; van der Hout AH; Meijers-Heijboer H; Marees T; Moll AC
Fertil Steril; 2012 Jan; 97(1):79-81. PubMed ID: 22112645
[TBL] [Abstract][Full Text] [Related]
12. DNA hypermethylation/boundary control loss identified in retinoblastomas associated with genetic and epigenetic inactivation of the
Raizis AM; Racher HM; Foucal A; Dimaras H; Gallie BL; George PM
Epigenetics; 2021 Sep; 16(9):940-954. PubMed ID: 33258708
[TBL] [Abstract][Full Text] [Related]
13. Etiology including epigenetic defects of retinoblastoma.
Zhou L; Tong Y; Ho BM; Li J; Chan HYE; Zhang T; Du L; He JN; Chen LJ; Tham CC; Yam JC; Pang CP; Chu WK
Asia Pac J Ophthalmol (Phila); 2024; 13(3):100072. PubMed ID: 38789041
[TBL] [Abstract][Full Text] [Related]
14. Clinical characteristics and germline mutation spectrum of RB1 in Chinese patients with retinoblastoma: A dual-center study of 145 patients.
Chai P; Luo Y; Yu J; Li Y; Yang J; Zhuang A; Fan J; Han M; Jia R
Exp Eye Res; 2021 Apr; 205():108456. PubMed ID: 33493472
[TBL] [Abstract][Full Text] [Related]
15. Biallelic and monoallelic deletion of the RB1 promoter in six isogenic clonal H9 hESC lines.
Döpper H; Horstmann M; Menges J; Bozet M; Kanber D; Steenpass L
Stem Cell Res; 2020 May; 45():101779. PubMed ID: 32268247
[TBL] [Abstract][Full Text] [Related]
16. Multiplex ligation-dependent probe amplification versus fluorescent in situ hybridization for screening
Eid OM; El Zomor H; Mohamed AM; El-Bassyouni HT; Afifi HH; El-Ayadi M; Sadek SH; Hammad SA; Salem SI; Mahrous R; Fadel IM; Refaat K; Afifi MA; Shelil AE; Ziko OAO; Abdel Azeem AA; El-Haddad A
Ophthalmic Genet; 2022 Dec; 43(6):789-794. PubMed ID: 36098066
[TBL] [Abstract][Full Text] [Related]
17. Methylation status of RB1 promoter in Indian retinoblastoma patients.
Joseph B; Mamatha G; Raman G; Shanmugam MP; Kumaramanickavel G
Cancer Biol Ther; 2004 Feb; 3(2):184-7. PubMed ID: 14726655
[TBL] [Abstract][Full Text] [Related]
18. Ectopic intracranial retinoblastoma in a 3.5-month-old infant without eye involvement and without evidence of heritability.
Römer T; Temming P; Lohmann DR; Sturm D; von Deimling A; Sellhaus B; Mull M; Kontny U; Moser O
Pediatr Blood Cancer; 2019 May; 66(5):e27599. PubMed ID: 30604586
[TBL] [Abstract][Full Text] [Related]
19. Impaired expression and promotor hypermethylation of O6-methylguanine-DNA methyltransferase in retinoblastoma tissues.
Choy KW; Pang CP; To KF; Yu CB; Ng JS; Lam DS
Invest Ophthalmol Vis Sci; 2002 May; 43(5):1344-9. PubMed ID: 11980845
[TBL] [Abstract][Full Text] [Related]
20. Association Between Genotype and Phenotype in Consecutive Unrelated Individuals With Retinoblastoma.
Salviat F; Gauthier-Villars M; Carton M; Cassoux N; Lumbroso-Le Rouic L; Dehainault C; Levy C; Golmard L; Aerts I; Doz F; Bonnet-Serrano F; Hayek S; Savignoni A; Stoppa-Lyonnet D; Houdayer C
JAMA Ophthalmol; 2020 Aug; 138(8):843-850. PubMed ID: 32556071
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]