Results 1 to 10 of about 41,917 (262)

Analysis of retinoblastoma-associated genes using bioinformatic methods

open access: yesDigital Diagnostics, 2023
BACKGROUND: Retinoblastoma is a common neoplasia that affects the visual organ in young children. The mortality rate is approximately 15%. In 91% of cases, surgery with enucleation is required, which significantly reduces the patients quality of life ...
Kirill Yu. Klimov
doaj   +2 more sources

A Meta-Analysis of Retinoblastoma Copy Numbers Refines the List of Possible Driver Genes Involved in Tumor Progression. [PDF]

open access: yesPLoS ONE, 2016
BACKGROUND:While RB1 loss initiates retinoblastoma development, additional somatic copy number alterations (SCNAs) can drive tumor progression. Although SCNAs have been identified with good concordance between studies at a cytoband resolution, accurate ...
Irsan E Kooi   +11 more
doaj   +2 more sources

Non-coding and Coding Transcriptional Profiles Are Significantly Altered in Pediatric Retinoblastoma Tumors [PDF]

open access: yesFrontiers in Oncology, 2019
Retinoblastoma is a rare pediatric tumor of the retina, caused by the homozygous loss of the Retinoblastoma 1 (RB1) tumor suppressor gene. Previous microarray studies have identified changes in the expression profiles of coding genes; however, our ...
Swetha Rajasekaran   +20 more
doaj   +4 more sources

BIRC5 drives cell-cycle dysregulation and represents a novel molecular target in retinoblastoma [PDF]

open access: yesFrontiers in Oncology
Aims and objectivesRetinoblastoma is the most common pediatric intraocular malignancy, although it remains a rare disease overall, yet the molecular targets and therapeutic vulnerabilities sustaining its most aggressive proliferative cell states remain ...
Yingtong Chen   +9 more
doaj   +2 more sources

BTG interacts with retinoblastoma to control cell fate in Dictyostelium. [PDF]

open access: yesPLoS ONE, 2010
BACKGROUND: In the genesis of many tissues, a phase of cell proliferation is followed by cell cycle exit and terminal differentiation. The latter two processes overlap: genes involved in the cessation of growth may also be important in triggering ...
Daniele Conte   +2 more
doaj   +3 more sources

Retinoblastoma [PDF]

open access: yesLancet, The, 2012
Retinoblastoma is the first tumor suppressor gene discovered ever. The discovery opened a new avenue in the field of oncology leading to the identification of 35 tumor suppressor genes, till date in our genome.
Helen Dimaras   +2 more
exaly   +3 more sources

RPL41 inhibits the proliferation and migration of retinoblastoma through the ARL5B-associated lysosomal trafficking [PDF]

open access: yesFrontiers in Immunology
PurposeRetinoblastoma is the most common intraocular cancer in infants and children, with a significant potential for metastasis. The mini-peptide ribosomal protein L41 (RPL41) has demonstrated extensive antitumor effects in vitro by promoting the ...
Ye Li   +6 more
doaj   +2 more sources

Transcriptome profiling of uterine leiomyosarcomas identifies a leiomyoma-like expression pattern that indicates better survival [PDF]

open access: yesBJC Reports
Background Uterine leiomyosarcomas are rare and aggressive cancers with poor survival. Their non-cancerous counterparts, uterine leiomyomas, are common tumors affecting many women during reproductive years.
Sara Khamaiseh   +7 more
doaj   +2 more sources

Genetics and Epigenetics of Human Retinoblastoma [PDF]

open access: yesAnnual Review of Pathology: Mechanisms of Disease, 2015
Retinoblastoma is a pediatric tumor of the developing retina from which the genetic basis for cancer development was first described. Inactivation of both copies of the RB1 gene is the predominant initiating genetic lesion in retinoblastoma and is rate ...
Claudia A Benavente, Michael A Dyer
exaly   +2 more sources

Epigenetic Factors in Pathogenesis of Retinoblastoma: DNA Methylation and Histone Acetylation [PDF]

open access: yesCurrent Issues in Molecular Biology
(Background) Retinoblastoma is the most common intraocular malignancy in childhood, primarily caused by mutations in the RB1 gene. However, increasing evidence highlights the significant role of epigenetic mechanisms, particularly DNA methylation and ...
Georgios Kiosis   +8 more
doaj   +2 more sources

Home - About - Disclaimer - Privacy