Results 61 to 70 of about 6,450 (234)

WWOX promotes osteosarcoma development via upregulation of Myc

open access: yesCell Death & Disease, 2023
Abstract Osteosarcoma is an aggressive bone tumor that primarily affects children and adolescents. This malignancy is highly aggressive, associated with poor clinical outcomes, and primarily metastasizes to the lungs.
Rania Akkawi   +7 more
openaire   +3 more sources

The RAG Model: a new paradigm for genetic risk stratification in multiple myeloma [PDF]

open access: yes, 2014
Molecular studies have shown that multiple myeloma is a highly genetically heterogonous disease which may manifest itself as any number of diverse subtypes each with variable clinicopathological features and outcomes.
Chevassut, Timothy J   +2 more
core   +3 more sources

The WWOX gene in brain development and pathology [PDF]

open access: yesExperimental Biology and Medicine, 2020
Shortly after its discovery in 2000, WWOX was hailed as a tumor suppressor gene. In subsequent years of research, this function was confirmed indisputably. Majority of tumors show high rate of loss of heterozygosity and decreased expression of WWOX.
K Kośla, Ż Kałuzińska, AK Bednarek
openaire   +2 more sources

Expression profile of CREB knockdown in myeloid leukemia cells. [PDF]

open access: yes, 2008
BackgroundThe cAMP Response Element Binding Protein, CREB, is a transcription factor that regulates cell proliferation, differentiation, and survival in several model systems, including neuronal and hematopoietic cells.
Cheng, Jerry C   +6 more
core   +2 more sources

Molecular Biology of the WWOX Gene That Spans Chromosomal Fragile Site FRA16D

open access: yesCells, 2021
It is now more than 20 years since the FRA16D common chromosomal fragile site was characterised and the WWOX gene spanning this site was identified. In this time, much information has been discovered about its contribution to disease; however, the normal
Cheng Shoou Lee   +4 more
doaj   +1 more source

Genome-Wide Copy Number Analysis in Esophageal Adenocarcinoma Using High-Density Single-Nucleotide Polymorphism Arrays [PDF]

open access: yes, 2008
We applied whole-genome single-nucleotide polymorphism arrays to define a comprehensive genetic profile of 23 esophageal adenocarcinoma (EAC) primary tumor biopsies based on loss of heterozygosity (LOH) and DNA copy number changes.
Clouston, Andrew D   +8 more
core   +1 more source

WWOX protein expression varies among ovarian carcinoma histotypes and correlates with less favorable outcome

open access: yesBMC Cancer, 2005
Background The putative tumor suppressor WWOX gene spans the common chromosomal fragile site 16D (FRA16D) at chromosome area 16q23.3-24.1. This region is a frequent target for loss of heterozygosity and chromosomal rearrangement in ovarian, breast ...
Liu Jinsong   +10 more
doaj   +1 more source

Copy number variants are produced in response to low‐dose ionizing radiation in cultured cells [PDF]

open access: yes, 2013
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/106089/1/em21840 ...
Arlt, Martin F.   +4 more
core   +1 more source

Dynamic expression of genes associated with schizophrenia and bipolar disorder across development [PDF]

open access: yes, 2019
Common genetic variation contributes a substantial proportion of risk for both schizophrenia and bipolar disorder. Furthermore, there is evidence of significant, but not complete, overlap in genetic risk between the two disorders.
Clifton, Nicholas E.   +10 more
core   +3 more sources

Molecular Alterations in Osteosarcomas of the Oral and Maxillofacial Region: A Scoping Review

open access: yesJournal of Oral Pathology &Medicine, EarlyView.
ABSTRACT Background Given the rarity and aggressive nature of osteosarcomas (OS) in the oral and maxillofacial region, understanding their molecular alterations is essential to improve diagnosis, prognosis, and guide targeted therapies. This study aimed to map molecular alterations associated with oral and maxillofacial OS, providing an overview of the
Iara Vieira Ferreira   +6 more
wiley   +1 more source

Home - About - Disclaimer - Privacy