Results 231 to 240 of about 1,081,535 (384)
TGF‐β has a complex role in cancer, exhibiting both tumor‐suppressive and tumor‐promoting properties. Using a series of differentiated tumoroids, derived from different stages and mutational background of colorectal cancer patients, we replicate this duality of TGF‐β in vitro. Notably, the atypical but highly aggressive KRASQ22K mutation rendered early‐
Theresia Mair+17 more
wiley +1 more source
Primary central nervous system tumors in patients with multiple sclerosis. [PDF]
Sabouri M+4 more
europepmc +1 more source
Multiple primary malignant neoplasms series: Recent results in cancer research
Joop W. Barents
openalex +1 more source
Multiple malignant primary neoplasms in patients with gastric neoplasms in the health district of León [PDF]
Alberto Muela Molinero+7 more
openalex +1 more source
Loss of the frequently mutated chromatin remodeler ARID1A, a subunit of the SWI/SNF cBAF complex, results in less open chromatin, alternative splicing, and the failure to stop cells from progressing through the cell cycle after DNA damage in bladder (cancer) cells. Created in BioRender. Epigenetic regulators, such as the SWI/SNF complex, with important
Rebecca M. Schlösser+11 more
wiley +1 more source
Characteristic Findings of Honeycomb-Like Structures in Patients With Chronic Coronary Syndrome Complicated With Myeloproliferative Neoplasms. [PDF]
Shimosato H+9 more
europepmc +1 more source
MULTIPLE PRIMARY MALIGNANT NEOPLASMS ASSOCIATED WITH GENITO-URINARY ORGANS
Hideo Kamada, Tsuyoshi Shiraga
openalex +2 more sources
Germline variants in CDKN2A wild‐type melanoma prone families
Among melanoma‐prone families, wild‐type for CDKN2A and CDK4, some have pathogenic variants in genes not usually linked to melanoma. Furthermore, rare XP‐related variants and variants in MC1R are enriched in such families. Germline pathogenic variants in CDKN2A are well established as an underlying cause of familial malignant melanoma. While pathogenic
Gjertrud T. Iversen+5 more
wiley +1 more source