titlesubmit dateissue date
Now showing items 1-20 of 25
DNA Methylomes Reveal Biological Networks Involved in Human Eye Development, Functions and Associated Disorders
Efficacy of ATR inhibitors as single agents in Ewing sarcoma
EWS-FLI1 confers exquisite sensitivity to NAMPT inhibition in Ewing sarcoma cells
EWS-FLI1 impairs aryl hydrocarbon receptor activation by blocking tryptophan breakdown via the kynurenine pathway.
EWS-FLI1-mediated suppression of the RAS-antagonist Sprouty 1 (SPRY1) confers aggressiveness to Ewing sarcoma
EWS/FLI1 Target Genes and Therapeutic Opportunities in Ewing Sarcoma
Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum
Frequency of low-level and high-level mosaicism in sporadic retinoblastoma: genotype-phenotype relationships.
Gene expression and immunohistochemical analyses identify SOX2 as major risk factor for overall survival and relapse in Ewing sarcoma patients
Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility
Helpful Criteria When Implementing NGS Panels in Childhood Lymphoblastic Leukemia.
Hippo pathway effectors YAP1/TAZ induce an EWS-FLI1-opposing gene signature and associate with disease progression in Ewing sarcoma.
Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma.
Lysyl oxidase is downregulated by the EWS/FLI1 oncoprotein and its propeptide domain displays tumor supressor activities in Ewing sarcoma cells
Periostin: A Matricellular Protein With Multiple Functions in Cancer Development and Progression
El plan de salud del estado de oregón para el acceso a los servicios sanitarios: contexto, elaboración y características
Primary intracranial spindle cell sarcoma with rhabdomyosarcoma-like features share a highly distinct methylation profile and DICER1 mutations.
Sarcoma classification by DNA methylation profiling.
Severe alpha-1 antitrypsin deficiency in composite heterozygotes inheriting a new splicing mutation QOMadrid
SpainUDP: The Spanish Undiagnosed Rare Diseases Program