Results 171 to 180 of about 13,841,936 (288)
The T cell‐inflamed gene expression profile (GEP) provides a biomarker for immunotherapy response across various cancers. We established a CT‐based radiomics model to predict the T cell‐inflamed GEP and immunotherapy response in hepatocellular carcinoma (HCC).
Mimi Tang +11 more
wiley +1 more source
Ancient DNA HLA typing reveals significant shifts in frequency in Europe since the Neolithic. [PDF]
Plascencia AG +2 more
europepmc +1 more source
Commentary: Identification of Repeat Region Ambiguities in HLA Typing and the Implications for Immunogenetics Research. [PDF]
Turner TR +4 more
europepmc +1 more source
The Value of HLA Typing in Severe Cutaneous Drug Reactions. [PDF]
Khan S, Ghosh B.
europepmc +1 more source
Human Leukocyte Antigen (HLA) Typing Study Identifies Maternal DQ2 Susceptibility Alleles among Infertile Women: Potential Associations with Autoimmunity and Micronutrients. [PDF]
Triggianese P +9 more
europepmc +1 more source
HLA typing in lung transplantation: does high resolution fit all? [PDF]
Deaglio S +3 more
europepmc +1 more source
Health in All Policies in Serbian Sectoral Legislation: A Document Analysis
ABSTRACT Health in All Policies (HiAP) seeks to integrate health considerations across sectors to improve population health and equity. This study examines how HiAP has been operationalised through legal instruments in Serbia, assessing the extent to which legislation incorporates health outcomes, intersectoral governance, equity, use of evidence, and ...
Predrag Duric +10 more
wiley +1 more source
Orthanq: transparent and uncertainty-aware haplotype quantification with application in HLA-typing. [PDF]
Uzuner H +3 more
europepmc +1 more source
Mendelian randomization (MR) studies were conducted using the inverse‐variance weighted (IVW) method, MR‐Egger and weighted median on juvenile myoclonic epilepsy (JME), and systemic lupus erythematosus (SLE) data from the Integrative Epidemiology Unit (IEU) Open genome‐wide association study (GWAS) database and the International League Against Epilepsy
Sirui Chen +10 more
wiley +1 more source
Abstract Lynch syndrome (LS) is the most common hereditary colorectal cancer syndrome, caused by a germline pathogenic variant in one of the mismatch repair (MMR) genes. Among these, MSH6‐associated LS represents a distinct subtype with unique molecular and clinical characteristics.
Salwa Ben Yahia +4 more
wiley +1 more source

