Results 321 to 330 of about 593,238 (360)
ABSTRACT Background The incidence of Nasopharyngeal carcinoma (NPC) is rising in recent years, especially in some non‐developed parts of the world. Hence, cost‐efficient means for sensitive detection of NPC are vital. Methods We recruited 646 participants, including healthy individuals, patients with benign nasopharyngeal diseases, and NPC patients for
Song Zhang+10 more
wiley +1 more source
Combining Clinical, Genetic and Protein Markers Using Machine Learning Models Discriminates Psoriatic Arthritis Patients From Those With Psoriasis. [PDF]
Ganatra D+11 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
Identification of loci associated with women's reproductive traits and exploration of a shared genetic basis with obesity. [PDF]
Kwon SA, Cho YS.
europepmc +1 more source
Mechanisms of enhancer‐driven oncogene activation
Abstract An aggressive subtype of acute myeloid leukemia (AML) is caused by enhancer hijacking resulting in MECOM overexpression. Several chromosomal rearrangements can lead to this: the most common (inv(3)/t(3;3)) results in a hijacked GATA2 enhancer, and there are several atypical MECOM rearrangements involving enhancers from other hematopoietic ...
Joyce Vriend+2 more
wiley +1 more source
Comprehensive genetic and epigenetic characterization of Lynch‐like syndrome patients
What's New? Lynch‐like syndrome is associated with development of colorectal cancer (CRC) with microsatellite instability and loss of expression of certain mismatch repair (MMR) genes, similar to Lynch syndrome, but unlike Lynch syndrome, the genetic cause of Lynch‐like syndrome (LLS) remains unknown.
Francesca Pirini+18 more
wiley +1 more source
ARMSprimer3: An open-source primer design Python program for amplification refractory mutation system PCR (ARMS-PCR). [PDF]
Guo J, Grojean J, Guo H.
europepmc +1 more source
What's New? Little is known about how genetic variation in human papillomavirus type 45 (HPV45) influences its ability to cause cancer. Here, the authors conducted the largest whole‐genome sequencing study to date of HPV45, looking for associations between viral genetic variation and precancer or cancer risk.
Aimee J. Koestler+14 more
wiley +1 more source
A Systematic Review of the Effect of Gene-Lifestyle Interactions on Metabolic-Disease-Related Traits in South Asian Populations. [PDF]
Bineid MM+8 more
europepmc +1 more source
What's New? TP53 is included in most cancer predisposition multigene panels, but analyzing the contribution of TP53 variants to cancer predisposition beyond the Li–Fraumeni syndrome remains challenging. This study, based on 53,085 hereditary breast and ovarian cancer panel analyses, explores the genotype–phenotype correlation of TP53 variants and ...
Edwige Kasper+46 more
wiley +1 more source