Results 211 to 220 of about 5,748,368 (263)

An artificial intelligence model integrating clinico-laboratory data and single nucleotide polymorphism-based genomic risk for prostate cancer diagnosis in Korean men. [PDF]

Investig Clin Urol
Jung JH, Han GH, So B, Hong M, Ahn SH, Lim SH, Han SM, Park H, Lee SW, Song G, Choi S, Chung HC, Chung H, Kang TW, Eom M, Koh SB, Kim JH.   +16 more
europepmc   +1 more source

The Prognostic Value of the XPC rs2228001 Single Nucleotide Polymorphism in Cholangiocarcinoma. [PDF]

Liver Int
Wang G, Mantas A, Liu D, Al-Masri TM, Lueong SS, Siveke J, Luedde T, Ulmer TF, Amygdalos I, Vondran FWR, Lurje G, Neumann UP, Heij LR, Bednarsch J.   +13 more
europepmc   +1 more source

Elevated Soybean Seed Oil Phenotype Associated with a Single Nucleotide Polymorphism in <i>GmNFR1α</i>. [PDF]

Plants (Basel)
Patibandla SV, Carrero-Colón M, Song Q, Qin Q, Clevinger E, Zhu H, Maroof MAS, Hudson K.   +7 more
europepmc   +1 more source

Sex Difference in Effect of the OPRM1 Gene A118G (rs1799971) Single-Nucleotide Polymorphism on the Requirement for Postoperative Fentanyl in Japanese Patients Who Underwent Laparoscopic-Assisted Colectomy. [PDF]

Neuropsychopharmacol Rep
Nakagawa H, Nishizawa D, Mieda T, Tsujita M, Kasai S, Hasegawa J, Nakayama K, Ebata Y, Kitamura A, Hayashida M, Ikeda K.   +10 more
europepmc   +1 more source

Association of <i>PLA2G2A</i> single nucleotide polymorphism and cardiometabolic diseases in an HIV-infected population. [PDF]

Biomed Rep
Ndonwi EN, Nqebelele U, Matsha TE, Kengne AP.   +3 more
europepmc   +1 more source

The causal relationship between systemic lupus erythematosus and juvenile myoclonic epilepsy: A Mendelian randomization study and mediation analysis

Ibrain, Volume 11, Issue 1, Page 98-105, Spring 2025.
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, Ningning Zhang, Ruirui Zhang, Lan Zhang, Dadong Luo, Junqiang Li, Yaqing Liu, Yunan Wang, Xinyue Duan, Xin Tian, Tiancheng Wang   +10 more
wiley   +1 more source

Sulfur Starvation, Sulfide Supplementation, and cysM Transcription in Campylobacter jejuni Strains with a Single Nucleotide Polymorphism. [PDF]

Microorganisms
Gunther NW, Abdul-Wakeel A, Guragain M.
europepmc   +1 more source

A multilevel perspective on MSH6‐associated Lynch syndrome: Integrating molecular, biological, and clinical insights

International Journal of Cancer, EarlyView.
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, Anne‐Sophie van der Werf‐'t Lam, Madalina Cabuta, Maartje Nielsen, Noah C. Helderman   +4 more
wiley   +1 more source

Preimplantation genetic testing and prenatal diagnosis of TANGO2 deficiency disorder with biallelic pathogenic variants using single-nucleotide polymorphism-based haplotyping and gap-polymerase chain reaction. [PDF]

Front Genet
Ke W, Wen X, Ou Z, Fang X, Huo J, Lin X, Zhang X, Li Z.   +7 more
europepmc   +1 more source

Clinical Relevance of BACH1 Expression in Non–Small Cell Lung Cancer

International Journal of Cancer, EarlyView.
ABSTRACT BTB and CNC homolog 1 (BACH1) is a redox‐sensitive transcription factor implicated in tumor progression, metabolic reprogramming, and therapy resistance in several cancers. However, its prognostic significance and role in therapy resistance in non–small cell lung cancer (NSCLC) remain unclear.
Jing Liu, Marc A. Schneider, Julia Held, Sabine Wrenger, Wenzhang Si, Michael Allgaeuer, Florian Eichhorn, Sabina Janciauskiene   +7 more
wiley   +1 more source