Results 221 to 230 of about 1,548,550 (297)

Cancer‐associated mutations in endometriosis reframe a benign disease through molecular oncology

Molecular Oncology, EarlyView.
This review aims to comprehensively analyse cancer‐associated somatic mutations (CAMs) present in endometriotic lesions, emphasizing their biological roles, spatial distribution and implications for translational applications in medicine. By contextualizing a benign state within a genomic framework, this analysis seeks to establish its value as a ...
Clarissa Mujacic, Maria Concetta Vitale, Rita Siino, Emilia Di Giovanni, Carla Ferrante Bannera, Enrico Di Marco, Andrea Gottardo, Tancredi Didier Bazan Russo, Nadia Barraco, Alessandro Perez, Valerio Gristina, Antonio Galvano, Giuseppe Badalamenti, Antonio Russo, Viviana Bazan, Lorena Incorvaia   +15 more
wiley   +1 more source

Father and son with a pathogenic variant c.614dup p.(Gln206Thrfs*20) in the <i>NR5A1</i> gene: a case report. [PDF]

Front Pediatr
Martinková J, Mihulová M, Balaščaková M, Trachta J, Křepelová A.   +4 more
europepmc   +1 more source

Preoperative circulating tumor cells integrated with imaging analysis for prognostic evaluation in head and neck squamous cell carcinoma

Molecular Oncology, EarlyView.
Detecting circulating tumor cells (CTCs) in blood before surgery may help predict outcomes in patients with head and neck squamous cell carcinoma (HNSCC). Here, we show when combined with tumor size and lymph node involvement from routine imaging, CTC status identifies high‐risk patients with poorer survival—offering a simple, minimally invasive tool ...
Susanne Flach, Gizem Abaci, Tom Huberty, Axel Lechner, Lukas Käsmann, Jens Ricke, Sophia Stöcklein, Martin Canis, Philipp Baumeister, Marianna Alunni‐Fabbroni   +9 more
wiley   +1 more source

Recent variant discoveries and emerging genetic mechanisms in autoinflammatory diseases. [PDF]

Front Immunol
Chen J, Zhou S, Xu T, Wu M.
europepmc   +1 more source

Genetic Sequencing in Saudi Patients with Systemic Lupus Erythematosus. [PDF]

Open Access Rheumatol
Al-Homood IA, Binhassan S, AlMatham K, Hassen LM, Samman M.   +4 more
europepmc   +1 more source

Genotype and Phenotype of 198 Korean Patients With Nonlethal Osteogenesis Imperfecta: A Retrospective Cohort Study. [PDF]

Hum Mutat
Lee J, Lee HR, Ko JM, Shin CH, Lee W, Song MH, Cho TJ.   +6 more
europepmc   +1 more source

Population prevalence of high-risk pharmacogenetic configurations in a healthy older Australian reference cohort. [PDF]

Front Pharmacol
Hooshmand K, Hughes S, Stocker SL, Somogyi AA, Ballinger ML, Thomas DM.   +5 more
europepmc   +1 more source

<i>STOML1</i> as an Exploratory Candidate Gene for Autosomal Dominant Iris and Chorioretinal Coloboma in a British Family. [PDF]

Genes (Basel)
Berry V, Ponnekanti MB, Aychoua N, Reddy MA, Michaelides M.   +4 more
europepmc   +1 more source

Genetic Monitoring of Tibial Hemimelia in Galloway Cattle. [PDF]

Anim Genet
Brenig B.
europepmc   +1 more source