Results 161 to 170 of about 24,775,971 (291)

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

Identification of novel <i>PROS1</i> variants through systematic analysis of patients with suspected hereditary protein S deficiency. [PDF]

Res Pract Thromb Haemost
Bartylla MM, Achenbach S, Hackstein H, Schneider S.   +3 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

Protein S deficiency

, 2017
Yuranga Weerakkody, Ian Bickle, Daniel Bell   +2 more
openaire   +1 more source

Acquired protein S deficiency. [PDF]

Archives of Disease in Childhood, 1993
openaire   +1 more source

Diffuse LAD and LV Thrombus as Possible Manifestation of Protein-S Deficiency in a Young Patient. [PDF]

JACC Case Rep, 2023
Kalogeras K, Kyvelou SM, Vythoulkas-Biotis N, Pesiridis T, Vogiatzi G, Katsianos E, Vavuranakis MA, Oikonomou E, Siasos G, Vavuranakis M.   +9 more
europepmc   +1 more source

Translating whole‐genome doubling into precision medicine in cancer

Molecular Oncology, EarlyView.
Whole‐genome doubling creates a WGD‐positive tumor state characterized by persistent chromosomal instability, karyotypic diversification, and cellular stress. These same biological pressures drive aggressive tumor evolution while exposing therapeutic vulnerabilities, providing a rationale for WGD‐informed precision medicine. Whole‐genome doubling (WGD)
Sejung Lee, Junghyeok Lim, Jinhyuk Bhin
wiley   +1 more source

Inherited protein S deficiency: from genotype to phenotype

Haematologica, 2003
ME Daly, NJ Beauchamp
doaj  

Acquired protein S deficiency in a patient with lupus nephritis

Saudi Journal of Medicine and Medical Sciences, 2019
Hajji Meriam, Beji Soumaya, Rais Lamia, Zouaghi Mohammed Karim   +3 more
doaj   +1 more source

Case Report: Severe protein S deficiency unmasks a cryptic <i>PROC</i> mutation with normal activity, triggering life-threatening pulmonary thromboembolism. [PDF]

Front Cardiovasc Med
Liu Y, Zhou B, Xue J, Zhang W, Liu J.
europepmc   +1 more source