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2.144  Articles
1 of 215 pages  |  10  records  |  more records»
This note provides a quiver which does not admit a maximal green sequence, but which is mutation-equivalent to a quiver which does admit a maximal green sequence. The proof uses the `scattering diagrams' of Gross-Hacking-Keel-Kontsevich to show that a max... see more

This note provides a quiver which does not admit a maximal green sequence, but which is mutation-equivalent to a quiver which does admit a maximal green sequence. The proof uses the `scattering diagrams' of Gross-Hacking-Keel-Kontsevich to show that a max... see more

Cluster automorphisms have been shown to have links to the mapping class groups of surfaces, maximal green sequences and to exchange graph automorphisms for skew-symmetric cluster algebras. In this paper we generalise these results to the s... see more

Cluster automorphisms have been shown to have links to the mapping class groups of surfaces, maximal green sequences and to exchange graph automorphisms for skew-symmetric cluster algebras. In this paper we generalise these results to the s... see more

 
Acute myeloid leukaemia (AML) is a clinically heterogeneous haematological cancer with increased incidence in the elderly. Genetic mutations remain important prognostic factors for treatment outcome. Our study determined the prevalence and clinical signif... see more

Colorectal carcinoma (CRC) represents a global health problem. The EGFR signaling pathway is very important in the initiation of different human epithelial cancers and plays a key role in colorectal carcinogenesis. Considering the role of EGFR as a mitoge... see more

Lipoid proteinosis is a rare multisystem genodermatosis inherited as autosomal recessive trait. We report a case of lipoid proteinosis in a 10-year-old boy born to first-degree consanguineous parents presented with marked hoarseness of voice, accelerated ... see more

Objective: To investigate the relationship between isocitrate dehydrogenase (IDH) 1/2 mutation, telomerase reverse transcriptase (TERT) gene promoter mutation and the prognosis of human glioma patients.Methods: One hundred fifteen patients with human glio... see more

BACKGROUND Retinoblastoma (RB) is an inherited disorder caused by the RB1 gene mutation in retinal cells or germline mutation. Identifying the specific mutation is crucial for prognosis, inheritance risk assessment, and treatment planning. This study aime... see more

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