Characterisation of somatic genetic alterations in sporadic medullary thyroid carcinoma
Hanna Langer-Macioł, Dagmara Rusinek, Małgorzata Kowalska, Aleksandra Pfeifer et autres
Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.
Hanna Langer-Macioł, Dagmara Rusinek, Małgorzata Kowalska, Aleksandra Pfeifer et autres
Beata Jurecka‐Lubieniecka, Małgorzata Roś-Mazurczyk, Aleksandra Syguła, Alexander Cortez et autres
Abstract Mutations in DNA repair genes are major drivers of both hereditary and sporadic malignancies, including breast, ovarian, prostate, colorectal adenocarcinoma, and pancreatic cancer. Familial tumors are typically associated with earlier onset and a more aggressive clinical phenotype. Advances in diagnostics and …
pl (code pays fourni par la source)
Agata Świętek, Joanna K. Strzelczyk, Dorota Hudy, Zenon Czuba et autres
Introduction: GEP-NETs constitute a heterogeneous group of rare cancers arising in biologically diverse microenvironments, while their cytokine profiles remain insufficiently characterized. Objectives: This study assessed IL-6, IL-8, IL-11 and leptin concentrations in tumor and corresponding surgical margins. Also, we aimed to determine …
pl, hu (code pays fourni par la source)
Agnieszka Piekiełko‐Witkowska, Rossella Elisei, Juliane Léger, Běla Bendlová et autres
BACKGROUND: Endocrine science remains underrepresented in European Union research programs despite the fundamental role of hormone health in human well-being. Analysis of the CORDIS database reveals a persistent gap between the societal impact of endocrine disorders and their research prioritization. At national …
pl, it, fr, cz, de, dk, se, nl, gb, be, hu, ch (code pays fourni par la source)
Beata Jurecka‐Lubieniecka, Małgorzata Roś-Mazurczyk, Aleksandra Syguła, Alexander Jorge Cortez et autres
Pancreatic neuroendocrine neoplasms (pNENs) are the second most common type of pancreatic cancer after pancreatic ductal adenocarcinoma. Germline mutations in DNA repair genes drive several hereditary and sporadic cancers; however, their role in pNENs remains poorly defined. This pilot study aimed to …
pl, hu (code pays fourni par la source)
Agnieszka Piekiełko‐Witkowska, Rossella Elisei, Juliane Léger, Běla Bendlová et autres
BACKGROUND: Endocrine science remains underrepresented in European Union research programs despite the fundamental role of hormone health in human well-being. Analysis of the CORDIS database reveals a persistent gap between the societal impact of endocrine disorders and their research prioritization. At national …
pl, it, fr, cz, de, dk, se, nl, gb, be, hu, ch (code pays fourni par la source)
Dagmara Rusinek, Aleksandra Pfeifer, Artur Zajkowicz, Karolina Tęcza et autres
The unique oncogenic duo of BRAF and TERT promoter ( TERT p) variants was demonstrated to be associated with aggressiveness and poor prognosis in several different cancer types, including melanoma and thyroid cancer. It has been shown that the coexistence of BRAF …
pl (code pays fourni par la source)
Marcin Kubeczko, Patrycja Tudrej, Tomasz Tyszkiewicz, Aleksandra Krzywon et autres
BACKGROUND: Liquid biopsy, including miRNA profiling, is a promising approach to identify breast cancer (BC) resistance. However, the effect of long-term storage on the quality of miRNA assessment in archival serum has not been fully addressed. OBJECTIVES: We aimed to determine whether …
pl (code pays fourni par la source)
Karolina Tęcza, Magdalena Kalinowska, Dagmara Rusinek, Artur Zajkowicz et autres
We studied the associations between 3′UTR genetic variants in ADME genes, clinical factors, and the risk of breast cancer chemotherapy toxicity. Those variants and factors were tested in relation to seven symptoms belonging to myelotoxicity (anemia, leukopenia, neutropenia), gastrointestinal side effects (vomiting, …
pl (code pays fourni par la source)
Elżbieta Szmida, Dorota Butkiewicz, Paweł Karpiński, Tomasz Rutkowski et autres
BACKGROUND: Head and neck squamous cell carcinoma (HNSCC) is one of the most prevalent cancers worldwide. The identification of molecular alterations adding to the individual risk of HNSCC development and progression is one of the most important challenges in studies on cancer …
pl (code pays fourni par la source)
Daria Handkiewicz-Junak, Marek Dedecjus, Urszula Ambroziak, Marcin Barczyński et autres
Advances in the diagnosis and treatment of adrenocortical carcinoma (ACC), along with the development of new therapeutic and diagnostic methods, have prompted a team of experts to formulate the first Polish guidelines for managing ACC. This article presents the diagnostic and therapeutic …
pl, hu (code pays fourni par la source)
Urszula Kacorzyk, Marek Kentnowski, Katarzyna Drosik‐Rutowicz, Dorota Słonina et autres
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