Results 111 to 120 of about 1,220,485 (237)
Rhabdomyosarcoma mimicking Wilms' tumor
, 1994 A case of a 6 year old child, with a pleomorphic rhabdomyosarcoma involving simultaneously the leg muscles and the kidney is reported. The renal tumor distorted the pyelocalycial system and Wilms' tumor was the clinical diagnosis.
Mendonça, Núbia [UNESP] +2 more
core +1 more source
Cancer Risk in Marfan Syndrome: A Swedish Population‐Based Cohort Study
International Journal of Cancer, Volume 159, Issue 7, Page 1707-1714, 1 October 2026.The cancer risk in Marfan syndrome, an autosomal dominant connective tissue disorder, largely remains to be explored. In this population‐based matched cohort study of 1544 Swedish patients, the overall cancer risk in adults with Marfan syndrome showed no significant increase, except for the risk of endocrine tumours with a nearly threefold increase ...
Ida Nordgren +8 more
wiley +1 more source
The Clinical Relevance of Age at Presentation in Nephroblastoma
, 2016 The most important prognostic factors for Wilms tumor (WT) patients seem to be stage, histological subtype, and 1p/16q loss of heterozygosity (LOH) in chemotherapy-naive WTs.
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MedComm, Volume 7, Issue 10, October 2026.• EV content maintains cellular homeostasis and is involved in several disease onset and progression. • miRNA export in EVs depends on: RNA‐binding proteins recognizing motif sequences and on epitranscriptomic modifications. • The disclosure of delivery mechanisms is crucial for developing personalized EV‐based therapeutic tools. ABSTRACT Extracellular
Sabrina Garbo +4 more
wiley +1 more source
Protein Science, Volume 35, Issue 10, October 2026.Abstract Autoantibodies against tumor‐associated autoantigens are clinically valuable biomarkers for cancer diagnosis; however, the structural determinants governing epitope selectivity remain unknown. Here, we investigated whether the intrinsic conformational stability of target autoantigens regulates the epitope propensity of tumor‐associated ...
Ai Miyamoto +13 more
wiley +1 more source
Annals of the New York Academy of Sciences, Volume 1564, Issue 1, October 2026.Epitranscriptomic marks are highly variable across life stages and tissues, complicating comparisons between species. Using m6A consensus motifs, we developed a genomic indicator reflecting transcript methylability, the DRACH o/e score, that we used to investigate epitranscriptomic features and associated functions across nine bilaterian species.
Natacha Clairet +4 more
wiley +1 more source
Diszregulált miRNS-ek Wilms-tumorban és lehetséges célpontjaik
Bevezetés: A Wilms-tumor a vese malignus daganatos elváltozása, mely leggyakrabban 10 év alatti gyermekek körében fordul elő. Célkitűzés: miRNS-profilozás 10 primer típusú Wilms-tumor szöveti FFPE mintából, valamint 10 kontrollmintából, és az ...
Kabai , Alexandra Barbara
core
Teratoid Wilms' tumor: a case report
, 2000 Teratoid Wilms' tumor is rarely seen and is a description used only recently. The term describes classical nephroma with a diversity of cell types and tissues.
Arzu Bostancı Şencan +4 more
core +2 more sources
Wilms’ tumor is also known as nephroblastoma. It is a rare cancer of the kidney which can be found exclusively in young children. It is fourth most common pediatric cancer found in children younger than five years old.
Pooja Rani
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