Results 21 to 30 of about 18,165 (198)
BARD1 Gene Polymorphisms Confer Nephroblastoma Susceptibility
EBioMedicine, 2017 BRCA1-associated RING domain protein 1 (BARD1) is a tumor suppressor, which forms a heterodimer with BRCA1. Three BARD1 gene polymorphisms (rs7585356 G>A, rs6435862 T>G and rs3768716 A>G) were initially identified as high-risk neuroblastoma ...
Wen Fu +10 more
doaj +1 more source
Di-san junyi daxue xuebao, 2020 Objective To investigate the role of long noncoding RNA LINC01006 in regulating the proliferation, invasion and apoptosis of nephroblastoma cells and explore the molecular mechanism.
ZHAO Ting +3 more
doaj +1 more source
Hemorrhagic shock due to rupture of a nephroblastoma in an infant: A case report
Journal of Pediatric Surgery Case Reports, 2023 Introduction: Nephroblastoma is the most common type of malignant renal tumor in children, but hemorrhage in ruptured nephroblastoma is rare. Case presentation: A three-month-old boy was admitted to our hospital with a large right renal tumor and ...
Yuko Hino +7 more
doaj +1 more source
Renal nephroblastoma in adult dog
Brazilian Journal of Veterinary Medicine, 2020 Nephroblastoma is a neoplasia originating from the poor differentiation of the metanephrogenic blastema, therefore neoplasia of embryonic origin. It is commonly reported in dogs less than two years old and is rare in adults.
Dayane Caicó Collares Araujo +3 more
doaj +1 more source
Clinical Case Reports, 2023 Key Clinical Message Renal cell carcinoma as a secondary malignant neoplasm is relatively rare; however, the possibility of secondary renal cell carcinoma following chemoradiotherapy for childhood nephroblastoma should be considered.
Shunsuke Fujisawa +8 more
doaj +1 more source
Cancer-prone syndrome of mosaic variegated aneuploidy and total premature chromatid separation: Report of five infants [PDF]
, 2001 Five infants (two girls and three boys) from four families all had severe pre- and post-natal growth retardation, profound developmental delay, microcephaly, hypoplasia of the brain with Dandy-Walker complex or other posterior fossa malformations, and ...
Galjaard, R-J.H. (Robert-Jan) +7 more
core +1 more source
miRNA profiles as a predictor of chemoresponsiveness in Wilms' tumor blastema. [PDF]
, 2013 The current SIOP treatment protocol for Wilms' tumor involves pre-operative chemotherapy followed by nephrectomy. Not all patients benefit equally from such chemotherapy.
Boccon-Gibod, L +9 more
core +6 more sources
Journal of the Egyptian National Cancer Institute, 2023 Objective Immunohistochemical expression of P53 protein is so closely related to status of mutation of P53 gene which is tightly linked with pathogenesis of nephroblastoma or Wilms tumor. This study aims to determine the immunohistochemical expression of
Emmanuel D. Morgan +4 more
doaj +1 more source
Cystic partially differentiated nephroblastoma: a rare pediatric renal tumor—case report
Radiology Case Reports, 2020 Cystic partially differentiated nephroblastoma is a rare renal tumor of childhood. It is part of a spectrum of multicystic renal tumors that also includes cystic nephroma and cystic Wilms’ tumor.
Leonardo Passos Vilares Cordeiro +5 more
doaj +1 more source
Wilms tumor: "State-of-the-art" update, 2016 [PDF]
, 2016 Despite an impressive increase in survival rate over the past decades, there is still a need to improve the survival of specific subgroups of Wilms tumor (anaplastic, metastatic, and bilateral) and to decrease the late effects of treatment in terms of ...
Ehrlich, PF +2 more
core +1 more source