Results 11 to 20 of about 78,942 (313)

IL‐34 in hepatoblastoma cells potentially promote tumor progression via autocrine and paracrine mechanisms

open access: yesCancer Medicine, 2022
Hepatoblastoma is the most common pediatric liver tumor, but little research has been done on the role of macrophages in hepatoblastoma. The purpose of this study was to gain insight into potential roles for macrophages in hepatoblastoma.
Tomoaki Irie   +10 more
doaj   +1 more source

Radiologic Pathologic Correlation of Primary Paratesticular Rhabdomyosarcoma

open access: yesJournal of Gastrointestinal and Abdominal Radiology, 2020
Rhabdomyosarcoma is the most common soft tissue sarcoma in childhood and adolescence, arising from the mesenchymal tissue. It is an intrascrotal tumor localized in the paratesticular structures such as the epididymis or spermatic cord.
Vignesh Kumar Mohan   +5 more
doaj   +1 more source

BLADDER EMBRYONAL RHABDOMYOSARCOMA IN AN 18-MONTHS-OLD BOY: A CASE REPORT

open access: yesJurnal Urologi Indonesia, 2023
Objective: This study aims to report a case of bladder embryonal rhabdomyosarcoma in an 18-months-old boy. Case(s) Presentation: An 18-months-old boy presented with complaint of difficult urinating since the last 2 months before presentation.
I Made Mahandita   +2 more
doaj   +1 more source

Interpretation on embryonal tumors in the 2021 WHO Classification of Tumors of the Central Nervous System (fifth edition)

open access: yesChinese Journal of Contemporary Neurology and Neurosurgery, 2021
Embryonal tumors of central nervous system (CNS) are a class of highly heterogeneous brain tumors and the most common malignant brain tumors in children. Researches based on histology and molecular genetics can classify them. This kind of researches only
WANG Yang
doaj   +1 more source

DAX-1 Expression in Pediatric Rhabdomyosarcomas: Another Immunohistochemical Marker Useful in the Diagnosis of Translocation Positive Alveolar Rhabdomyosarcoma [PDF]

open access: yes, 2015
OBJECTIVES: The aim of this study was to investigate the expression of DAX-1 in a series of pediatric rhabdomyosarcomas (RMS) with known translocation and compare it to Ap2\u3b2, known to be selectively expressed in ARMS. DESIGN: We revised a series of
Alaggio, Rita   +10 more
core   +9 more sources

Early life factors and risk of childhood rhabdomyosarcoma. [PDF]

open access: yes, 2013
Although little is known about etiology of childhood rhabdomyosarcoma (RMS), early life factors are suspected in the etiology. We explored this hypothesis using linked data from the California Cancer Registry and the California birth rolls.
Anshu eShrestha   +6 more
core   +2 more sources

Giant Rhabdomyosarcoma in A Child: A Rare Entity

open access: yesNepal Journal of Neuroscience, 2018
Rhabdomyosarcoma (RMS) is a highly aggressive and rapidly progressive sarcoma. RMS can occur in any part of the human body, however, paraspinal or paravertebral or epidural RMS is very rare in children.
Gopal Raman Sharma   +3 more
doaj   +1 more source

DNMT3B in vitro knocking-down is able to reverse embryonal rhabdomyosarcoma cell phenotype through inhibition of proliferation and induction of myogenic differentiation [PDF]

open access: yes, 2016
Aberrant DNA methylation has been frequently observed in many human cancers, including rhabdomyosarcoma (RMS), the most common soft tissue sarcoma in children.
Camero, Simona   +11 more
core   +1 more source

PRDM14 is expressed in germ cell tumors with constitutive overexpression altering human germline differentiation and proliferation. [PDF]

open access: yes, 2018
Germ cell tumors (GCTs) are a heterogeneous group of tumors occurring in gonadal and extragonadal locations. GCTs are hypothesized to arise from primordial germ cells (PGCs), which fail to differentiate.
Chen, Di   +4 more
core   +2 more sources

Key role of MEK/ERK pathway in sustaining tumorigenicity and in vitro radioresistance of embryonal rhabdomyosarcoma stem-like cell population [PDF]

open access: yes, 2016
The identification of signaling pathways that affect the cancer stem-like phenotype may provide insights into therapeutic targets for combating embryonal rhabdomyosarcoma.
Ciccarelli, Carmela   +10 more
core   +9 more sources

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