Results 111 to 120 of about 19,884 (196)

Low PRKAB2 Expression Is Associated with Poor Outcomes in Pediatric Adrenocortical Tumors, and Treatment with Rottlerin Increases the PRKAB2 Level and Inhibits Tumorigenic Aspects in the NCI-H295R Adrenocortical Cancer Cell Line

Cancers
Simple Summary Adrenocortical tumors are rare neoplasms with an uncertain prognosis. A greater understanding of the biology of these tumors will allow new therapeutic targets to be identified and the prognosis of these patients to be better understood ...
Alcides Euzebio Tavares Xavier, L. Veronez, Luis F. P. Nagano, C. Corrêa, Mirela Baroni, M. Ramos, Rosane Gomes Queiroz, C. A. Fernandes Molina, J. A. Yunes, S. Brandalise, S. Antonini, L. Tone, E. Valera, C. Scrideli   +13 more
semanticscholar   +1 more source

Spongiosolysis [PDF]

, 1987
Gilbert, P., Stief, Christian Georg
core   +1 more source

Abstracts

Cancer Science, Volume 117, Issue S1, Page 1-2148, January 2026.
wiley   +1 more source

A case report of neonatal adrenocortical carcinoma [PDF]

, 2015

core   +1 more source

Functional adrenocortical carcinoma with adrenohepatic fusion: A case report

Journal of Pediatric Surgery Case Reports
Introduction: Adrenocortical carcinoma (ACC) is rare, aggressive, and metastasizes mainly to the lungs, liver, and regional lymph nodes. This is the first reported case of a pediatric patient with adrenohepatic fusion (AHF) and functional ACC that solely
Pastor Escárcega-Fujigaki, Guillermo Hernández-Peredo Rezk, José de Jesús Loeza- Oliva, Anallely Luna-Hernández, Bethsaida Natali Arreguín-Cortés, Rafael López-Cruz   +5 more
doaj   +1 more source

Clinical features and treatment options for pediatric adrenal incidentalomas: a retrospective single center study

BMC Pediatrics
Background The aim of this study was to investigate the clinical features and treatment options for pediatric adrenal incidentalomas(AIs) to guide the diagnosis and treatment of these tumors.
Xiaojiang Zhu, Saisai Liu, Yimin Yuan, Nannan Gu, Jintong Sha, Yunfei Guo, Yongji Deng   +6 more
doaj   +1 more source

Genomic landscape of paediatric adrenocortical tumours [PDF]

, 2015
et al,, Mardis, Elaine R, Wilson, Richard K   +2 more
core   +2 more sources

Transperitoneal Laparoscopic Adrenalectomy in Children – Initial Experience in an Emerging Tertiary Center in Eastern India

Journal of Indian Association of Pediatric Surgeons
Background: Adrenal tumors account for 0.2%–1% of all tumors in children. They can be benign or malignant, secretory or nonsecretory, and can arise either from the cortex or medulla. The common indication in children undergoing laparoscopic adrenalectomy
Avilash Sahu, Aditya Arvind Manekar, Subrat Kumar Sahoo, Bikasha Bihary Tripathy, Manoj Kumar Mohanty   +4 more
doaj   +1 more source

Characterization of p53 p.T253I as a pathogenic mutation underlying Li-Fraumeni Syndrome.

PLoS ONE
We identified a germline TP53 c.758C > T (p.T253I) mutation in the TP53 tumor suppressor gene in a pediatric adrenocortical carcinoma (ACC) patient. Characteristic of pathogenic p53 mutations, we observed upregulation of total p53 protein levels in the ...
Nathaniel C Holcomb, Amanda M Harrington, Hong Pu, Berina Halilovic, Nathan R Shelman, Shulin Zhang, Catherine Sears, Terra Armstrong, Brent Shelton, Lauren Corum, John A D'Orazio   +10 more
doaj   +1 more source

Mechanisms and functions of chemerin in cancer: Potential roles in therapeutic intervention [PDF]

, 2018
Pachynski, Russell K, Shin, Woo Jae, Zabel, Brian A   +2 more
core   +1 more source