Genomic landscape of pheochromocytoma and paraganglioma
I Jochmanova, K Pacak - Trends in cancer, 2018 - cell.com
Recent comprehensive molecular analysis allowed the identification of unique molecular
signatures in pheochromocytomas (PHEOs) and paragangliomas (PGLs). Here we …
signatures in pheochromocytomas (PHEOs) and paragangliomas (PGLs). Here we …
[HTML][HTML] Comprehensive molecular characterization of pheochromocytoma and paraganglioma
L Fishbein, I Leshchiner, V Walter, L Danilova… - Cancer cell, 2017 - cell.com
We report a comprehensive molecular characterization of pheochromocytomas and
paragangliomas (PCCs/PGLs), a rare tumor type. Multi-platform integration revealed that …
paragangliomas (PCCs/PGLs), a rare tumor type. Multi-platform integration revealed that …
New perspectives on pheochromocytoma and paraganglioma: toward a molecular classification
A molecular biology–based taxonomy has been proposed for pheochromocytoma and
paraganglioma (PPGL). Data from the Cancer Genome Atlas revealed clinically relevant …
paraganglioma (PPGL). Data from the Cancer Genome Atlas revealed clinically relevant …
Rethinking pheochromocytomas and paragangliomas from a genomic perspective
LJ Castro-Vega, C Lepoutre-Lussey… - Oncogene, 2016 - nature.com
Pheochromocytomas (PCC) and paragangliomas (PGL) are rare neuroendocrine tumors of
neural crest origin. These tumors are caused by germline or somatic mutations in known …
neural crest origin. These tumors are caused by germline or somatic mutations in known …
Pheochromocytoma and paraganglioma pathogenesis: learning from genetic heterogeneity
PLM Dahia - Nature Reviews Cancer, 2014 - nature.com
The neuroendocrine tumours pheochromocytomas and paragangliomas carry the highest
degree of heritability in human neoplasms, enabling genetic alterations to be traced to …
degree of heritability in human neoplasms, enabling genetic alterations to be traced to …
An update on the genetics of paraganglioma, pheochromocytoma, and associated hereditary syndromes
AP Gimenez-Roqueplo, PL Dahia… - Hormone and …, 2012 - thieme-connect.com
Pheochromocytomas (PCCs) and paragangliomas (PGLs) are catecholamine-secreting
tumors of neural crest origin. Once collectively known as the '10% tumor', based on the …
tumors of neural crest origin. Once collectively known as the '10% tumor', based on the …
Multi-omics analysis defines core genomic alterations in pheochromocytomas and paragangliomas
Abstract Pheochromocytomas and paragangliomas (PCCs/PGLs) are neural crest-derived
tumours with a very strong genetic component. Here we report the first integrated genomic …
tumours with a very strong genetic component. Here we report the first integrated genomic …
The genomic landscape of phaeochromocytoma
A Flynn, D Benn, R Clifton‐Bligh… - The Journal of …, 2015 - Wiley Online Library
Abstract Phaeochromocytomas (PCCs) and paragangliomas (PGLs) are rare neural crest‐
derived tumours originating from adrenal chromaffin cells or extra‐adrenal sympathetic and …
derived tumours originating from adrenal chromaffin cells or extra‐adrenal sympathetic and …
[HTML][HTML] New insights on the pathogenesis of paraganglioma and pheochromocytoma
V Kantorovich, K Pacak - F1000Research, 2018 - ncbi.nlm.nih.gov
Abstract Pheochromocytomas (PCCs) and paragangliomas (PGLs) are rare chromaffin cell
tumors (PPGLs) that at times raise significant challenges in clinical recognition, diagnosis …
tumors (PPGLs) that at times raise significant challenges in clinical recognition, diagnosis …
Genetic bases of pheochromocytoma and paraganglioma
The genetics of pheochromocytoma and paraganglioma (PPGL) has become increasingly
complex over the last two decades. The list of genes involved in the development of these …
complex over the last two decades. The list of genes involved in the development of these …