P. M. Dahia

发表

A HIF1α Regulatory Loop Links Hypoxia and Mitochondrial Signals in Pheochromocytomas

Sandro Santagata, Marta Barontini, Gabriela Sanso, 2005, PLoS genetics.

Insights into Mechanisms of Pheochromocytomas and Paragangliomas Driven by Known or New Genetic Drivers

P. M. Dahia, Shahida K. Flores, C. M. Estrada-Zúñiga, 2021, Cancers.

Transcription Association of VHL and SDH Mutations Link Hypoxia and Oxidoreductase Signals in Pheochromocytomas

P. M. Dahia, P. Dahia, 2006, Annals of the New York Academy of Sciences.

Mutation and deletion analysis of GFRα-1, encoding the co-receptor for the GDNF/RET complex, in human brain tumours

L. Mulligan, A. Deimling, C. Eng, 1999, British Journal of Cancer.

Absence of germline mutations in MINPP1, a phosphatase encoding gene centromeric of PTEN, in patients with Cowden and Bannayan-Riley- Ruvalcaba syndrome without germlinePTEN mutations

P. Reynolds, C. Eng, D. Marsh, 2000, Journal of medical genetics.

Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas.

S. Gruber, C. Ricketts, M. Vikkula, 2010, JAMA.

Novel pheochromocytoma susceptibility loci identified by integrative genomics.

M. Pujana, C. Stiles, N. Aronin, 2005, Cancer research.

A RET::GRB2 fusion in pheochromocytoma defies the classic paradigm of RET oncogenic fusions

R. Aguiar, N. Aronin, Xiaojing Wang, 2022, Cell reports. Medicine.

P. M. Dahia, M. Barontini, P. Dahia, 2010, Best practice & research. Clinical endocrinology & metabolism.

Allelic imbalance, including deletion of PTEN/MMAC1, at the Cowden disease locus on 10q22‐23, in hamartomas from patients with cowden syndrome and germline PTEN mutation

R. Eeles, A. Goldstein, C. Eng, 1998, Genes, chromosomes & cancer.

Case report: Two sisters with a germline CHEK2 variant and distinct endocrine neoplasias

J. Bishop, P. Söderkvist, A. Alli, 2022, Frontiers in Endocrinology.

A HIF1-alpha Regulatory Loop Links Hypoxiaand Mitochondrial Signals in Pheochromocytomas

Andrew L. Kung, Sandro Santagata, James F. Powers, 2005 .

Next‐generation sequencing for the genetic screening of phaeochromcytomas and paragangliomas: riding the new wave, but with caution

P. M. Dahia, R. Toledo, P. Dahia, 2014, Clinical endocrinology.

Pheochromocytomas: from genetic diversity to new paradigms.

K. Buddavarapu, P. M. Dahia, Y. Qin, 2009, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

Endocrine and Neuroendocrine Tumors Special Issue—Checkpoint Inhibitors for Adrenocortical Carcinoma and Metastatic Pheochromocytoma and Paraganglioma: Do They Work?

Yang Lu, M. Habra, C. Jimenez, 2022, Cancers.

The TMEM127 human tumor suppressor is a component of the mTORC1 lysosomal nutrient-sensing complex

S. Srikantan, K. Vogel, E. Wang, 2018, Human molecular genetics.

Acute and Subacute Effects of Endotoxin on Hypothalamic Gaseous Neuromodulators

M. Forsling, A. Grossman, S. Chew, 1998, Annals of the New York Academy of Sciences.