- Home
- Publications
- Publication Search
- Publication Details
Title
Genomic Alterations in Sporadic Pituitary Tumors
Authors
Keywords
Pituitary adenoma, Craniopharyngioma, Genomics, Precision medicine
Journal
Current Neurology and Neuroscience Reports
Volume 18, Issue 1, Pages -
Publisher
Springer Nature
Online
2018-02-02
DOI
10.1007/s11910-018-0811-0
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- From pituitary adenoma to pituitary neuroendocrine tumor (PitNET): an International Pituitary Pathology Club proposal
- (2017) S L Asa et al. ENDOCRINE-RELATED CANCER
- Clinical Identification of Oncogenic Drivers and Copy-Number Alterations in Pituitary Tumors
- (2017) Wenya Linda Bi et al. ENDOCRINOLOGY
- Hyperfractionated high-dose proton beam radiotherapy for clival chordomas after surgical removal
- (2016) Yasutaka Hayashi et al. BRITISH JOURNAL OF RADIOLOGY
- The genome-wide mutational landscape of pituitary adenomas
- (2016) Zhi-Jian Song et al. CELL RESEARCH
- Landscape of Genomic Alterations in Pituitary Adenomas
- (2016) Wenya Linda Bi et al. CLINICAL CANCER RESEARCH
- Recurrent gain-of-function USP8 mutations in Cushing's disease
- (2015) Zeng-Yi Ma et al. CELL RESEARCH
- Landscape of somatic mutations in sporadic GH-secreting pituitary adenomas
- (2015) Cristina L Ronchi et al. EUROPEAN JOURNAL OF ENDOCRINOLOGY
- Pronounced response of papillary craniopharyngioma to treatment with vemurafenib, a BRAF inhibitor
- (2015) Simon J. B. Aylwin et al. Pituitary
- BRAF V600E mutations are characteristic for papillary craniopharyngioma and may coexist with CTNNB1-mutated adamantinomatous craniopharyngioma
- (2014) Sarah Jane Larkin et al. ACTA NEUROPATHOLOGICA
- Exome sequencing identifies BRAF mutations in papillary craniopharyngiomas
- (2014) Priscilla K Brastianos et al. NATURE GENETICS
- Mutations in the deubiquitinase gene USP8 cause Cushing's disease
- (2014) Martin Reincke et al. NATURE GENETICS
- Gigantism and Acromegaly Due to Xq26 Microduplications and GPR101 Mutation
- (2014) Giampaolo Trivellin et al. NEW ENGLAND JOURNAL OF MEDICINE
- A Novel Mutation in the Upstream Open Reading Frame of the CDKN1B Gene Causes a MEN4 Phenotype
- (2013) Gianluca Occhi et al. PLoS Genetics
- Cyclin-dependent kinase inhibitor 1B (CDKN1B) gene variants in AIP mutation-negative familial isolated pituitary adenoma kindreds
- (2012) Maria A Tichomirowa et al. ENDOCRINE-RELATED CANCER
- The pituitary tumour epigenome: aberrations and prospects for targeted therapy
- (2012) Kiren Yacqub-Usman et al. Nature Reviews Endocrinology
- Combined BRAF and MEK Inhibition in Melanoma with BRAF V600 Mutations
- (2012) Keith T. Flaherty et al. NEW ENGLAND JOURNAL OF MEDICINE
- Survival in BRAF V600–Mutant Advanced Melanoma Treated with Vemurafenib
- (2012) Jeffrey A. Sosman et al. NEW ENGLAND JOURNAL OF MEDICINE
- Inhibition of Mutated, Activated BRAF in Metastatic Melanoma
- (2010) Keith T. Flaherty et al. NEW ENGLAND JOURNAL OF MEDICINE
- Menin, Histone H3 Methyltransferases, and Regulation of Cell Proliferation: Current Knowledge and Perspective
- (2008) Xinjiang Wu et al. CURRENT MOLECULAR MEDICINE
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now