Germline NF1 mutational spectra and loss-of-heterozygosity analyses in patients with pheochromocytoma and neurofibromatosis type 1.
about
Pheochromocytoma: implications in tumorigenesis and the actual managementA Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes.Paragangliomas/Pheochromocytomas: clinically oriented genetic testingSolid tumors associated with multiple endocrine neoplasias.The NF1 gene revisited - from bench to bedside.10 rare tumors that warrant a genetics referral.The use of next-generation sequencing in molecular diagnosis of neurofibromatosis type 1: a validation study.Hereditary paragangliomas.SDH mutations in tumorigenesis and inherited endocrine tumours: lesson from the phaeochromocytoma-paraganglioma syndromesExploring the somatic NF1 mutational spectrum associated with NF1 cutaneous neurofibromasRare vertebral metastasis in a case of Hereditary Paraganglioma.Protein kinase Cδ inactivation inhibits cellular proliferation and decreases survival in human neuroendocrine tumors.Multiplicity of hormone-secreting tumors: common themes about cause, expression, and management.Cutaneous squamous cell carcinoma in a patient with neurofibromatosis type 1: A case reportThe approach to the patient with paraganglioma.Hypoxia-inducible factor signaling in pheochromocytoma: turning the rudder in the right direction.Neuroendocrine tumors and tumor syndromes in childhood.Neurofibromatosis type 1-associated tumours: their somatic mutational spectrum and pathogenesis.Genetics and molecular pathogenesis of pheochromocytoma and paraganglioma.Neurofibromatosis type 1: diagnosis and recent advances.Translational research in endocrine surgery.Microarray-based copy number analysis of neurofibromatosis type-1 (NF1)-associated malignant peripheral nerve sheath tumors reveals a role for Rho-GTPase pathway genes in NF1 tumorigenesis.PheoSeq: A Targeted Next-Generation Sequencing Assay for Pheochromocytoma and Paraganglioma Diagnostics.Rare diseases in clinical endocrinology: a taxonomic classification system.Sporadic or familial head neck paragangliomas enrolled in a single center: clinical presentation and genotype/phenotype correlations.Alu-Alu recombination underlies the vast majority of large VHL germline deletions: Molecular characterization and genotype-phenotype correlations in VHL patients.RETRACTED: Repeated Multiple Neurofibromatosis Type 1 in the Right Lower Limb: A Case Report.Extent of surgery for phaeochromocytomas in the genomic era.Mutation screening in a Norwegian cohort with pheochromocytoma.The mutational spectrum of the NF1 gene in neurofibromatosis type I patients from UAE.A Clinical Roadmap to Investigate the Genetic Basis of Pediatric Pheochromocytoma: Which Genes Should Physicians Think About?Molecular Genetics of Gastroenteropancreatic Neuroendocrine TumoursIntegrative genomics reveals frequent somatic NF1 mutations in sporadic pheochromocytomas
P2860
Q27024128-D70A1F0F-C324-4539-B163-A40A5837BF25Q30252766-5B4F45A6-86C3-436E-A430-87C5460C3772Q33679204-0471A0ED-0566-4511-A963-0A443204B67FQ34213017-AECE364E-E78B-4139-A864-9EAB95C216CFQ34227509-A1746DDF-86A6-42F6-B977-3FF0C90306BBQ34325954-34EFDBC2-42C4-46A0-B778-E9F704DBFEFCQ34439859-9736B622-7CF5-47B6-A41C-ABB7978E626FQ34456420-09646B24-2565-40FF-AA2D-AD5AC18A06F4Q35185252-E6FAF20F-3139-4FB7-BA37-0845435AA9B7Q35837640-27621C5D-7794-41D4-8538-337C0C5807E8Q36367439-3EF1798E-3798-46E3-A689-A78C92227CCCQ36480150-B9A7A7FC-B222-4EF5-828C-7AA4C7B293DCQ37071229-4FEF43C0-8BFF-4A76-9908-4AFA01E4717CQ37229417-BD0F1AA1-B926-4747-A79C-C393619C7A21Q37315681-7D3C84E6-98DF-41DC-92CC-FA382E5C62D3Q37464073-C1F58561-F7D0-4B58-A08C-8F94DB48DFC8Q37587164-08D69CBA-D544-4E53-83BA-A814A38083CDQ37966599-DF5BCF4D-8B8D-4673-93E5-5C1D3A44A0AFQ38051726-AD9F0FF1-A299-450B-A7CF-258048795A5CQ38089870-60D2A037-3325-4471-9195-58BB252A2C9AQ38135137-E3622A9B-DCFF-4A2B-8191-65651887148FQ38327730-77ABFDD1-EB5B-44BC-895F-D79CE1EC389DQ38759395-35794603-823B-4140-8EA8-FE397941D4D9Q39102141-08AE338B-8E66-4C65-BD66-D76A74B36AA0Q44951490-4201A1F3-493F-403D-B925-D6981B65CADDQ46091220-6CE88569-AFA9-4FBA-B9E2-E440C90AD31EQ47120997-A91C1102-EA44-4386-AAEB-646368320402Q47552587-3705A66A-E0DF-4679-83D6-7E5217A36735Q50871805-735734FB-A8D0-4C11-A858-B8F4ACB42ECAQ54228124-A7DA10A4-5D1E-4AF6-9986-63086EEE01BBQ55263855-96E8124A-2712-4130-B93F-47BC6684E54BQ55981792-1D72E6DC-D115-48BC-91AF-F17E03672452Q56697959-9B3A2B0B-2C43-4948-AB03-414C24510A6C
P2860
Germline NF1 mutational spectra and loss-of-heterozygosity analyses in patients with pheochromocytoma and neurofibromatosis type 1.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
2007年學術文章
@zh-hant
name
Germline NF1 mutational spectr ...... and neurofibromatosis type 1.
@en
Germline NF1 mutational spectr ...... and neurofibromatosis type 1.
@nl
type
label
Germline NF1 mutational spectr ...... and neurofibromatosis type 1.
@en
Germline NF1 mutational spectr ...... and neurofibromatosis type 1.
@nl
prefLabel
Germline NF1 mutational spectr ...... and neurofibromatosis type 1.
@en
Germline NF1 mutational spectr ...... and neurofibromatosis type 1.
@nl
P2093
P50
P356
P1476
Germline NF1 mutational spectr ...... and neurofibromatosis type 1.
@en
P2093
Ambrogio Fassina
Andrzej Januszewicz
Ann-Cathrin Koschker
Bernhard Kremens
Birke Bausch
Christian Pawlu
Detlef Boehm
European-American Phaeochromocytoma Registry Study Group
F Fausto Palazzo
Felix Lohoefner
P304
P356
10.1210/JC.2006-2833
P407
P50
P577
2007-04-10T00:00:00Z