Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology.
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The candidate neuroprotective agent artemin induces autonomic neural dysplasia without preventing peripheral nerve dysfunctionRare germline mutations identified by targeted next-generation sequencing of susceptibility genes in pheochromocytoma and paraganglioma.SDHA is a tumor suppressor gene causing paraganglioma.Genetic analysis of Pten and Ink4a/Arf interactions in the suppression of tumorigenesis in miceMicroRNA expression profiling in benign (sporadic and hereditary) and recurring adrenal pheochromocytomas.Chromosomal changes in sporadic and familial head and neck paragangliomas.Copy number alterations in small intestinal neuroendocrine tumors determined by array comparative genomic hybridizationSDH mutations in tumorigenesis and inherited endocrine tumours: lesson from the phaeochromocytoma-paraganglioma syndromesProfiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysis.Patterns of chromosomal imbalances in parathyroid carcinomasDifferential loss of chromosome 11q in familial and sporadic parasympathetic paragangliomas detected by comparative genomic hybridizationOverexpression of ERBB-2 was more frequently detected in malignant than benign pheochromocytomas by multiplex ligation-dependent probe amplification and immunohistochemistry.Molecular and therapeutic advances in the diagnosis and management of malignant pheochromocytomas and paragangliomasPhenylethanolamine N-methyltransferase downregulation is associated with malignant pheochromocytoma/paraganglioma.Phaeochromocytomas and sympathetic paragangliomas.Paraganglioma of the bladder in a kidney transplant recipient: A case reportUpdate on tumours of the adrenal cortex, phaeochromocytoma and extra-adrenal paraganglioma.Malignant pheochromocytomas and paragangliomas: a diagnostic challenge.Pheochromocytoma and paraganglioma: understanding the complexities of the genetic background.Rethinking pheochromocytomas and paragangliomas from a genomic perspective.Neuroendocrine Tumors of the Urinary Bladder According to the 2016 World Health Organization Classification: Molecular and Clinical Characteristics.Pheochromocytomas and paragangliomas in humans and dogs.Molecular cytogenetic characterization in four pediatric pheochromocytomas and paragangliomas.Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array-CGH.Composite tumor with pheochromocytoma and immature neuroblastoma: report of two cases with cytogenetic analysis and discussion of current terminology.Loss of maternal chromosome 11 is a signature event in SDHAF2, SDHD, and VHL-related paragangliomas, but less significant in SDHB-related paragangliomas.Adrenal medullary hyperplasia is a precursor lesion for pheochromocytoma in MEN2 syndromeAlterations of the SDHD gene locus in midgut carcinoids, Merkel cell carcinomas, pheochromocytomas, and abdominal paragangliomas.Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families.Conditional Pten knock-out mice: a model for metastatic phaeochromocytoma.Malignant pheochromocytoma in a young adult forming the structure simulating Homer Wright rosette: differentiation from neuroblastoma on repeating fluorescence in situ hybridization.Characteristic genomic imbalances in pediatric pheochromocytoma.ARHI is a novel epigenetic silenced tumor suppressor in sporadic pheochromocytoma.CGH and CD 44/MIB-1 immunohistochemistry are helpful to distinguish metastasized from nonmetastasized sporadic pheochromocytomas.Multiple locations on chromosome 3 are the targets of specific deletions in uveal melanoma.Allelic loss of chromosomes 8 and 19 in MENX-associated rat pheochromocytoma.Frequent loss of 17p, but no p53 mutations or protein overexpression in benign and malignant pheochromocytomas.
P2860
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P2860
Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
2000年论文
@zh
2000年论文
@zh-cn
name
Comparative genomic hybridizat ...... ing a common genetic etiology.
@ast
Comparative genomic hybridizat ...... ing a common genetic etiology.
@en
type
label
Comparative genomic hybridizat ...... ing a common genetic etiology.
@ast
Comparative genomic hybridizat ...... ing a common genetic etiology.
@en
prefLabel
Comparative genomic hybridizat ...... ing a common genetic etiology.
@ast
Comparative genomic hybridizat ...... ing a common genetic etiology.
@en
P2093
P2860
P1476
Comparative genomic hybridizat ...... ing a common genetic etiology.
@en
P2093
E Mahlamäki
M Bäckdahl
M Kjellman
N Goncharov
P2860
P304
P356
10.1016/S0002-9440(10)64769-4
P407
P50
P577
2000-02-01T00:00:00Z