Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL.
about
von Hippel-Lindau disease: a clinical and scientific reviewGene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paragangliomaPhaeochromocytoma: an unusual cause of hypertension in pregnancy.The spectrum of mutations in TSC1 and TSC2 in women with tuberous sclerosis and lymphangiomyomatosis.Haploinsufficiency in tumor predisposition syndromes: altered genomic transcription in morphologically normal cells heterozygous for VHL or TSC mutation.Molecular markers of paragangliomas/pheochromocytomasMutation analysis of HIF prolyl hydroxylases (PHD/EGLN) in individuals with features of phaeochromocytoma and renal cell carcinoma susceptibilityFounder effect at PGL1 in hereditary head and neck paraganglioma families from the Netherlands.Hereditary paraganglioma targets diverse paraganglia.Pheochromocytoma: the expanding genetic differential diagnosis.Cryptic von Hippel-Lindau disease: germline mutations in patients with haemangioblastoma onlyFamilial clear cell renal cell carcinoma (FCRC): clinical features and mutation analysis of the VHL, MET, and CUL2 candidate genes.Investigation of the role of SDHB inactivation in sporadic phaeochromocytoma and neuroblastoma.Long-term outcomes, branch-specific expressivity, and disease-related mortality in von Hippel-Lindau type 2A.Von hippel-lindau disease: a genetic and clinical review.Identification of novel VHL targets that are associated with the development of renal cell carcinoma.Genetic analysis of RET, GFR alpha 1 and GDNF genes in Spanish families with multiple endocrine neoplasia type 2A.Hirschsprung associated GDNF mutations do not prevent RET activation.Paraganglioma genes.RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours.Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility.Molecular genetic analysis of von Hippel-Lindau disease.Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytoma.Familial nonsyndromic pheochromocytoma.Effects of point mutations in pVHL on the binding of HIF-1α.Von Hippel-Lindau disease.Von Hippel-Lindau Disease.
P2860
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P2860
Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Genetic predisposition to phae ...... idate genes GDNF, RET and VHL.
@en
type
label
Genetic predisposition to phae ...... idate genes GDNF, RET and VHL.
@en
prefLabel
Genetic predisposition to phae ...... idate genes GDNF, RET and VHL.
@en
P2093
P356
P1476
Genetic predisposition to phae ...... didate genes GDNF, RET and VHL
@en
P2093
B A Ponder
E R Woodward
N A Affara
P304
P356
10.1093/HMG/6.7.1051
P577
1997-07-01T00:00:00Z