(Q36678858)

15 August 2017

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title

Recent insights into the molecular pathogenesis of pheochromocytoma and paraganglioma (English)

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15 August 2017

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2

William G Kaelin

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15 August 2017

Eijiro Nakamura

1

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15 August 2017

publication date

1 January 2006

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15 August 2017

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15 August 2017

volume

17

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15 August 2017

issue

2

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15 August 2017

page(s)

97-106

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Seminars in medicine of the Beth Israel Hospital, Boston. The RET proto-oncogene in multiple endocrine neoplasia type 2 and Hirschsprung's disease

15 August 2017

cites work

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12 December 2020

Extensive mutation scanning of RET in sporadic medullary thyroid carcinoma and of RET and VHL in sporadic pheochromocytoma reveals involvement of these genes in only a minority of cases.

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12 December 2020

Direct Interaction of the β-Domain of VHL Tumor Suppressor Protein with the Regulatory Domain of Atypical PKC Isotypes

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12 December 2020

Inhibition of hypoxia-inducible factor is sufficient for growth suppression of VHL-/- tumors.

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12 December 2020

Protein kinase C-zeta reverts v-raf transformation of NIH-3T3 cells

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12 December 2020

Molecular basis of the VHL hereditary cancer syndrome

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12 December 2020

Genetic aberrance of sporadic MEN 2A component tumours: analysis of RET.

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12 December 2020

Recent advances in genetics, diagnosis, localization, and treatment of pheochromocytoma

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12 December 2020

Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease

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12 December 2020

Altered gene expression in neurons during programmed cell death: identification of c-jun as necessary for neuronal apoptosis

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12 December 2020

Hypoxia-inducible factor-1 (HIF-1) promotes its degradation by induction of HIF-alpha-prolyl-4-hydroxylases.

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12 December 2020

The von Hippel Lindau/hypoxia-inducible factor (HIF) pathway regulates the transcription of the HIF-proline hydroxylase genes in response to low oxygen

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12 December 2020

Opposing effects of ERK and JNK-p38 MAP kinases on apoptosis

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12 December 2020

Sporadic phaeochromocytomas are rarely associated with germline mutations in the von Hippel-Lindau and RET genes

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12 December 2020

Neuronal apoptosis linked to EglN3 prolyl hydroxylase and familial pheochromocytoma genes: developmental culling and cancer

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12 December 2020

Von Recklinghausen neurofibromatosis

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12 December 2020

AP-1 as a regulator of cell life and death

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12 December 2020

The role of Jun transcription factor expression and phosphorylation in neuronal differentiation, neuronal cell death, and plastic adaptations in vivo

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12 December 2020

Activation of Sp1-mediated vascular permeability factor/vascular endothelial growth factor transcription requires specific interaction with protein kinase C zeta

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12 December 2020

The contribution of VHL substrate binding and HIF1-alpha to the phenotype of VHL loss in renal cell carcinoma

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12 December 2020

AP-1: a double-edged sword in tumorigenesis

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12 December 2020

Analysis of the SDHD gene, the susceptibility gene for familial paraganglioma syndrome (PGL1), in pheochromocytomas

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12 December 2020

Sporadic pheochromocytomas are rarely associated with germline mutations in the vhl tumor suppressor gene or the ret protooncogene

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12 December 2020

Expression of the SM-20 gene promotes death in nerve growth factor-dependent sympathetic neurons

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12 December 2020

Differential genetic alterations in von Hippel-Lindau syndrome-associated and sporadic pheochromocytomas

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12 December 2020

Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma

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12 December 2020

SM-20 is a novel mitochondrial protein that causes caspase-dependent cell death in nerve growth factor-dependent neurons

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12 December 2020

The von Hippel-Lindau protein, HIF hydroxylation, and oxygen sensing

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12 December 2020

The pressure rises: update on the genetics of phaeochromocytoma

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12 December 2020

Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas.

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12 December 2020

Clusterin is a secreted marker for a hypoxia-inducible factor-independent function of the von Hippel-Lindau tumor suppressor protein

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12 December 2020

Inhibition of HIF is necessary for tumor suppression by the von Hippel-Lindau protein

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12 December 2020

NGF utilizes c-Ret via a novel GFL-independent, inter-RTK signaling mechanism to maintain the trophic status of mature sympathetic neurons.

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12 December 2020

von Hippel-Lindau disease

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12 December 2020

Loss of neurofibromin results in neurotrophin-independent survival of embryonic sensory and sympathetic neurons

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12 December 2020

Germline SDHD mutation in familial phaeochromocytoma

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12 December 2020

The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis

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12 December 2020

Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma

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12 December 2020

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

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12 December 2020

Chat in the trophic web: NGF activates Ret by inter-RTK signaling

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12 December 2020

Inhibition of HIF2alpha is sufficient to suppress pVHL-defective tumor growth

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12 December 2020

The RET protooncogene in sporadic pheochromocytomas: frequent MEN 2-like mutations and new molecular defects

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12 December 2020

Succinate links TCA cycle dysfunction to oncogenesis by inhibiting HIF-alpha prolyl hydroxylase

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12 December 2020

von Hippel-Lindau protein mutants linked to type 2C VHL disease preserve the ability to downregulate HIF.

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12 December 2020

A c-Jun dominant negative mutant protects sympathetic neurons against programmed cell death

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12 December 2020

Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families: comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytoma

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12 December 2020

Mitochondrial tumour suppressors: a genetic and biochemical update

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12 December 2020

HIF prolyl-hydroxylase 2 is the key oxygen sensor setting low steady-state levels of HIF-1alpha in normoxia

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12 December 2020

Hereditary paraganglioma targets diverse paraganglia

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12 December 2020

The von Hippel-Lindau gene product inhibits vascular permeability factor/vascular endothelial growth factor expression in renal cell carcinoma by blocking protein kinase C pathways

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12 December 2020

Von Hippel-Lindau gene alterations in sporadic benign and malignant pheochromocytomas

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12 December 2020

Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma

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12 December 2020

Regulation of HIF prolyl hydroxylases by hypoxia-inducible factors

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12 December 2020

A simplified diagnostic approach to pheochromocytoma. A review of the literature and report of one institution's experience

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12 December 2020

Contrasting effects on HIF-1alpha regulation by disease-causing pVHL mutations correlate with patterns of tumourigenesis in von Hippel-Lindau disease.

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12 December 2020

Germ-line mutations in nonsyndromic pheochromocytoma

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12 December 2020

Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility

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12 December 2020

Induction of SM-20 in PC12 cells leads to increased cytochrome c levels, accumulation of cytochrome c in the cytosol, and caspase-dependent cell death

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12 December 2020

Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas

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12 December 2020

Role of VHL gene mutation in human cancer

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12 December 2020

Identifiers

DOI

10.1385/EP:17:2:97

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Dimensions Publication ID

15 August 2017

1006291766

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Fatcat ID

release_sncge43nzvbkrnsucnq4gp7x3i

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Fatcat

https://api.fatcat.wiki/v0/release/sncge43nzvbkrnsucnq4gp7x3i

24 November 2022

mapped directly with Wikidata item

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