EZH2 and ZFX oncogenes in malignant behaviour of parathyroid neoplasms. (Q53005136)

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8 March 2020

title

EZH2 and ZFX oncogenes in malignant behaviour of parathyroid neoplasms (English)

1 reference

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8 March 2020

author

Federico Pio Fabrizio

8

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8 March 2020

Lucia Anna Muscarella

11

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8 March 2020

Vito Guarnieri

12

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8 March 2020

Paolo Graziano

7

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8 March 2020

author name string

E Sanpaolo

1

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8 March 2020

M Miroballo

2

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8 March 2020

S Corbetta

3

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8 March 2020

C Verdelli

4

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8 March 2020

F Baorda

5

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8 March 2020

T Balsamo

6

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8 March 2020

L Cinque

9

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8 March 2020

A Scillitani

10

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publication date

15 February 2016

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8 March 2020

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8 March 2020

volume

54

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8 March 2020

page(s)

55-59

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8 March 2020

issue

1

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https://scigraph.springernature.com/pub.10.1007/s12020-016-0892-y

8 March 2020

exact match

0 references

cites work

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Stabilizing mutation of CTNNB1/beta-catenin and protein accumulation analyzed in a large series of parathyroid tumors of Swedish patients.

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Evidence of a stabilizing mutation of β-catenin encoded by CTNNB1 exon 3 in a large series of sporadic parathyroid adenomas.

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Identification of somatic mutations in parathyroid tumors using whole-exome sequencing

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The control of histone lysine methylation in epigenetic regulation

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Histone methyltransferase activity of a Drosophila Polycomb group repressor complex

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Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin

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Zfx controls the self-renewal of embryonic and hematopoietic stem cells.

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The zinc finger transcription factor ZFX is required for maintaining the tumorigenic potential of glioblastoma stem cells

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Overexpression of ZFX confers self-renewal and chemoresistance properties in hepatocellular carcinoma

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Dysregulation of zinc finger protein, X-linked (ZFX) impairs cell proliferation and induces apoptosis in human oral squamous cell carcinorma

21 January 2018

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HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome

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New role for ZFX in oncogenesis

21 January 2018

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Challenging lesions in the differential diagnosis of endocrine tumors: parathyroid carcinoma

21 January 2018

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The clinical importance of parathyroid atypia: is long-term surveillance necessary?

21 January 2018

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Prognostic factors in parathyroid cancer: a review of 95 cases

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Mutations in EZH2 cause Weaver syndrome

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Epigenetic alterations in human parathyroid tumors

21 January 2018

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A rare S33C mutation of CTNNB1 encoding β-catenin in a parathyroid adenoma found in an Italian primary hyperparathyroid cohort

21 January 2018

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CDC73 mutations and parafibromin immunohistochemistry in parathyroid tumors: clinical correlations in a single-centre patient cohort

21 January 2018

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Diverse involvement of EZH2 in cancer epigenetics

21 January 2018

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12 December 2020

Frequent Large GermlineHRPT2Deletions in a French National Cohort of Patients With Primary Hyperparathyroidism

1 reference

12 December 2020

Lack of S37A CTNNB1/β-catenin mutations in a Swedish cohort of 98 parathyroid adenomas

1 reference

12 December 2020

Recurrent ZFX mutations in human sporadic parathyroid adenomas

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12 December 2020