(Q28241168)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21685915%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

title

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma (English)

1 reference

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5 February 2020

1 reference

4

1 reference

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5 February 2020

IÑAKI COMINO-MENDEZ

1

1 reference

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5 February 2020

Francesca Schiavi

3

1 reference

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5 February 2020

Luis J Leandro-García

5

1 reference

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5 February 2020

Emiliano Honrado

7

1 reference

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5 February 2020

Lucia Inglada-Pérez

13

1 reference

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5 February 2020

Lucia Inglada

14

1 reference

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5 February 2020

Elisa Taschin

16

1 reference

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5 February 2020

Anna González-Neira

23

1 reference

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5 February 2020

Giovanna Roncador

24

1 reference

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Cristina Rodríguez-Antona

5 February 2020

25

1 reference

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5 February 2020

Massimo Mannelli

27

1 reference

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5 February 2020

Giuseppe Opocher

28

1 reference

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5 February 2020

Mercedes Robledo

29

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5 February 2020

Alberto Cascón

30

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5 February 2020

6

Rocío Letón

1 reference

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5 February 2020

10

Guillermo Pita

1 reference

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5 February 2020

11

Alvaro Gómez-Graña

1 reference

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5 February 2020

17

Sara Bobisse

1 reference

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5 February 2020

author name string

Francisco J Gracia-Aznárez

2

1 reference

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5 February 2020

Rocío Ramos-Medina

8

1 reference

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5 February 2020

Daniela Caronia

9

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5 February 2020

Aguirre A de Cubas

12

1 reference

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5 February 2020

Agnieszka Maliszewska

15

1 reference

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5 February 2020

Giuseppe Pica

18

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5 February 2020

Paola Loli

19

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5 February 2020

Rafael Hernández-Lavado

20

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5 February 2020

José A Díaz

21

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5 February 2020

Mercedes Gómez-Morales

22

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5 February 2020

Javier Benítez

26

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5 February 2020

language of work or name

English

0 references

publication date

19 June 2011

1 reference

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5 February 2020

1 reference

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5 February 2020

volume

43

1 reference

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5 February 2020

issue

7

1 reference

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5 February 2020

page(s)

663-667

1 reference

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SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma

5 February 2020

cites work

1 reference

A HIF1alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas

20 April 2017

1 reference

Myc and Max: molecular evolution of a family of proto-oncogene products and their dimerization partner

20 April 2017

1 reference

The Myc/Max/Mad network and the transcriptional control of cell behavior

20 April 2017

1 reference

Germline mutations in TMEM127 confer susceptibility to pheochromocytoma

20 April 2017

1 reference

The Sequence Alignment/Map format and SAMtools

20 April 2017

1 reference

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

20 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG.861

The NF1 tumor suppressor critically regulates TSC2 and mTOR.

20 April 2017

1 reference

12 December 2020

Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas.

1 reference

12 December 2020

c-Myc inhibits Ras-mediated differentiation of pheochromocytoma cells by blocking c-Jun up-regulation

1 reference

12 December 2020

Allelic variant at -79 (C>T) in CDKN1B (p27Kip1) confers an increased risk of thyroid cancer and alters mRNA levels.

1 reference

12 December 2020

Gross SDHB deletions in patients with paraganglioma detected by multiplex PCR: a possible hot spot?

1 reference

12 December 2020

Research resource: Transcriptional profiling reveals different pseudohypoxic signatures in SDHB and VHL-related pheochromocytomas

1 reference

12 December 2020

Regulation of gene expression in hepatic cells by the mammalian Target of Rapamycin (mTOR).

1 reference

12 December 2020

Genetics of pheochromocytoma and paraganglioma in Spanish patients.

1 reference

12 December 2020

Transposition and amplification of oncogene-related sequences in human neuroblastomas

1 reference

12 December 2020

Identification of casein kinase II phosphorylation sites in Max: effects on DNA-binding kinetics of Max homo- and Myc/Max heterodimers

1 reference

12 December 2020

c-Myc Does Not Require Max for Transcriptional Activity in PC-12 Cells

1 reference

12 December 2020

Activation of PI3K/Akt and MAPK pathways regulates Myc-mediated transcription by phosphorylating and promoting the degradation of Mad1.

1 reference

12 December 2020

The Warburg effect is genetically determined in inherited pheochromocytomas

1 reference

12 December 2020

Loss of heterozygosity associated with uniparental disomy in breast carcinoma

1 reference

12 December 2020

Paternal UPD14 is responsible for a distinctive malformation complex

1 reference

12 December 2020

Epigenetic alteration at the DLK1-GTL2 imprinted domain in human neoplasia: analysis of neuroblastoma, phaeochromocytoma and Wilms' tumour

1 reference

12 December 2020

New lesions detected by single nucleotide polymorphism array-based chromosomal analysis have important clinical impact in acute myeloid leukemia

1 reference

12 December 2020

Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals

1 reference

12 December 2020

The clinical phenotype of mosaicism for genome-wide paternal uniparental disomy: two new reports

1 reference

12 December 2020

X-ray structures of Myc-Max and Mad-Max recognizing DNA. Molecular bases of regulation by proto-oncogenic transcription factors

1 reference

12 December 2020

The nerve growth factor-responsive PC12 cell line does not express the Myc dimerization partner Max

1 reference

12 December 2020

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

1 reference

12 December 2020

SDHA is a tumor suppressor gene causing paraganglioma

1 reference

12 December 2020

Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic event.

1 reference

12 December 2020

Germ-line mutations in nonsyndromic pheochromocytoma

1 reference

12 December 2020

Clinically guided genetic screening in a large cohort of italian patients with pheochromocytomas and/or functional or nonfunctional paragangliomas

1 reference

12 December 2020

Transforming ability of MEN2A-RET requires activation of the phosphatidylinositol 3-kinase/AKT signaling pathway.

1 reference

12 December 2020

Biphasic effect of Max on Myc cotransformation activity and dependence on amino- and carboxy-terminal Max functions

1 reference

12 December 2020

Involvement of the 'leucine zipper' region in the oligomerization and transforming activity of human c-myc protein.

1 reference

12 December 2020

Identifiers

DOI

10.1038/NG.861

2 references

Consolidated OpenCitations Corpus – April 2017

92042

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21685915%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

92042

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

92042

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21685915%20AND%20SRC:MED&resulttype=core&format=json