Pin1-mediated Runx2 modification is critical for skeletal development (Q33733296)

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1 March 2020

title

Pin1-mediated Runx2 modification is critical for skeletal development (English)

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1 March 2020

2

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1 March 2020

Kyung Mi Woo

4

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1 March 2020

Takafumi Uchida

6

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1 March 2020

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Gary S Stein

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1 March 2020

author name string

Won-Joon Yoon

1

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1 March 2020

Young-Dan Cho

3

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1 March 2020

Jeong-Hwa Baek

5

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1 March 2020

Toshihisa Komori

7

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1 March 2020

Andre van Wijnen

8

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1 March 2020

Janet L Stein

9

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1 March 2020

Jane B Lian

10

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1 March 2020

Je-Yong Choi

12

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1 March 2020

Suk-Chul Bae

13

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1 March 2020

Hyun-Mo Ryoo

14

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1 March 2020

publication date

1 December 2013

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Journal of Cellular Physiology

1 March 2020

published in

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1 March 2020

volume

228

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issue

12

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1 March 2020

page(s)

2377-2385

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Elevated PIN1 expression by C/EBPalpha-p30 blocks C/EBPalpha-induced granulocytic differentiation through c-Jun in AML

1 March 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4051422

FGF2-activated ERK mitogen-activated protein kinase enhances Runx2 acetylation and stabilization

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4051422

Dipentamethylene thiuram monosulfide is a novel inhibitor of Pin1.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4051422

Essential role of Pin1 in the regulation of TRF1 stability and telomere maintenance

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4051422

A Runx2 threshold for the cleidocranial dysplasia phenotype

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4051422

Prolyl cis-trans isomerization as a molecular timer

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4051422

Critical role of the extracellular signal-regulated kinase-MAPK pathway in osteoblast differentiation and skeletal development

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4051422

Establishment and characterization of a stable cell line to evaluate cellular Runx2 activity

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4051422

Functional analysis of RUNX2 mutations in Japanese patients with cleidocranial dysplasia demonstrates novel genotype-phenotype correlations

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4051422

Mice lacking Pin1 develop normally, but are defective in entering cell cycle from G(0) arrest

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4051422

Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4051422

Function of WW domains as phosphoserine- or phosphothreonine-binding modules

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4051422

Sequence-specific and phosphorylation-dependent proline isomerization: a potential mitotic regulatory mechanism

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4051422

Structural and functional analysis of the mitotic rotamase Pin1 suggests substrate recognition is phosphorylation dependent

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4051422

Differential staining of cartilage and bone in whole mouse fetuses by alcian blue and alizarin red S.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4051422

The Drosophila segmentation gene runt acts as a position-specific numerator element necessary for the uniform expression of the sex-determining gene Sex-lethal

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4051422

Drosophila Pin1 prolyl isomerase Dodo is a MAP kinase signal responder during oogenesis

28 July 2018

1 reference

The protein kinase C pathway plays a central role in the fibroblast growth factor-stimulated expression and transactivation activity of Runx2

21 January 2018

1 reference

Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts

21 January 2018

1 reference

The prolyl isomerase PIN1: a pivotal new twist in phosphorylation signalling and disease

21 January 2018

1 reference

Copy number variation analysis in single-suture craniosynostosis: multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosis.

21 January 2018

1 reference

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

21 January 2018

1 reference

PIN1, the cell cycle and cancer.

21 January 2018

1 reference

Functional analysis of RUNX2 mutations in cleidocranial dysplasia: novel insights into genotype–phenotype correlations

21 January 2018

1 reference

RUNX2 quadruplication: additional evidence toward a new form of syndromic craniosynostosis

21 January 2018

1 reference

The prolyl isomerase Pin1 is a novel prognostic marker in human prostate cancer.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4051422

Biallelic and heterozygous point mutations in the runt domain of the AML1/PEBP2alphaB gene associated with myeloblastic leukemias

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23702614

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/JCP.24403

1 reference

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1 March 2020

1 reference

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1 March 2020

PubMed publication ID

23702614

1 reference