p57(Kip2) knock-in mouse reveals CDK-independent contribution in the development of Beckwith-Wiedemann syndrome. (Q50525407)

http://europepmc.org/abstract/MED/27015986

14 March 2018

title

p57(Kip2) knock-in mouse reveals CDK-independent contribution in the development of Beckwith-Wiedemann syndrome. (English)

1 reference

http://europepmc.org/abstract/MED/27015986

14 March 2018

author

Arnaud Besson

8

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2 June 2020

Pauline Jeannot

3

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2 June 2020

author name string

Nicolas Duquesnes

1

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2 June 2020

Caroline Callot

2

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2 June 2020

Virginie Daburon

4

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2 June 2020

Keiichi I Nakayama

5

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2 June 2020

Stephane Manenti

6

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2 June 2020

Alice Davy

7

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2 June 2020

publication date

25 March 2016

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http://europepmc.org/abstract/MED/27015986

14 March 2018

published in

Journal of Pathology

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2 June 2020

volume

239

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2 June 2020

page(s)

250-261

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2 June 2020

issue

3

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CDK inhibitors: cell cycle regulators and beyond

2 June 2020

cites work

1 reference

p57KIP2: "Kip"ing the cell under control.

21 January 2018

1 reference

Ablation of the CDK inhibitor p57Kip2 results in increased apoptosis and delayed differentiation during mouse development.

21 January 2018

1 reference

Common and specific roles of the related CDK inhibitors p27 and p57 revealed by a knock-in mouse model

21 January 2018

1 reference

Mutations of the Imprinted CDKN1C Gene as a Cause of the Overgrowth Beckwith-Wiedemann Syndrome: Clinical Spectrum and Functional Characterization

21 January 2018

1 reference

CDKN1C mutations: two sides of the same coin.

21 January 2018

1 reference

Silver-Russell syndrome without body asymmetry in three patients with duplications of maternally derived chromosome 11p15 involving CDKN1C.

21 January 2018

1 reference

CDKN1C mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndrome.

21 January 2018

1 reference

Imprinted anomalies in fetal and childhood growth disorders: the model of Russell-Silver and Beckwith-Wiedemann syndromes

21 January 2018

1 reference

Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome

21 January 2018

1 reference

A novel variant in CDKN1C is associated with intrauterine growth restriction, short stature, and early-adulthood-onset diabetes

21 January 2018

1 reference

An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

New p57KIP2 mutations in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

Functional analysis of the p57KIP2 gene mutation in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

Regulation of the cytoskeleton: an oncogenic function for CDK inhibitors?

21 January 2018

1 reference

A pathway in quiescent cells that controls p27Kip1 stability, subcellular localization, and tumor suppression

21 January 2018

1 reference

Suppression of cell transformation by the cyclin-dependent kinase inhibitor p57KIP2 requires binding to proliferating cell nuclear antigen

21 January 2018

1 reference

Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse

21 January 2018

1 reference

Stabilization of MyoD by direct binding to p57(Kip2)

21 January 2018

1 reference

p57(Kip2) and cancer: time for a critical appraisal.

21 January 2018

1 reference

Beckwith-Wiedemann syndrome: growth pattern and tumor risk according to molecular mechanism, and guidelines for tumor surveillance

21 January 2018

1 reference

Silver-Russell and Beckwith-Wiedemann syndromes: opposite (epi)mutations in 11p15 result in opposite clinical pictures

21 January 2018

1 reference

Paradoxical NSD1 mutations in Beckwith-Wiedemann syndrome and 11p15 anomalies in Sotos syndrome

21 January 2018

1 reference

Expanding the clinical spectrum of B4GALT7 deficiency: homozygous p.R270C mutation with founder effect causes Larsen of Reunion Island syndrome

21 January 2018

1 reference

Confirmation of an epilepsy modifier locus on mouse chromosome 11 and candidate gene analysis by RNA-Seq

21 January 2018

1 reference

Distinctive phenotype in 9 patients with deletion of chromosome 1q24-q25

21 January 2018

1 reference

Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration

21 January 2018

1 reference

Glycogen synthase: a putative locus for diet-induced hyperglycemia.

21 January 2018

1 reference

Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination

21 January 2018

1 reference

Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas

21 January 2018

1 reference

Gene expression profiling of mesoblastic nephroma and Wilms tumors--comparison and clinical implications

21 January 2018

1 reference

Identification of sequence polymorphisms in two sulfation-related genes, PAPSS2 and SLC26A2, and an association analysis with knee osteoarthritis

21 January 2018

1 reference

Frameshift mutation in p53 regulator RPL26 is associated with multiple physical abnormalities and a specific pre-ribosomal RNA processing defect in diamond-blackfan anemia

21 January 2018

1 reference

Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse

21 January 2018

1 reference

The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia

21 January 2018

1 reference

A murine model of Denys-Drash syndrome reveals novel transcriptional targets of WT1 in podocytes.

21 January 2018

1 reference

22q11.2 deletion syndrome: DiGeorge, velocardiofacial, and conotruncal anomaly face syndromes

21 January 2018

1 reference

Characterizing the functional consequences of haploinsufficiency of NELF-A (WHSC2) and SLBP identifies novel cellular phenotypes in Wolf-Hirschhorn syndrome

21 January 2018

1 reference

Altered cell differentiation and proliferation in mice lacking p57KIP2 indicates a role in Beckwith–Wiedemann syndrome

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/PATH.4721

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27015986%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

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