(Q38271699)

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Disruption of the histone acetyltransferase MYST4 leads to a Noonan syndrome-like phenotype and hyperactivated MAPK signaling in humans and mice

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Europe PubMed Central

PMC publication ID

1 September 2017

Disruption of the histone acetyltransferase MYST4 leads to a Noonan syndrome-like phenotype and hyperactivated MAPK signaling in humans and mice (English)

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Europe PubMed Central

PMC publication ID

1 September 2017

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Noonan syndrome

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inferred from title

9

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1 September 2017

Marco Tartaglia

13

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1 September 2017

15

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1 September 2017

Christian T Thiel

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Christian Thomas Thiel

18

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Hamish S. Scott

object named as

Hamish Scott

8

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object named as

Bilal N Sheikh

6

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14

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Arif Ekici

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1 September 2017

12

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Martin Zenker

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1 September 2017

17

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Anita Rauch

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1 September 2017

author name string

Michael Kraft

1

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1 September 2017

Ion Cristian Cirstea

2

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1 September 2017

Anne Kathrin Voss

3

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1 September 2017

Tim Thomas

4

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1 September 2017

Ina Goehring

5

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Europe PubMed Central

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1 September 2017

Lavinia Gordon

7

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1 September 2017

Mohammad Reza Ahmadian

10

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1 September 2017

Udo Trautmann

11

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1 September 2017

Helmuth-Guenther Dörr

16

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1 September 2017

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publication date

1 August 2011

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1 September 2017

Journal of Clinical Investigation

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1 September 2017

121

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Europe PubMed Central

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1 September 2017

9

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1 September 2017

3479-3491

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1 September 2017

describes a project that uses

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Europe PubMed Central

22 June 2022

https://europepmc.org/article/PMC/3163944

based on heuristic

inferred from PubMed Central ID database lookup

Noonan syndrome: clinical aspects and molecular pathogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163944

6 September 2017

A restricted spectrum of NRAS mutations causes Noonan syndrome

1 reference

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Epigenetic mechanisms in neurological diseases: genes, syndromes, and therapies

1 reference

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6 September 2017

MYST family histone acetyltransferases take center stage in stem cells and development.

1 reference

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6 September 2017

Lysine acetylation targets protein complexes and co-regulates major cellular functions

1 reference

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6 September 2017

Histone acetylation: where to go and how to get there

1 reference

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Inhibition of histone deacetylases: a pharmacological approach to the treatment of non-cancer disorders.

1 reference

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Regulation of cartilage formation and maturation by mitogen-activated protein kinase signaling

1 reference

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Mof (MYST1 or KAT8) is essential for progression of embryonic development past the blastocyst stage and required for normal chromatin architecture.

1 reference

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KEGG for linking genomes to life and the environment

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MOZ and MORF, two large MYSTic HATs in normal and cancer stem cells

1 reference

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Aberrant forms of histone acetyltransferases in human disease

1 reference

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Development of histone deacetylase inhibitors for cancer treatment

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6 September 2017

Histone acetyltransferase complexes: one size doesn't fit all

1 reference

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6 September 2017

Germline gain-of-function mutations in SOS1 cause Noonan syndrome

1 reference

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Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations

1 reference

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The natural history of Noonan syndrome: a long-term follow-up study

1 reference

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Monocytic leukemia zinc finger protein is essential for the development of long-term reconstituting hematopoietic stem cells

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1 reference

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6 September 2017

The p38 MAPK signaling pathway: a major regulator of skeletal muscle development

1 reference

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6 September 2017

A phosphatase holoenzyme comprised of Shoc2/Sur8 and the catalytic subunit of PP1 functions as an M-Ras effector to modulate Raf activity

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Genome-wide analysis of HDAC function

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6 September 2017

The diverse superfamily of lysine acetyltransferases and their roles in leukemia and other diseases

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6 September 2017

Querkopf, a histone acetyltransferase, is essential for embryonic neurogenesis.

1 reference

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Spatial and temporal patterns of ERK signaling during mouse embryogenesis

1 reference

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Neuronal p38 MAPK signalling: an emerging regulator of cell fate and function in the nervous system

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MOZ and MORF histone acetyltransferases interact with the Runt-domain transcription factor Runx2

1 reference

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Mitogen-activated protein (MAP) kinase pathways: regulation and physiological functions

1 reference

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Mammalian MAP kinase signalling cascades

1 reference

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Fusion of the MORF and CBP genes in acute myeloid leukemia with the t(10;16)(q22;p13)

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Querkopf, a MYST family histone acetyltransferase, is required for normal cerebral cortex development

1 reference

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Mice lacking HSP90beta fail to develop a placental labyrinth

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Uterine leiomyomata with t(10;17) disrupt the histone acetyltransferase MORF

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Yeast SAS silencing genes and human genes associated with AML and HIV-1 Tat interactions are homologous with acetyltransferases

1 reference

https://pubmed.ncbi.nlm.nih.gov/21804188

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Noonan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21804188

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Efficiency assessment of the gene trap approach

1 reference

https://pubmed.ncbi.nlm.nih.gov/21804188

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI43428

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

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