Structural and functional insights into the human Börjeson-Forssman-Lehmann syndrome-associated protein PHF6. (Q31814788)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24554700%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

title

Structural and functional insights into the human Börjeson-Forssman-Lehmann syndrome-associated protein PHF6 (English)

1 reference

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8 March 2020

1 reference

GOA release 2020-03-11

sequence-specific DNA binding

1 reference

GOA release 2020-03-11

1 reference

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8 March 2020

Jiahai Zhang

1 reference

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8 March 2020

Yunyu Shi

1 reference

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8 March 2020

Zhonghua Liu

1 reference

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8 March 2020

Fudong Li

series ordinal

1 reference

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8 March 2020

Yide Mei

series ordinal

1 reference

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8 March 2020

Jihui Wu

series ordinal

1 reference

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8 March 2020

language of work or name

English

0 references

publication date

19 February 2014

1 reference

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Journal of Biological Chemistry

8 March 2020

published in

1 reference

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8 March 2020

volume

289

1 reference

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8 March 2020

issue

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8 March 2020

page(s)

10069-10083

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The X-linked intellectual disability protein PHF6 associates with the PAF1 complex and regulates neuronal migration in the mammalian brain.

8 March 2020

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The Methyltransferase NSD3 Has Chromatin-binding Motifs, PHD5-C5HCH, That Are Distinct from Other NSD (Nuclear Receptor SET Domain) Family Members in Their Histone H3 Recognition

14 July 2018

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PHF6 regulates cell cycle progression by suppressing ribosomal RNA synthesis

14 July 2018

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Solution structure of an atypical PHD finger in BRPF2 and its interaction with DNA

14 July 2018

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PHF6 interacts with the nucleosome remodeling and deacetylation (NuRD) complex

14 July 2018

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A Poised Chromatin Platform for TGF-β Access to Master Regulators

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Many keys to push: diversifying the 'readership' of plant homeodomain fingers

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PHF6 Deletions May Cause Borjeson-Forssman-Lehmann Syndrome in Females

14 July 2018

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Mutations of PHF6 are associated with mutations of NOTCH1, JAK1 and rearrangement of SET-NUP214 in T-cell acute lymphoblastic leukemia

14 July 2018

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A cooperative microRNA-tumor suppressor gene network in acute T-cell lymphoblastic leukemia (T-ALL).

14 July 2018

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The PHD finger: a versatile epigenome reader

14 July 2018

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iMOSFLM: a new graphical interface for diffraction-image processing with MOSFLM

14 July 2018

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Insights into association of the NuRD complex with FOG-1 from the crystal structure of an RbAp48·FOG-1 complex

14 July 2018

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PHF6 mutations in adult acute myeloid leukemia

14 July 2018

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T-cell acute lymphoblastic leukemia in association with Börjeson-Forssman-Lehmann syndrome due to a mutation in PHF6.

14 July 2018

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Dali server: conservation mapping in 3D

14 July 2018

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Features and development of Coot

14 July 2018

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PHF6 mutations in T-cell acute lymphoblastic leukemia

14 July 2018

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Behavioural phenotype in Börjeson-Forssman-Lehmann syndrome

14 July 2018

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Automated macromolecular model building for X-ray crystallography using ARP/wARP version 7

14 July 2018

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Histone H3K4me3 Binding Is Required for the DNA Repair and Apoptotic Activities of ING1 Tumor Suppressor

14 July 2018

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Decoding of methylated histone H3 tail by the Pygo-BCL9 Wnt signaling complex

14 July 2018

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14 July 2018

A short history of SHELX

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Protein and gene expression analysis of Phf6, the gene mutated in the Börjeson-Forssman-Lehmann Syndrome of intellectual disability and obesity

14 July 2018

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NOTCH1 directly regulates c-MYC and activates a feed-forward-loop transcriptional network promoting leukemic cell growth

14 July 2018

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The Börjeson-Forssman-Lehman syndrome (BFLS, MIM #301900).

14 July 2018

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14 July 2018

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Clinical and behavioral features of patients with Borjeson-Forssman-Lehmann syndrome with mutations in PHF6.

14 July 2018

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A novel PHF6 mutation results in enhanced exon skipping and mild Börjeson-Forssman-Lehmann syndrome

14 July 2018

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Refinement of macromolecular structures by the maximum-likelihood method

14 July 2018

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14 July 2018

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The clinical picture of the Börjeson-Forssman-Lehmann syndrome in males and heterozygous females with PHF6 mutations.

14 July 2018

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An X-linked, recessively inherited syndrome characterized by grave mental deficiency, epilepsy, and endocrine disorder

14 July 2018

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Novel PHF6 mutation p.D333del causes Börjeson-Forssman-Lehmann syndrome

14 July 2018

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Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome

14 July 2018

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Solution structure of the PHD domain from the KAP-1 corepressor: structural determinants for PHD, RING and LIM zinc-binding domains

14 July 2018

1 reference

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Biochemical analyses of the AF10 protein: the extended LAP/PHD-finger mediates oligomerisation

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3974978

Measurement of J and dipolar couplings from simplified two-dimensional NMR spectra

14 July 2018

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NMRPipe: a multidimensional spectral processing system based on UNIX pipes

14 July 2018

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The PHD finger: implications for chromatin-mediated transcriptional regulation

14 July 2018

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1024C> T (R342X) is a recurrent PHF6 mutation also found in the original Börjeson-Forssman-Lehmann syndrome family

14 July 2018

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Börjeson-Forssman-Lehmann Syndrome due to a novel plant homeodomain zinc finger mutation in the PHF6 gene

21 January 2018

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Gene mutation profiles and prognostic implications in Korean patients with T-lymphoblastic leukemia.

21 January 2018

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NMR: prediction of molecular alignment from structure using the PALES software

21 January 2018

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HAT3.1, a novel Arabidopsis homeodomain protein containing a conserved cysteine-rich region

21 January 2018

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A simple apparatus for generating stretched polyacrylamide gels, yielding uniform alignment of proteins and detergent micelles

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24554700

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Further clinical delineation of the Börjeson-Forssman-Lehmann syndrome in patients with PHF6 mutations

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24554700

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Refinement of the background genetic map of Xq26-q27 and gene localisation for Börjeson-Forssman-Lehmann Syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24554700

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1074/JBC.M113.535351

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24554700%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24554700%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

PubMed publication ID

24554700

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24554700%20AND%20SRC:MED&resulttype=core&format=json