(Q34241216)

31 July 2017

title

Mutations in EZH2 cause Weaver syndrome (English)

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31 July 2017

7

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31 July 2017

William T Gibson

1

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Kym M Boycott

14

object named as

Kym M Boycott

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31 July 2017

12

FORGE Canada Consortium

1 reference

31 July 2017

Rebecca L Hood

2

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31 July 2017

Shing Hei Zhan

3

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31 July 2017

Dennis E Bulman

4

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31 July 2017

Anthony P Fejes

5

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31 July 2017

Richard Moore

6

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31 July 2017

Patrice Eydoux

8

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31 July 2017

Riyana Babul-Hirji

9

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31 July 2017

Jianghong An

10

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31 July 2017

Marco A Marra

11

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31 July 2017

David Chitayat

13

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31 July 2017

David D Weaver

15

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31 July 2017

Steven J M Jones

16

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31 July 2017

language of work or name

English

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publication date

15 December 2011

1 reference

American Journal of Human Genetics

31 July 2017

published in

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31 July 2017

volume

90

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31 July 2017

issue

1

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31 July 2017

page(s)

110-118

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SMART 7: recent updates to the protein domain annotation resource

31 July 2017

cites work

1 reference

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6 July 2018

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The functional spectrum of low-frequency coding variation

6 July 2018

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Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma

6 July 2018

1 reference

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Polycomb EZH2 controls self-renewal and safeguards the transcriptional identity of skeletal muscle stem cells

6 July 2018

1 reference

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6 July 2018

1 reference

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Somatic mutations at EZH2 Y641 act dominantly through a mechanism of selectively altered PRC2 catalytic activity, to increase H3K27 trimethylation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257956

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6 July 2018

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Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome

6 July 2018

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6 July 2018

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Structural Biology of Human H3K9 Methyltransferases

6 July 2018

1 reference

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Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin

6 July 2018

1 reference

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Detection of nonneutral substitution rates on mammalian phylogenies

6 July 2018

1 reference

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Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

6 July 2018

1 reference

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The Sequence Alignment/Map format and SAMtools

6 July 2018

1 reference

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Fast and accurate short read alignment with Burrows-Wheeler transform

6 July 2018

1 reference

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Polycomb protein Ezh2 regulates pancreatic beta-cell Ink4a/Arf expression and regeneration in diabetes mellitus.

6 July 2018

1 reference

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DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

6 July 2018

1 reference

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InterPro: the integrative protein signature database

6 July 2018

1 reference

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The SWISS-MODEL workspace: a web-based environment for protein structure homology modelling

6 July 2018

1 reference

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Detection of large-scale variation in the human genome

6 July 2018

1 reference

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SIFT: Predicting amino acid changes that affect protein function

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257956

Spectrum of NSD1 mutations in Sotos and Weaver syndromes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257956

NSD1 mutations are the major cause of Sotos syndrome and occur in some cases of Weaver syndrome but are rare in other overgrowth phenotypes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257956

The active site of the SET domain is constructed on a knot

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257956

dbSNP: the NCBI database of genetic variation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257956

Regulation of chromatin structure by site-specific histone H3 methyltransferases

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257956

Weaver syndrome: autosomal dominant inheritance of the disorder

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257956

Autosomal dominant inheritance of Weaver syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257956

A new overgrowth syndrome with accelerated skeletal maturation, unusual facies, and camptodactyly

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257956

Ezh2 regulates anteroposterior axis specification and proximodistal axis elongation in the developing limb

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257956

Acute lymphoblastic leukemia in Weaver syndrome.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257956

Clinical and molecular overlap in overgrowth syndromes.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257956

Novel homo- and hemizygous mutations in EZH2 in myeloid malignancies

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22177091

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.AJHG.2011.11.018

1 reference

31 July 2017

1 reference

31 July 2017

1 reference