The landscape of somatic mutations in Down syndrome-related myeloid disorders. (Q53089292)

11 May 2018

title

The landscape of somatic mutations in Down syndrome-related myeloid disorders. (English)

1 reference

11 May 2018

author

Kenichi Yoshida

1

1 reference

11 May 2018

Yusuke Okuno

3

1 reference

11 May 2018

Daisuke Hasegawa

20

1 reference

11 May 2018

Hirokazu Kanegane

22

object named as

Hirokazu Kanegane

1 reference

11 May 2018

author name string

Tsutomu Toki

2

1 reference

11 May 2018

Rika Kanezaki

4

1 reference

11 May 2018

Yuichi Shiraishi

5

1 reference

11 May 2018

Aiko Sato-Otsubo

6

1 reference

11 May 2018

Masashi Sanada

7

1 reference

11 May 2018

Myoung-ja Park

8

1 reference

11 May 2018

Kiminori Terui

9

1 reference

11 May 2018

Hiromichi Suzuki

10

1 reference

11 May 2018

Ayana Kon

11

1 reference

11 May 2018

Yasunobu Nagata

12

1 reference

11 May 2018

Yusuke Sato

13

1 reference

11 May 2018

RuNan Wang

14

1 reference

11 May 2018

Norio Shiba

15

1 reference

11 May 2018

Kenichi Chiba

16

1 reference

11 May 2018

Hiroko Tanaka

17

1 reference

11 May 2018

Asahito Hama

18

1 reference

11 May 2018

Hideki Muramatsu

19

1 reference

11 May 2018

Kazuhiro Nakamura

21

1 reference

11 May 2018

Keiko Tsukamoto

23

1 reference

11 May 2018

Souichi Adachi

24

1 reference

11 May 2018

Kiyoshi Kawakami

25

1 reference

11 May 2018

Koji Kato

26

1 reference

11 May 2018

Ryosei Nishimura

27

1 reference

11 May 2018

Shai Izraeli

28

1 reference

11 May 2018

Yasuhide Hayashi

29

1 reference

11 May 2018

Satoru Miyano

30

1 reference

11 May 2018

Seiji Kojima

31

1 reference

11 May 2018

Etsuro Ito

32

1 reference

11 May 2018

Seishi Ogawa

33

1 reference

11 May 2018

language of work or name

English

0 references

publication date

22 September 2013

1 reference

11 May 2018

published in

Nature Genetics

1 reference

11 May 2018

volume

45

1 reference

11 May 2018

page(s)

1293-1299

1 reference

11 May 2018

issue

11

1 reference

11 May 2018

https://scigraph.springernature.com/pub.10.1038/ng.2759

exact match

0 references

cites work

MPLW515L mutation in acute megakaryoblastic leukaemia.

1 reference

12 December 2020

Chromosomal cohesin forms a ring

1 reference

12 December 2020

Effects of sister chromatid cohesion proteins on cut gene expression during wing development in Drosophila

1 reference

12 December 2020

Acute megakaryoblastic leukemia with a four-way variant translocation originating the RBM15-MKL1 fusion gene.

1 reference

12 December 2020

BLAT—The BLAST-Like Alignment Tool

1 reference

12 December 2020

Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.

1 reference

12 December 2020

CTCF physically links cohesin to chromatin

1 reference

12 December 2020

The role of p53 in megakaryocyte differentiation and the megakaryocytic leukemias of Down syndrome

1 reference

12 December 2020

Characterization of novel genomic alterations and therapeutic approaches using acute megakaryoblastic leukemia xenograft models

1 reference

12 December 2020

An empirical Bayesian framework for somatic mutation detection from cancer genome sequencing data

1 reference

12 December 2020

Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemia.

1 reference

12 December 2020

A prospective study of the natural history of transient leukemia (TL) in neonates with Down syndrome (DS): Children's Oncology Group (COG) study POG-9481.

1 reference

12 December 2020

The cohesin complex is required for the DNA damage-induced G2/M checkpoint in mammalian cells

1 reference

12 December 2020

Involvement of a human gene related to the Drosophila spen gene in the recurrent t(1;22) translocation of acute megakaryocytic leukemia

1 reference

12 December 2020

Cohesin: its roles and mechanisms

1 reference

12 December 2020

Circos: an information aesthetic for comparative genomics

1 reference

12 December 2020

Activating mutations in human acute megakaryoblastic leukemia.

1 reference

12 December 2020

Treatment and prognostic impact of transient leukemia in neonates with Down syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Exome sequencing identifies putative drivers of progression of transient myeloproliferative disorder to AMKL in infants with Down syndrome.

1 reference

12 December 2020

The origin and evolution of mutations in acute myeloid leukemia

1 reference

12 December 2020

Patterns of somatic mutation in human cancer genomes

1 reference

12 December 2020

Risk factors for early death in neonates with Down syndrome and transient leukaemia

1 reference

12 December 2020

COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer

1 reference

12 December 2020

Frequent pathway mutations of splicing machinery in myelodysplasia

1 reference

12 December 2020

BioGPS: an extensible and customizable portal for querying and organizing gene annotation resources

1 reference

12 December 2020

Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype

1 reference

12 December 2020

The Sequence Alignment/Map format and SAMtools

1 reference

12 December 2020

DYRK1A binds to an evolutionarily conserved WD40-repeat protein WDR68 and induces its nuclear translocation

1 reference

12 December 2020

Cytogenetic features of acute lymphoblastic and myeloid leukemias in pediatric patients with Down syndrome: an iBFM-SG study

1 reference

12 December 2020

Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing

1 reference

12 December 2020

An Inv(16)(p13.3q24.3)-encoded CBFA2T3-GLIS2 fusion protein defines an aggressive subtype of pediatric acute megakaryoblastic leukemia

1 reference

12 December 2020

NUP98/JARID1A is a novel recurrent abnormality in pediatric acute megakaryoblastic leukemia with a distinct HOX gene expression pattern.

1 reference

12 December 2020

Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia

1 reference

12 December 2020

Two mammalian MOF complexes regulate transcription activation by distinct mechanisms

1 reference

12 December 2020

CTCF shapes chromatin by multiple mechanisms: the impact of 20 years of CTCF research on understanding the workings of chromatin

1 reference

12 December 2020

Identification of distinct molecular phenotypes in acute megakaryoblastic leukemia by gene expression profiling.

1 reference

12 December 2020

Integrated molecular analysis of clear-cell renal cell carcinoma

1 reference

12 December 2020

Myeloid leukemia in Down syndrome

1 reference

12 December 2020

Frequency and prognostic implications of JAK 1-3 aberrations in Down syndrome acute lymphoblastic and myeloid leukemia

1 reference

12 December 2020

Mutational screen reveals a novel JAK2 mutation, L611S, in a child with acute lymphoblastic leukemia

1 reference

12 December 2020

Postreplicative Formation of Cohesion Is Required for Repair and Induced by a Single DNA Break

1 reference

12 December 2020

Detection of JAK2 mutations in paraffin marrow biopsies by high resolution melting analysis: identification of L611S alone and in cis with V617F in polycythemia vera

1 reference

12 December 2020

Integrative genomics viewer

1 reference

12 December 2020

A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays

1 reference

12 December 2020

Role of histone H3 lysine 27 methylation in Polycomb-group silencing

1 reference

12 December 2020

Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays

1 reference

12 December 2020

Cohesins functionally associate with CTCF on mammalian chromosome arms

1 reference

12 December 2020

Comprehensive molecular portraits of human breast tumours

1 reference

12 December 2020

Cohesins localize with CTCF at the KSHV latency control region and at cellular c-myc and H19/Igf2 insulators

1 reference

12 December 2020

Molecular lesions in childhood and adult acute megakaryoblastic leukaemia

1 reference

12 December 2020

Prognostic relevance of integrated genetic profiling in acute myeloid leukemia

1 reference

12 December 2020

JAK mutations in high-risk childhood acute lymphoblastic leukemia

1 reference

12 December 2020

Mutational inactivation of STAG2 causes aneuploidy in human cancer

1 reference

12 December 2020

Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders

1 reference

12 December 2020

Mutations of JAK2 in acute lymphoblastic leukaemias associated with Down's syndrome

1 reference

12 December 2020

Frequent mutations in the GATA-1 gene in the transient myeloproliferative disorder of Down syndrome

1 reference

12 December 2020

Cohesin mediates transcriptional insulation by CCCTC-binding factor

1 reference

12 December 2020

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

1 reference

12 December 2020

Activating alleles of JAK3 in acute megakaryoblastic leukemia

1 reference

12 December 2020

How cohesin and CTCF cooperate in regulating gene expression

1 reference

12 December 2020

Diagnosis and management of acute myeloid leukemia in children and adolescents: recommendations from an international expert panel

1 reference

12 December 2020

Acquired mutations in GATA1 in the megakaryoblastic leukemia of Down syndrome

1 reference

12 December 2020

CTCF: master weaver of the genome

1 reference

12 December 2020

The viral oncogene Np9 acts as a critical molecular switch for co-activating β-catenin, ERK, Akt and Notch1 and promoting the growth of human leukemia stem/progenitor cells

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.2759

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/NG.2759

1 reference

11 May 2018

PubMed ID

24056718

1 reference

11 May 2018