(Q44998179)

8 December 2017

title

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

1 reference

8 December 2017

1 reference

Kenichi Yoshida

4

0 references

Yusuke Okuno

object named as

Yusuke Okuno

2

0 references

author name string

Hirotoshi Sakaguchi

1

1 reference

8 December 2017

Hideki Muramatsu

3

1 reference

8 December 2017

Yuichi Shiraishi

5

1 reference

8 December 2017

Mariko Takahashi

6

1 reference

8 December 2017

Ayana Kon

7

1 reference

8 December 2017

Masashi Sanada

8

1 reference

8 December 2017

Kenichi Chiba

9

1 reference

8 December 2017

Hiroko Tanaka

10

1 reference

8 December 2017

Hideki Makishima

11

1 reference

8 December 2017

Xinan Wang

12

1 reference

8 December 2017

Yinyan Xu

13

1 reference

8 December 2017

Sayoko Doisaki

14

1 reference

8 December 2017

Asahito Hama

15

1 reference

8 December 2017

Koji Nakanishi

16

1 reference

8 December 2017

Yoshiyuki Takahashi

17

1 reference

8 December 2017

Nao Yoshida

18

1 reference

8 December 2017

Jaroslaw P Maciejewski

19

1 reference

8 December 2017

Satoru Miyano

20

1 reference

8 December 2017

Seishi Ogawa

21

1 reference

8 December 2017

Seiji Kojima

22

1 reference

8 December 2017

language of work or name

English

0 references

publication date

7 July 2013

1 reference

8 December 2017

1 reference

8 December 2017

volume

45

1 reference

8 December 2017

issue

8

1 reference

8 December 2017

page(s)

937-941

1 reference

https://scigraph.springernature.com/pub.10.1038/ng.2698

8 December 2017

exact match

0 references

cites work

Reactome knowledgebase of human biological pathways and processes

1 reference

12 December 2020

Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1.

1 reference

12 December 2020

Differentiating juvenile myelomonocytic leukemia from infectious disease

1 reference

12 December 2020

BLAT—The BLAST-Like Alignment Tool

1 reference

12 December 2020

Loss-of-function JAK3 mutations in TMD and AMKL of Down syndrome

1 reference

12 December 2020

Prevention of Organ Allograft Rejection by a Specific Janus Kinase 3 Inhibitor

1 reference

12 December 2020

SETBP1 overexpression is a novel leukemogenic mechanism that predicts adverse outcome in elderly patients with acute myeloid leukemia.

1 reference

12 December 2020

SETBP1 mutations in 658 patients with myelodysplastic syndromes, chronic myelomonocytic leukemia and secondary acute myeloid leukemias.

1 reference

12 December 2020

Mutations in CBL occur frequently in juvenile myelomonocytic leukemia

1 reference

12 December 2020

Analysis of JAK3, JAK2, and C-MPL mutations in transient myeloproliferative disorder and myeloid leukemia of Down syndrome blasts in children with Down syndrome

1 reference

12 December 2020

Functional analysis of JAK3 mutations in transient myeloproliferative disorder and acute megakaryoblastic leukaemia accompanying Down syndrome

1 reference

12 December 2020

Mutations of an E3 ubiquitin ligase c-Cbl but not TET2 mutations are pathogenic in juvenile myelomonocytic leukemia

1 reference

12 December 2020

Fusion of NUP98 and the SET binding protein 1 (SETBP1) gene in a paediatric acute T cell lymphoblastic leukaemia with t(11;18)(p15;q12).

1 reference

12 December 2020

Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration

1 reference

12 December 2020

Frequent pathway mutations of splicing machinery in myelodysplasia

1 reference

12 December 2020

Drosophila haematopoiesis

1 reference

12 December 2020

SETBP1 mutation analysis in 944 patients with MDS and AML.

1 reference

12 December 2020

The Sequence Alignment/Map format and SAMtools

1 reference

12 December 2020

MutationTaster evaluates disease-causing potential of sequence alterations

1 reference

12 December 2020

Genome-wide single-nucleotide polymorphism analysis in juvenile myelomonocytic leukemia identifies uniparental disomy surrounding the NF1 locus in cases associated with neurofibromatosis but not in cases with mutant RAS or PTPN11.

1 reference

12 December 2020

A method and server for predicting damaging missense mutations

1 reference

12 December 2020

De novo mutations of SETBP1 cause Schinzel-Giedion syndrome

1 reference

12 December 2020

The genetic basis of early T-cell precursor acute lymphoblastic leukaemia

1 reference

12 December 2020

Recurrent SETBP1 mutations in atypical chronic myeloid leukemia

1 reference

12 December 2020

Janus kinase 3-activating mutations identified in natural killer/T-cell lymphoma

1 reference

12 December 2020

Evi-1 is a critical regulator for hematopoietic stem cells and transformed leukemic cells.

1 reference

12 December 2020

FERM domain mutations induce gain of function in JAK3 in adult T-cell leukemia/lymphoma

1 reference

12 December 2020

Genetic typing of CBL, ASXL1, RUNX1, TET2 and JAK2 in juvenile myelomonocytic leukaemia reveals a genetic profile distinct from chronic myelomonocytic leukaemia

1 reference

12 December 2020

Identification and characterization of SEB, a novel protein that binds to the acute undifferentiated leukemia-associated protein SET

1 reference

12 December 2020

Somatic SETBP1 mutations in myeloid malignancies

1 reference

12 December 2020

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

1 reference

12 December 2020

SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations

1 reference

12 December 2020

A novel retinoblastoma therapy from genomic and epigenetic analyses

1 reference

12 December 2020

Fast and accurate short read alignment with Burrows-Wheeler transform

1 reference

12 December 2020

Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome

1 reference

12 December 2020

CAP3: A DNA sequence assembly program

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

SETBP1 mutations in 415 patients with primary myelofibrosis or chronic myelomonocytic leukemia: independent prognostic impact in CMML.

1 reference

12 December 2020

JAK3 mutations occur in acute megakaryoblastic leukemia both in Down syndrome children and non-Down syndrome adults

1 reference

12 December 2020

Inhibition of intracellular dipeptidyl peptidases 8 and 9 enhances parthenolide's anti-leukemic activity.

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.2698

7 January 2021

inferred from DOI database lookup

From in vitro to in vivo: intracellular determination of imatinib and nilotinib may be related with clinical outcome.

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.2698

7 January 2021

inferred from DOI database lookup

The secondary FLT3-ITD F691L mutation induces resistance to AC220 in FLT3-ITD+ AML but retains in vitro sensitivity to PKC412 and Sunitinib

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.2698

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/NG.2698

1 reference

Dimensions Publication ID

8 December 2017

1029513939

0 references

1 reference