Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia (Q44998179)

8 December 2017

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

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8 December 2017

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Kenichi Yoshida

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Yusuke Okuno

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Yusuke Okuno

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author name string

Hirotoshi Sakaguchi

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8 December 2017

Hideki Muramatsu

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8 December 2017

Yuichi Shiraishi

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8 December 2017

Mariko Takahashi

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8 December 2017

Ayana Kon

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8 December 2017

Masashi Sanada

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8 December 2017

Kenichi Chiba

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8 December 2017

Hiroko Tanaka

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8 December 2017

Hideki Makishima

11

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8 December 2017

Xinan Wang

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8 December 2017

Yinyan Xu

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8 December 2017

Sayoko Doisaki

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8 December 2017

Asahito Hama

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8 December 2017

Koji Nakanishi

16

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8 December 2017

Yoshiyuki Takahashi

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8 December 2017

Nao Yoshida

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8 December 2017

Jaroslaw P Maciejewski

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8 December 2017

Satoru Miyano

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8 December 2017

Seishi Ogawa

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8 December 2017

Seiji Kojima

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8 December 2017

language of work or name

English

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publication date

7 July 2013

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8 December 2017

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8 December 2017

45

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8 December 2017

8

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8 December 2017

937-941

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

8 December 2017

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

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12 December 2020

Differentiating juvenile myelomonocytic leukemia from infectious disease

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12 December 2020

BLAT—The BLAST-Like Alignment Tool

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Mutations in CBL occur frequently in juvenile myelomonocytic leukemia

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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

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12 December 2020

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

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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).

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12 December 2020

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

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12 December 2020

Frequent pathway mutations of splicing machinery in myelodysplasia

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12 December 2020

Drosophila haematopoiesis

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12 December 2020

SETBP1 mutation analysis in 944 patients with MDS and AML.

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12 December 2020

The Sequence Alignment/Map format and SAMtools

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12 December 2020

MutationTaster evaluates disease-causing potential of sequence alterations

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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.

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12 December 2020

A method and server for predicting damaging missense mutations

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12 December 2020

De novo mutations of SETBP1 cause Schinzel-Giedion syndrome

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12 December 2020

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

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12 December 2020

Recurrent SETBP1 mutations in atypical chronic myeloid leukemia

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12 December 2020

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

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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

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12 December 2020

Somatic SETBP1 mutations in myeloid malignancies

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12 December 2020

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

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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

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12 December 2020

A novel retinoblastoma therapy from genomic and epigenetic analyses

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12 December 2020

Fast and accurate short read alignment with Burrows-Wheeler transform

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12 December 2020

Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome

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12 December 2020

CAP3: A DNA sequence assembly program

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12 December 2020

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

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12 December 2020

Activating alleles of JAK3 in acute megakaryoblastic leukemia

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12 December 2020

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

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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

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

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Identifiers

DOI

10.1038/NG.2698

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Dimensions Publication ID

8 December 2017

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