(Q42589188)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

title

GATA2 and secondary mutations in familial myelodysplastic syndromes and pediatric myeloid malignancies (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

3

1 reference

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15 February 2020

Kenichi Yoshida

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

author name string

Xinan Wang

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Hideki Muramatsu

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Hirotoshi Sakaguchi

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Nozomu Kawashima

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Yinyan Xu

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Yuichi Shiraishi

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Kenichi Chiba

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Hiroko Tanaka

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Shoji Saito

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Yozo Nakazawa

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Taro Masunari

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Tadashi Hirose

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Shaimaa Elmahdi

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Atsushi Narita

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Sayoko Doisaki

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Olfat Ismael

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Hideki Makishima

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Asahito Hama

20

1 reference

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15 February 2020

Satoru Miyano

21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Yoshiyuki Takahashi

22

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Seishi Ogawa

23

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Seiji Kojima

24

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

language of work or name

1 reference

28 May 2015

1 reference

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15 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

volume

100

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

issue

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

page(s)

e398-401

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

Mutations in GATA2 are rare in juvenile myelomonocytic leukemia

15 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4591774

Landscape of genetic lesions in 944 patients with myelodysplastic syndromes

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4591774

Somatic SETBP1 mutations in myeloid malignancies

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4591774

GATA2 haploinsufficiency caused by mutations in a conserved intronic element leads to MonoMAC syndrome

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4591774

Germ-line GATA2 p.THR354MET mutation in familial myelodysplastic syndrome with acquired monosomy 7 and ASXL1 mutation demonstrating rapid onset and poor survival.

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4591774

Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4591774

Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4591774

Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency.

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4591774

Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome.

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4591774

Gain-of-function mutation of GATA-2 in acute myeloid transformation of chronic myeloid leukemia

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4591774

Haploinsufficiency of GATA-2 perturbs adult hematopoietic stem-cell homeostasis

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4591774

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

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4591774

Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4591774

GATA2 mutations are frequent in intermediate-risk karyotype AML with biallelic CEBPA mutations and are associated with favorable prognosis

16 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26022708

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3324/HAEMATOL.2015.127092

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

PubMed publication ID

26022708

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26022708%20AND%20SRC:MED&resulttype=core&format=json