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English
Validation of two clinically useful assays for evaluation of JAK2 V617F mutation in chronic myeloproliferative disorders
scientific article published on 01 January 2006
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
16270039
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16270039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
title
Validation of two clinically useful assays for evaluation of JAK2 V617F mutation in chronic myeloproliferative disorders
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
16270039
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16270039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
main subject
myeloproliferative disorders
1 reference
based on heuristic
inferred from title
author name string
McClure R
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
16270039
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16270039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
Mai M
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
16270039
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16270039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
Lasho T
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
16270039
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16270039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
publication date
1 January 2006
1 reference
stated in
Europe PubMed Central
PubMed ID
16270039
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16270039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
published in
Leukemia
1 reference
stated in
Europe PubMed Central
PubMed ID
16270039
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16270039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
volume
20
1 reference
stated in
Europe PubMed Central
PubMed ID
16270039
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16270039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
16270039
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16270039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
page(s)
168-171
1 reference
stated in
Europe PubMed Central
PubMed ID
16270039
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16270039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
exact match
https://scigraph.springernature.com/pub.10.1038/sj.leu.2404007
0 references
cites work
A gain-of-function mutation of JAK2 in myeloproliferative disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.LEU.2404007
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.LEU.2404007
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.LEU.2404007
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both "atypical" myeloproliferative disorders and myelodysplastic syndromes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.LEU.2404007
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
JAK2 mutation 1849G>T is rare in acute leukemias but can be found in CMML, Philadelphia chromosome-negative CML, and megakaryocytic leukemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.LEU.2404007
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The JAK2V617F activating mutation occurs in chronic myelomonocytic leukemia and acute myeloid leukemia, but not in acute lymphoblastic leukemia or chronic lymphocytic leukemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.LEU.2404007
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.LEU.2404007
retrieved
7 January 2021
based on heuristic
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Identifiers
DOI
10.1038/SJ.LEU.2404007
1 reference
stated in
Europe PubMed Central
PubMed ID
16270039
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16270039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
Dimensions Publication ID
1051176897
0 references
PubMed ID
16270039
1 reference
stated in
Europe PubMed Central
PubMed ID
16270039
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16270039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
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