(Q33587677)

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Hereditary thrombocytosis caused by MPLSer505Asn is associated with a high thrombotic risk, splenomegaly and progression to bone marrow fibrosis

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Hereditary thrombocytosis caused by MPLSer505Asn is associated with a high thrombotic risk, splenomegaly and progression to bone marrow fibrosis (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

1 reference

based on heuristic

inferred from title

Luigi Maria Larocca

object named as

Luigi Maria Larocca

11

0 references

Maurizio Martini

object named as

Maurizio Martini

10

0 references

Luciana Teofili

object named as

Luciana Teofili

1

0 references

object named as

Giuseppe Leone

9

0 references

8

object named as

Robin Foà

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

author name string

Fiorina Giona

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Lorenza Torti

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Tonia Cenci

4

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Bianca Maria Ricerca

5

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Carlo Rumi

6

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Vittorio Nunes

7

1 reference

Europe PubMed Central

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28 July 2017

publication date

27 August 2009

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Europe PubMed Central

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28 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

95

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Europe PubMed Central

PubMed publication ID

28 July 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

65-70

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Evidence for a founder effect of the MPL-S505N mutation in eight Italian pedigrees with hereditary thrombocythemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805752

21 June 2018

Therapeutic targeting of Janus kinases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805752

21 June 2018

MPL mutations in myeloproliferative disorders: analysis of the PT-1 cohort.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805752

21 June 2018

MPLW515L is a novel somatic activating mutation in myelofibrosis with myeloid metaplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805752

21 June 2018

Lessons from familial myeloproliferative disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805752

21 June 2018

European consensus on grading bone marrow fibrosis and assessment of cellularity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805752

21 June 2018

Mpl Baltimore: a thrombopoietin receptor polymorphism associated with thrombocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805752

21 June 2018

Translational pathophysiology: a novel molecular mechanism of human disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805752

21 June 2018

Essential thrombocythaemia in children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805752

21 June 2018

Familial essential thrombocythemia associated with one-base deletion in the 5'-untranslated region of the thrombopoietin gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805752

21 June 2018

An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805752

21 June 2018

Characteristics and clinical correlates of MPL 515W>L/K mutation in essential thrombocythemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805752

31 October 2018

A de novo splice donor mutation in the thrombopoietin gene causes hereditary thrombocythemia in a Polish family.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805752

31 October 2018

Childhood polycythemia vera and essential thrombocythemia: does their pathogenesis overlap with that of adult patients?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805752

31 October 2018

MPL515 mutations in myeloproliferative and other myeloid disorders: a study of 1182 patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805752

31 October 2018

Increased platelet and leukocyte activation as contributing mechanisms for thrombosis in essential thrombocythemia and correlation with the JAK2 mutational status.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805752

31 October 2018

Familial essential thrombocythemia associated with a dominant-positive activating mutation of the c-MPL gene, which encodes for the receptor for thrombopoietin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805752

31 October 2018

Thrombopoietin production is inhibited by a translational mechanism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805752

31 October 2018

A single-base deletion in the thrombopoietin (TPO) gene causes familial essential thrombocythemia through a mechanism of more efficient translation of TPO mRNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/19713221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Essential thrombocythemia beyond the first decade: life expectancy, long-term complication rates, and prognostic factors

1 reference

https://pubmed.ncbi.nlm.nih.gov/19713221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Markers of myeloproliferative diseases in childhood polycythemia vera and essential thrombocythemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/19713221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

V617F JAK-2 mutation in patients with essential thrombocythemia: relation to platelet, granulocyte, and plasma hemostatic and inflammatory molecules

1 reference

https://pubmed.ncbi.nlm.nih.gov/19713221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The revised WHO diagnostic criteria for Ph-negative myeloproliferative diseases are not appropriate for the diagnostic screening of childhood polycythemia vera and essential thrombocythemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/19713221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New mutations of MPL in primitive myelofibrosis: only the MPL W515 mutations promote a G1/S-phase transition

1 reference

https://pubmed.ncbi.nlm.nih.gov/19713221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial thrombocytosis caused by the novel germ-line mutation p.Pro106Leu in the MPL gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/19713221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary thrombocythaemia in a Japanese family is caused by a novel point mutation in the thrombopoietin gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/19713221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.3324/HAEMATOL.2009.007542

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

0 references

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