(Q54270566)

27 May 2018

title

MYD88 L265P is a marker highly characteristic of, but not restricted to, Waldenström's macroglobulinemia. (English)

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27 May 2018

author

Miguel Alcoceba

11

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27 May 2018

Norma C. Gutiérrez

18

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27 May 2018

Ramón García-Sanz

21

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27 May 2018

Elena Sebastián

object named as

E Sebastián

2

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M. Carmen Chillón

3

object named as

M C Chillón

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27 May 2018

author name string

C Jiménez

1

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27 May 2018

P Giraldo

4

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27 May 2018

J Mariano Hernández

5

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27 May 2018

F Escalante

6

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27 May 2018

T J González-López

7

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27 May 2018

C Aguilera

8

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27 May 2018

A G de Coca

9

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27 May 2018

I Murillo

10

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27 May 2018

A Balanzategui

12

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27 May 2018

M E Sarasquete

13

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27 May 2018

R Corral

14

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27 May 2018

L A Marín

15

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27 May 2018

B Paiva

16

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27 May 2018

E M Ocio

17

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27 May 2018

M González

19

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27 May 2018

J F San Miguel

20

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27 May 2018

publication date

28 February 2013

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27 May 2018

published in

Leukemia

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27 May 2018

volume

27

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27 May 2018

issue

8

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27 May 2018

page(s)

1722-1728

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27 May 2018

https://scigraph.springernature.com/pub.10.1038/leu.2013.62

exact match

0 references

cites work

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The incidence and survival of Waldenström's Macroglobulinaemia in South East England

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Molecular pathogenesis of Waldenstrom's macroglobulinemia.

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MYD88 L265P somatic mutation in Waldenström's macroglobulinemia.

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Oncogenically active MYD88 mutations in human lymphoma

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Discovery and prioritization of somatic mutations in diffuse large B-cell lymphoma (DLBCL) by whole-exome sequencing

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MYD88 somatic mutation is a genetic feature of primary cutaneous diffuse large B-cell lymphoma, leg type

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Recurrent mutations of MYD88 and TBL1XR1 in primary central nervous system lymphomas

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Activating L265P mutations of the MYD88 gene are common in primary central nervous system lymphoma.

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Differential diagnosis of IgM MGUS and WM according to B-lymphoid infiltration by morphology and flow cytometry

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Multiparameter flow cytometry quantification of bone marrow plasma cells at diagnosis provides more prognostic information than morphological assessment in myeloma patients.

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Post-treatment bone marrow residual disease > 5% by flow cytometry is highly predictive of short progression-free and overall survival in patients with Waldenström's macroglobulinemia

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6q deletion in Waldenström macroglobulinemia is associated with features of adverse prognosis

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IGHV gene features and MYD88 L265P mutation separate the three marginal zone lymphoma entities and Waldenström macroglobulinemia/lymphoplasmacytic lymphomas

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Prevalence and clinical significance of the MYD88 (L265P) somatic mutation in Waldenstrom's macroglobulinemia and related lymphoid neoplasms.

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Development of high-resolution melting analysis for the detection of the MYD88 L265P mutation

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7 January 2021

MYD88 L265P in Waldenström macroglobulinemia, immunoglobulin M monoclonal gammopathy, and other B-cell lymphoproliferative disorders using conventional and quantitative allele-specific polymerase chain reaction

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Immunophenotypic and Cytogenetic Comparison of Waldenström's Macroglobulinemia with Splenic Marginal Zone Lymphoma

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CD27 in defining memory B-cell origins in Waldenström's macroglobulinemia

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7 January 2021

Clonotypic IgM V/D/J sequence analysis in Waldenstrom macroglobulinemia suggests an unusual B-cell origin and an expansion of polyclonal B cells in peripheral blood.

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https://api.crossref.org/works/10.1038%2FLEU.2013.62

7 January 2021

Lymphoplasmacytic lymphoma/Waldenström's macroglobulinemia derives from an extensively hypermutated B cell that lacks ongoing somatic hypermutation.

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https://api.crossref.org/works/10.1038%2FLEU.2013.62

7 January 2021

Response assessment in Waldenström macroglobulinaemia: update from the VIth International Workshop

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7 January 2021

Identifiers

DOI

10.1038/LEU.2013.62

1 reference

27 May 2018

1 reference

27 May 2018