Further cytogenetic characterization of multiple myeloma confirms that 14q32 translocations are a very rare event in hyperdiploid cases (Q79079259)

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19 December 2019

title

Further cytogenetic characterization of multiple myeloma confirms that 14q32 translocations are a very rare event in hyperdiploid cases (English)

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19 December 2019

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author name string

Nicole Véronique Smadja

1

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19 December 2019

Dominique Leroux

2

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19 December 2019

Jean Soulier

3

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19 December 2019

Sylvie Dumont

4

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19 December 2019

Catherine Arnould

5

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19 December 2019

Sylvie Taviaux

6

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19 December 2019

Jean Louis Taillemite

7

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19 December 2019

Christian Bastard

8

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19 December 2019

language of work or name

English

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National Center for Biotechnology Information

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13 March 2024

publication date

1 November 2003

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full work available at URL

19 December 2019

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002/gcc.10275

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https://onlinelibrary.wiley.com/doi/pdf/10.1002/gcc.10275

13 March 2024

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Genes, Chromosomes and Cancer

13 March 2024

published in

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19 December 2019

volume

38

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19 December 2019

issue

3

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19 December 2019

page(s)

234-239

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High incidence of cryptic translocations involving the Ig heavy chain gene in multiple myeloma, as shown by fluorescence in situ hybridization

19 December 2019

cites work

1 reference

7 January 2021

Oncogenesis of multiple myeloma: 14q32 and 13q chromosomal abnormalities are not randomly distributed, but correlate with natural history, immunological features, and clinical presentation

1 reference

7 January 2021

Promiscuous translocations into immunoglobulin heavy chain switch regions in multiple myeloma

1 reference

7 January 2021

Frequent translocation t(4;14)(p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3

1 reference

7 January 2021

A clinical staging system for multiple myeloma correlation of measured myeloma cell mass with presenting clinical features, response to treatment, and survival

1 reference

7 January 2021

The t(4;14)(p16.3;q32) is strongly associated with chromosome 13 abnormalities in both multiple myeloma and monoclonal gammopathy of undetermined significance

1 reference

7 January 2021

Myeloma and the t(11;14)(q13;q32); evidence for a biologically defined unique subset of patients.

1 reference

7 January 2021

Illegitimate switch recombinations are present in approximately half of primary myeloma tumors, but do not relate to known prognostic indicators or survival

1 reference

7 January 2021

Deregulation of MUM1/IRF4 by chromosomal translocation in multiple myeloma

1 reference

7 January 2021

Recurrent 14q32 translocations determine the prognosis of multiple myeloma, especially in patients receiving intensive chemotherapy

1 reference

7 January 2021

Insertional events as well as translocations may arise during aberrant immunoglobulin switch recombination in a patient with multiple myeloma.

1 reference

7 January 2021

Cytogenetic study in multiple myeloma at diagnosis: comparison of two techniques

1 reference

7 January 2021

Chromosomal analysis in multiple myeloma: cytogenetic evidence of two different diseases

1 reference

7 January 2021

Hypodiploidy is a major prognostic factor in multiple myeloma

1 reference

7 January 2021

High incidence of translocations t(11;14)(q13;q32) and t(4;14)(p16;q32) in patients with plasma cell malignancies

1

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13 March 2024

Identifiers

DOI

10.1002/GCC.10275

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19 December 2019

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