Genome-wide detection of recurring sites of uniparental disomy in follicular and transformed follicular lymphoma (Q40134048)

17 September 2017

title

Genome-wide detection of recurring sites of uniparental disomy in follicular and transformed follicular lymphoma (English)

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17 September 2017

J Fitzgibbon

1

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17 September 2017

S Iqbal

2

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17 September 2017

A Davies

3

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17 September 2017

D O'shea

4

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E Carlotti

5

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T Chaplin

6

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J Matthews

7

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M Raghavan

8

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A Norton

9

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T A Lister

10

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B D Young

11

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17 September 2017

publication date

10 May 2007

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17 September 2017

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17 September 2017

volume

21

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17 September 2017

issue

7

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17 September 2017

page(s)

1514-1520

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Histological transformation of non-hodgkin's lymphoma.A prospective study

17 September 2017

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Copy number gain at 12q12-14 may be important in the transformation from follicular lymphoma to diffuse large B cell lymphoma

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A p21/WAF1 mutation favors the appearance of drug resistance to paclitaxel in human noncancerous epithelial mammary cells

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A fascination with chromosome rescue in uniparental disomy: Mendelian recessive outlaws and imprinting copyrights infringements

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Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic event.

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Prediction of Survival in Follicular Lymphoma Based on Molecular Features of Tumor-Infiltrating Immune Cells

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An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays

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High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping

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E mu-BRD2 transgenic mice develop B-cell lymphoma and leukemia.

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Splicing factor SRP20 is a novel partner of BCL6 in a t(3;6)(q27;p21) translocation in transformed follicular lymphoma.

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Cyclin D3 at 6p21 is dysregulated by recurrent chromosomal translocations to immunoglobulin loci in multiple myeloma.

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7 January 2021

Histologic conversion in the non-Hodgkin's lymphomas

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7 January 2021

Incidence, predictive factors, and outcome of lymphoma transformation in follicular lymphoma patients.

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7 January 2021

Transformation of follicular lymphoma to diffuse large cell lymphoma is associated with a heterogeneous set of DNA copy number and gene expression alterations

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7 January 2021

The use of real-time quantitative polymerase chain reaction and comparative genomic hybridization to identify amplification of the REL gene in follicular lymphoma

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7 January 2021

Genetic instability is associated with histological transformation of follicle center lymphoma

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7 January 2021

Partial uniparental disomy: a recurrent genetic mechanism alternative to chromosomal deletion in malignant lymphoma

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7 January 2021

Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias

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7 January 2021

A limited role for TP53 mutation in the transformation of follicular lymphoma to diffuse large B-cell lymphoma

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7 January 2021

Loss of heterozygosity associated with uniparental disomy in breast carcinoma

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7 January 2021

Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays

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7 January 2021

Mutations in the HLA class�II genes leading to loss of expression of HLA-DR and HLA-DQ in diffuse large B-cell lymphoma

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7 January 2021

Development of a human acute myeloid leukaemia screening panel and consequent identification of novel gene mutation in FLT3 and CCND3

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7 January 2021

Identifiers

DOI

10.1038/SJ.LEU.2404696

1 reference

Dimensions Publication ID

17 September 2017

1036113809

0 references

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