(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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17 September 2017

E Carlotti

5

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17 September 2017

T Chaplin

6

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17 September 2017

J Matthews

7

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17 September 2017

M Raghavan

8

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17 September 2017

A Norton

9

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17 September 2017

T A Lister

10

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17 September 2017

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

cites work

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Higher grade transformation of follicular lymphoma: phenotypic tumor progression associated with diverse genetic lesions

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Identification of cytogenetic subgroups and karyotypic pathways of clonal evolution in follicular lymphomas

21 January 2018

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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

21 January 2018

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Identifying allelic loss and homozygous deletions in pancreatic cancer without matched normals using high-density single-nucleotide polymorphism arrays

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Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex changes and multiple forms of chromosomal instability in colorectal cancers

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Molecular karyotyping of human hepatocellular carcinoma using single-nucleotide polymorphism arrays.

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A JAK2 mutation in myeloproliferative disorders: pathogenesis and therapeutic and scientific prospects.

21 January 2018

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A gain-of-function mutation of JAK2 in myeloproliferative disorders

21 January 2018

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Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders

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Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis

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PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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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.

21 January 2018

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

21 January 2018

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Alteration of SMRT tumor suppressor function in transformed non-Hodgkin lymphomas

21 January 2018

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Clonal evolution of B cells in transformation from low- to high-grade lymphoma

21 January 2018

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Follicular lymphoma: prognostic factors for response and survival

21 January 2018

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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.

1 reference

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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

Mechanisms leading to uniparental disomy and their clinical consequences

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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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https://api.crossref.org/works/10.1038%2FSJ.LEU.2404696

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404696

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404696

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404696

7 January 2021

Identifiers

DOI

10.1038/SJ.LEU.2404696

1 reference

Dimensions Publication ID

17 September 2017

1036113809

0 references

1 reference