(Q34456199)

English

The FOXP1 transcription factor is expressed in the majority of follicular lymphomas but is rarely expressed in classical and lymphocyte predominant Hodgkin's lymphoma

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scholarly article

1 reference

Europe PubMed Central

2 August 2017

The FOXP1 transcription factor is expressed in the majority of follicular lymphomas but is rarely expressed in classical and lymphocyte predominant Hodgkin's lymphoma (English)

1 reference

Europe PubMed Central

2 August 2017

Alison H Banham

4

1 reference

Europe PubMed Central

2 August 2017

author name string

Philip Brown

1

1 reference

Europe PubMed Central

2 August 2017

Teresa Marafioti

2

1 reference

Europe PubMed Central

2 August 2017

Rajko Kusec

3

1 reference

Europe PubMed Central

2 August 2017

publication date

1 May 2005

1 reference

Europe PubMed Central

2 August 2017

Journal of Molecular Histology

1 reference

Europe PubMed Central

2 August 2017

36

1 reference

Europe PubMed Central

2 August 2017

4

1 reference

Europe PubMed Central

2 August 2017

249-256

1 reference

Europe PubMed Central

2 August 2017

The amount of scurfin protein determines peripheral T cell number and responsiveness

1 reference

https://api.crossref.org/works/10.1007%2FS10735-005-6521-3

21 January 2018

FoxP4, a novel forkhead transcription factor

1 reference

https://api.crossref.org/works/10.1007%2FS10735-005-6521-3

21 January 2018

Forkhead transcription factors: key players in development and metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The FOXP1 winged helix transcription factor is a novel candidate tumor suppressor gene on chromosome 3p.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lymphoid malignancies: the dark side of B-cell differentiation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A forkhead-domain gene is mutated in a severe speech and language disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Down-regulation of BOB.1/OBF.1 and Oct2 in classical Hodgkin disease but not in lymphocyte predominant Hodgkin disease correlates with immunoglobulin transcription

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Foxp3 programs the development and function of CD4+CD25+ regulatory T cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of Hodgkin and Reed-Sternberg cell-specific genes by gene expression profiling

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transcriptional regulation during B cell development

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of clonal T-cell receptor gamma-chain gene rearrangements in Reed-Sternberg cells of classic Hodgkin disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of the B-lineage-specific gene expression program in Hodgkin and Reed-Sternberg cells of Hodgkin lymphoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rare occurrence of classical Hodgkin's disease as a T cell lymphoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hodgkin and Reed-Sternberg cells in lymphocyte predominant Hodgkin disease represent clonal populations of germinal center-derived tumor B cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotype and genotype of interfollicular large B cells, a subpopulation of lymphocytes often with dendritic morphology

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An essential role for Scurfin in CD4+CD25+ T regulatory cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hodgkin disease: Hodgkin and Reed-Sternberg cells picked from histological sections show clonal immunoglobulin gene rearrangements and appear to be derived from B cells at various stages of development

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Control of regulatory T cell development by the transcription factor Foxp3

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Scurfin (FOXP3) acts as a repressor of transcription and regulates T cell activation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Origin of nodular lymphocyte-predominant Hodgkin's disease from a clonal expansion of highly mutated germinal-center B cells.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple Domains Define the Expression and Regulatory Properties of Foxp1 Forkhead Transcriptional Repressors

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Classical Hodgkin's disease and follicular lymphoma originating from the same germinal center B cell

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The use of molecular profiling to predict survival after chemotherapy for diffuse large-B-cell lymphoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hodgkin and reed-sternberg cells represent an expansion of a single clone originating from a germinal center B-cell with functional immunoglobulin gene rearrangements but defective immunoglobulin transcription

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of a new subfamily of winged-helix/forkhead (Fox) genes that are expressed in the lung and act as transcriptional repressors

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oct-2 and Bob-1 deficiency in Hodgkin and Reed Sternberg cells.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16200457

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10735-005-6521-3

1 reference

Europe PubMed Central

2 August 2017

1 reference

Europe PubMed Central

2 August 2017

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