(Q33412120)

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Integrated genomic analysis implicates haploinsufficiency of multiple chromosome 5q31.2 genes in de novo myelodysplastic syndromes pathogenesis

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Europe PubMed Central

PubMed publication ID

26 July 2017

Integrated genomic analysis implicates haploinsufficiency of multiple chromosome 5q31.2 genes in de novo myelodysplastic syndromes pathogenesis (English)

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Europe PubMed Central

PubMed publication ID

26 July 2017

Haploinsufficiency

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Timothy A. Graubert

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Timothy A Graubert

1

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author name string

Michelle A Payton

2

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Europe PubMed Central

PubMed publication ID

26 July 2017

Jin Shao

3

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Europe PubMed Central

PubMed publication ID

26 July 2017

Richard A Walgren

4

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Ryan S Monahan

5

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

John L Frater

6

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Europe PubMed Central

PubMed publication ID

26 July 2017

Mark A Walshauser

7

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Mike G Martin

8

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Yumi Kasai

9

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Europe PubMed Central

PubMed publication ID

26 July 2017

Matthew J Walter

10

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Europe PubMed Central

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26 July 2017

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publication date

25 February 2009

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Europe PubMed Central

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26 July 2017

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Europe PubMed Central

PubMed publication ID

26 July 2017

4

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Europe PubMed Central

PubMed publication ID

26 July 2017

2

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Europe PubMed Central

PubMed publication ID

26 July 2017

e4583

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Europe PubMed Central

PubMed publication ID

26 July 2017

copyright license

Creative Commons Attribution 4.0 International

25 February 2009

1 reference

April 2022 Public Data File from Crossref

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wuHMM: a robust algorithm to detect DNA copy number variation using long oligonucleotide microarray data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2642994

21 June 2018

Somatic mutations and germline sequence variants in the expressed tyrosine kinase genes of patients with de novo acute myeloid leukemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2642994

21 June 2018

Identification of RPS14 as a 5q- syndrome gene by RNA interference screen

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2642994

21 June 2018

Distinct patterns of mutations occurring in de novo AML versus AML arising in the setting of severe congenital neutropenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2642994

21 June 2018

Haploinsufficiency of EGR1, a candidate gene in the del(5q), leads to the development of myeloid disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2642994

21 June 2018

Evaluation of recurring cytogenetic abnormalities in the treatment of myelodysplastic syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2642994

21 June 2018

Chromosome 5q deletion and epigenetic suppression of the gene encoding alpha-catenin (CTNNA1) in myeloid cell transformation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2642994

21 June 2018

A lentiviral RNAi library for human and mouse genes applied to an arrayed viral high-content screen

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2642994

21 June 2018

A lentiviral microRNA-based system for single-copy polymerase II-regulated RNA interference in mammalian cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2642994

21 June 2018

Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2642994

21 June 2018

Circular binary segmentation for the analysis of array-based DNA copy number data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2642994

21 June 2018

Evaluation of ETF1/eRF1, mapping to 5q31, as a candidate myeloid tumor suppressor gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2642994

21 June 2018

A novel nuclear protein, 5qNCA (LOC51780) is a candidate for the myeloid leukemia tumor suppressor gene on chromosome 5 band q31.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2642994

21 June 2018

Human mortalin (HSPA9): a candidate for the myeloid leukemia tumor suppressor gene on 5q31

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2642994

21 June 2018

Transcript map and comparative analysis of the 1.5-Mb commonly deleted segment of human 5q31 in malignant myeloid diseases with a del(5q)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2642994

21 June 2018

Molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases to 1-1.5 Mb and preparation of a PAC-based physical map.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2642994

21 June 2018

Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2642994

21 June 2018

Loss of Hspa9b in zebrafish recapitulates the ineffective hematopoiesis of the myelodysplastic syndrome

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0004583

21 January 2018

Delineation of a minimal interval and identification of 9 candidates for a tumor suppressor gene in malignant myeloid disorders on 5q31

1 reference

https://pubmed.ncbi.nlm.nih.gov/19240791

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multilineage involvement in the 5q- syndrome: a fluorescent in situ hybridization study on bone marrow smears

1 reference

https://pubmed.ncbi.nlm.nih.gov/19240791

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Narrowing and genomic annotation of the commonly deleted region of the 5q- syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19240791

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fluorescence in situ hybridization for the study of cell lineage involvement in myelodysplastic syndromes with chromosome 5 anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/19240791

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular signature of MDS stem cells supports a stem-cell origin of 5q myelodysplastic syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19240791

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Combined immunophenotyping and FISH identifies the involvement of B-cells in 5q- syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19240791

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0004583

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

2009PLoSO...4.4583G

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

ResearchGate publication ID

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