(Q40791054)

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Identification of candidate genes on chromosome band 20q12 by physical mapping of translocation breakpoints found in myeloid leukemia cell lines

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Europe PubMed Central

PubMed publication ID

23 September 2017

Identification of candidate genes on chromosome band 20q12 by physical mapping of translocation breakpoints found in myeloid leukemia cell lines (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

author name string

MacGrogan D

1

1 reference

Europe PubMed Central

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23 September 2017

Alvarez S

2

1 reference

Europe PubMed Central

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23 September 2017

DeBlasio T

3

1 reference

Europe PubMed Central

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23 September 2017

Jhanwar SC

4

1 reference

Europe PubMed Central

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23 September 2017

Nimer SD

5

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Europe PubMed Central

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23 September 2017

language of work or name

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publication date

1 July 2001

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Europe PubMed Central

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23 September 2017

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Europe PubMed Central

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23 September 2017

20

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Europe PubMed Central

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23 September 2017

31

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

4150-4160

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Basic local alignment search tool

1 reference

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21 January 2018

Deletions of chromosome 20q and the pathogenesis of myeloproliferative disorders

1 reference

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Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

1 reference

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21 January 2018

A physical map of 30,000 human genes

1 reference

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A comprehensive genetic map of the human genome based on 5,264 microsatellites

1 reference

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Cell lineage involvement of recurrent chromosomal abnormalities in hematologic neoplasms

1 reference

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A human homolog of Drosophila lethal(3)malignant brain tumor (l(3)mbt) protein associates with condensed mitotic chromosomes

1 reference

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21 January 2018

Identification of novel human genes evolutionarily conserved in Caenorhabditis elegans by comparative proteomics

1 reference

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21 January 2018

cDNAs with long CAG trinucleotide repeats from human brain

1 reference

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21 January 2018

Characterization of 20q deletions in patients with myeloproliferative disorders or myelodysplastic syndromes

1 reference

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21 January 2018

Mybl2 (Bmyb) maps to mouse chromosome 2 and human chromosome 20q 13.1.

1 reference

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21 January 2018

Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers

1 reference

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21 January 2018

Identification by representational difference analysis of a homozygous deletion in pancreatic carcinoma that lies within the BRCA2 region.

1 reference

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21 January 2018

A yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1, and a myeloid leukemia related gene

1 reference

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21 January 2018

Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus.

1 reference

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21 January 2018

Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients

1 reference

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21 January 2018

A Detailed Physical and Transcriptional Map of the Region of Chromosome 20 That Is Deleted in Myeloproliferative Disorders and Refinement of the Common Deleted Region

1 reference

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21 January 2018

Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes

1 reference

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21 January 2018

Refinement of the Smallest Commonly Deleted Segment of Chromosome 20 in Malignant Myeloid Diseases and Development of a PAC-Based Physical and Transcription Map

1 reference

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21 January 2018

Clinical significance of the del(20q) chromosome in hematologic disorders

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204540

7 January 2021

based on heuristic

inferred from DOI database lookup

Physical mapping of a translocation breakpoint in neurofibromatosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204540

7 January 2021

based on heuristic

inferred from DOI database lookup

Deletion 20q in association with Philadelphia chromosome positive acute lymphoblastic leukemia. A report of two cases

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Hematologic disorders associated with deletions of chromosome 20q: a clinicopathologic study of 107 patients

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204540

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.ONC.1204540

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

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