(Q36243996)

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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.

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scholarly article

1 reference

Europe PubMed Central

13 August 2017

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. (English)

1 reference

Europe PubMed Central

13 August 2017

Michelle M Le Beau

7

object named as

M M Le Beau

1 reference

Europe PubMed Central

13 August 2017

Richard A. Larson

6

object named as

R A Larson

1 reference

Europe PubMed Central

13 August 2017

author name string

N Zhao

1

1 reference

Europe PubMed Central

13 August 2017

A Stoffel

2

1 reference

Europe PubMed Central

13 August 2017

P W Wang

3

1 reference

Europe PubMed Central

13 August 2017

J D Eisenbart

4

1 reference

Europe PubMed Central

13 August 2017

R Espinosa

5

1 reference

Europe PubMed Central

13 August 2017

language of work or name

0 references

publication date

1 June 1997

1 reference

Europe PubMed Central

13 August 2017

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

13 August 2017

94

1 reference

Europe PubMed Central

13 August 2017

6948-6953

1 reference

Europe PubMed Central

13 August 2017

13

1 reference

Europe PubMed Central

13 August 2017

A Gene Map of the Human Genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21265

1 October 2017

Cytogenetic and molecular delineation of a region of chromosome 7 commonly deleted 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=21265

1 October 2017

Therapy-related myeloid leukemia

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1 October 2017

Mad-related genes in the human

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1 October 2017

A human Mad protein acting as a BMP-regulated transcriptional activator

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21265

1 October 2017

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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21265

1 October 2017

The secondary leukemias: challenges and research directions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21265

1 October 2017

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=21265

1 October 2017

Deletion of IRF-1, mapping to chromosome 5q31.1, in human leukemia and preleukemic myelodysplasia

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1 October 2017

The tumor suppressor genes

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1 October 2017

The balanced and the unbalanced chromosome aberrations of acute myeloid leukemia may develop in different ways and may contribute differently to malignant transformation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21265

1 October 2017

The 5q-syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21265

1 October 2017

Antioncogenes and human cancer

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1 October 2017

The zinc finger transcription factor Egr-1 is essential for and restricts differentiation along the macrophage lineage

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21265

1 October 2017

Physical mapping of the minimal region of loss in 5q- chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21265

1 October 2017

Cytogenetic deletion maps of hematologic neoplasms: circumstantial evidence for tumor suppressor loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21265

1 October 2017

Clinical and cytogenetic correlations in 63 patients with therapy-related myelodysplastic syndromes and acute nonlymphocytic leukemia: further evidence for characteristic abnormalities of chromosomes no. 5 and 7

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21265

1 October 2017

1 reference

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1 October 2017

The 5q- abnormality

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21265

1 October 2017

Human homolog of fission yeast cdc25 mitotic inducer is predominantly expressed in G2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21265

1 October 2017

Fluorescence in situ hybridization of YAC clones after Alu-PCR amplification

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21265

1 October 2017

Specific chromosomal abnormalities in acute nonlymphocytic leukemia correlate with drug susceptibility in vivo.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21265

29 June 2018

Chromosomal translocations in human cancer.

1 reference

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22 September 2018

The Fourth International Workshop on Chromosomes in Leukemia: a prospective study of acute nonlymphocytic leukemia. Chicago, Illinois, U.S.A., September 2-7, 1982

1 reference

https://pubmed.ncbi.nlm.nih.gov/9192672

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence-independent amplification and labeling of yeast artificial chromosomes for fluorescence in situ hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/9192672

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic loss of IRF1 in myelodysplasia and acute myeloid leukemia: retention of IRF1 on the 5q- chromosome in some patients with the 5q- syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9192672

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two simple procedures for releasing chromatin from routinely fixed cells for fluorescence in situ hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/9192672

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular Mapping of Uncharacteristically Small 5q Deletions in Two Patients with the 5q- Syndrome: Delineation of the Critical Region on 5q and Identification of a 5q- Breakpoint

1 reference

https://pubmed.ncbi.nlm.nih.gov/9192672

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.94.13.6948

1 reference

Europe PubMed Central

13 August 2017

1997PNAS...94.6948Z

0 references

release_kbeshjnfmnatfh7tdqmphn35pq

1 reference

https://api.fatcat.wiki/v0/release/kbeshjnfmnatfh7tdqmphn35pq

24 November 2022

based on heuristic

mapped directly with Wikidata item

1 reference

Europe PubMed Central

13 August 2017

1 reference

Europe PubMed Central

13 August 2017

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