(Q73343620)

English

Loss of heterozygosity and heterogeneity of its appearance and persisting in the course of acute myeloid leukemia and myelodysplastic syndromes

scientific article published on 01 January 2001

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Europe PubMed Central

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3 November 2019

Loss of heterozygosity and heterogeneity of its appearance and persisting in the course of acute myeloid leukemia and myelodysplastic syndromes (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11137560%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference

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acute myeloid leukemia

1 reference

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1 reference

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author name string

L Krsková-Honzátková

1

1 reference

Europe PubMed Central

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3 November 2019

J Cermák

2

1 reference

Europe PubMed Central

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3 November 2019

J Sajdová

3

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Europe PubMed Central

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3 November 2019

J Starý

4

1 reference

Europe PubMed Central

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3 November 2019

P Sedlácek

5

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Europe PubMed Central

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3 November 2019

Z Sieglová

6

1 reference

Europe PubMed Central

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3 November 2019

publication date

1 January 2001

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Europe PubMed Central

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3 November 2019

Leukemia Research

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11137560%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

25

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3 November 2019

1

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3 November 2019

45-53

1 reference

Europe PubMed Central

PubMed publication ID

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3 November 2019

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Study of p53 in elderly patients with myelodysplastic syndromes by immunohistochemistry and DNA analysis

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The non-random distribution of point mutations in leukaemia and myelodysplasia--a possible pointer to their aetiology

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No concomitant occurrence of the N-ras and p53 gene mutations in myelodysplastic syndromes

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Methylation status of the p15INK4B gene in hematopoietic progenitors and peripheral blood cells in myelodysplastic syndromes

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Hypermethylation of calcitonin gene in adult acute leukemia at diagnosis and during complete remission

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Rapid and sensitive minimal residual disease detection in acute leukemia by quantitative real-time RT-PCR exemplified by t(12;21) TEL-AML1 fusion transcript

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Deletions of the long arm of chromosome 7 in myeloid disorders: loss of band 7q32 implies worst prognosis

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Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

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A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5.

1 reference

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High-resolution allelotype analysis of childhood B-lineage acute lymphoblastic leukemia

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Identifiers

10.1016/S0145-2126(00)00086-2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11137560%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11137560%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

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