(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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scholarly article

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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

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3 November 2019

1 reference

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acute myeloid leukemia

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author name string

L Krsková-Honzátková

1

1 reference

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3 November 2019

J Cermák

2

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3 November 2019

J Sajdová

3

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3 November 2019

J Starý

4

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3 November 2019

P Sedlácek

5

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3 November 2019

Z Sieglová

6

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3 November 2019

publication date

1 January 2001

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3 November 2019

Leukemia Research

1 reference

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3 November 2019

25

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3 November 2019

1

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3 November 2019

45-53

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Molecular themes in oncogenesis

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LOH at the APC/MCC gene (5Q21) in gastric cancer and preneoplastic lesions. Prognostic implications

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

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Molecular alterations in the TP53 gene of peripheral blood cells of patients with chronic myeloid leukemia

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p53 loss and point mutations are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis.

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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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Correlation of N-ras point mutations with specific chromosomal abnormalities in primary myelodysplastic syndrome.

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RAS mutations and clonality analysis in children with juvenile myelomonocytic leukemia (JMML)

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Molecular analysis of the retinoblastoma (RB1) gene in acute myeloid leukemia patients

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

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P15INK4b gene methylation and myelodysplastic syndromes

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

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FISH analysis of an AML-M5a with segmental rearrangements involving 11q23-MLL region

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Use of dual-color interphase FISH for the detection of inv(16) in acute myeloid leukemia at diagnosis, relapse and during follow-up: a study of 23 patients

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Light microscopic detection of BCR-ABL transcripts after in-cell RT-PCR: fusion gene expression might correlate with clinical evolution of chronic myeloid leukemia

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Quantitation of minimal residual disease in acute promyelocytic leukemia patients with t(15;17) translocation using real-time RT-PCR

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A rapid practical RT-PCR-based approach for the detection of the PML/RAR alpha fusion transcript in acute promyelocytic leukemia

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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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Significantly lower relapse rate for TEL/AML1-positive ALL

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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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Nonrandom chromosomal abnormalities in acute lymphoblastic leukemia of childhood.

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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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Allelic loss in childhood acute lymphoblastic leukemia

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

1 reference

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DNA methylation and chromatin structure

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Identifiers

10.1016/S0145-2126(00)00086-2

1 reference

Europe PubMed Central

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1 reference

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3 November 2019

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