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Low frequency of NRAS and KRAS2 gene mutations in childhood myelodysplastic syndromes

Authorized Users Only
2004
Authors
Jekić, B.
Novaković, I.
Luković, L
Kuzmanović, M
Popović, Branka
Pastar, I
Milašin, Jelena
Bunjevacki, G
Bunjevački, Vera
Article (Published version)
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Abstract
In children, myelodysplastic syndromes (MDS) represent less then 10% of all hematological malignancies; consequently, molecular genetic studies dealing with this group of patients are scarce. We have analyzed 35 archival bone marrow samples of children with MDS for the presence of mutations in the first and second exons of the NRAS and KRAS2 genes. Mutations were detected with single-strand conformation polymorphism analysis in three patients. One patient harbored a mutation in the second exon of NRAS and two patients in the second exon of KRAS2. Sequencing was performed in two samples and novel mutations were found in both. One patient had a missense mutation in codon 45 of NRAS; the other had a silent mutation in codon 53 and a missense mutation in codon 55 of KRAS2.
Source:
Cancer Genetics & Cytogenetics, 2004, 154, 2, 180-182
Publisher:
  • Elsevier Science Inc, New York

DOI: 10.1016/j.cancergencyto.2004.02.025

ISSN: 0165-4608

PubMed: 15474158

WoS: 000224907000015

Scopus: 2-s2.0-5144234239
[ Google Scholar ]
10
9
URI
https://smile.stomf.bg.ac.rs/handle/123456789/1224
Collections
  • Radovi istraživača
Institution/Community
Stomatološki fakultet
TY  - JOUR
AU  - Jekić, B.
AU  - Novaković, I.
AU  - Luković, L
AU  - Kuzmanović, M
AU  - Popović, Branka
AU  - Pastar, I
AU  - Milašin, Jelena
AU  - Bunjevacki, G
AU  - Bunjevački, Vera
PY  - 2004
UR  - https://smile.stomf.bg.ac.rs/handle/123456789/1224
AB  - In children, myelodysplastic syndromes (MDS) represent less then 10% of all hematological malignancies; consequently, molecular genetic studies dealing with this group of patients are scarce. We have analyzed 35 archival bone marrow samples of children with MDS for the presence of mutations in the first and second exons of the NRAS and KRAS2 genes. Mutations were detected with single-strand conformation polymorphism analysis in three patients. One patient harbored a mutation in the second exon of NRAS and two patients in the second exon of KRAS2. Sequencing was performed in two samples and novel mutations were found in both. One patient had a missense mutation in codon 45 of NRAS; the other had a silent mutation in codon 53 and a missense mutation in codon 55 of KRAS2.
PB  - Elsevier Science Inc, New York
T2  - Cancer Genetics & Cytogenetics
T1  - Low frequency of NRAS and KRAS2 gene mutations in childhood myelodysplastic syndromes
VL  - 154
IS  - 2
SP  - 180
EP  - 182
DO  - 10.1016/j.cancergencyto.2004.02.025
ER  - 
@article{
author = "Jekić, B. and Novaković, I. and Luković, L and Kuzmanović, M and Popović, Branka and Pastar, I and Milašin, Jelena and Bunjevacki, G and Bunjevački, Vera",
year = "2004",
abstract = "In children, myelodysplastic syndromes (MDS) represent less then 10% of all hematological malignancies; consequently, molecular genetic studies dealing with this group of patients are scarce. We have analyzed 35 archival bone marrow samples of children with MDS for the presence of mutations in the first and second exons of the NRAS and KRAS2 genes. Mutations were detected with single-strand conformation polymorphism analysis in three patients. One patient harbored a mutation in the second exon of NRAS and two patients in the second exon of KRAS2. Sequencing was performed in two samples and novel mutations were found in both. One patient had a missense mutation in codon 45 of NRAS; the other had a silent mutation in codon 53 and a missense mutation in codon 55 of KRAS2.",
publisher = "Elsevier Science Inc, New York",
journal = "Cancer Genetics & Cytogenetics",
title = "Low frequency of NRAS and KRAS2 gene mutations in childhood myelodysplastic syndromes",
volume = "154",
number = "2",
pages = "180-182",
doi = "10.1016/j.cancergencyto.2004.02.025"
}
Jekić, B., Novaković, I., Luković, L., Kuzmanović, M., Popović, B., Pastar, I., Milašin, J., Bunjevacki, G.,& Bunjevački, V.. (2004). Low frequency of NRAS and KRAS2 gene mutations in childhood myelodysplastic syndromes. in Cancer Genetics & Cytogenetics
Elsevier Science Inc, New York., 154(2), 180-182.
https://doi.org/10.1016/j.cancergencyto.2004.02.025
Jekić B, Novaković I, Luković L, Kuzmanović M, Popović B, Pastar I, Milašin J, Bunjevacki G, Bunjevački V. Low frequency of NRAS and KRAS2 gene mutations in childhood myelodysplastic syndromes. in Cancer Genetics & Cytogenetics. 2004;154(2):180-182.
doi:10.1016/j.cancergencyto.2004.02.025 .
Jekić, B., Novaković, I., Luković, L, Kuzmanović, M, Popović, Branka, Pastar, I, Milašin, Jelena, Bunjevacki, G, Bunjevački, Vera, "Low frequency of NRAS and KRAS2 gene mutations in childhood myelodysplastic syndromes" in Cancer Genetics & Cytogenetics, 154, no. 2 (2004):180-182,
https://doi.org/10.1016/j.cancergencyto.2004.02.025 . .

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