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Low frequency of PIM3 gene in patients with monoclonal gammopathies

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1996
Authors
Jelić-Ivanović, Zorana
Spasojević-Kalimanovska, Vesna
Stanković, B
Topić, Aleksandra
Spasić, S
Article (Published version)
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Abstract
The distribution of PI (protease inhibitor) phenotypes and PI M subtypes was studied in 200 patients with monoclonal gammopathies and 320 healthy blood donors by isoelectric focusing in thin-layer polyacrylamide gels, pH range 4-5. The distribution of PI phenotypes and gene frequencies in the patients differed significantly from the corresponding values found in the blood donors, as shown by the chi(2) test (chi(2) = 16.5, p = 0.02 and chi(2) = 17.6, p = 0.0014, respectively). A lower frequency of the M3 variant was observed in patients, both in homozygous (PI M3) and heterozygous forms (PI M1M3 and PI M2M3). No significant difference between PIz allele frequencies in patients and healthy controls was found.
Source:
Human Heredity, 1996, 46, 2, 115-117
Publisher:
  • Karger, Basel

DOI: 10.1159/000154337

ISSN: 0001-5652

PubMed: 8666412

WoS: A1996TY47900009

Scopus: 2-s2.0-0029664902
[ Google Scholar ]
1
URI
https://farfar.pharmacy.bg.ac.rs/handle/123456789/143
Collections
  • Radovi istraživača / Researchers’ publications
Institution/Community
Pharmacy
TY  - JOUR
AU  - Jelić-Ivanović, Zorana
AU  - Spasojević-Kalimanovska, Vesna
AU  - Stanković, B
AU  - Topić, Aleksandra
AU  - Spasić, S
PY  - 1996
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/143
AB  - The distribution of PI (protease inhibitor) phenotypes and PI M subtypes was studied in 200 patients with monoclonal gammopathies and 320 healthy blood donors by isoelectric focusing in thin-layer polyacrylamide gels, pH range 4-5. The distribution of PI phenotypes and gene frequencies in the patients differed significantly from the corresponding values found in the blood donors, as shown by the chi(2) test (chi(2) = 16.5, p = 0.02 and chi(2) = 17.6, p = 0.0014, respectively). A lower frequency of the M3 variant was observed in patients, both in homozygous (PI M3) and heterozygous forms (PI M1M3 and PI M2M3). No significant difference between PIz allele frequencies in patients and healthy controls was found.
PB  - Karger, Basel
T2  - Human Heredity
T1  - Low frequency of PIM3 gene in patients with monoclonal gammopathies
VL  - 46
IS  - 2
SP  - 115
EP  - 117
DO  - 10.1159/000154337
ER  - 
@article{
author = "Jelić-Ivanović, Zorana and Spasojević-Kalimanovska, Vesna and Stanković, B and Topić, Aleksandra and Spasić, S",
year = "1996",
abstract = "The distribution of PI (protease inhibitor) phenotypes and PI M subtypes was studied in 200 patients with monoclonal gammopathies and 320 healthy blood donors by isoelectric focusing in thin-layer polyacrylamide gels, pH range 4-5. The distribution of PI phenotypes and gene frequencies in the patients differed significantly from the corresponding values found in the blood donors, as shown by the chi(2) test (chi(2) = 16.5, p = 0.02 and chi(2) = 17.6, p = 0.0014, respectively). A lower frequency of the M3 variant was observed in patients, both in homozygous (PI M3) and heterozygous forms (PI M1M3 and PI M2M3). No significant difference between PIz allele frequencies in patients and healthy controls was found.",
publisher = "Karger, Basel",
journal = "Human Heredity",
title = "Low frequency of PIM3 gene in patients with monoclonal gammopathies",
volume = "46",
number = "2",
pages = "115-117",
doi = "10.1159/000154337"
}
Jelić-Ivanović, Z., Spasojević-Kalimanovska, V., Stanković, B., Topić, A.,& Spasić, S.. (1996). Low frequency of PIM3 gene in patients with monoclonal gammopathies. in Human Heredity
Karger, Basel., 46(2), 115-117.
https://doi.org/10.1159/000154337
Jelić-Ivanović Z, Spasojević-Kalimanovska V, Stanković B, Topić A, Spasić S. Low frequency of PIM3 gene in patients with monoclonal gammopathies. in Human Heredity. 1996;46(2):115-117.
doi:10.1159/000154337 .
Jelić-Ivanović, Zorana, Spasojević-Kalimanovska, Vesna, Stanković, B, Topić, Aleksandra, Spasić, S, "Low frequency of PIM3 gene in patients with monoclonal gammopathies" in Human Heredity, 46, no. 2 (1996):115-117,
https://doi.org/10.1159/000154337 . .

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