TY  - CONF
AU  - Spremo-Potparević, Biljana
AU  - Želježić, Davor
AU  - Bajić, Vladan
AU  - Popović, Petar
AU  - Živković, Lada
PY  - 2023
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/5471
AB  - Background: Chromosome instability (CIN) in Alzheimer’s disease has been found in peripheral blood lymphocytes, and also in neurons of affected individuals. CIN is a result of errors in chromosome segregation during mitosis leading to numerical and structural chromosomal abnormalities. Material and Methods: Fluorescent In Situ Hybridization. (FISH) has been a method of choice for the evaluation of CIN in various diseases. We have studied a specific type of X chromosome instability, or premature centromere division (PCD) in interphase nuclei of the hippocampus brain tissue neurons from sporadic AD females. PCD was studied by using a new approach to FISH. Results: Namely, we have established a methodology that allows quantitative analysis of centromere fluorescence intensity, i.e. the size of individual FISH spots, thus giving a more focused view of the centromere region of interest. By using the micro image system, our results show that quantitative FISH can distinguish PCD positive signals vs. PCD negative signals in cells of brain tissue. Conclusion: This could be a specific biomarker in affected cells in order to verify CIN, thus supporting the established qualitative analysis of FISH spots in the study of centromere and chromosomal alterations in interphase nuclei of patients affected by AD.
PB  - Macedonian Academy of Sciences and Arts
C3  - 14th Balkan Congress o14th Balkan Congress of Human Genetics & 9th Rare Disease SEE Meeting 2023 Supplement Skopje, October 05-07, ABSTRACT BOOK
T1  - New approach in quantitative estimation  of x chromosome centromere instability  in Alzheimer disease
VL  - 26
IS  - Supplement
SP  - 88
EP  - 88
UR  - https://hdl.handle.net/21.15107/rcub_farfar_5471
ER  - 

@conference{
author = "Spremo-Potparević, Biljana and Želježić, Davor and Bajić, Vladan and Popović, Petar and Živković, Lada",
year = "2023",
abstract = "Background: Chromosome instability (CIN) in Alzheimer’s disease has been found in peripheral blood lymphocytes, and also in neurons of affected individuals. CIN is a result of errors in chromosome segregation during mitosis leading to numerical and structural chromosomal abnormalities. Material and Methods: Fluorescent In Situ Hybridization. (FISH) has been a method of choice for the evaluation of CIN in various diseases. We have studied a specific type of X chromosome instability, or premature centromere division (PCD) in interphase nuclei of the hippocampus brain tissue neurons from sporadic AD females. PCD was studied by using a new approach to FISH. Results: Namely, we have established a methodology that allows quantitative analysis of centromere fluorescence intensity, i.e. the size of individual FISH spots, thus giving a more focused view of the centromere region of interest. By using the micro image system, our results show that quantitative FISH can distinguish PCD positive signals vs. PCD negative signals in cells of brain tissue. Conclusion: This could be a specific biomarker in affected cells in order to verify CIN, thus supporting the established qualitative analysis of FISH spots in the study of centromere and chromosomal alterations in interphase nuclei of patients affected by AD.",
publisher = "Macedonian Academy of Sciences and Arts",
journal = "14th Balkan Congress o14th Balkan Congress of Human Genetics & 9th Rare Disease SEE Meeting 2023 Supplement Skopje, October 05-07, ABSTRACT BOOK",
title = "New approach in quantitative estimation  of x chromosome centromere instability  in Alzheimer disease",
volume = "26",
number = "Supplement",
pages = "88-88",
url = "https://hdl.handle.net/21.15107/rcub_farfar_5471"
}

Spremo-Potparević, B., Želježić, D., Bajić, V., Popović, P.,& Živković, L.. (2023). New approach in quantitative estimation  of x chromosome centromere instability  in Alzheimer disease. in 14th Balkan Congress o14th Balkan Congress of Human Genetics & 9th Rare Disease SEE Meeting 2023 Supplement Skopje, October 05-07, ABSTRACT BOOK
Macedonian Academy of Sciences and Arts., 26(Supplement), 88-88.
https://hdl.handle.net/21.15107/rcub_farfar_5471

Spremo-Potparević B, Želježić D, Bajić V, Popović P, Živković L. New approach in quantitative estimation  of x chromosome centromere instability  in Alzheimer disease. in 14th Balkan Congress o14th Balkan Congress of Human Genetics & 9th Rare Disease SEE Meeting 2023 Supplement Skopje, October 05-07, ABSTRACT BOOK. 2023;26(Supplement):88-88.
https://hdl.handle.net/21.15107/rcub_farfar_5471 .

Spremo-Potparević, Biljana, Želježić, Davor, Bajić, Vladan, Popović, Petar, Živković, Lada, "New approach in quantitative estimation  of x chromosome centromere instability  in Alzheimer disease" in 14th Balkan Congress o14th Balkan Congress of Human Genetics & 9th Rare Disease SEE Meeting 2023 Supplement Skopje, October 05-07, ABSTRACT BOOK, 26, no. Supplement (2023):88-88,
https://hdl.handle.net/21.15107/rcub_farfar_5471 .

TY  - JOUR
AU  - Ziauddin, M.F.
AU  - Guo, Z.S.
AU  - O'Malley, M.E.
AU  - Austin, F.
AU  - Popović, Petar
AU  - Kavanagh, M.A.
AU  - Li, J.
AU  - Sathaiah, M.
AU  - Thirunavukarasu, P.
AU  - Fang, B.
AU  - Lee, Y.J.
AU  - Bartlett, D.L.
PY  - 2010
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/5537
AB  - We have explored a unique combination therapy for metastatic colorectal cancer. This strategy combines a potent and new oncolytic poxvirus expressing a membrane-bound tumor necrosis factor-related apoptosis-inducing ligand (TRAIL or TNFSF10) and oxaliplatin (Ox) chemotherapy. We hypothesized that TRAIL expression would increase the efficacy of the oncolytic poxvirus, and that the therapeutic efficacy would be further enhanced by combination with chemotherapy. The cytotoxicity to cancer cells by Ox, oncolytic vaccinia virus (VV) and trail gene-armed VV alone or in combination was tested in vitro. The trail gene armed oncolytic VV-expressed high levels of TRAIL in infected cancer cells and had greater potency as a cytotoxic agent compared with the parent VV. Ox alone exerted concentration-dependent cytotoxicity. In vitro, the combination of the two agents applied at suboptimal concentrations for individual therapy displayed synergy in inducing cancer cells into enhanced levels of apoptosis/necrosis. Western blot analyses were consistent with the notion that TRAIL induced cancer cell death mainly through apoptosis, whereas Ox and vJS6 induced cell death more through non-apoptotic death pathways. In two aggressive colorectal carcinomatosis models derived from human HCT116 and murine MC38 cells, the combination therapy displayed synergistic or additive antitumor activity and prolonged the survival of the tumor-bearing mice compared with either Ox chemotherapy or vvTRAIL-mediated oncolytic gene therapy alone. This combination strategy may provide a new avenue to treating peritoneal carcinomatosis and other types of metastases of colorectal cancer.
PB  - Nature
T2  - Gene Therapy
T1  - TRAIL gene-armed oncolytic poxvirus and oxaliplatin can work synergistically against colorectal cancer
VL  - 17
IS  - 4
SP  - 550
EP  - 559
DO  - 10.1038/gt.2010.5
ER  - 

@article{
author = "Ziauddin, M.F. and Guo, Z.S. and O'Malley, M.E. and Austin, F. and Popović, Petar and Kavanagh, M.A. and Li, J. and Sathaiah, M. and Thirunavukarasu, P. and Fang, B. and Lee, Y.J. and Bartlett, D.L.",
year = "2010",
abstract = "We have explored a unique combination therapy for metastatic colorectal cancer. This strategy combines a potent and new oncolytic poxvirus expressing a membrane-bound tumor necrosis factor-related apoptosis-inducing ligand (TRAIL or TNFSF10) and oxaliplatin (Ox) chemotherapy. We hypothesized that TRAIL expression would increase the efficacy of the oncolytic poxvirus, and that the therapeutic efficacy would be further enhanced by combination with chemotherapy. The cytotoxicity to cancer cells by Ox, oncolytic vaccinia virus (VV) and trail gene-armed VV alone or in combination was tested in vitro. The trail gene armed oncolytic VV-expressed high levels of TRAIL in infected cancer cells and had greater potency as a cytotoxic agent compared with the parent VV. Ox alone exerted concentration-dependent cytotoxicity. In vitro, the combination of the two agents applied at suboptimal concentrations for individual therapy displayed synergy in inducing cancer cells into enhanced levels of apoptosis/necrosis. Western blot analyses were consistent with the notion that TRAIL induced cancer cell death mainly through apoptosis, whereas Ox and vJS6 induced cell death more through non-apoptotic death pathways. In two aggressive colorectal carcinomatosis models derived from human HCT116 and murine MC38 cells, the combination therapy displayed synergistic or additive antitumor activity and prolonged the survival of the tumor-bearing mice compared with either Ox chemotherapy or vvTRAIL-mediated oncolytic gene therapy alone. This combination strategy may provide a new avenue to treating peritoneal carcinomatosis and other types of metastases of colorectal cancer.",
publisher = "Nature",
journal = "Gene Therapy",
title = "TRAIL gene-armed oncolytic poxvirus and oxaliplatin can work synergistically against colorectal cancer",
volume = "17",
number = "4",
pages = "550-559",
doi = "10.1038/gt.2010.5"
}

Ziauddin, M.F., Guo, Z.S., O'Malley, M.E., Austin, F., Popović, P., Kavanagh, M.A., Li, J., Sathaiah, M., Thirunavukarasu, P., Fang, B., Lee, Y.J.,& Bartlett, D.L.. (2010). TRAIL gene-armed oncolytic poxvirus and oxaliplatin can work synergistically against colorectal cancer. in Gene Therapy
Nature., 17(4), 550-559.
https://doi.org/10.1038/gt.2010.5

Ziauddin M, Guo Z, O'Malley M, Austin F, Popović P, Kavanagh M, Li J, Sathaiah M, Thirunavukarasu P, Fang B, Lee Y, Bartlett D. TRAIL gene-armed oncolytic poxvirus and oxaliplatin can work synergistically against colorectal cancer. in Gene Therapy. 2010;17(4):550-559.
doi:10.1038/gt.2010.5 .

Ziauddin, M.F., Guo, Z.S., O'Malley, M.E., Austin, F., Popović, Petar, Kavanagh, M.A., Li, J., Sathaiah, M., Thirunavukarasu, P., Fang, B., Lee, Y.J., Bartlett, D.L., "TRAIL gene-armed oncolytic poxvirus and oxaliplatin can work synergistically against colorectal cancer" in Gene Therapy, 17, no. 4 (2010):550-559,
https://doi.org/10.1038/gt.2010.5 . .

TY  - CHAP
AU  - Popović, Petar
AU  - Benjamin, Matta M.
AU  - Juan, Ochoa B.
PY  - 2009
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/5535
AB  - The main physiologic function of the immune system - protection of the host from infection for many years characterized the immune response in its ability to distinguish between “foreign” and “self”, the key issue being that foreign was to be attacked and eradicated, while self was not to be
attacked. In recent years, however, from the wide range of diseases that are consequent to inappropriate immune functions, we have learned that the ability of the immune system to distinguish between harmful and harmless molecules or cells rather than characterizing the dichotomy as foreign and self is essential for mounting protective immune responses and preventing the induction of pathology.
PB  - Lippincott Williams & Wilkins, a Wolters Kluwer Business
T2  - Civetta, Taylor, & Kirby’s critical care / edited by Andrea Gabrielli, A. Joseph Layon, Mihae Yu. — 4th ed.
T1  - Allergy and Immunology
SP  - 749
EP  - 760
UR  - https://hdl.handle.net/21.15107/rcub_farfar_5535
ER  - 

@inbook{
author = "Popović, Petar and Benjamin, Matta M. and Juan, Ochoa B.",
year = "2009",
abstract = "The main physiologic function of the immune system - protection of the host from infection for many years characterized the immune response in its ability to distinguish between “foreign” and “self”, the key issue being that foreign was to be attacked and eradicated, while self was not to be
attacked. In recent years, however, from the wide range of diseases that are consequent to inappropriate immune functions, we have learned that the ability of the immune system to distinguish between harmful and harmless molecules or cells rather than characterizing the dichotomy as foreign and self is essential for mounting protective immune responses and preventing the induction of pathology.",
publisher = "Lippincott Williams & Wilkins, a Wolters Kluwer Business",
journal = "Civetta, Taylor, & Kirby’s critical care / edited by Andrea Gabrielli, A. Joseph Layon, Mihae Yu. — 4th ed.",
booktitle = "Allergy and Immunology",
pages = "749-760",
url = "https://hdl.handle.net/21.15107/rcub_farfar_5535"
}

Popović, P., Benjamin, M. M.,& Juan, O. B.. (2009). Allergy and Immunology. in Civetta, Taylor, & Kirby’s critical care / edited by Andrea Gabrielli, A. Joseph Layon, Mihae Yu. — 4th ed.
Lippincott Williams & Wilkins, a Wolters Kluwer Business., 749-760.
https://hdl.handle.net/21.15107/rcub_farfar_5535

Popović P, Benjamin MM, Juan OB. Allergy and Immunology. in Civetta, Taylor, & Kirby’s critical care / edited by Andrea Gabrielli, A. Joseph Layon, Mihae Yu. — 4th ed.. 2009;:749-760.
https://hdl.handle.net/21.15107/rcub_farfar_5535 .

Popović, Petar, Benjamin, Matta M., Juan, Ochoa B., "Allergy and Immunology" in Civetta, Taylor, & Kirby’s critical care / edited by Andrea Gabrielli, A. Joseph Layon, Mihae Yu. — 4th ed. (2009):749-760,
https://hdl.handle.net/21.15107/rcub_farfar_5535 .

TY  - CHAP
AU  - Popović, Petar
AU  - Dubois, Diane
AU  - Rabin, Bruce S.
AU  - Shurin, Michael R.
PY  - 2005
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/5536
AB  - Immunoglobulins (antibodies) are a group of heterogeneous proteins that exhibit the unique property of being able to bind to proteins or polysaccharides that stimulated the production of the antibody. Antibodies are one of two important antigen recognition components of the immune system. Antibodies recognize antigen directly in a three-dimensional conformation. Evaluation of the titers of each immunoglobulin subclasses as well as the levels of specific antibodies is essential for diagnosis of many immunological diseases.
PB  - Elsevier Academic Press
T2  - Measuring Immunity: Basic Biology and Clinical Assessment / Edited by Michael T. Lotze and Angus W. Thomson
T1  - Immunoglobulin Titers and Immunoglobulin Subtypes
SP  - 158
EP  - 171
UR  - https://hdl.handle.net/21.15107/rcub_farfar_5536
ER  - 

@inbook{
author = "Popović, Petar and Dubois, Diane and Rabin, Bruce S. and Shurin, Michael R.",
year = "2005",
abstract = "Immunoglobulins (antibodies) are a group of heterogeneous proteins that exhibit the unique property of being able to bind to proteins or polysaccharides that stimulated the production of the antibody. Antibodies are one of two important antigen recognition components of the immune system. Antibodies recognize antigen directly in a three-dimensional conformation. Evaluation of the titers of each immunoglobulin subclasses as well as the levels of specific antibodies is essential for diagnosis of many immunological diseases.",
publisher = "Elsevier Academic Press",
journal = "Measuring Immunity: Basic Biology and Clinical Assessment / Edited by Michael T. Lotze and Angus W. Thomson",
booktitle = "Immunoglobulin Titers and Immunoglobulin Subtypes",
pages = "158-171",
url = "https://hdl.handle.net/21.15107/rcub_farfar_5536"
}

Popović, P., Dubois, D., Rabin, B. S.,& Shurin, M. R.. (2005). Immunoglobulin Titers and Immunoglobulin Subtypes. in Measuring Immunity: Basic Biology and Clinical Assessment / Edited by Michael T. Lotze and Angus W. Thomson
Elsevier Academic Press., 158-171.
https://hdl.handle.net/21.15107/rcub_farfar_5536

Popović P, Dubois D, Rabin BS, Shurin MR. Immunoglobulin Titers and Immunoglobulin Subtypes. in Measuring Immunity: Basic Biology and Clinical Assessment / Edited by Michael T. Lotze and Angus W. Thomson. 2005;:158-171.
https://hdl.handle.net/21.15107/rcub_farfar_5536 .

Popović, Petar, Dubois, Diane, Rabin, Bruce S., Shurin, Michael R., "Immunoglobulin Titers and Immunoglobulin Subtypes" in Measuring Immunity: Basic Biology and Clinical Assessment / Edited by Michael T. Lotze and Angus W. Thomson (2005):158-171,
https://hdl.handle.net/21.15107/rcub_farfar_5536 .

TY  - JOUR
AU  - Čolić, Miodrag
AU  - Jandrić, Dušan
AU  - Stojić-Vukanić, Zorica
AU  - Antić-Stanković, Jelena
AU  - Popović, Petar
AU  - Vasilijić, Saša
AU  - Milosavljević, Petar
AU  - Balint, Bela
PY  - 2003
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/465
AB  - Several laboratories have developed culture systems that allow the generation of large numbers of human dendritic cells (DC) from monocytes using granulocyte-macrophage colony stimulating factor (GM-CSF), and interleukin-4 (IL-4). In this work we provided evidence that GM-CSF (100 ng/ml) in combination with a low concentration of IL-4 (5 ng/ml) was efficient in the generation of immature, non-adherent, monocyte-derived DC as the same concentration of GM-CSF, and ten times higher concentration of IL-4 (50 ng/ml). This conclusion was based on the similar phenotype profile of DC such as the expression of CD1a, CD80, CD86, and HLA-DR, down-regulation of CD14, and the absence of CD83, as well as on their similar allostimulatory activity for T cells. A higher number of cells remained adherent in cultures with lower concentrations of IL-4 than in cultures with higher concentrations of the cytokine. However, most of these adherent cells down-regulated CD14 and stimulated the proliferation of alloreactive T cells. In contrast adherent cells cultivated with GM-CSF alone were predominantly macrophages as judged by the expression of CD14 and the inefficiency to stimulate alloreactive T cells. DC generated in the presence of lower concentrations of IL-4 had higher proapoptotic potential for the Jurkat cell line than DC differentiated with higher concentrations of IL-4, suggesting their stronger cytotoxic, anti-tumor effect.
AB  - U više laboratorija su uspostavljeni sistemi za kultivaciju velikog broja humanih dendritičnih ćelija (DĆ) od monocita korišćenjem faktora stimulacije granulocitno--makrofagnih kolonija (GM-CSF) i interleukina-4 (IL-4). U ovom radu je pokazano da je kombinacija GM-CSF (100 ng/ml) i mala koncentracija IL-4 (5 ng/ml) podjednako efikasna za dobijanje nezrelih, neadherentnih, DĆ monocitnog porekla kao i kombinacija GM-CSF sa deset puta većom koncentracijom IL-4 (50 ng/ml). Ovaj zaključak izveden je na osnovu sličnog fenotipskog profila DĆ (ispoljavanje CD1a, CD80, CD86 i HLA-DR, smanjenje ekspresije CD14 i odsustva CD83), kao i slične alostimulatorne aktivnosti ovih ćelija za limfocite T. U kulturama sa nižim koncentracijama IL-4 prisutan je bio veći broj adherentnih ćelija nego u kulturama sa većim koncentracijama IL-4. Međutim, većina ovih ćelija je smanjivala ekspresiju CD14 i stimulisala proliferaciju aloreaktivnih limfocita T. Nasuprot njima adherentne ćelije, diferentovane samo u prisustvu GM-CSF, koje su ispoljavale CD14 i nisu imale sposobnost stimulacije aloreakativnih limfocita T pokazivale su karakteristike makrofaga. DĆ obrazovane u prisustvu manjih koncentracija IL-4 imale su veći potencijal za indukciju apoptoze Jurkat ćelijske linije, a time i snažniji citotoksični, antitumorski efekat nego DĆ diferentovane u prisustvu većih koncentracija IL-4.
PB  - Vojnomedicinska akademija - Institut za naučne informacije, Beograd
T2  - Vojnosanitetski pregled
T1  - Differentiation of human dendritic cells from monocytes in vitro using granulocyte-macrophage colony stimulating factor and low concentration of interleukin-4
T1  - Diferencijacija humanih dendritičnih ćelija od monocita in vitro korišćenjem faktora stimulacije granulocitno-makrofagnih kolonija i niske koncentracije interleukina-4
VL  - 60
IS  - 5
SP  - 531
EP  - 538
DO  - 10.2298/VSP0305531C
ER  - 

@article{
author = "Čolić, Miodrag and Jandrić, Dušan and Stojić-Vukanić, Zorica and Antić-Stanković, Jelena and Popović, Petar and Vasilijić, Saša and Milosavljević, Petar and Balint, Bela",
year = "2003",
abstract = "Several laboratories have developed culture systems that allow the generation of large numbers of human dendritic cells (DC) from monocytes using granulocyte-macrophage colony stimulating factor (GM-CSF), and interleukin-4 (IL-4). In this work we provided evidence that GM-CSF (100 ng/ml) in combination with a low concentration of IL-4 (5 ng/ml) was efficient in the generation of immature, non-adherent, monocyte-derived DC as the same concentration of GM-CSF, and ten times higher concentration of IL-4 (50 ng/ml). This conclusion was based on the similar phenotype profile of DC such as the expression of CD1a, CD80, CD86, and HLA-DR, down-regulation of CD14, and the absence of CD83, as well as on their similar allostimulatory activity for T cells. A higher number of cells remained adherent in cultures with lower concentrations of IL-4 than in cultures with higher concentrations of the cytokine. However, most of these adherent cells down-regulated CD14 and stimulated the proliferation of alloreactive T cells. In contrast adherent cells cultivated with GM-CSF alone were predominantly macrophages as judged by the expression of CD14 and the inefficiency to stimulate alloreactive T cells. DC generated in the presence of lower concentrations of IL-4 had higher proapoptotic potential for the Jurkat cell line than DC differentiated with higher concentrations of IL-4, suggesting their stronger cytotoxic, anti-tumor effect., U više laboratorija su uspostavljeni sistemi za kultivaciju velikog broja humanih dendritičnih ćelija (DĆ) od monocita korišćenjem faktora stimulacije granulocitno--makrofagnih kolonija (GM-CSF) i interleukina-4 (IL-4). U ovom radu je pokazano da je kombinacija GM-CSF (100 ng/ml) i mala koncentracija IL-4 (5 ng/ml) podjednako efikasna za dobijanje nezrelih, neadherentnih, DĆ monocitnog porekla kao i kombinacija GM-CSF sa deset puta većom koncentracijom IL-4 (50 ng/ml). Ovaj zaključak izveden je na osnovu sličnog fenotipskog profila DĆ (ispoljavanje CD1a, CD80, CD86 i HLA-DR, smanjenje ekspresije CD14 i odsustva CD83), kao i slične alostimulatorne aktivnosti ovih ćelija za limfocite T. U kulturama sa nižim koncentracijama IL-4 prisutan je bio veći broj adherentnih ćelija nego u kulturama sa većim koncentracijama IL-4. Međutim, većina ovih ćelija je smanjivala ekspresiju CD14 i stimulisala proliferaciju aloreaktivnih limfocita T. Nasuprot njima adherentne ćelije, diferentovane samo u prisustvu GM-CSF, koje su ispoljavale CD14 i nisu imale sposobnost stimulacije aloreakativnih limfocita T pokazivale su karakteristike makrofaga. DĆ obrazovane u prisustvu manjih koncentracija IL-4 imale su veći potencijal za indukciju apoptoze Jurkat ćelijske linije, a time i snažniji citotoksični, antitumorski efekat nego DĆ diferentovane u prisustvu većih koncentracija IL-4.",
publisher = "Vojnomedicinska akademija - Institut za naučne informacije, Beograd",
journal = "Vojnosanitetski pregled",
title = "Differentiation of human dendritic cells from monocytes in vitro using granulocyte-macrophage colony stimulating factor and low concentration of interleukin-4, Diferencijacija humanih dendritičnih ćelija od monocita in vitro korišćenjem faktora stimulacije granulocitno-makrofagnih kolonija i niske koncentracije interleukina-4",
volume = "60",
number = "5",
pages = "531-538",
doi = "10.2298/VSP0305531C"
}

Čolić, M., Jandrić, D., Stojić-Vukanić, Z., Antić-Stanković, J., Popović, P., Vasilijić, S., Milosavljević, P.,& Balint, B.. (2003). Differentiation of human dendritic cells from monocytes in vitro using granulocyte-macrophage colony stimulating factor and low concentration of interleukin-4. in Vojnosanitetski pregled
Vojnomedicinska akademija - Institut za naučne informacije, Beograd., 60(5), 531-538.
https://doi.org/10.2298/VSP0305531C

Čolić M, Jandrić D, Stojić-Vukanić Z, Antić-Stanković J, Popović P, Vasilijić S, Milosavljević P, Balint B. Differentiation of human dendritic cells from monocytes in vitro using granulocyte-macrophage colony stimulating factor and low concentration of interleukin-4. in Vojnosanitetski pregled. 2003;60(5):531-538.
doi:10.2298/VSP0305531C .

Čolić, Miodrag, Jandrić, Dušan, Stojić-Vukanić, Zorica, Antić-Stanković, Jelena, Popović, Petar, Vasilijić, Saša, Milosavljević, Petar, Balint, Bela, "Differentiation of human dendritic cells from monocytes in vitro using granulocyte-macrophage colony stimulating factor and low concentration of interleukin-4" in Vojnosanitetski pregled, 60, no. 5 (2003):531-538,
https://doi.org/10.2298/VSP0305531C . .