Maja Stojiljkovic

Maja Stojiljkovic

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Maja Stojiljkovic

Maja Stojiljkovic

Publications by authors named "Maja Stojiljkovic"

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30Publications

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Impact of genotype on neutropenia in a large cohort of Serbian patients with glycogen storage disease type Ib.

Eur J Med Genet 2019 Sep 16:103767. Epub 2019 Sep 16.

Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Serbia.

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http://dx.doi.org/10.1016/j.ejmg.2019.103767DOI Listing
September 2019

CRISPR/Cas9 genome editing of SLC37A4 gene elucidates the role of molecular markers of endoplasmic reticulum stress and apoptosis in renal involvement in glycogen storage disease type Ib.

Gene 2019 Jun 3;703:17-25. Epub 2019 Apr 3.

Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, 11010 Belgrade, Serbia. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S03781119193034
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http://dx.doi.org/10.1016/j.gene.2019.04.002DOI Listing
June 2019

Functional Characterization of Novel Phenylalanine Hydroxylase p.Gln226Lys Mutation Revealed Its Non-responsiveness to Tetrahydrobiopterin Treatment in Hepatoma Cellular Model.

Biochem Genet 2018 Oct 13;56(5):533-541. Epub 2018 Apr 13.

Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, Belgrade, 11010, Serbia.

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http://dx.doi.org/10.1007/s10528-018-9858-5DOI Listing
October 2018

Intra-articular injection of autologous adipose-derived mesenchymal stem cells in the treatment of knee osteoarthritis.

J Gene Med 2018 01 22;20(1). Epub 2018 Jan 22.

Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Serbia.

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http://dx.doi.org/10.1002/jgm.3002DOI Listing
January 2018

Functional and structural characterisation of 5 missense mutations of the phenylalanine hydroxylase.

Gen Physiol Biophys 2017 Oct 27;36(4):361-371. Epub 2017 Jun 27.

Department of Molecular Biology, Faculty of Natural Sciences, Comenius University, Ilkovicova 6, 842 15 Bratislava, Slovakia.

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http://dx.doi.org/10.4149/gpb_2017003DOI Listing
October 2017

New PAH gene promoter KLF1 and 3'-region C/EBPalpha motifs influence transcription in vitro.

J Appl Genet 2017 Feb 22;58(1):79-85. Epub 2016 Jul 22.

Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, 11010, Belgrade, Serbia.

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http://dx.doi.org/10.1007/s13353-016-0359-0DOI Listing
February 2017

Functional Analysis of an (A)γ-Globin Gene Promoter Variant (HBG1: g.-225_-222delAGCA) Underlines Its Role in Increasing Fetal Hemoglobin Levels Under Erythropoietic Stress.

Hemoglobin 2016 16;40(1):48-52. Epub 2015 Nov 16.

a Laboratory for Molecular Biomedicine , Institute of Molecular Genetics and Genetic Engineering, University of Belgrade , Belgrade , Serbia .

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http://dx.doi.org/10.3109/03630269.2015.1107842DOI Listing
October 2016

Novel patched 1 mutations in patients with nevoid basal cell carcinoma syndrome--case report.

Croat Med J 2015 Feb;56(1):63-7

Vesna Spasovski, Laboratory for Molecular Biomedicine, Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, 11000 Belgrade, Serbia,

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4364350PMC
http://dx.doi.org/10.3325/cmj.2015.56.63DOI Listing
February 2015

6th Golden Helix Pharmacogenomics Day: pharmacogenomics and individualized therapy.

Hum Genomics 2012 Sep 25;6:19. Epub 2012 Sep 25.

Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, Belgrade 11010, Republic of Serbia.

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http://dx.doi.org/10.1186/1479-7364-6-19DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3505187PMC
September 2012

Clinical applicability of sequence variations in genes related to drug metabolism.

Curr Drug Metab 2011 Jun;12(5):445-54

Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Serbia.

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June 2011

Thalassemia syndromes in Serbia: an update.

Hemoglobin 2010 ;34(5):477-85

Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Serbia.

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http://dx.doi.org/10.3109/03630269.2010.513637DOI Listing
March 2011

Novel transcriptional regulatory element in the phenylalanine hydroxylase gene intron 8.

Mol Genet Metab 2010 Sep 9;101(1):81-3. Epub 2010 Jun 9.

Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, Belgrade, Serbia.

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http://dx.doi.org/10.1016/j.ymgme.2010.05.014DOI Listing
September 2010

Functional analysis of the role of the TPMT gene promoter VNTR polymorphism in TPMT gene transcription.

Pharmacogenomics 2010 Apr;11(4):547-57

Institute for Molecular Genetics & Genetic Engineering, Laboratory of Molecular Hematology, Vojvode Stepe 444a, 11010 Belgrade, Serbia.

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http://dx.doi.org/10.2217/pgs.10.7DOI Listing
April 2010

Acute myeloid leukemia with NUP98-HOXC13 fusion and FLT3 internal tandem duplication mutation: case report and literature review.

Cancer Genet Cytogenet 2009 Sep;193(2):98-103

Laboratory for Molecular Hematology, Institute of Molecular Genetics and Genetic Engineering, Vojvode Stepe 444a, P.O. Box 23, 11010 Belgrade, Serbia.

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http://dx.doi.org/10.1016/j.cancergencyto.2009.03.007DOI Listing
September 2009

The Missense p.S231F phenylalanine hydroxylase gene mutation causes complete loss of enzymatic activity in vitro.

Protein J 2009 Aug;28(6):294-9

Institute of Molecular Genetics and Genetic Engineering, Vojvode Stepe 444a, 11000, Belgrade, Serbia.

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http://link.springer.com/10.1007/s10930-009-9194-z
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http://dx.doi.org/10.1007/s10930-009-9194-zDOI Listing
August 2009

Characterization of 9L glioma model of the Wistar rat.

J Neurooncol 2003 May;63(1):1-7

ICN Galenika Institute, Biomedical Research Center, Belgrade, Serbia, Yugoslavia.

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http://dx.doi.org/10.1023/a:1023732619651DOI Listing
May 2003