Goran Kungulovski
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Explore the profile of Goran Kungulovski including associated specialties, affiliations and a list of published articles.
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21
Citations
496
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Recent Articles
1.
Compound Heterozygosity in Cerebellar Ataxia, Mental Retardation, and Disequilibrium Syndrome Type 4
Teov B, Janchevska A, Beqiri-Jasari A, Tasic V, Kungulovski G, Gucev Z
Pril (Makedon Akad Nauk Umet Odd Med Nauki)
. 2023 Dec;
44(3):85-90.
PMID: 38109455
Cerebellar ataxia, mental retardation, and disequilibrium syndrome (CAMRQ) is a genetically and clinically heterogeneous disorder with four described subtypes. Autosomal recessive syndrome of cerebellar ataxia, mental retardation, and disequilibrium type...
2.
Choudalakis M, Kungulovski G, Mauser R, Bashtrykov P, Jeltsch A
Protein Sci
. 2023 Aug;
32(9):e4760.
PMID: 37593997
UHRF1 is an essential chromatin protein required for DNA methylation maintenance, mammalian development, and gene regulation. We investigated the Tandem-Tudor domain (TTD) of human UHRF1 that is known to bind...
3.
Lozo J, Ristovic N, Kungulovski G, Jovanovic Z, Rakic T, Stankovic S, et al.
World J Microbiol Biotechnol
. 2023 Jul;
39(10):256.
PMID: 37474779
Rhizosphere microbial communities play an important role in maintaining the health and productivity of the plant host. The rhizobacteria Pseudomonas putida P2 of Ramonda serbica and Bacillus cereus P5 of...
4.
Gjorgjievska M, Mehandziska S, Stajkovska A, Pecioska-Dokuzovska S, Dimovska A, Durmish I, et al.
Front Genet
. 2022 May;
13:892682.
PMID: 35495156
Trends from around the world suggest that the omicron BA.2 subvariant is increasing in proportion to the original BA.1 subvariant. Here we report two cases of co-infection with omicron BA.1...
5.
Broche J, Kungulovski G, Bashtrykov P, Rathert P, Jeltsch A
Nucleic Acids Res
. 2020 Dec;
49(1):158-176.
PMID: 33300025
Chromatin properties are regulated by complex networks of epigenome modifications. Currently, it is unclear how these modifications interact and if they control downstream effects such as gene expression. We employed...
6.
Mehandziska S, Stajkovska A, Stavrevska M, Jakovleva K, Janevska M, Rosalia R, et al.
Front Genet
. 2020 Jul;
11:619.
PMID: 32695137
To enable the implementation of precise genomics in a local healthcare system, we devised a pipeline for filtering and reporting of relevant genetic information to healthy individuals based on exome...
7.
Stajkovska A, Mehandziska S, Rosalia R, Stavrevska M, Janevska M, Markovska M, et al.
Front Genet
. 2019 Nov;
10:952.
PMID: 31749828
Targeted gene panel testing has the power to interrogate hundreds of genes and evaluate the genetic risk for many types of hereditary cancers simultaneously. We screened a 13-year-old male patient...
8.
Stajkovska A, Mehandziska S, Stavrevska M, Jakovleva K, Nikchevska N, Mitrev Z, et al.
Front Genet
. 2018 Apr;
9:113.
PMID: 29675035
Exome sequencing can interrogate thousands of genes simultaneously and it is becoming a first line diagnostic tool in genomic medicine. Herein, we applied trio clinical exome sequencing (CES) in a...
9.
Jurkowska R, Qin S, Kungulovski G, Tempel W, Liu Y, Bashtrykov P, et al.
Nat Commun
. 2017 Dec;
8(1):2057.
PMID: 29234025
SETDB1 is an essential H3K9 methyltransferase involved in silencing of retroviruses and gene regulation. We show here that its triple Tudor domain (3TD) specifically binds to doubly modified histone H3...
10.
Mauser R, Kungulovski G, Meral D, Maisch D, Jeltsch A
Biochimie
. 2017 Nov;
146:14-19.
PMID: 29133117
The N-terminal tails of histone proteins are massively decorated with post-translational modifications (PTMs), which play important roles in the regulation of gene expression. Several highly conserved chromatin interacting proteins can...