Researchers
Klaassen Ljubičić, Kristel
Results 61-80 of 91
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2019 | Genomic profiling of glycogen storage diseases: from NGS method to the CRISPR/Cas9 technology | Skakić, Anita   ; Anđelković, Marina ; Tošić, Nataša ; Kristel Klaassen ; Spasovski, Vesna ; Đorđević, Maja; Sarajlija, Adrijan; Pavlović, Sonja ; Stojiljković, Maja | Conference Paper | Mp. category will be shown later |
| 2019 | Genomic profiling of glycogen storage diseases | Skakic, Anita ; Anđelković, Marina ; Tošic, Natasa ; Kristel Klaassen ; Spasovski, Vesna ; Ristivojević, Bojan ; Đorđević, Maja; Sarajlija, Adrijan; Pavlović, Sonja ; Stojiljković, Maja | Conference Paper | Mp. category will be shown later |
| 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 | Skakic, Anita ; Andjelkovic, Marina ; Tošić, Nataša ; Klaassen, Kristel ; Djordjevic, Maja; Pavlović, Sonja ; Stojiljković, Maja | Article | 22M22 |
| 2019 | GENOMIC PROFILING OF GLYCOGEN STORAGE DISEASES: FROM THE NGS METHOD TO THE CRISPR/CAS9 TECHNOLOGY | Skakić, Anita ; Anđelković, Marina ; Tošic, Nataša ; Kristel Klaassen ; Vesna Spasovski ; Ristivojevic, Bojan ; Đordjevic, Maja; Adrijan Sarajlija; Pavlović, Sonja ; Stojiljković, Maja | Conference Paper | Mp. category will be shown later |
| 2018 | Functional Characterization of Novel Phenylalanine Hydroxylase p.Gln226Lys Mutation Revealed Its Non-responsiveness to Tetrahydrobiopterin Treatment in Hepatoma Cellular Model | Klaassen, Kristel ; Djordjevic, Maja; Skakić, Anita ; Desviat, Lourdes R.; Pavlović, Sonja ; Perez, Belen; Stojiljković, Maja | Article | 22M22 |
| 2018 | Importance of TLR9-IL23-1L17 axis in inflammatory bowel disease development: Gene expression profiling study | Dragašević, Sanja ; Stanković, Biljana ; Sokić-Milutinović, Aleksandra ; Milosavljević, Tomica ; Milovanović, Tamara ; Lukić, Snežana ; Srzentić Dražilov, Sanja ; Klaassen, Kristel ; Kotur, Nikola ; Pavlović, Sonja ;
Popović, Dragan
; | Article | 21M21 |
| 2018 | Genetic characterization of GSD I in Serbian population revealed unexpectedly high incidence of GSD Ib and 3 novel SLC37A4 variants | Skakić, Anita ; Đorđević, M.; Sarajlija, A. ; Klaassen, Kristel ; Tošić, Nataša ; Kecman, B.; Ugrin, Milena ; Spasovski, Vesna ; Pavlović, Sonja ; Stojiljković, Maja | Article | 21M21 |
| 2017 | Precision molecular diagnostic of hepatic GSD revealed unexpectedly high incidence of gsd ib in serbian population and three novel variants in the SLC37A4 gene | Skakic, Anita ; Djordjevic, Maja; Adrijan Sarajlija; Kristel Klaassen ; Tosic, Natasa ; Bozica Kecman; Milena Ugrin; Vesna Spasovski ; Pavlovic, Sonja ; Stojiljkovic, Maja | Conference Paper | Mp. category will be shown later |
| 2017 | Molecular genetic strategy for diagnosis of congenital adrenal hyperplasia in Serbia | Ugrin, Milena ; Milačić, Iva; Skakić, Anita ; Klaassen, Kristel ; Komazec, Jovana ; Pavlović, Sonja ; Stojiljković, Maja | Article | 23M23 |
| 2017 | New PAH gene promoter KLF1 and 3'-region C/EBPalpha motifs influence transcription in vitro | Klaassen, Kristel ; Stanković, Biljana ; Kotur, Nikola ; Đorđević, Maja; Zukić, Branka ; Nikčević, Gordana ; Ugrin, Milena ; Spasovski, Vesna ; Srzentić Dražilov, Sanja ; Pavlović, Sonja ;
Stojiljković, Maja
; | Article | 22M22 |
| 2017 | Genetic modifiers of -thalassemia: a rise of a novel therapy approaches | Ugrin M. ; Stojiljković M.; Zukić B. ; Klaassen K. ; Jovana Komazec ; Skakić A. ; Dokmanović, L.; Janić D.; Patrinos GP.; Pavlović S. | Conference Paper | Mp. category will be shown later |
| 2017 | Genetic modifiers of beta-thalassemia: a rise of a novel therapy approaches. | Milena Ugrin; Stojiljkovic, Maja ; Zukic, Branka; Kristel Klaassen ; Jovana Komazec; Skakic, Anita ; Dokmanovic, Lidija; Janic, Dragana; George Patrinos; Pavlovic, Sonja | Conference Paper | Mp. category will be shown later |
| 2016 | Functional Analysis of an (A)gamma-Globin Gene Promoter Variant (HBG1: g.-225_-222delAGCA) Underlines Its Role in Increasing Fetal Hemoglobin Levels Under Erythropoietic Stress | Ugrin, Milena ; Stojiljković, Maja ; Zukić, Branka ; Klaassen, Kristel ; Katsila, Theodora; Komazec, Jovana ; Dokmanović, Lidija ; Janić, Dragana ; Patrinos, George P.; Pavlović, Sonja | Article | 23M23 |
| 2016 | Molecular and phenotypic characteristics of seven novel mutations causing branched-chain organic acidurias | Stojiljković, Maja ; Klaassen, Kristel ; Đorđević, Maja ; Sarajlija, Adrijan ; Brasil, S.; Kecman, Božica; Grković, Sanja; Perić, Jelena ; Rodriguez-Pombo, P.; Desviat, L.R.;
Pavlović, Sonja
; Perez, B.; | Article | 21M21 |
| 2016 | Molecular genetic testing of inborn metabolic diseases in Serbia | Stojiljkovic, Maja ; Kristel Klaassen ; Skakic, Anita ; Kostic, Jelena; Tosic, Natasa ; Pavlovic, Sonja | Conference Paper | Mp. category will be shown later |
| 2016 | Functional analysis of an Aγ-globin gene promoter variant (HBG1: g.-225_-222delAGCA) underlines its role in increasing fetal hemoglobin levels under erythropoietic stress | Jovana Komazec ; Ugrin M ; Stojiljkovic, M; Zukic, B ; Klaassen K ; Katsila T; Dokmanovic, L; Janic, D; Patrinos GP; Pavlovic, S | Conference Paper | Mp. category will be shown later |
| 2015 | Molecular characterization of mutations in Serbian patients with glycogen storage diseases. | Skakic, Anita ; Kristel Klaassen ; Kostić, Jelena; Đorđević, Maja; Sarajlija, Adrijan; Boyica Kecman; Kotur, Nikola ; Stanković, Biljana; Srzentić, Sanja ; Pavlović, Sonja ;
Stojiljković, Maja
; | Conference Paper | Mp. category will be shown later |
| 2015 | Molecular characterization of mutations in Serbian patients with glycogen storage diseases - an NGS approach | Skakic, Anita ; Kristel Klaassen ; Kostić, Jelena; Đorđević, Maja; Adrijan Sarajlija; Kecman, Božica; Spasovski, Vesna ; Anđelković, Marina ; Vreca, Misa; Pavlović, Sonja ;
Stojiljković, Maja
; | Conference Paper | Mp. category will be shown later |
| 2015 | Molecular genetic study of congenital adrenal hyperplasia in Serbia: novel p.Leu129Pro and p.Ser165Pro CYP21A2 gene mutations | Milačić, I.; Barać, M.; Milenković, Tatjana; Ugrin, Milena ; Klaassen, Kristel ; Skakić, Anita ; Ješić, Maja ; Joksić, Ivana ; Mitrović, Katarina; Todorović, Slađana;
Vujović, Svetlana
; Pavlović, Sonja ; Stojiljković, Maja ; | Article | 22M22 |
| 2015 | Molecular genetic study of congenital adrenal hyperplasia in serbia: two novel CYP21A2 gene mutations | Skakic, Anita ; Milacic, Iva; M Barac; Milenkovic, Tatjana; Milena Ugrin ; Kristel Klaassen ; Jesic, Maja; Joksic, I; Mitrovic, K; Todorovic, S;
Vujovic, S; Pavlovic, Sonja
; Stojiljkovic, Maja ; | Conference Paper | Mp. category will be shown later |