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The Role of Autophagy and Apoptosis in Affected Skin and Lungs in Patients with Systemic Sclerosis

International journal of molecular sciences, 2023-07, Vol.24 (13), p.11212

2023

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Identification and Classification of Novel Genetic Variants: En Route to the Diagnosis of Primary Ciliary Dyskinesia

International journal of molecular sciences, 2021-08, Vol.22 (16), p.8821

2021

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Genomic profiling supports the diagnosis of primary ciliary dyskinesia and reveals novel candidate genes and genetic variants

PloS one, 2018-10, Vol.13 (10), p.e0205422-e0205422

2018

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Expression of TLR7, TLR9, JAK2, and STAT3 genes in peripheral blood mononuclear cells from patients with systemic sclerosis

Journal of applied genetics, 2018-02, Vol.59 (1), p.59-66

2018

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Seven-Year Longitudinal Study: Clinical Evaluation of Knee Osteoarthritic Patients Treated with Mesenchymal Stem Cells

Journal of clinical medicine, 2024-06, Vol.13 (13), p.3861

2024

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Crosstalk between Glycogen-Selective Autophagy, Autophagy and Apoptosis as a Road towards Modifier Gene Discovery and New Therapeutic Strategies for Glycogen Storage Diseases

Life (Basel, Switzerland), 2022-09, Vol.12 (9), p.1396

2022

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PB2037: NEW TERT VARIANT IN A FAMILY WITH APLASTIC ANEMIA

HemaSphere, 2023-08, Vol.7 (S3), p.e62401c5-n/a

2023

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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, 2019-06, Vol.703, p.17-25

2019

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Genetic variants in TNFA, LTA, TLR2 and TLR4 genes and risk of sepsis in patients with severe trauma: nested case-control study in a level-1 trauma centre in SERBIA

Injury, 2021-03, Vol.52 (3), p.419-425

2021

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Impact of alterations in X-linked IRAK1gene and miR-146a on susceptibility and clinical manifestations in patients with systemic sclerosis

Immunology letters, 2018-12, Vol.204, p.1-8

2018

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Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic Strategies

Molecular diagnosis & therapy, 2024-09, Vol.28 (5), p.645-663

2024

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Association between the -174 C/G polymorphism in the interleukin-6 (IL-6) gene and gastrointestinal involvement in patients with systemic sclerosis

Clinical rheumatology, 2018-09, Vol.37 (9), p.2447-2454

2018

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The importance of combined NGS and MLPA genetic tests for differential diagnosis of maturity onset diabetes of the young

Endokrynologia polska, 2019-01, Vol.70 (1), p.28-36

2019

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Genes and metabolic pathway of sarcoidosis: identification of key players and risk modifiers

Archives of medical science, 2019-09, Vol.15 (5), p.1138-1146

2019

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Genetic basis of otosclerosis

Srpski arhiv za celokupno lekarstvo, 2020-09, Vol.148 (9-10), p.621-625

2020

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The importance of genomic profiling for differential diagnosis of pediatric lung disease patients with suspected ciliopathies

Srpski arhiv za celokupno lekarstvo, 2019-03, Vol.147 (3-4), p.160-166

2019

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Opis przypadku — występujący rodzinnie wewnątrzczaszkowo germinoma

Endokrynologia polska, 2018-09, Vol.69 (5), p.612-618

2018

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Clinical case seminar: Familial intracranial germinoma

Endokrynologia Polska, 2018, Vol.69 (5), p.612-618

2018

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Variants in VDR and NRAMP1 genes as susceptibility factors for tuberculosis in the population of Serbia

Genetika (Beograd), 2015, Vol.47 (3), p.1021-1028

2015

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Mating behavior as an indicator of quality of Drosophila subobscura males

Insect science, 2017-02, Vol.24 (1), p.122-132

2017

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Alternative respiratory chain enzymes: Therapeutic potential and possible pitfalls

Biochimica et biophysica acta. Molecular basis of disease, 2019-04, Vol.1865 (4), p.854-866

2019

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Myocardial perfusion scintigraphy in the prediction of the existence of hemodynamically significant coronary artery stenosis

Acta Facultatis Medicae Naissensis, 2024, Vol.41 (1), p.29-41

2024

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Affinity chromatography on monolithic supports for simultaneous and high‐throughput isolation of immunoglobulins from human serum

Electrophoresis, 2017-11, Vol.38 (22-23), p.2909-2913

2017

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MEASLES OUTBREAK IN THE NIŠAVA AND TOPLICA DISTRICTS FROM 2017 TO 2018

Acta Medica Medianae, 2021-06, Vol.60 (2), p.35-43

2021

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Antitumor effect of mifepristone on human endometrial stromal cell line

Vojnosanitetski pregled, 2021, Vol.78 (6), p.615-620

2021

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The Role of Autophagy and Apoptosis in Affected Skin and Lungs in Patients with Systemic Sclerosis

Identification and Classification of Novel Genetic Variants: En Route to the Diagnosis of Primary Ciliary Dyskinesia

Genomic profiling supports the diagnosis of primary ciliary dyskinesia and reveals novel candidate genes and genetic variants

Expression of TLR7, TLR9, JAK2, and STAT3 genes in peripheral blood mononuclear cells from patients with systemic sclerosis

Seven-Year Longitudinal Study: Clinical Evaluation of Knee Osteoarthritic Patients Treated with Mesenchymal Stem Cells

Crosstalk between Glycogen-Selective Autophagy, Autophagy and Apoptosis as a Road towards Modifier Gene Discovery and New Therapeutic Strategies for Glycogen Storage Diseases

PB2037: NEW TERT VARIANT IN A FAMILY WITH APLASTIC ANEMIA

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

Genetic variants in TNFA, LTA, TLR2 and TLR4 genes and risk of sepsis in patients with severe trauma: nested case-control study in a level-1 trauma centre in SERBIA

Impact of alterations in X-linked IRAK1gene and miR-146a on susceptibility and clinical manifestations in patients with systemic sclerosis

Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic Strategies

Association between the -174 C/G polymorphism in the interleukin-6 (IL-6) gene and gastrointestinal involvement in patients with systemic sclerosis

The importance of combined NGS and MLPA genetic tests for differential diagnosis of maturity onset diabetes of the young

Genes and metabolic pathway of sarcoidosis: identification of key players and risk modifiers

Genetic basis of otosclerosis

The importance of genomic profiling for differential diagnosis of pediatric lung disease patients with suspected ciliopathies

Opis przypadku — występujący rodzinnie wewnątrzczaszkowo germinoma

Clinical case seminar: Familial intracranial germinoma

Variants in VDR and NRAMP1 genes as susceptibility factors for tuberculosis in the population of Serbia

Mating behavior as an indicator of quality of Drosophila subobscura males

Alternative respiratory chain enzymes: Therapeutic potential and possible pitfalls

Myocardial perfusion scintigraphy in the prediction of the existence of hemodynamically significant coronary artery stenosis

Affinity chromatography on monolithic supports for simultaneous and high‐throughput isolation of immunoglobulins from human serum

MEASLES OUTBREAK IN THE NIŠAVA AND TOPLICA DISTRICTS FROM 2017 TO 2018

Antitumor effect of mifepristone on human endometrial stromal cell line

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