D. Vujić

发表

A Single-Cell Raman Spectroscopy Analysis of Bone Marrow Mesenchymal Stem/Stromal Cells to Identify Inter-Individual Diversity

D. Bugarski, U. Ralević, T. Kukolj, 2022, International journal of molecular sciences.

The mutational spectrum of human malignant autosomal recessive osteopetrosis.

A. Villa, M. Vihinen, L. Notarangelo, 2001, Human molecular genetics.

Severe Combined Immunodeficiency in Serbia and Montenegro Between Years 1986 and 2010: A Single-Center Experience

S. Giliani, A. Villa, M. Mostarica‐Stojković, 2014, Journal of Clinical Immunology.

Radiation-induced mitotic catastrophe in FANCD2 primary fibroblasts

G. Joksiċ, D. Vujić, S. Petrović, 2014, International journal of radiation biology.

Influence of applied CD34+ cell dose on the survival of Hodgkin's lymphoma and multiple myeloma patients following autologous stem cell transplants

B. Balint, D. Antić, B. Mihaljević, 2020, Vojnosanitetski pregled.

Dysfunctional telomeres in primary cells from Fanconi anemia FANCD2 patients

G. Joksiċ, J. Surrallés, P. Slijepcevic, 2012, Genome Integrity.

G. Joksiċ, J. Kotur-Stevuljević, D. Vujić, 2011, Biological chemistry.

Evaluation of the SIOPEN semi-quantitative scoring system in planar simpatico-adrenal MIBG scintigraphy in children with neuroblastoma.

D. Sobic-Saranovic, B. Radovic, U. Beogradu, 2015, Neoplasma.

Chloride Channel ClCN7 Mutations Are Responsible for Severe Recessive, Dominant, and Intermediate Osteopetrosis

L. Notarangelo, A. Flanagan, T. Young, 2003, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Complex karyotype with cryptic FUS gene rearrangement and deletion of NR3C1 and VPREB1 genes in childhood B-cell acute lymphoblastic leukemia: A case report.

T. Liehr, B. Meyer, M. Othman, 2020, Oncology letters.

Vitamin D3 Stimulates Proliferation Capacity, Expression of Pluripotency Markers, and Osteogenesis of Human Bone Marrow Mesenchymal Stromal/Stem Cells, Partly through SIRT1 Signaling

D. Bugarski, S. Mojsilović, B. Gobeljić, 2022, Biomolecules.

Autologous stem cell transplants - single center standpoints for lymphoma patients

B. Balint, B. Mihaljević, B. Andjelic, 2017 .

Comet assay and cytogenetic findings in differential diagnosis of Fanconi anemia

B. Vuković-Gačić, K. Sunjog, D. Vujić, 2019, Genetika.

A cryptic three-way translocation t(10;19;11)(p12.31;q13.31;q23.3) with a derivative Y-chromosome in an infant with acute myeloblastic leukemia (M5b).

T. Liehr, B. Meyer, M. Othman, 2015, Gene.

Chromosomal instability in patients with Fanconi anemia from Serbia.

D. Vujić, S. Ćirković, D. Mićić, 2014, Vojnosanitetski pregled.

Cytogenetic diepoxybutane sensitivity in Serbian children with Fanconi anemia

D. Vujić, S. Ćirković, D. Mićić, 2006 .

Prognostic value of clinical, genetic and cytogenetic findings in neuroblastoma patients from Serbia and Montenegro

S. Djuricic, D. Vujić, M. Guć-Šćekić, 2005 .

BIRC3 alterations in chronic and B-cell acute lymphocytic leukemia patients

G. Joksiċ, T. Liehr, S. Hauke, 2016, Oncology letters.

Risk factors for thrombosis in Serbian children

D. Radojkovic, G. Kovačević, J. Kosutić, 2014, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Fanconi anemia is characterized by delayed repair kinetics of DNA double-strand breaks.

G. Joksiċ, P. Slijepcevic, D. Vujić, 2010, The Tohoku journal of experimental medicine.

Enhanced frequency of sister chromatid exchanges induced by diepoxybutane is specific characteristic of Fanconi anemia cellular phenotype

G. Joksiċ, D. Vujić, S. Petrović, 2013 .

Monitoring of Pediatric Patients With Malignant Hematological Diseases After Allogeneic HSCT: Serbian Experience

A. Krstic, O. Stojković, D. Vujić, 2012, Journal of pediatric hematology/oncology.

Atypical Strain of Toxoplasma gondii Causing Fatal Reactivation after Hematopoietic Stem Cell Transplantion in a Patient with an Underlying Immunological Deficiency

S. Pašić, Z. Vasiljevic, D. Ajzenberg, 2013, Journal of Clinical Microbiology.

Cytomegalovirus glycoprotein B and N genotypes in pediatric recipients of the hematopoietic stem cell transplant.

T. Jovanović, I. Soldatovic, M. Ćupić, 2020, Virology.

Aggressive human neuroblastomas show a massive increase in the numbers of autophagic vacuoles and damaged mitochondria

T. Martinović, S. Djuricic, V. Bumbasirevic, 2016, Ultrastructural pathology.

Independent role of interleukin-6 and interleukin-8 in the etiology of transfusion reactions to platelet concentrates in children

M. Životić, Nic, Dragana Gojkov, 2018 .

Independent role of interleukin IL-6 and IL-8 in the etiology of transfusion reactions to platelet concentrates in children

M. Životić, M. Kuzmanović, D. Vujić, 2016 .

Acute leukemia of childhood: A single institution's experience

A. Krstic, S. Djuricic, M. Kuzmanović, 2005 .

Severe Combined Immunodeficiency in Serbia and Montenegro Between Years 1986 and 2010: A Single-Center Experience

S. Giliani, A. Villa, M. Mostarica‐Stojković, 2014, Journal of Clinical Immunology.

Genotyping Fanconi anemia patients from Serbia reveals three novel FANCD2 variants

G. Joksiċ, V. Mandušić, D. Vujić, 2017 .

Cell cycle analysis in patients with Fanconi anemia from Serbia

T. Srdić-Rajić, D. Vujić, S. Ćirković, 2013 .

Diagnosis of Fanconi’s Anemia by Diepoxybutane Analysis in Children from Serbia

N. Ilić, A. Jovanovic, D. Vujić, 2011, Balkan journal of medical genetics : BJMG.

Assessment of single nucleotide polymorphisms in screening 52 DNA repair and cell cycle control genes in Fanconi anemia patients

G. Joksiċ, D. Vujić, S. Petrović, 2015 .

Mobilization and Harvesting of Peripheral Blood Stem Cells in Pediatric Patients With Solid Tumors

E. Lazic, D. Veljković, D. Vujić, 2011, Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy.

Haploidentical bone marrow transplantation in leukemia and genetic diseases.

A. Beorchia, C. Vidali, M. Rabusin, 2000, Haematologica.

First molecular-cytogenetic characterization of Fanconi anemia fragile sites in primary lymphocytes of FA-D2 patients in different stages of the disease

G. Joksiċ, K. Mrasek, T. Liehr, 2016, Molecular Cytogenetics.

Non-Hodgkin's lymphoma of the uterus and CNS.

G. Vujanić, D. Vujić, D. Zamurović, 2000, Pediatric neurology.

Coagulation disturbances in paediatric patients with hepatic veno-occlusive disease after stem cells transplantation.

I. Elezović, D. Veljković, D. Vujić, 2010, Srpski arhiv za celokupno lekarstvo.

Subclinical hypothyroidism in children and adolescents after hematopoietic stem cells transplantation without irradiation.

I. Soldatovic, T. Milenković, R. Vuković, 2014, Vojnosanitetski pregled.

Pediatric hematopoietic stem cell transplantation in Serbia - 25 years of experience

E. Lazic, D. Vujić, G. Samardžija, 2022, Medical review.