Zobrazeno 1 - 10
of 68
pro vyhledávání: '"Zorana Grubic"'
Autor:
Martina Held, Katarina Stingl Jankovic, Mario Sestan, Matej Sapina, Nastasia Kifer, Sasa Srsen, Marijan Frkovic, Alenka Gagro, Zorana Grubic, Marija Jelusic
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 2, p 882 (2024)
Studies concerning the genetic background of IgA vasculitis (IgAV), a small-vessel vasculitis occurring predominantly in childhood, have confirmed that the HLA-DRB1 gene showed a strong association with disease susceptibility. The objective was to in
Externí odkaz:
https://doaj.org/article/8efed6c2b9c84e0fb3b008ca5f7c7259
Autor:
Katja K. Dumic, Zorana Grubic, Vesna Kusec, Duje Braovac, Kristina Gotovac, Maja Vinkovic, Maja Vucinic, Miroslav Dumic
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
ObjectiveCongenital adrenal hyperplasia (CAH) owing to 21-hydroxylase deficiency (21-OHD) is a rare autosomal recessive disorder caused by pathological variants in the CYP21A2 gene. After a high prevalence of classic 21-OHD CAH in the Romani populati
Externí odkaz:
https://doaj.org/article/e78401ebd2f44716a9af33ec243da054
Mapping the Human Leukocyte Antigen Diversity among Croatian Regions: Implication in Transplantation
Autor:
Zorana Grubic, Marija Maskalan, Katarina Stingl Jankovic, Marija Burek Kamenaric, Renata Zunec
Publikováno v:
Journal of Immunology Research, Vol 2021 (2021)
In the present study, HLA allele and haplotype frequencies were studied using the HLA data of 9277 Croatian unrelated individuals, typed using high-resolution methods for the HLA-A, -B, -C, and -DRB1 loci. The total numbers of observed alleles were 4
Externí odkaz:
https://doaj.org/article/36bb9e6e82cb4996953e66b3bd19b9ff
Autor:
Atifete Ramosaj-Morina, Marija Burek Kamenaric, Mehmedali Azemi, Lidvana Spahiu, Zorana Grubic, Renata Zunec
Publikováno v:
Gastroenterology Research and Practice, Vol 2019 (2019)
Genetic predisposition to celiac disease (CD) is strongly associated with the presence of HLA alleles in the individual genotype encoding HLA-DQ2 and/or HLA-DQ8 heterodimers. The main aim of this study was to analyze the HLA-A, -B, -DRB1, and -DQ all
Externí odkaz:
https://doaj.org/article/27b7af2dfadb47ea94824a991feff9af
Publikováno v:
International Journal of Endocrinology, Vol 2014 (2014)
Steroid 11β-hydroxylase deficiency (11β-OHD) is the second most common cause of congenital adrenal hyperplasia. Mutations in the CYP11B1 gene, which encodes steroid 11β-hydroxylase, are responsible for this autosomal recessive disorder. Here, we d
Externí odkaz:
https://doaj.org/article/fee902ffd99a4f7291d7f267b7cd5fb1
Autor:
Katja K. Dumic, Zorana Grubic, Vesna Kusec, Duje Braovac, Kristina Gotovac, Maja Vinkovic, Maja Vucinic, Miroslav Dumic
ObjectiveCongenital adrenal hyperplasia (CAH) owing to 21-hydroxylase deficiency (21-OHD) is a rare autosomal recessive disorder caused by pathological variants in the CYP21A2 gene. After a high prevalence of classic 21-OHD CAH in the Romani populati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b573021d0394e6cde07ff3d667bbd8a
https://doi.org/10.3389/fendo.2023.1170449
https://doi.org/10.3389/fendo.2023.1170449
Autor:
Zorana Grubic, Marija Burek Kamenaric, Marija Maskalan, Nadira Durakovic, Radovan Vrhovac, Katarina Stingl Jankovic, Ranka Serventi Seiwerth, Renata Zunec
Introduction We investigated the association of HLA on clinical outcomes in our cohort of patients in the haplo-HSCT program using the HLAMatchmaker (EM) and PIRCHE score (PS) algorithms. Methods The group comprised 64 patients (male = 35–54.7%, fe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0c606353582c9ffcc7fd92085632f77
https://www.bib.irb.hr/1194296
https://www.bib.irb.hr/1194296
Autor:
Marija Maskalan, Renata Zunec, Marija Burek Kamenaric, Nadira Duraković, Radovan Vrhovac, Mirta Mikulić, Zorana Grubic, Ranka Serventi Seiwerth, Katarina Stingl Jankovic
Publikováno v:
Human Immunology. 81:12-17
Matching for HLA-A, -B, -C, -DRB1, -DQB1 alleles is the gold standard in hematopoietic stem cell transplantation (HSCT). However, this is often not enough to prevent postransplantational complications. The HLA mismatches (MM) have been associated wit
Autor:
Zorana Grubic, Marija Maskalan, Renata Zunec, Marija Burek Kamenaric, Nadira Duraković, Ranka Serventi-Seiwerth, Radovan Vrhovac, Katarina Stingl Jankovic
Publikováno v:
HLA. 94:16-20
Chimerism status evaluation is a routine test performed in post-hematopoietic stem cell transplantation (HSCT) period. The aim of the study was to evaluate a quantitative polymerase chain reaction (qPCR) method (GenDx, Utrecht, the Netherlands) appli
Autor:
Zorana Grubic
Publikováno v:
ISBT Science Series. 15:164-173