Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Blanka Vidan Jeras"'
Publikováno v:
Zdravniški Vestnik, Vol 81, Iss SUPL II (2012)
Background: HSC transplantation outcome is associated with the level of HLA matching between donor and recipient. A search for HSC donor starts in the patient’s family. In the absence of related donor, HLA matched unrelated donors are searched in r
Externí odkaz:
https://doaj.org/article/b3ba5da69d8c46eaab31f156c108113b
Autor:
Jožef Pretnar, Mihael Tonejc, Blanka Vidan Jeras, Cvetka Cotič Flajs, Irena Preložnik Zupan, Matjaž Sever
Publikováno v:
Zdravniški Vestnik, Vol 81, Iss SUPL II (2012)
Objectives: Allogeneic stem-cell transplantation is an efficient treatment modality for adult patients with various leukemias. Due to the lack of family donors, stem-cell transplantation with unrelated HLA identical donors is on the increase. In the
Externí odkaz:
https://doaj.org/article/0a3ced5522f744608da3932862ebb279
Autor:
Annette Fink, Dianne De Santis, Manuela Testi, Marcel G.J. Tilanus, Blanka Vidan-Jeras, Thuong Hien Tran, Gottfried Fischer, Mathijs Groeneweg, Ingrid Fae, Marco Andreani, Ben M. Matern, Christina E.M. Voorter, R. Whidborne, Sendi Montanic
Publikováno v:
Human Immunology. 79(11):763-772
The gold standard for typing at the allele level of the highly polymorphic Human Leucocyte Antigen (HLA) gene system is sequence based typing. Since sequencing strategies have mainly focused on identification of the peptide binding groove, full-lengt
Autor:
Katja Goričar, Darja Smigoc Schweiger, Andrijana Mendez, Tadej Battelino, Blanka Vidan-Jeras, Vita Dolzan, Tinka Hovnik, Natasa Bratina, Jernej Brecelj
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
Genetic polymorphisms in genes coding for inflammasome components nucleotide-binding oligomerization domain leucine rich repeat and pyrin domain-containing protein 3 (NLRP3) and caspase recruitment domain-containing protein 8 (CARD8) have been associ
Autor:
Blanka Vidan-Jeras
Publikováno v:
HLA. 92
Type1 diabetes (T1D) and celiac disease (CD) may occur together. HLA-DQ8 and DQ2 are key genetic risk factors in both. Overall, the patients with co-existing T1D and CD (T1D+CD) were shown to have HLA profile more similar to patients with T1D than th
Autor:
Andrijana Mendez, Jernej Brecelj, Tadej Battelino, D. Smigoc Schweiger, S. Kunilo Jamnik, Nina Bratanic, Blanka Vidan-Jeras, Natasa Bratina
Publikováno v:
Tissue Antigens. 84:471-478
The prevalence of celiac disease (CD) in patients with type 1 diabetes (T1D) has been reported to be 5-7 times higher than in the general population. Risk factors for co-occurrence of both diseases have not been entirely established. The aim of our s
Autor:
Miha Arnol, Nika Kojc, Aljoša Kandus, Gregor Mlinšek, Blanka Vidan-Jeras, Manca Oblak, Jadranka Buturović-Ponikvar
Publikováno v:
Transplantation. 102:S210-S211
Autor:
Nina Bratanic, Sabina Kunilo Jamnik, Andrijana Mendez, Natasa Bratina, Blanka Vidan-Jeras, Darja Smigoc Schweiger, Jernej Brecelj, Tadej Battelino
Publikováno v:
Autoimmunity. 49(4)
Shared susceptibility alleles in the HLA region contribute to the co-existence of type 1 diabetes (T1D) and celiac disease (CD). The aim of our study was to identify HLA genotype variations that influence co-occurrence of T1D and CD (T1D + CD) and th
Publikováno v:
Clinical and Vaccine Immunology. 18:1435-1440
Major histocompatibility complex (MHC) class I and class II genes regulate the balance between appropriate aggressive responses and invading pathogens while minimizing the destruction of host tissue. Several studies have shown that in hemorrhagic fev
Publikováno v:
Open Life Sciences, Vol 5, Iss 3, Pp 324-330 (2010)
The Major Histocompatibility Complex (MHC) is a large gene family that is found in most vertebrates and has an important influence on body odour preference and mate selection in animals. In this research we found, that human leukocyte antigen (HLA) p