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Tissue Antigens

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https://www.readbyqxmd.com/read/26707816/description-of-the-novel-hla-dqb1-02-02-01-02-allele-in-a-spanish-individual
#1
G Montero-Martín, I Cervera, A Teniente-Serra, M Fonolleda, J Martinez-Laso
HLA-DQB1*02:02:01:02 has an intron sequences coming from a combination of DQB1*02:01:01 and DQB1*02:02:01:01.
December 28, 2015: Tissue Antigens
https://www.readbyqxmd.com/read/26648393/a-novel-hla-c-null-allele-hla-c-08-121n
#2
X Zhang, E F Reed
HLA-C*08:121N results from two-nucleotide loss compared with its closest allele HLA-C*08:01:01.
December 9, 2015: Tissue Antigens
https://www.readbyqxmd.com/read/26638973/identification-of-a-novel-hla-a-02-allele-hla-a-02-432-in-a-chinese-individual
#3
S-Z Jin, Z Li, H-Y Zou
A*02:432 differs from A*02:07:01 by one nucleotide change at nucleotide 572 in exon 3 from G to C.
December 7, 2015: Tissue Antigens
https://www.readbyqxmd.com/read/26625936/the-profile-of-hla-drb1-alleles-in-arabs-with-type-1-diabetes-meta-analyses
#4
A R Hamzeh, P Nair, M T Al Ali
Genes from the HLA complex have a major contribution in type 1 diabetes (T1D), which results from an interplay between environmental and genetic factors. The latter can explain some of the geographic variability in T1D occurrence around the world. Of a particular importance in this regard are the HLA-DR, -DP and -DQ loci. Consequently, we aimed at elucidating the collective genetic profiles of various alleles relating to HLA-DRB1 and -DP in T1D patients throughout the Arab World using the tools of meta-analysis...
December 2, 2015: Tissue Antigens
https://www.readbyqxmd.com/read/26628408/increasing-polymorphism-of-the-raet1e-ulbp4-gene-in-humans
#5
H Pearson, J Alejandro Madrigal, A Saudemont, S T Cox
Description of three novel RAET1E/ULBP4 allele and promoter polymorphisms identified by sequence-based typing.
December 1, 2015: Tissue Antigens
https://www.readbyqxmd.com/read/26628274/genomic-full-length-sequence-of-two-hla-a-alleles-a-23-01-01-and-a-24-02-01-01-identified-by-cloning-and-sequencing
#6
S X Wang, Y P Xu, H Zhang
Genomic full-length sequences of HLA-A*23:01:01 and A*24:02:01:01, identified by cloning and sequencing from Chinese donors.
December 1, 2015: Tissue Antigens
https://www.readbyqxmd.com/read/26628075/genomic-full-length-sequence-of-two-hla-a-alleles-a-24-03-01-and-a-24-07-01-identified-by-cloning-and-sequencing
#7
Y P Xu, S X Wang
Genomic full length sequences of HLA-A*24:03:01 and A*24:07:01, identified by cloning and sequencing Chinese donors.
December 1, 2015: Tissue Antigens
https://www.readbyqxmd.com/read/26625719/hla-a-02-06-21-a-novel-variant-of-hla-a-02-06-discovered-in-a-taiwanese-bone-marrow-hematopoietic-stem-cell-donor
#8
K L Yang, J Ng, A Lazaro, J H Hung, P Y Lin
One nucleotide substitution at residue 318 of the HLA-A*02:06:01:01 results in a new allele, HLA-A*02:06:21.
December 1, 2015: Tissue Antigens
https://www.readbyqxmd.com/read/26593759/corrigendum
#9
(no author information available yet)
No abstract text is available yet for this article.
December 2015: Tissue Antigens
https://www.readbyqxmd.com/read/26593758/nomenclature-for-factors-of-the-hla-system-update-september-2015
#10
Steven G E Marsh
No abstract text is available yet for this article.
December 2015: Tissue Antigens
https://www.readbyqxmd.com/read/26593757/nomenclature-for-factors-of-the-hla-system-update-august-2015
#11
Steven G E Marsh
No abstract text is available yet for this article.
December 2015: Tissue Antigens
https://www.readbyqxmd.com/read/26593756/nomenclature-for-factors-of-the-hla-system-update-july-2015
#12
Steven G E Marsh
No abstract text is available yet for this article.
December 2015: Tissue Antigens
https://www.readbyqxmd.com/read/26593755/four-amino-acid-exchanges-located-in-the-alpha-2-domain-specify-the-novel-hla-b-50-20-allele
#13
COMPARATIVE STUDY
P S A Becker, E Seifried, C Seidl
HLA-B*50:20 contains seven nucleotide substitutions leading to four amino acid changes in the alpha-2 domain.
December 2015: Tissue Antigens
https://www.readbyqxmd.com/read/26593754/a-novel-hla-a-02-variant-hla-a-02-575-detected-in-a-taiwanese-bone-marrow-hematopoietic-stem-cell-donor
#14
COMPARATIVE STUDY
K L Yang, J H Hung, P Y Lin
One nucleotide substitution at residue 410 of HLA-A*02:07:01 results in a new allele, HLA-A*02:575.
December 2015: Tissue Antigens
https://www.readbyqxmd.com/read/26593753/identification-of-a-novel-hla-a-02-06-01-02-allele-in-a-chinese-individual-by-sequence-based-typing
#15
COMPARATIVE STUDY
J Kwok, J C Y Ho, Y S Chan, A Soormally, S G E Marsh
The new HLA-A*02:06:01:02 allele differs from HLA-A*02:06:01 by a C→G substitution in Intron 1.
December 2015: Tissue Antigens
https://www.readbyqxmd.com/read/26593752/genetic-variation-of-the-mhc-class-ii-drb-genes-in-the-japanese-weasel-mustela-itatsi-endemic-to-japan-compared-with-the-siberian-weasel-mustela-sibirica
#16
Y Nishita, A V Abramov, P A Kosintsev, L-K Lin, S Watanabe, K Yamazaki, Y Kaneko, R Masuda
Major histocompatibility complex (MHC) genes encode proteins that play a critical role in vertebrate immune system and are highly polymorphic. To further understand the molecular evolution of the MHC genes, we compared MHC class II DRB genes between the Japanese weasel (Mustela itatsi), a species endemic to Japan, and the Siberian weasel (Mustela sibirica), a closely related species on the continent. We sequenced a 242-bp region of DRB exon 2, which encodes antigen-binding sites (ABS), and found 24 alleles from 31 M...
December 2015: Tissue Antigens
https://www.readbyqxmd.com/read/26593751/changes-to-tissue-antigens
#17
EDITORIAL
James McCluskey, Redmond Barry
No abstract text is available yet for this article.
December 2015: Tissue Antigens
https://www.readbyqxmd.com/read/26555242/questionable-expression-of-unstable-dq-heterodimer-containing-hla-dqa1-01-07
#18
COMPARATIVE STUDY
H Miyadera, L B Bungener, S Kusano, S Yokoyama, K Tokunaga, B G Hepkema
Human leukocyte antigens (HLA)-DQA1*01:07 was identified as an HLA-DQ blank specificity that segregated with the serological HLA-A2, -B7, -DR14, -DR52 haplotype, which carried DQB1*05:03. The blank specificity of DQA1*01:07-DQB1*05:03 may be because of lack of reactivity of available typing sera, or disruption of proper assembly of DQ heterodimer. The cDNA sequence of DQA1*01:07 is nearly identical to DQA1*01:04 except for a variant at position 304, which results in the replacement of an arginine with a cysteine at 79α...
December 2015: Tissue Antigens
https://www.readbyqxmd.com/read/26514650/characterization-of-bovine-mhc-class-ii-drb3-diversity-in-south-american-holstein-cattle-populations
#19
COMPARATIVE STUDY
S-N Takeshima, G Giovambattista, N Okimoto, Y Matsumoto, A Rogberg-Muñoz, T J Acosta, M Onuma, Y Aida
Holstein cattle dominate the global milk production industry because of their outstanding milk production, however, this breed is susceptible to tropical endemic pathogens and suffers from heat stress and thus fewer Holstein populations are raised in tropical areas. The bovine major histocompatibility complex (BoLA)-DRB3 class II gene is used as a marker for disease and immunological traits, and its polymorphism has been studied extensively in Holstein cattle from temperate and cold regions. We studied the genetic diversity of the BoLA-DRB3 gene in South American Holstein populations to determine whether tropical populations have diverged from those bred in temperate and cold regions by selection and/or crossbreeding with local native breeds...
December 2015: Tissue Antigens
https://www.readbyqxmd.com/read/26514448/group-1-cd1-restricted-t-cells-and-the-pathophysiological-implications-of-self-lipid-antigen-recognition
#20
REVIEW
P Dellabona, M Consonni, C de Lalla, G Casorati
T cell responses are generally regarded as specific for protein-derived peptide antigens. This is based on the molecular paradigm dictated by the T cell receptor (TCR) recognition of peptide-major histocompatibility complexs, which provides the molecular bases of the specificity and restriction of the T cell responses. An increasing number of findings in the last 20 years have challenged this paradigm, by showing the existence of T cells specific for lipid antigens presented by CD1 molecules. CD1-restricted T cells have been proven to be frequent components of the immune system and to recognize exogenous lipids, derived from pathogenic bacteria, as well as cell-endogenous self-lipids...
December 2015: Tissue Antigens
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