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1.
Int J Immunogenet ; 45(3): 140-142, 2018 Jun.
Article in English | MEDLINE | ID: mdl-29516629

ABSTRACT

Three new HLA class I alleles were described in the Spanish population. HLA-A*68:169 and -B*39:129 show one amino acid replacement at the α1-domain, compared to A*68:02 (P47 > L47) and -B*39:06 (S11 > A11), respectively. HLA-B*07:298 presents one nucleotide mutation within exon 1, resulting in a new amino acid position -14, L>Q, which has not been previously described in any HLA protein. Prediction of the B*07:298 signal peptide cleavage did not show significant differences in comparison with that obtained for the rest of HLA-B genes.


Subject(s)
Alleles , Base Sequence , HLA-A Antigens/genetics , HLA-B Antigens/genetics , HLA-B7 Antigen/genetics , Sequence Analysis, DNA , Amino Acid Sequence , HLA-A Antigens/chemistry , HLA-B Antigens/chemistry , HLA-B7 Antigen/chemistry , Haplotypes , Humans , Peptides/chemistry
3.
Int J Immunogenet ; 44(3): 148-150, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28383785

ABSTRACT

Three new HLA class I alleles, HLA-A*02:620, HLA-B*27:150 and HLA-B*07:05:01:02, were described in the Spanish Caucasoid population.


Subject(s)
Alleles , HLA-A Antigens/genetics , HLA-B Antigens/genetics , Genes, MHC Class I/immunology , HLA-A Antigens/immunology , HLA-B Antigens/immunology , Humans , Spain , White People/genetics
5.
Tissue Antigens ; 85(2): 141-2, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25626608

ABSTRACT

HLA-B*18:105 shows two nucleotide differences regarding B*18:22 (97 AGC>AGG, 99 TAC>TAT) and B*18:52 (94 ACC>ATC, 95 CTC>ATC).


Subject(s)
Alleles , HLA-B Antigens/genetics , Hispanic or Latino/genetics , White People/genetics , Base Sequence , Exons/genetics , Humans , Molecular Sequence Data , Sequence Alignment
8.
Tissue Antigens ; 86(5): 385-6, 2015 Nov.
Article in English | MEDLINE | ID: mdl-26399227

ABSTRACT

Two new HLA-B*35 alleles, B*35:270 and B*35:273, were characterized in the Spanish population.


Subject(s)
Alleles , HLA-B35 Antigen/genetics , Female , Humans , Male , Spain
11.
Tissue Antigens ; 83(4): 297-8, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24410056

ABSTRACT

HLA-DRB1*11:153 differs from DRB1*11:131 by one nucleotide at position 286 where C > A, (codon 67 CTC>ATC), resulting in an amino acid substitution, 67L>67I.


Subject(s)
Alleles , Databases, Nucleic Acid , HLA-DRB1 Chains/genetics , Base Sequence , Humans , Molecular Sequence Data
14.
Tissue Antigens ; 81(3): 177-8, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23360107

ABSTRACT

HLA-B*49:24 shows one nucleotide difference regarding B*49:10 at codon 12 (ATG>GTG). DRB1*03:64 differs from DRB1*03:01:01 in one amino acid residue at position 59, E>Q.


Subject(s)
Alleles , HLA-B Antigens/genetics , HLA-DRB1 Chains/genetics , Sequence Analysis, DNA , Amino Acid Sequence , HLA-B Antigens/chemistry , HLA-DRB1 Chains/chemistry , Humans , Molecular Sequence Data , Protein Structure, Tertiary
15.
Tissue Antigens ; 82(3): 211-2, 2013 Sep.
Article in English | MEDLINE | ID: mdl-24032732

ABSTRACT

The new HLA-DPB1*142:01 allele differs from DPB1*26:01:02 and DPB1*56:01 at codons 65 (I65>L65) and 35 (F35>Y35), respectively.


Subject(s)
Alleles , Graft Rejection , HLA-DP beta-Chains/genetics , Kidney Transplantation , Polymorphism, Single Nucleotide , Base Sequence , Codon , Exons , Fatal Outcome , Histocompatibility Testing , Humans , Molecular Sequence Data , Peru , Sequence Alignment , Sequence Analysis, DNA , Tissue Donors
18.
Tissue Antigens ; 80(3): 268-70, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22724558

ABSTRACT

B*08:79 is composed by partial B*08:01:01 and B*07:06 sequences because of a possible recombination event within intron 2.


Subject(s)
Alleles , Exons/genetics , Genome, Human/genetics , HLA-B7 Antigen/genetics , HLA-B8 Antigen/genetics , Recombination, Genetic/genetics , Base Sequence , Humans , Molecular Sequence Data
19.
Tissue Antigens ; 79(4): 291-4, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22251067

ABSTRACT

To determine the complete sequence of a newly identified human leukocyte antigen (HLA)-C allele, we designed a method where the full genomic sequence of HLA-C*04 was amplified in isolation from the patient second HLA-C allele in a single polymerase chain reaction (PCR), using primers spanning its 5'- and 3'-untranslated regions. The new allele, officially designated HLA-C*04:71, differs from HLA-C*04:01:01:01 by two single-nucleotide polymorphisms: one determines substitution of phenylalanine for serine 9 at the B pocket of the peptide-binding site; the second substitution is a new polymorphism in intron 5. Phe-9 is characteristic of Cw1 alleles and its presence in C*04:71 most likely affects its peptide-binding repertoire. The principle we have used for C*04:71 isolation could be adapted for unambiguous sequence-based HLA-C typing of selected samples in a clinical setting.


Subject(s)
Alleles , HLA-C Antigens/genetics , Peptides/chemistry , Amino Acid Motifs , Base Sequence , Crystallography, X-Ray , Female , Genomics , HLA-C Antigens/chemistry , Humans , Molecular Sequence Data , Protein Binding , Sequence Alignment
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