Identification of a new HLA‐B null allele, B*1817 N, in a family
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References (14)
SEROTYPING FOR HOMOTRANSPLANTATION XVIII. REFINEMENT OF MICRODROPLET LYMPHOCYTE CYTOTOXICITY TEST
1968 • 1,151 citations
IMGT/HLA Database – a sequence database for the human major histocompatibility complex
2000 • 687 citations
Nomenclature for factors of the HLA system, 2000
2001 • 163 citations
Natural inactivation of a common HLA allele (A*2402) has occurred on at least three separate occasions.
1997 • 80 citations
HLA-A null allele with a stop codon, HLA-A * 0215N, identified in a homozygous state in a healthy adult
1995 • 54 citations
HLA class I allele (HLA-A2) expression defect associated with a mutation in its enhancer B inverted cat box in two families
1994 • 47 citations
Aberrant splicing of intron 1 creates a novel null HLA‐B*1501 allele
1999 • 44 citations
Filling in the blanks
1997 • 39 citations
Identification of the null HLA‐A2 allele, A*0232N
2000 • 24 citations
Non‐expression of HLA‐B*5111N is caused by an insertion into the cytosine island at exon 4 creating a frameshift stop codon
2001 • 17 citations
Sequence of a new class I null allele within the HLA‐B44 specificity
2000 • 17 citations
An HLA‐B null allele (B*0808N) caused by a nucleotide deletion in exon 3, found in the family of a bone marrow transplant recipient
2000 • 16 citations
Presence of the DRB4*0103102N null allele in different DRB1*04‐positive individuals
2000 • 14 citations
A novel HLA‐B null allele (B*4022N) generated by a nonsense codon in the α1 domain
2000 • 13 citations