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Identification of a new HLA‐B null allele, B*1817 N, in a family

Data up to Jan 2025

Published2002
Citations8
References14

Total Citations Per Year

Abstract

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

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Identification of a new HLA‐B null allele, B*1817 N, in a family (2002) – Tissue Antigens | Metascience Observatory Explorer