PMID- 27984624
OWN - NLM
STAT- MEDLINE
DCOM- 20170710
LR  - 20170713
IS  - 1003-9406 (Print)
IS  - 1003-9406 (Linking)
VI  - 33
IP  - 6
DP  - 2016 Dec 10
TI  - [Progress in research on genetic polymorphisms and sequence-based typing of KIR 
      genes].
PG  - 867-870
AB  - Killer cell immunoglobulin-like receptors (KIRs) are members of the 
      immunoglobulin superfamily expressed on natural killer (NK) cells and a subset of 
      T cells. Given the receptor-ligand relationship between certain KIR and human 
      leukocyte antigen (HLA) classⅠmolecules, the KIRs are involved in the regulation 
      of NK cell activation through conveying activating or inhibitory signals, which 
      plays an important role in immunities involved in transplantation, tumor, 
      infection as well as autoimmune diseases. This paper has provided a review for 
      the research on KIR gene polymorphisms and summarized the characteristics of the 
      sequence-based typing method for KIR genes.
FAU - Zhen, Jianxin
AU  - Zhen J
AD  - Shenzhen Blood Center, Shenzhen, Guangdong 518035, China. zhihui_deng@aliyun.com.
FAU - Yu, Qiong
AU  - Yu Q
LA  - chi
PT  - Journal Article
PT  - Review
PL  - China
TA  - Zhonghua Yi Xue Yi Chuan Xue Za Zhi
JT  - Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese 
      journal of medical genetics
JID - 9425197
RN  - 0 (HLA Antigens)
RN  - 0 (Histocompatibility Antigens Class I)
RN  - 0 (Receptors, KIR)
SB  - IM
MH  - HLA Antigens/genetics
MH  - Histocompatibility Antigens Class I/*genetics
MH  - Humans
MH  - Killer Cells, Natural/metabolism
MH  - Polymorphism, Genetic/*genetics
MH  - Receptors, KIR/*genetics
EDAT- 2016/12/17 06:00
MHDA- 2017/07/14 06:00
CRDT- 2016/12/17 06:00
PHST- 2016/12/17 06:00 [entrez]
PHST- 2016/12/17 06:00 [pubmed]
PHST- 2017/07/14 06:00 [medline]
AID - 940633181 [pii]
AID - 10.3760/cma.j.issn.1003-9406.2016.06.027 [doi]
PST - ppublish
SO  - Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Dec 10;33(6):867-870. doi: 
      10.3760/cma.j.issn.1003-9406.2016.06.027.