Characterization of a novel MICB variant in an individual from the Chinese Uyghur population, MICB*005:09, by cloning and sequencing.

Abstract:

:A new allelic variant in MICB*005 lineage, MICB*005:09, has been identified in a male Uyghur individual recruited from Xinjiang Uyghur Autonomous Region, China by PCR-sequence-based typing (Sanger sequencing) and confirmed by cloning and sequencing. Aligned with MICB*005:03, this new allelic variant shows a synonymous T substitution at nucleotide position 8 in exon 2, corresponding to codon 3 (CAC→CAT) of the mature MICB mRNA transcript.

journal_name

Int J Immunogenet

authors

Tursun M,Wang Z,Guo W,Hasim A,Tian W

doi

10.1111/iji.12410

subject

Has Abstract

pub_date

2019-02-01 00:00:00

pages

17-19

issue

1

eissn

1744-3121

issn

1744-313X

journal_volume

46

pub_type

杂志文章
  • CTLA-4 gene polymorphism of exon 1(+49 A/G) in Turkish systemic lupus erythematosus patients.

    abstract::Cytotoxic T lymphocyte-associated antigen-4 is a cell-surface molecule providing a negative signal for T cell activation. CTLA-4 gene polymorphisms are known to be related with genetic susceptibility to various autoimmune diseases, including systemic lupus erythematosus (SLE). However, the effects of this polymorphism...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2009.00856.x

    authors: Ulker M,Yazisiz V,Sallakci N,Avci AB,Sanlioglu S,Yegin O,Terzioglu E

    更新日期:2009-08-01 00:00:00

  • The complement-mediated prozone effect in the Luminex single-antigen bead assay and its impact on HLA antibody determination in patient sera.

    abstract::The Luminex xMAP system has become an important tool for HLA antibody screening and identification in sera of transplant patients. Recently, the Luminex single antigen bead assay was shown to be prone to an artefact, the so called prozone phenomenon: Sera with high titer HLA antibodies gave negative results when teste...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章,评审

    doi:10.1111/j.1744-313X.2012.01147.x

    authors: Weinstock C,Schnaidt M

    更新日期:2013-06-01 00:00:00

  • Presence of the functional CASPASE-12 allele in Indian subpopulations.

    abstract::Most humans lack a functional CASP12 gene, with the nonfunctional variant (CASP12p1), found in 100% of the Caucasian and east Asian population, and in approximately 80% of people of African descent. However, 20% of Africans carry an intact allele of CASP12, which produces a full-length pro-enzyme and increases the ris...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2012.01107.x

    authors: Yavari M,Brinkley G,Klapstein KD,Hartwig WC,Rao R,Hermel E

    更新日期:2012-10-01 00:00:00

  • IL-18 gene promoter -137C/G and -607C/A polymorphisms in Chinese Han children with type 1 diabetes mellitus.

    abstract::Type 1 diabetes mellitus (T1DM) is a heterogeneous autoimmune disease, and both environmental and genetic factors play a role in its pathogenesis. Interleukin (IL)-18 is a potent pro-inflammatory cytokine capable of inducing interferon-gamma production that is associated with the development of T1DM. The gene for IL-1...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2007.00665.x

    authors: Dong GP,Yu ZS,Liang L,Zou CC,Fu JF,Wang CL

    更新日期:2007-04-01 00:00:00

  • FcγRIIB-nt645+25A/G gene polymorphism and periodontitis in Japanese women with preeclampsia.

    abstract::FcγRIIB contains a unique immunoreceptor tyrosine-based inhibition motif (ITIM) and functions as a negative feedback regulator of leucocyte activation and antibody production. We have previously reported FcγRIIB-nt645+25A/G gene polymorphism to be associated with prevalence and severity of periodontitis, FcγRIIB expre...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2012.01124.x

    authors: Wang Y,Sugita N,Kikuchi A,Iwanaga R,Hirano E,Shimada Y,Sasahara J,Tanaka K,Yoshie H

    更新日期:2012-12-01 00:00:00

  • Analysis of ERCC2/XPD functional polymorphisms in systemic lupus erythematosus.

    abstract::Sunlight/ultraviolet (UV) irradiation has been recognized as an important risk factor for developing systemic lupus erythematosus (SLE). However, the interpretation of genetic variations involved in UV-light sensitivity is largely unknown. Recent studies indicated that two genetic variations of ERCC2/XPD gene (rs17997...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2008.00817.x

    authors: Wan L,Lin YJ,Sheu JJ,Huang CM,Tsai Y,Tsai CH,Wong W,Tsai FJ

    更新日期:2009-02-01 00:00:00

  • Association between FokI, ApaI and TaqI RFLP polymorphisms in VDR gene and Hashimoto's thyroiditis: preliminary data from female patients in Serbia.

    abstract::Hashimoto's thyroiditis (HT) is the most prevalent autoimmune thyroid disorder caused by an interaction between genes and environmental triggers. Intrathyroid lymphocytic infiltration may lead to progressive destruction of thyroid tissue and consequently to hypothyroidism. Many studies in different populations have sh...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12199

    authors: Djurovic J,Stojkovic O,Ozdemir O,Silan F,Akurut C,Todorovic J,Savic K,Stamenkovic G

    更新日期:2015-06-01 00:00:00

  • Region 1p13.2 including the RSBN1, PTPN22, AP4B1 and long non-coding RNA genes does not bear risk factors for endemic pemphigus foliaceus (fogo selvagem).

    abstract::Pemphigus foliaceus (PF) is an autoimmune skin disease characterized by autoantibodies directed mainly against desmoglein-1. The purpose of this study was to determine whether differential susceptibility to endemic PF in Brazil (fogo selvagem) is associated with polymorphisms at the cytogenetic location 1p13.2. Four s...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12423

    authors: Lobo-Alves SC,de Oliveira LA,Petzl-Erler ML

    更新日期:2019-06-01 00:00:00

  • The clinical implications of HLA mismatches in unrelated donor haematopoietic cell transplantation.

    abstract::Haematopoietic stem cell transplantation (HSCT), using unrelated donors (UD), is now a common modality of treatment for individuals with a variety of different diseases. HLA matching has been shown to have a significant impact on patient outcome. This study includes 423 unrelated UK patient/donor pairs. The patients a...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2008.00793.x

    authors: Shaw BE

    更新日期:2008-08-01 00:00:00

  • Association of mannose-binding lectin polymorphisms and HBV outcome in a South Indian population.

    abstract::Mannose binding lectin (MBL) is an important innate immune system pattern recognition molecule. The MBL gene polymorphisms are reported to play a crucial role in outcome of hepatitis B virus (HBV) infection. In this study, we ascertained the association of MBL genotypes with HBV outcome in a South Indian population. T...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2010.00908.x

    authors: Fletcher GJ,Gnanamony M,Samuel P,Ismail AM,Kannangai R,Daniel D,Eapen CE,Abraham P

    更新日期:2010-06-01 00:00:00

  • A clinical case-control study on the association between mannose-binding lectin and susceptibility to HIV-1 infection among northern Han Chinese population.

    abstract::Mannose-binding lectin (MBL) is a key molecule of the innate immune system and a competent to bind carbohydrates of a variety of microorganisms, resulting in complement activation and opsonophagocytosis against various pathogens. However, there is no systemic investigation on the MBL's role in innate immune responses ...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2010.00946.x

    authors: Sheng A,Lan J,Wu H,Lu J,Wang Y,Chu Q,Jia Z,Song M,Liu L,Wang W

    更新日期:2010-12-01 00:00:00

  • Coenzyme Q plays opposing roles on bacteria/fungi and viruses in Drosophila innate immunity.

    abstract::Coenzyme Q (CoQ or ubiquinone) is a lipid-soluble component of virtually all types of cell membranes and has been shown to play multiple metabolic functions. Several clinical diseases including encephalomyopathy, cerebellar ataxia and isolated myopathy were shown to be associated with CoQ deficiency. However, the role...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2011.01012.x

    authors: Cheng W,Song C,Anjum KM,Chen M,Li D,Zhou H,Wang W,Chen J

    更新日期:2011-08-01 00:00:00

  • Frequencies of MICA alleles in patients from southern Brazil with multibacillary and paucibacillary leprosy.

    abstract::Leprosy is a chronic infectious disease caused by Mycobacterium leprae, which mainly affects the skin and nervous system. The disease has several clinical forms. This study investigated the MICA and HLA-B genes in 223 samples from leprosy patients and 201 samples from healthy individuals matched for age, gender and et...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2011.01074.x

    authors: do Sacramento WS,Mazini PS,Franceschi DA,de Melo FC,Braga MA,Sell AM,Tsuneto LT,Visentainer JE

    更新日期:2012-06-01 00:00:00

  • CCR5 genetic variants and epidemiological determinants for HPV infection and cervical premalignant lesions.

    abstract::Human papillomavirus (HPV) infection can lead to the development of productive epithelial lesions and cervical cancer. Most cervical HPV infections are solved by cell-mediated immunity within 1-2 years, and it is known that chronic inflammation predisposes to lesions progression and tumour development. In this context...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12444

    authors: Mangieri LFL,Sena MM,Cezar-Dos-Santos F,Trugilo KP,Okuyama NCM,Pereira ÉR,Maria GCQ,Watanabe MAE,de Oliveira KB

    更新日期:2019-10-01 00:00:00

  • A chromosomal event resulting in possession and expression of multiple HLA-B and Cw genes in a renal patient.

    abstract::Routine HLA typing of a renal patient for purposes of registration for transplantation revealed an unusual human leucocyte antigen (HLA)-B and Cw genotype, with three specificities detected. Results were confirmed in a second sample, and in a second laboratory. The possibility of these results reflecting a chimaeric s...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2006.00610.x

    authors: Poole K,Montague B,Roberts R,Stoves J,Bendukidze N,Clark B

    更新日期:2006-08-01 00:00:00

  • Molecular diversity of HLA-A, -B and -C alleles in a North Indian population as determined by PCR-SSOP.

    abstract::We have used molecular methods to determine the frequencies of human leukocyte antigen (HLA)-A, -B and -C alleles in normal, healthy, unrelated individuals from North India using polymerase chain reaction and hybridization with sequence-specific oligonucleotide probes as there is no comprehensive report showing molecu...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2007.00677.x

    authors: Rani R,Marcos C,Lazaro AM,Zhang Y,Stastny P

    更新日期:2007-06-01 00:00:00

  • Study on the polymorphisms of HLA-ABCDQB1DRB1 alleles and haplotypes in Hubei Han population of China.

    abstract::The present study aimed to analyse the frequencies of human leukocyte antigen HLA-ABCDQB1 and HLA-DRB1 alleles and haplotypes in a subset of 3,732 Han population from Hubei of China. All samples were typed in the HLA-ABCDQB1 and HLA-DRB1 loci using the sequence-based typing method; subsequently, the HLA polymorphisms ...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12516

    authors: Zou J,Shen G,Qiang W,Zhu YY,Li WX

    更新日期:2021-02-01 00:00:00

  • Phenotypic and allelic profile of ABO and Rhésus D blood group system among blood donor in Antananarivo.

    abstract::This study assessed the phenotypic and allelic profiles of ABO and Rhesus D blood group system among first time blood donors at the National Centre of Blood Supply of Antananarivo. We collected through this retrospective study all data registered during 7 years of practice (from 2003 to 2009). Age and sex were analyse...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2012.01120.x

    authors: Randriamanantany ZA,Rajaonatahina DH,Razafimanantsoa FE,Rasamindrakotroka MT,Andriamahenina R,Rasoarilalamanarivo FB,Hanitriniala SP,Herisoa FR,Rasamindrakotroka A,Rakoto Alson OA

    更新日期:2012-12-01 00:00:00

  • Th-1 cytokines gene polymorphism in human brucellosis.

    abstract::Brucellosis is a worldwide zoonosis. Infection with Brucella species results in the activation of cell-mediated immune response. The interaction between Th1and Th2 cytokines determines the outcome of disease. Production of each cytokine is in turn affected by genetic factors. In this study, we investigated the possibl...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2006.00626.x

    authors: Davoudi S,Amirzargar AA,Hajiabdolbaghi M,Rasoolinejad M,Soodbakhsh A,Jafari S,Piri H,Maleknejad P,Bagherian H,Madadi N,Nikbin B

    更新日期:2006-10-01 00:00:00

  • Solid phase testing in the HLA laboratory: implications for organ allocation.

    abstract::This piece was originally requested as a white paper from the Scientific and Clinical Affairs Committee of the American Society for Histocompatibility and Immunogenetics (ASHI), of which the author was then Chairman. Upon review by the ASHI Board of Directors and the Editors of their journal, it was considered too con...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章,评审

    doi:10.1111/j.1744-313X.2008.00768.x

    authors: Eckels DD

    更新日期:2008-08-01 00:00:00

  • The molecular characterization of a catalase from Chinese mitten crab Eriocheir sinensis.

    abstract::Catalase (CAT) is an antioxidant enzyme and plays a significant role in the protection against oxidative stress by reducing hydrogen peroxide. The CAT cDNA of Eriocheir sinensis (EsCAT) was cloned via RACE technique. The complete sequence of EsCAT cDNA consisted of a 5' untranslated regions (UTR) of 224 bp, a 3' UTR o...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12019

    authors: Wang M,Wang L,Zhou Z,Gao Y,Wang L,Shi X,Gai Y,Mu C,Song L

    更新日期:2013-06-01 00:00:00

  • Characterization of the novel HLA-DQB1*06:48 allele by group-specific sequencing.

    abstract::HLA-DQB1*06:48 has single nucleotide polymorphisms within codons 70 and 62 of exon 2 (GGG>AGG and AAG>AAC) relative to HLA-DQB1*06:02:01 and HLA-DQB1*06:37. This results in amino acid differences (G>R and K>N) that will change the polarity and charge of the encoded antigen and may therefore affect its peptide repertoi...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12004

    authors: Foster L,Tate D,Poulton K

    更新日期:2013-08-01 00:00:00

  • HLA and disease: guilt by association.

    abstract::It is now over forty years since the first associations between particular HLA antigens and disease susceptibility were described, and the identification of large numbers HLA-associated diseases parallels our increased understanding of the genetic complexity of the HLA system and its extensive polymorphism. However, s...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章,评审

    doi:10.1111/iji.12088

    authors: Howell WM

    更新日期:2014-02-01 00:00:00

  • Discovery of the novel HLA-DRB1*09:01:08 allele in a Taiwanese volunteer bone marrow donor and identification of the probable HLA-A, HLA-B and HLA-DRB1 haplotype in association with DRB1*09:01:08.

    abstract::We report here the novel variant of HLA-DRB1*09:01, DRB1*09:01:08, discovered in a Taiwanese volunteer bone marrow donor by a sequence-based typing (SBT) method. The DNA sequence of DRB1*09:01:08 is identical to the sequence of DRB1*09:01:02 in exon 2 except a silent mutation at nucleotide position 261(C→T) (GCC→GCT a...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2012.01143.x

    authors: Yang KL,Lee SK,Yang SY,Kao RH,Lin CL,Lin PY

    更新日期:2013-04-01 00:00:00

  • Association of tumour necrosis factor-alpha -308 G/A promoter polymorphism with susceptibility and disease profile of rheumatoid arthritis.

    abstract::The objective was to analyze the possible involvement of tumour necrosis factor-alpha (TNF-α) -308 G/A promoter polymorphism in the susceptibility and/or the disease profile of rheumatoid arthritis (RA) in Egyptian patients. TNF-α-308 G/promoter polymorphism detection by amplification refractory mutation system (ARMS)...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2011.01028.x

    authors: Mosaad YM,Abdelsalam A,El-Bassiony SR

    更新日期:2011-10-01 00:00:00

  • TNF microsatellite alleles may confer protection against the development of lipodystrophy syndrome in Brazilian HIV patients.

    abstract::The aim of this study was to evaluate the frequency of TNFa-e microsatellites and the promoter region (TNF-308 and TNF-238) in HIV/AIDS-infected patients presenting or not lipodystrophy syndrome (LS). The design is the genetic case-control association study. Microsatellite and the TNF promoter region polymorphisms wer...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2010.00937.x

    authors: Silva MM,Simões RT,Castelli EC,Mendes-Junior CT,Deghaide NH,Tsuda LC,Machado AA,Donadi EA,Fernandes AP

    更新日期:2010-10-01 00:00:00

  • Distribution of KIR genes in the Czech population.

    abstract::Killer cells immunoglobulin-like receptors (KIRs) are a family of inhibitory and activating receptors expressed mainly by natural killer (NK) cells and few subsets of T lymphocytes. KIRs regulate NK cells' activity through interactions with specific HLA class I molecules and other yet unknown ligands presented on targ...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2007.00737.x

    authors: Pavlova Y,Kolesar L,Striz I,Jabor A,Slavcev A

    更新日期:2008-02-01 00:00:00

  • Promoter polymorphism of IL-18 gene in pulmonary tuberculosis in South Indian population.

    abstract::Interleukin-18 (IL-18) plays a vital role in both innate and acquired immunity. We analysed polymorphisms at -607(C/A) and -137(G/A) in the promoter region of IL-18 gene by allele-specific polymerase chain reaction in normal healthy subjects (n = 173) and patients with pulmonary tuberculosis (n = 165). Allele, genotyp...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2007.00714.x

    authors: Harishankar M,Selvaraj P,Rajeswari DN,Anand SP,Narayanan PR

    更新日期:2007-10-01 00:00:00

  • Association study of polymorphisms within matrix metalloproteinase 9 with bronchial asthma.

    abstract::Matrix metalloproteinase 9 plays an important role in the development of bronchial asthma. We were interested in whether the polymorphisms -T1702A, -C1562T, R279Q and +C6T within the matrix metalloproteinase 9 (MMP-9) gene were associated with asthma in a population of 231 asthmatic children. However, we found no asso...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2005.00516.x

    authors: Ganter K,Deichmann KA,Heinzmann A

    更新日期:2005-08-01 00:00:00

  • Killer cell immunoglobulin-like receptors on NK cells: the how, where and why.

    abstract::Natural killer (NK) cells have killer cell immunoglobulin-like receptors (KIR) that recognize and interact with HLA class I antigen. The KIRs are a multigene family and its members are often highly polymorphic. Evidence is emerging from disease-association studies that KIR receptors can play beneficial roles in viral ...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章,评审

    doi:10.1111/j.1744-313X.2007.00739.x

    authors: Gardiner CM

    更新日期:2008-02-01 00:00:00