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Characterisation of the Novel HLA‐B*58:139 Allele by Next‐Generation Sequencing.
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- HLA: Immune Response Genetics, 2024, v. 104, n. 4, p. 1, doi. 10.1111/tan.15721
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- Article
Establishment and Application of a Multiplex PCR NGS Method for the Genotyping of HLA‐Class I and HPA.
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- HLA: Immune Response Genetics, 2024, v. 104, n. 4, p. 1, doi. 10.1111/tan.15716
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- Article
Analysis of KIR and HLA Polymorphism in Chinese Individuals With COVID‐19.
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- HLA: Immune Response Genetics, 2024, v. 104, n. 4, p. 1, doi. 10.1111/tan.15715
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- Article
Full annotation of viral metagenomics in different components from chinese blood donors using next-generation sequencing.
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- Blood Transfusion (17232007), 2024, v. 22, n. 5, p. 140, doi. 10.2450/BloodTransfus.451
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- Article
Full annotation of viral metagenomics in different components from Chinese blood donors using next-generation sequencing.
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- Blood Transfusion (17232007), 2024, v. 22, n. 2, p. 140, doi. 10.2450/BloodTransfus.451
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- Article
Seroprevalence of transfusion-transmissible infectious agents among volunteer blood donors between 2006 and 2012 in Zhejiang, China.
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- Blood Transfusion (17232007), 2015, v. 13, n. 3, p. 401, doi. 10.2450/2015.0271-14
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- Article
Variants of CD36 gene and their association with CD36 protein expression in platelets.
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- Blood Transfusion (17232007), 2014, v. 12, n. 4, p. 557, doi. 10.2450/2014.0209-13
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- Article
A pilot study on screening blood donors with individual-donation nucleic acid testing in China.
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- Blood Transfusion (17232007), 2014, v. 12, n. 2, p. 172, doi. 10.2450/2013.0095-13
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- Article
Genotyping of human neutrophil antigens by polymerase chain reaction sequence-based typing.
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- Blood Transfusion (17232007), 2014, v. 12, p. s292, doi. 10.2450/2013.0308-12
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- Article
Mechanism evaluation for an amino acid substitution p.Y246C of B‐glycosyltransferase enzyme with Bweak phenotype.
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- Vox Sanguinis, 2021, v. 116, n. 4, p. 464, doi. 10.1111/vox.13041
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- Article
HLA‐A*02:06 allele may be susceptible to myelodysplastic syndrome in Zhejiang Han population, China.
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- International Journal of Immunogenetics, 2023, v. 50, n. 5, p. 233, doi. 10.1111/iji.12629
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- Article
The polymorphism of HLA-A, -C, -B, -DRB3/4/5, -DRB1, -DQB1 loci in Zhejiang Han population, China using NGS technology.
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- International Journal of Immunogenetics, 2021, v. 48, n. 6, p. 485, doi. 10.1111/iji.12554
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- Article
The distributions of HLA‐A, HLA‐B, HLA‐C, HLA‐DRB1 and HLA‐DQB1 allele and haplotype at high‐resolution level in Zhejiang Han population of China.
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- International Journal of Immunogenetics, 2019, v. 46, n. 1, p. 7, doi. 10.1111/iji.12411
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- Article
Characterization of three new HLA Class I Alleles in Chinese individuals, HLA‐B*46:68,‐B*46:71,‐B*46:72.
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- International Journal of Immunogenetics, 2018, v. 45, n. 6, p. 351, doi. 10.1111/iji.12394
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- Article
Characterization of a novel allelic variant in HLA‐B*46:01 lineage, HLA‐B*46:01:25, by cloning, phasing and sequencing.
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- International Journal of Immunogenetics, 2018, v. 45, n. 6, p. 347, doi. 10.1111/iji.12392
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- Article
Analysis of the Genomic Sequence of ABO Allele Using Next-Generation Sequencing Method.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.814263
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- Article
The Significance of RHD Genotyping and Characteristic Analysis in Chinese RhD Variant Individuals.
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- Frontiers in Immunology, 2021, v. 12, p. 1, doi. 10.3389/fimmu.2021.755661
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- Article
Cord Blood Banking and Transplantation in China: A Ten Years Experience of a Single Public Bank.
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- Transfusion Medicine & Hemotherapy, 2012, v. 39, n. 1, p. 23, doi. 10.1159/000335720
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- Article
Molecular basis for para-Bombay phenotypes in Chinese persons, including a novel nonfunctional FUT1 allele.
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- Transfusion, 2005, v. 45, n. 5, p. 725, doi. 10.1111/j.1537-2995.2005.04305.x
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- Article
Bacterial Analysis of the Whole Blood in Chinese Healthy Donors Using 16S rDNA–Targeted Metagenomic Sequencing.
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- Canadian Journal of Infectious Diseases & Medical Microbiology, 2024, v. 2024, p. 1, doi. 10.1155/2024/6635560
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- Article
Prevalence and Residual Risk of HIV in Volunteer Blood Donors of Zhejiang Province, China, from 2018 to 2022.
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- Canadian Journal of Infectious Diseases & Medical Microbiology, 2024, v. 2024, p. 1, doi. 10.1155/2024/4749097
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- Article
A Novel c.796 A>C Mutation in the ABO*B.01 Allele Responsible for CisAB Phenotype.
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- Transfusion Medicine & Hemotherapy, 2020, v. 47, n. 4, p. 288, doi. 10.1159/000501107
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- Article
Seroprevalence of human T-lymphotropic virus infection among blood donors in China: a first nationwide survey.
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- Retrovirology, 2021, v. 18, n. 1, p. 1, doi. 10.1186/s12977-020-00546-w
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- Article
Determination for KIR genotype and allele copy number via real-time quantitative PCR method.
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- Immunogenetics, 2024, v. 76, n. 2, p. 137, doi. 10.1007/s00251-023-01331-7
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- Article
The characteristic of HLA-A, HLA-B, HLA-C, HLA-DRB1, HLA-DRB3/4/5, HLA-DQA1, HLA-DQB1, HLA-DPA1, and HLA-DPB1 alleles in Zhejiang Han population.
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- Immunogenetics, 2024, v. 76, n. 5/6, p. 305, doi. 10.1007/s00251-024-01349-5
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- Article
High-Resolution Analysis Identifies High Frequency of KIR-A Haplotypes and Inhibitory Interactions of KIR With HLA Class I in Zhejiang Han.
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- Frontiers in Immunology, 2021, v. 12, p. N.PAG, doi. 10.3389/fimmu.2021.640334
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- Article
MICA Gene Deletion in 3411 DNA Samples from Five Distinct Populations in Mainland China and Lack of Association with Nasopharyngeal Carcinoma (NPC) in a Southern Chinese Han population.
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- Annals of Human Genetics, 2016, v. 80, n. 6, p. 319, doi. 10.1111/ahg.12175
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- Article
Six splice site variations, three of them novel, in the ABO gene occurring in nine individuals with ABO subtypes.
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- 2021
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- journal article
Multiple low‐frequency and rare HLA‐B allelic variants are associated with reduced risk in 1,105 nasopharyngeal carcinoma patients in Hunan province, southern China.
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- International Journal of Cancer, 2020, v. 147, n. 5, p. 1397, doi. 10.1002/ijc.32992
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- Article
A new allele with 303 base pairs insertion in B3GALT1 gene identified in an individual with P<sub>1</sub><sup>k</sup> phenotype.
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- Transfusion, 2023, v. 63, n. 8, p. E43, doi. 10.1111/trf.17455
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- Article
A novel B allele with c.736T>C, c.738C>A, and c.930A>G variations identified in a Chinese individual with Bw phenotype.
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- Transfusion, 2023, v. 63, n. 4, p. E25, doi. 10.1111/trf.17299
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- Article
Identification of a novel A allele with initiator codon variant (c.2T > A) in the ABO gene associated with weak A phenotype.
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- Transfusion, 2023, v. 63, n. 4, p. E23, doi. 10.1111/trf.17295
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- Article
Identification of a novel A allele with a c.102C > A variation on the ABO*A1.02 allele.
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- Transfusion, 2023, v. 63, n. 4, p. E15, doi. 10.1111/trf.17257
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- Article
Identification of a novel A allele with a c.977A>C variation on the ABO*A1.02 allele.
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- 2022
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- journal article
Identification of a novel B allele with a c.256G>A mutation on the ABO*B.01 allele.
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- Transfusion, 2022, v. 62, n. 2, p. E10, doi. 10.1111/trf.16760
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- Article
Identification of a novel B allele with c.10‐14dupGTGTT and c.17G>A variants in a Chinese individual with a weak B phenotype.
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- Transfusion, 2021, v. 61, n. 9, p. E67, doi. 10.1111/trf.16616
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- Article
Two novel A alleles with c.322C>T or c.410C>T mutations on the ABO*A1.02 allele were identified in the Chinese individuals.
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- Transfusion, 2020, v. 60, n. 10, p. E38, doi. 10.1111/trf.16036
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- Article
Identification of a novel A allele with a c.731T>C mutation on the ABO*A1.02 allele.
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- 2020
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- journal article
Identification of a novel B allele with a c.586T>C mutation on the ABO*B.01 allele.
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- 2020
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- journal article
c.426G>C mutation in ABO*A1.02 allele was associated with Aw phenotype.
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- 2019
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- journal article
c.830T>C mutation on the ABO*A1.02 allele responsible for Aw phenotype.
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- 2019
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- journal article
Identification of a novel missense mutation c.29G>T in the ABO*A1.02 allele from a Chinese individual with an A subtype.
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- 2019
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- journal article
Identification of a novel B allele with a nucleotide deletion (c.3_4 del G) in the ABO gene associated with a Bx phenotype individual.
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- 2019
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- journal article
c.125_126insT mutation in ABO*B.01 allele responsible for Bel phenotype.
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- 2018
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- journal article
c.49T>C mutation on the α-(1,2)-fucosyltransferase gene responsible for an individual with para-Bombay phenotype.
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- 2018
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- journal article
Two novel mutations in KLF1 were identified in Chinese individuals with In(Lu) phenotype.
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- 2018
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- journal article
c.518T > C missense mutation in the B glycosyltransferase gene responsible for a weak B variant.
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- 2018
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- journal article
A novel mutation in A4GALT was identified in a Chinese individual with p phenotype.
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- 2017
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- journal article
Identification of a novel B allele with missense mutation (c.98G > C) in the ABO gene.
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- 2017
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- Publication type:
- journal article
Molecular basis and zygosity determination of D variants including identification of four novel alleles in Chinese individuals.
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- Transfusion, 2015, v. 55, n. 1, p. 137, doi. 10.1111/trf.12797
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- Article