详情页 - 昆明医科大学第一附属医院知识库

当前位置：首页 > 详情页

Identification of the novel HLA-B*38:97 allele in a Chinese individual

7| 导出 | 链接全文 |

文献详情

资源类型：

WOS体系：

Pubmed体系：

收录情况： ◇ SCIE

作者：

机构： [1]Kunming Med Univ, Affiliated Hosp 1, Dept Dermatol, 295 Xichang Rd, Kunming 650032, Yunnan, Peoples R China [2]Kunming Med Univ, Affiliated Hosp 1, NHC Key Lab Drug Addict Med, 295 Xichang Rd, Kunming 650032, Yunnan, Peoples R China [3]Kunming Med Univ, Affiliated Hosp 1, Sci Res Lab Ctr, Kunming, Yunnan, Peoples R China [4]Second Peoples Hosp Dali City, Dept Dermatol, Dali, Peoples R China

出处：

DOI：

ISSN：

关键词： HLA-B*38:97 new HLA allele next-generation sequencing

摘要：

Compared with the HLA-B*38:02:01:01 allele, HLA-B*38:97 differs by a single nucleotide substitution.

基金：

基金编号： L-201613 32060177 81860553 YNWRMY-2018-039 ZX2019-03-02 2019ZF012

语种：

被引次数：

WOS：

PubmedID：

中科院(CAS)分区：

出版当年[2023]版：

大类 | 4 区医学

小类 | 4 区细胞生物学 4 区免疫学 4 区病理学

最新[2023]版：

大类 | 4 区医学

小类 | 4 区细胞生物学 4 区免疫学 4 区病理学

JCR分区：

出版当年[2022]版：

Q1 CELL BIOLOGY Q1 IMMUNOLOGY Q1 PATHOLOGY

最新[2023]版：

Q1 IMMUNOLOGY Q1 CELL BIOLOGY Q1 PATHOLOGY Q2 CELL BIOLOGY

影响因子： 6.5 最新[2023版] 3.8 最新五年平均 8 出版当年[2022版] 4.3 出版当年五年平均 9.2 出版前一年[2021版] 6.5 出版后一年[2023版]

第一作者：

第一作者机构： [1]Kunming Med Univ, Affiliated Hosp 1, Dept Dermatol, 295 Xichang Rd, Kunming 650032, Yunnan, Peoples R China

通讯作者：

通讯机构： [1]Kunming Med Univ, Affiliated Hosp 1, Dept Dermatol, 295 Xichang Rd, Kunming 650032, Yunnan, Peoples R China

推荐引用方式(GB/T 7714)：

APA：

MLA：

相关文献

[1]Identification of the novel HLA-B*38:97 allele in a Chinese individual. [2]Next-generation sequencing-based microRNA profiling of mice testis subjected to transient heat stress [3]The diagnostic value of metagenomic next-generation sequencing in critically ill patients with sepsis: A retrospective cohort study [4]Analysis of gene landscape of small cell lung cancer of Chinese through next-generation sequencing [5]Analysis of gene landscape of small cell lung cancer of Chinese through next-generation sequencing. [6]Next-Generation Sequencing Reveals High Uncommon EGFR Mutations and Tumour Mutation Burden in a Subgroup of Lung Cancer Patients [7]Evaluation of high-throughput next-generation sequencing applied in the pathogenic diagnosis of bloodstream infections(Open Access) [8]Next-generation sequencing identifies HOXA6 as a novel oncogenic gene in low grade glioma [9]Mutational Profile of Multiple Lung Cancers in Xuanwei by Next-Generation Sequencing [10]Detecting trisomy in products of conception from first-trimester spontaneous miscarriages by next-generation sequencing (NGS)