Výsledky vyhledávání - "Hongfei Kang"

[Diagnosis of a Chinese pedigree affected with autosomal recessive deafness 4 with enlarged vestibular aqueduct due to compound heterozygous variants of FOXI1 gene]

Autor: Jingjing, Li, Hongfei, Kang, Xiangdong, Kong

Publikováno v: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 39(10)

To explore the genetic basis for a Chinese pedigree affected with congenital deafness pedigree in conjunct with enlarged vestibular aqueduct.Whole-exome sequencing was carried out for the proband to analyze the genes associated with hereditary deafne

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::5b349fe1373b405afc79adb51a0862f6
https://pubmed.ncbi.nlm.nih.gov/36184087

Zobrazit plný text záznamu

[Genetic diagnosis of a pedigree affected with Usher syndrome type 1D/F]

Autor: Hongfei, Kang, Kaihui, Zhao, Xiangdong, Kong

Publikováno v: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 38(10)

To explore the genetic basis for a pedigree affected with congenital sensorineural deafness.High-throughput sequencing was carried out to analyze the coding regions of 415 genes associated with hereditary deafness in the proband. Suspected variants w

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::377d76a3bda25cd7b3dd0e29fc1ff408
https://pubmed.ncbi.nlm.nih.gov/34625930

Zobrazit plný text záznamu

Engineering hollow carbon spheres: directly from solid resin spheres to porous hollow carbon spheres via air induced linker cleaving

Autor: Suping Huang, Neng Li, Bihui Qin, Qi Xiao, Hongfei Kang, Nana Cai

Publikováno v: Nanoscale. 13(32)

Hollow carbon spheres (HCSs) have broad application in many fields such as catalysis, adsorption and energy storage. Due to various restrictions on hard and soft templates, self-templating methods have received extensive attention. Generally, the con

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f59f6bfd274b2fdc5b4b83d33d2af41
https://pubmed.ncbi.nlm.nih.gov/34477661

Zobrazit plný text záznamu

[Genetic testing of a Chinese pedigree affected with non-syndromic autosomal dominant deafness 15]

Autor: Hongfei, Kang, Kaihui, Zhao, Xiangdong, Kong

Publikováno v: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 38(7)

To explore the genetic basis of a Chinese pedigree affected with progressive non-syndromic sensorineural hearing loss.High-throughput DNA sequencing was carried out to analyze 415 genes associated with hereditary deafness in the proband. Sanger seque

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::131dc85365a7df5e1507a70150e48e47
https://pubmed.ncbi.nlm.nih.gov/34247367

Zobrazit plný text záznamu

Modification-scavenging hydroxyl groups of natural mineral fiber separators to boost initial coulombic efficiency of lithium-ion battery

Autor: Hongfei Kang, Nana Cai, Bihui Qin, Yan Li, Neng Li, Suping Huang, Qi Xiao

Publikováno v: Materials Chemistry and Physics. 284:126056

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7ff683cd5f3ef28e69c40ee02189dd41
https://doi.org/10.1016/j.matchemphys.2022.126056

Zobrazit plný text záznamu

FVIII inhibitor risk correlated with F8 gene variants in 296 unrelated male Chinese patients with haemophilia A

Autor: Bai Li, Shengmei Chen, Yin Feng, Hongfei Kang, Xiangdong Kong, Jingjing Li

Publikováno v: Haemophilia. 27

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a96b473fd7138baf28a4241ee0215d8
https://doi.org/10.1111/hae.14141

Zobrazit plný text záznamu

Subunit Vaccines Consisting of Antigens from Dormant and Replicating Bacteria Show Promising Therapeutic Effect againstMycobacterium BovisBCG Latent Infection

Autor: Hongxia Niu, Bingdong Zhu, Chao Gan, Xingming Ma, Dengcai Zhang, Lan Ma, Fei Li, Jiying Tan, Xun Liu, Hongfei Kang, Ruitian Tang, Ying Zhang, Arthur M. Dannenberg, Xue Han, Jingjing Li

Publikováno v: Scandinavian Journal of Immunology. 85:425-432

To screen effective antigens as therapeutic subunit vaccines against Mycobacterium latent infection, we did bioinformatics analysis and literature review to identify effective antigens and evaluated the immunogenicity of five antigens highly expresse

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::121e7b5aa77a0d69b62c7d8c0bf77746
https://doi.org/10.1111/sji.12556

Zobrazit plný text záznamu

Plný text ve formátu HTML

[Genetic and prenatal diagnosis of a retinitis pigmentosa pedigree]

Autor: Hongfei, Kang, Nan, Bai, Shiyue, Mei, Xiangdong, Kong

Publikováno v: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 35(2)

To explore the genetic etiology of a pedigree affected with hereditary retinitis pigmentosa.High-throughput DNA sequencing was used to analyze the sequences of 173 genes associated with hereditary eye diseases in the proband. Suspected mutation was v

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c098e15bd9b7d191f9544f16ec9e23b2
https://pubmed.ncbi.nlm.nih.gov/29652988

Zobrazit plný text záznamu

Loss of Heterozygosity in Thyroid Hormone Receptor Beta in Invasive Breast Cancer

Autor: Yaqin Ling, Hui Yang, Yonghe Wang, Fabing Tang, Hongfei Kang, Yong Wang, Qing Li

Publikováno v: Tumori Journal. 101:572-577

Background Loss of heterozygosity (LOH) on chromosome arm 3p, where the gene of thyroid hormone receptor beta (THRB) is located, has been reported in breast cancer. Although some studies performed in vitro have suggested that THRB could act as a tumo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89683c3ef9aa3a018bb6f4edb12a1596
https://doi.org/10.5301/tj.5000272

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání