Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Huikun Duan"'
Autor:
Ying Bai, Yue Sun, Ning Liu, Li Wang, Zhihui Jiao, Yaqin Hou, Huikun Duan, Qianqian Li, Xiaofan Zhu, Jingjing Meng, Xiangdong Kong
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-12 (2022)
Abstract Background Fetal skeletal dysplasia (SD) is a common congenital disability comprising a complex group of skeletal disorders with substantial clinical and genetic heterogeneity. Many of these defects are detected prenatally using ultrasound (
Externí odkaz:
https://doaj.org/article/1ffb5a473f8148aa87b820387570201d
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-7 (2020)
Abstract Background X-linked agammaglobulinaemia (XLA) is a rare immunodeficiency disease for which recurrent severe infection is the major clinical symptom. BTK is the main causative gene, with X chromosome recessive inheritance. However, the mutati
Externí odkaz:
https://doaj.org/article/0892142975534122867e96e7cc0d01d0
Identification of quantitative trait loci controlling high Calcium response in Arabidopsis thaliana.
Publikováno v:
PLoS ONE, Vol 9, Iss 11, p e112511 (2014)
Natural variation for primary root growth response to high Ca stress in Arabidopsis thaliana was studied by screening a series of accessions (ecotypes) under high Calcium (40 mM CaCl2) conditions. The genetic basis of this variation was further inves
Externí odkaz:
https://doaj.org/article/8bcc960063934b88a8644f88c6f5c62c
Autor:
Huikun Duan, Xiangdong Kong, Xiaofan Zhu, Zhihui Jiao, Xiaohua Fang, Yin Feng, Ning Liu, Chaofeng Zhu
Publikováno v:
Clinica Chimica Acta. 524:194-200
Background Mucopolysaccharidosis (MPS) refers to a group of lysosomal storage disorders for which seven types and 11 subtypes are currently recognized. Targeted next-generation sequencing (NGS) offers an important method of disease typing, diagnosis,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::168eabeb79f0f545f50da0eff1ee8385
https://doi.org/10.1016/j.cca.2021.11.019
https://doi.org/10.1016/j.cca.2021.11.019
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 38(5)
To explore the genetic basis for two Chinese pedigrees affected with Huntington disease and provide prenatal diagnosis for them.Peripheral venous blood samples were collected from the probands. PCR and capillary gel electrophoresis were used to deter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b5c7791ecda7a4e32a9343f4cbc4cdb1
https://pubmed.ncbi.nlm.nih.gov/33974252
https://pubmed.ncbi.nlm.nih.gov/33974252
Background: X-linked agammaglobulinaemia (XLA) is a rare immunodeficiency disease, and the main clinical symptoms is recurrent severe infections. BTK is the main disease-causing gene, and the genetic mode is X chromosome recessive inheritance. But th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb304444b1f664429b4ad088cb9587bf
https://doi.org/10.21203/rs.2.22278/v1
https://doi.org/10.21203/rs.2.22278/v1
Additional file 1: Table S1.BTK gene primers.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be5e3018c5bb53a3d7c9e06d3bd9742f
Autor:
Huikun Duan, Zhenhua Zhao, Xiangdong Kong, Yiqian Liu, David S. Cram, Ning Liu, Mengnan Xu, Zhifeng Li, Yin Wang
Publikováno v:
Archives of Disease in Childhood - Fetal and Neonatal Edition. 104:F24-F29
BackgroundPhenylketonuria (PKU) is a common metabolic disorder caused predominately by mutations in the phenylalanine hydroxylase (PAH) gene. The aim of the study was to design and validate the performance of a non-invasive prenatal test (NIPT) for P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::656e53068aa2de798341c2270d1d8e25
https://doi.org/10.1136/archdischild-2017-313929
https://doi.org/10.1136/archdischild-2017-313929
Autor:
Qian Wei, Zaizhong Ni, Xiaofeng Ma, Xiangzhen Ji, Minggang Li, Huikun Duan, Bin Wang, Xiaodan Li, Pingzhe Jiang
Publikováno v:
Applied Biochemistry and Biotechnology. 180:1276-1285
5rolGLP-HV had an ideal therapeutic potential in the prevention of hyperglycemia in type 2 diabetes and delay of the thrombosis. The objective of the study was to investigate the toxicology effects of 5rolGLP-HV and guarantee its safety. In acute tox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::691fe73e5cca958048c9d61ffc5f9e55
https://doi.org/10.1007/s12010-016-2166-9
https://doi.org/10.1007/s12010-016-2166-9
Autor:
Xiaodan Li, Dong Zhen, Zaizhong Ni, Huikun Duan, Qian Wei, Xiaofeng Ma, Bin Wang, Minggang Li, Pingzhe Jiang, Baicheng Ma, Xiangzhen Ji
Publikováno v:
Applied Biochemistry and Biotechnology. 180:841-851
Diabetes has been cited as the most challenging health problem in the twenty-first century. Accordingly, it is urgent to develop a new type of efficient and low-toxic antidiabetic medication. Since vanadium compounds have insulin-mimetic and potentia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1451ce840f592970d82fbd83078787f0
https://doi.org/10.1007/s12010-016-2137-1
https://doi.org/10.1007/s12010-016-2137-1