Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Xiufen Bu"'
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Paternal uniparental disomy (UPD) of chromosome 7 is extremely rare, and only a few postnatal cases have been reported. The effects on growth were discordant in these cases, and the relevance of paternal UPD(7) to growth caused by imprint
Externí odkaz:
https://doaj.org/article/59a95c3d530b48d08721912969121f3b
Publikováno v:
Molecular Cytogenetics, Vol 15, Iss 1, Pp 1-5 (2022)
Abstract Background Tetrasomy 18p syndrome is a rare chromosomal disorder that is caused by the presence of isochromosome 18p. Most tetrasomy 18p cases are de novo cases and maternal origin of trisomy 18p is a rare condition. At present, only four ca
Externí odkaz:
https://doaj.org/article/640e9bfef4f7421fab33662731689d9a
Publikováno v:
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-5 (2021)
Abstract Background Uniparental disomy (UPD) is defined as an inheritance of two chromosomes from only one of the parents with no representative copy from the other. Paternal-origin UPD of chromosome 3 is a very rare condition, with only five cases o
Externí odkaz:
https://doaj.org/article/160a431cc5cf43b6baabb5895448eab3
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
This study explored the diagnostic efficiency of different prenatal diagnostic approaches for women with positive non-invasive prenatal screening (NIPS) results by analyzing their clinical information and pregnancy outcomes. We collected data on 626
Externí odkaz:
https://doaj.org/article/df887346640a4f998a9657d7a0de886a
Background: This study explores the diagnostic efficiency of different prenatal diagnostic approaches for women with positive non-invasive prenatal testing (NIPT) results by analyzing their clinical information and pregnancy outcome. Methods: We coll
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46affe2326d26214c8a2e6a9d97dd1b6
https://doi.org/10.21203/rs.3.rs-1641089/v1
https://doi.org/10.21203/rs.3.rs-1641089/v1
Background: Tetrasomy 18p syndrome is a very rare chromosomal disorder that is caused by the presence of isochromosome 18p.Most tetrasomy 18p cases are de novo cases,maternal origin trisomy 18p is a very rare condition.At present, only 4 cases of mat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7893ad6dcff327ea7bcd1fc4d5ffd215
https://doi.org/10.21203/rs.3.rs-1629060/v1
https://doi.org/10.21203/rs.3.rs-1629060/v1
Publikováno v:
Molecular Cytogenetics
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-5 (2021)
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-5 (2021)
Background Uniparental disomy (UPD) is defined as an inheritance of two chromosomes from only one of the parents with no representative copy from the other. Paternal-origin UPD of chromosome 3 is a very rare condition, with only five cases of paterna
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::981d6e644209cd16b4cd660e342ae015
https://pubmed.ncbi.nlm.nih.gov/34742342
https://pubmed.ncbi.nlm.nih.gov/34742342
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 38(6)
To explore the value of chromosomal microarray analysis (CMA) for the diagnosis of fetuses with high risk signaled by non-invasive prenatal testing (NIPT).From June 2017 to August 2019, 628 pregnant women with high risk signaled by NIPT underwent inv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fd2aa234bf6ee64d6f1af1af90f448c6
https://pubmed.ncbi.nlm.nih.gov/34096021
https://pubmed.ncbi.nlm.nih.gov/34096021
Autor:
Lanping, Hu, Weihong, Wang, Hongyu, Li, Shihao, Zhou, Shan, Liu, Mengyue, Yang, Xiufen, Bu, Jun, He
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 37(10)
To carry out prenatal diagnosis on a fetus with abnormal findings by ultrasonography and non-invasive prenatal testing.The fetus and both parents were subjected to chromosomal karyotyping and single nucleotide polymorphism array (SNP-array) analysis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8f0df2dad41778b5961ea53930d4dbc7
https://pubmed.ncbi.nlm.nih.gov/32924106
https://pubmed.ncbi.nlm.nih.gov/32924106
Publikováno v:
World Journal of Microbiology and Biotechnology. 35
In this study, the cDNA of immunomodulatory protein from Poria cocos (PCP) was amplified by reverse transcription polymerase chain reaction and used to transform P. Pastoris cells, resulting in rPCP expression as a secreted protein to a concentration
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18a209f3ab243c6eebd84dcb2c7226c5
https://doi.org/10.1007/s11274-019-2602-4
https://doi.org/10.1007/s11274-019-2602-4