Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Suihan Wu"'
Publikováno v:
Stem Cell Research, Vol 62, Iss , Pp 102801- (2022)
Human induced pluripotent stem cells (iPSC) resemble human embryonic stem cells with potential to differentiate into cells of all adult tissues. Nonetheless human iPSCs may have an epigenetic memory of their donor tissue origin, are easier to differe
Externí odkaz:
https://doaj.org/article/4c13d79b1d164db98d44dbcdcff6590d
Publikováno v:
Stem Cell Research, Vol 54, Iss , Pp 102390- (2021)
Variants in FBN1 are associated with Marfan Syndrome, an autosomal dominant disorder with clinical features that involve the musculoskeletal, cardiovascular and ocular systems. We generated a human iPSC line QDMHi001-A from a patient with Marfan synd
Externí odkaz:
https://doaj.org/article/6435d0b44be1460f9c5b4bc817580b14
Publikováno v:
Stem Cell Research, Vol 54, Iss , Pp 102397- (2021)
The 46, XX male sex reversal syndrome (SRS) is a rare disease with a gender dysplasia phenotype. Scientists concur that SRS is associated with translocation of the sex-determining region Y gene (SRY). We obtained peripheral blood mononuclear cells (P
Externí odkaz:
https://doaj.org/article/5d23961fff494872bad13af6090704d4
Publikováno v:
Stem Cell Research, Vol 49, Iss , Pp 102074- (2020)
β-thalassemia is mostly caused by homozygous or compound heterozygous variants in HBB. We generated a human iPSC line CIBi008-A from amniotic fluid-derived cells of a fetus with β-thalassemia major, carrying compound heterozygous −28A > G and IVS
Externí odkaz:
https://doaj.org/article/754f1368faa44d999005b7161ad9a024
Autor:
Yubo Yan, Suihan Wu, Lixiang Jiang, Bo Yang, Xuhui Chen, Yuqing Liu, Baorong Yu, Jian Fu, Jin Yu, Hui Ning, Meng Chu, Jiayin Yang
Publikováno v:
Stem Cell Research, Vol 47, Iss , Pp 101905- (2020)
Variations in PRKN or HTRA2 are associated with Parkinson’s disease. We generated a human induced pluripotent stem cell (iPSC) line CIBi007-A from a patient with young-onset Parkinson’s disease (YOPD) who carried variants in PRKN and HTRA2. The g
Externí odkaz:
https://doaj.org/article/80285d9b073d4bdc8e02c64f3e31768b
Background The placental anticoagulant protein Annexin A5 is highly expressed on the apical surfaces of syncytiotrophoblasts and plays an important role in maintaining blood fluidity in the placental circulation. We investigated the expression of Ann
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4eaf1b9069f54e25b5dd086d9eb4c8c
https://doi.org/10.21203/rs.3.rs-1349894/v1
https://doi.org/10.21203/rs.3.rs-1349894/v1
Publikováno v:
Stem Cell Research, Vol 54, Iss, Pp 102397-(2021)
The 46, XX male sex reversal syndrome (SRS) is a rare disease with a gender dysplasia phenotype. Scientists concur that SRS is associated with translocation of the sex-determining region Y gene (SRY). We obtained peripheral blood mononuclear cells (P
Publikováno v:
Stem Cell Research, Vol 54, Iss, Pp 102390-(2021)
Variants in FBN1 are associated with Marfan Syndrome, an autosomal dominant disorder with clinical features that involve the musculoskeletal, cardiovascular and ocular systems. We generated a human iPSC line QDMHi001-A from a patient with Marfan synd
Publikováno v:
Stem Cell Research, Vol 49, Iss, Pp 102074-(2020)
β-thalassemia is mostly caused by homozygous or compound heterozygous variants in HBB. We generated a human iPSC line CIBi008-A from amniotic fluid-derived cells of a fetus with β-thalassemia major, carrying compound heterozygous −28A > G and IVS
Autor:
Yan Yubo, Liu Yuqing, Bo Yang, Jiang Lixiang, Hui Ning, Fu Jian, Jiayin Yang, Jin Yu, Suihan Wu, Baorong Yu, Meng Chu, Xuhui Chen
Publikováno v:
Stem Cell Research, Vol 47, Iss, Pp 101905-(2020)
Variations in PRKN or HTRA2 are associated with Parkinson’s disease. We generated a human induced pluripotent stem cell (iPSC) line CIBi007-A from a patient with young-onset Parkinson’s disease (YOPD) who carried variants in PRKN and HTRA2. The g