Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Wen-Wen Jia"'
Autor:
Zhi-Bin Qiao, Ji-Zhen Lu, Lu Zhang, Hong-Xia Cao, Zhi-Hui Bai, Yi-Yao Qi, Han-Yu Zhu, Shou-Mei Zhang, Yan Bao, Wen-Wen Jia, Zhong-Min Liu
Publikováno v:
Stem Cell Research, Vol 56, Iss , Pp 102519- (2021)
SUV39H1 is a histone methyltransferase involve numerous biological processes, including of aging, embryo development, tumor growth and mitosis via catalysis of dimethylation and trimethylation of lysine 9 of histone H3. Here we report a human induced
Externí odkaz:
https://doaj.org/article/046332ec6b5c4e4093d5785cb247f21a
Autor:
Ji-Zhen Lu, Zhi-Bin Qiao, Lu Zhang, Hong-Xia Cao, Zhi-Hui Bai, Yi-Yao Qi, Han-Yu Zhu, Ya-Qi Chen, Shou-Mei Zhang, Xiu-Hua Yan, Yan Bao, Wen-Wen Jia, Zhong-Min Liu
Publikováno v:
Stem Cell Research, Vol 56, Iss , Pp 102530- (2021)
LAMIN A/C, encoded by the LMNA gene, supports the normal structure of the cell nucleus and regulates the connection between the nucleus and the cytoskeleton as a component of the nucleus envelope. The loss of expression and function of the LMNA gene
Externí odkaz:
https://doaj.org/article/ccf4aa14cea6478f840b2670f2437f48
Autor:
Wen-Wen Jia, Ji-Zhen Lu, Lu Zhang, Hong-Xia Cao, Yi-Yao Qi, Han-Yu Zhu, Zhi-Hui Bai, Shou-Mei Zhang, Zhi-Bin Qiao, Yan Bao, Zhong-Min Liu
Publikováno v:
Stem Cell Research, Vol 53, Iss , Pp 102328- (2021)
Hypertrophic cardiomyopathy (HCM) is an autosomal dominant heart disease. An induced pluripotent stem cell line (EHTJUi003-A) was generated from umbilical cord blood mononuclear cells (UCBMCs) of a female neonate with heterozygous mutation of p.L460W
Externí odkaz:
https://doaj.org/article/566e981ff8484463b1a26ae8a380a158
Autor:
Yi-Yao Qi, Ji-Zhen Lu, Lu Zhang, Hong-Xia Cao, Han-Yu Zhu, Zhi-Hui Bai, Shou-Mei Zhang, Zhi-Bin Qiao, Wen-Wen Jia, Zhong-Min Liu
Publikováno v:
Stem Cell Research, Vol 53, Iss , Pp 102369- (2021)
Familial Arrhythmogenic Right Ventricular Dysplasia (ARVD) is a primary cardiomyopathy characterized by the abnormality of the right ventricular muscle. ARVD may be life-threatening due to the induction of paroxysmal refractory ventricular tachycardi
Externí odkaz:
https://doaj.org/article/2f02d3b8a9f64bc6948fdee1f5b830e5
Publikováno v:
Stem Cell Research, Vol 48, Iss , Pp 101932- (2020)
Familial exudative vitreoretinopathy (FEVR) is an autosomal dominant genetic disease. An induced pluripotent stem cell line (EHTJUi002-A) was generated from umbilical cord blood mononuclear cells (UCBMCs) of a neonate with heterozygous mutation of p.
Externí odkaz:
https://doaj.org/article/cbf58f9db52f410394e2cf25f54ad29c
Publikováno v:
Stem Cell Research, Vol 43, Iss , Pp - (2020)
Long QT syndrome type 8 is an uncommon inherited condition .An induced pluripotent stem cell (iPSC) line was generated from Peripheral blood mononuclear cells (PBMCs) of a 10-year-old patient with heterozygous mutation of p.R858H(c.2573G > A)in the C
Externí odkaz:
https://doaj.org/article/369147dff1c04dd68ee9509557ff0531
Autor:
Su-Qin Zhu, Xiu-Hua Liao, Wen-Wen Jiang, Yan Sun, Hui-Ling Xu, Xiao-Jing Chen, Bei-Hong Zheng
Publikováno v:
Asian Journal of Andrology, Vol 26, Iss 4, Pp 415-420 (2024)
This study aimed to investigate the effects of male hepatitis B virus (HBV) infection on male fertility, embryonic development, and in vitro fertilization/intracytoplasmic sperm injection (IVF/ICSI) outcomes. We performed a retrospective cohort study
Externí odkaz:
https://doaj.org/article/e85b1e87f0b1407994ca46c29f12ecb7
Autor:
Zhi-Bin Qiao, Lu Zhang, Hong-Xia Cao, Han-Yu Zhu, Shou-Mei Zhang, Wen-Wen Jia, Ji-Zhen Lu, Zhi-Hui Bai, Yi-Yao Qi, Zhong-Min Liu, Yan Bao
Publikováno v:
Stem Cell Research, Vol 53, Iss, Pp 102328-(2021)
Hypertrophic cardiomyopathy (HCM) is an autosomal dominant heart disease. An induced pluripotent stem cell line (EHTJUi003-A) was generated from umbilical cord blood mononuclear cells (UCBMCs) of a female neonate with heterozygous mutation of p.L460W
Autor:
Ji-Zhen Lu, Shou-Mei Zhang, Lu Zhang, Zhong-Min Liu, Zhi-Hui Bai, Yi-Yao Qi, Hong-Xia Cao, Zhi-Bin Qiao, Wen-Wen Jia, Han-Yu Zhu
Publikováno v:
Stem Cell Research, Vol 53, Iss, Pp 102369-(2021)
Familial Arrhythmogenic Right Ventricular Dysplasia (ARVD) is a primary cardiomyopathy characterized by the abnormality of the right ventricular muscle. ARVD may be life-threatening due to the induction of paroxysmal refractory ventricular tachycardi
Publikováno v:
Stem Cell Research, Vol 43, Iss, Pp-(2020)
Long QT syndrome type 8 is an uncommon inherited condition .An induced pluripotent stem cell (iPSC) line was generated from Peripheral blood mononuclear cells (PBMCs) of a 10-year-old patient with heterozygous mutation of p.R858H(c.2573G > A)in the C