Therapeutics Development for Alagille Syndrome

por Sanchez, Phillip, Farkhondeh, Atena, Pavlinov, Ivan, Baumgaertel, Karsten, Rodems, Steven, Zheng, Wei
Publicado 2021

An induced pluripotent stem cell line (TRNDi010-C) from a patient carrying a homozygous p.R401X mutation in the NGLY1 gene

por Yang, Shu, Cheng, Yu-Shan, Li, Rong, Pradhan, Manisha, Hong, Junjie, Beers, Jeanette, Zou, Jizhong, Liu, Chengyu, Might, Matt, Rodems, Steven, Zheng, Wei
Publicado 2019

An induced pluripotent stem cell line (NCATS-CL9075) from a patient carrying compound heterozygote mutations, p.R390P and p.L318P, in the NGLY1 gene

por Pradhan, Manisha, Farkhondeh, Atena, Cheng, Yu-Shan, Xu, Miao, Beers, Jeanette, Zou, Jizhong, Liu, Chengyu, Might, Matthew, Rodems, Steven, Baumgärtel, Karsten, Zheng, Wei
Publicado 2021

Generation of an induced pluripotent stem cell line (TRNDi002-B) from a patient carrying compound heterozygous p.Q208X and p.G310G mutations in the NGLY1 gene

por Li, Rong, Pradhan, Manisha, Xu, Miao, Baskfield, Amanda, Farkhondeh, Atena, Cheng, Yu-Shan, Beers, Jeanette, Zou, Jizhong, Liu, Chengyu, Might, Matthew, Rodems, Steven, Zheng, Wei
Publicado 2018

Generation of an induced pluripotent stem cell line (TRNDi031-A) from a patient with Alagille syndrome type 1 carrying a heterozygous p. C312X (c. 936 T > A) mutation in JAGGED-1

por Brooks, Brianna M., Pradhan, Manisha, Cheng, Yu-Shan, Gorshkov, Kirill, Farkhondeh, Atena, Chen, Catherine Z., Beers, Jeanette, Liu, Chengyu, Baumgaertel, Karsten, Rodems, Steven, Zheng, Wei
Publicado 2021

Generation and characterization of NGLY1 patient-derived midbrain organoids

por Abbott, Joshua, Tambe, Mitali, Pavlinov, Ivan, Farkhondeh, Atena, Nguyen, Ha Nam, Xu, Miao, Pradhan, Manisha, York, Tate, Might, Matthew, Baumgärtel, Karsten, Rodems, Steven, Zheng, Wei
Publicado 2023