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International Journal of Environmental Research and Public Health
|
August 5, 2020
Development of the Chinese Version of Medication Adherence Reasons Scale (ChMAR-Scale)
Pin-Fang Chen, Elizabeth H Chang, Elizabeth J Unni, et al.
Scientific Reports
|
May 6, 2016
RBFOX1 and RBFOX2 are dispensable in iPSCs and iPSC-derived neurons and do not contribute to neural-specific paternal UBE3A silencing
Pin-Fang Chen, Jack S Hsiao, Carissa L Sirois, et al.
Biology Open
|
April 15, 2014
Colchicine-induced degeneration of the micronucleus during conjugation in Tetrahymena
Pin-Fang Chen, Sita Singhal, Daniel Bushyhead, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
December 19, 2014
Modeling Genomic Imprinting Disorders Using Induced Pluripotent Stem Cells
Stormy J Chamberlain, Noelle D Germain, Pin-Fang Chen, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 30, 2010
Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes
Stormy J Chamberlain, Pin-Fang Chen, Khong Y Ng, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 9, 2019
Biallelic Mutations in <i>TSC2</i> Lead to Abnormalities Associated with Cortical Tubers in Human iPSC-Derived Neurons
Kellen D Winden, Maria Sundberg, Cindy Yang, et al.
Stem Cell Reports
|
April 16, 2021
Balancing serendipity and reproducibility: Pluripotent stem cells as experimental systems for intellectual and developmental disorders
Nickesha C Anderson, Pin-Fang Chen, Kesavan Meganathan, et al.
Stem Cell Research
|
September 17, 2019
Generation and characterization of six human induced pluripotent stem cell lines (iPSC) from three families with AP4B1-associated hereditary spastic paraplegia (SPG47)
Julian Teinert, Robert Behne, Angelica D'Amore, et al.
Human Molecular Genetics
|
December 24, 2013
Imprinted expression of UBE3A in non-neuronal cells from a Prader-Willi syndrome patient with an atypical deletion
Kristen Martins-Taylor, Jack S Hsiao, Pin-Fang Chen, et al.
Stem Cell Research
|
April 27, 2024
Generation and characterization of six human induced pluripotent stem cell lines (hiPSCs) from three individuals with SSADH Deficiency and CRISPR-corrected isogenic controls
Wardiya Afshar-Saber, Cidi Chen, Nicole A Teaney, et al.
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Search research articles
Search
Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
International Journal of Environmental Research and Public Health
|
August 5, 2020
Development of the Chinese Version of Medication Adherence Reasons Scale (ChMAR-Scale)
Pin-Fang Chen, Elizabeth H Chang, Elizabeth J Unni, et al.
Scientific Reports
|
May 6, 2016
RBFOX1 and RBFOX2 are dispensable in iPSCs and iPSC-derived neurons and do not contribute to neural-specific paternal UBE3A silencing
Pin-Fang Chen, Jack S Hsiao, Carissa L Sirois, et al.
Biology Open
|
April 15, 2014
Colchicine-induced degeneration of the micronucleus during conjugation in Tetrahymena
Pin-Fang Chen, Sita Singhal, Daniel Bushyhead, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
December 19, 2014
Modeling Genomic Imprinting Disorders Using Induced Pluripotent Stem Cells
Stormy J Chamberlain, Noelle D Germain, Pin-Fang Chen, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 30, 2010
Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes
Stormy J Chamberlain, Pin-Fang Chen, Khong Y Ng, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 9, 2019
Biallelic Mutations in <i>TSC2</i> Lead to Abnormalities Associated with Cortical Tubers in Human iPSC-Derived Neurons
Kellen D Winden, Maria Sundberg, Cindy Yang, et al.
Stem Cell Reports
|
April 16, 2021
Balancing serendipity and reproducibility: Pluripotent stem cells as experimental systems for intellectual and developmental disorders
Nickesha C Anderson, Pin-Fang Chen, Kesavan Meganathan, et al.
Stem Cell Research
|
September 17, 2019
Generation and characterization of six human induced pluripotent stem cell lines (iPSC) from three families with AP4B1-associated hereditary spastic paraplegia (SPG47)
Julian Teinert, Robert Behne, Angelica D'Amore, et al.
Human Molecular Genetics
|
December 24, 2013
Imprinted expression of UBE3A in non-neuronal cells from a Prader-Willi syndrome patient with an atypical deletion
Kristen Martins-Taylor, Jack S Hsiao, Pin-Fang Chen, et al.
Stem Cell Research
|
April 27, 2024
Generation and characterization of six human induced pluripotent stem cell lines (hiPSCs) from three individuals with SSADH Deficiency and CRISPR-corrected isogenic controls
Wardiya Afshar-Saber, Cidi Chen, Nicole A Teaney, et al.
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of 2