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[HTML][HTML] Directly reprogrammed human neurons retain aging-associated transcriptomic signatures and reveal age-related nucleocytoplasmic defects

J Mertens, ACM Paquola, M Ku, E Hatch, L Böhnke… - Cell stem cell, 2015 - cell.com
Aging is a major risk factor for many human diseases, and in vitro generation of human
neurons is an attractive approach for modeling aging-related brain disorders. However …
被引用次数：677 相关文章

Directly Reprogrammed Human Neurons Retain Aging-Associated Transcriptomic Signatures and Reveal Age-Related Nucleocytoplasmic Defects.

J Mertens, ACM Paquola, M Ku, E Hatch, L Böhnke… - Cell Stem …, 2015 - europepmc.org
Aging is a major risk factor for many human diseases, and in vitro generation of human
neurons is an attractive approach for modeling aging-related brain disorders. However …

Directly Reprogrammed Human Neurons Retain Aging-Associated Transcriptomic Signatures and Reveal Age-Related Nucleocytoplasmic Defects

J Mertens, ACM Paquola, M Ku, E Hatch… - Cell stem …, 2015 - pubmed.ncbi.nlm.nih.gov
Aging is a major risk factor for many human diseases, and in vitro generation of human
neurons is an attractive approach for modeling aging-related brain disorders. However …

[引用][C] Directly Reprogrammed Human Neurons Retain Aging-Associated Transcriptomic Signatures and Reveal Age-Related Nucleocytoplasmic Defects

J Mertens, ACM Paquola, M Ku, E Hatch, L Böhnke… - Cell Stem Cell, 2015 - cir.nii.ac.jp
Directly Reprogrammed Human Neurons Retain Aging-Associated Transcriptomic Signatures
and Reveal Age-Related Nucleocytoplasmic Defects | CiNii Research CiNii 国立情報学研究所 …

Directly Reprogrammed Human Neurons Retain Aging-Associated Transcriptomic Signatures and Reveal Age-Related Nucleocytoplasmic Defects

J Mertens, ACM Paquola, M Ku, E Hatch… - Cell Stem …, 2015 - einstein.elsevierpure.com
Aging is a major risk factor for many human diseases, and in vitro generation of human
neurons is an attractive approach for modeling aging-related brain disorders. However …
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[HTML][HTML] Directly Reprogrammed Human Neurons Retain Aging-Associated Transcriptomic Signatures and Reveal Age-Related Nucleocytoplasmic Defects

J Mertens, ACM Paquola, M Ku, E Hatch, L Böhnke… - Cell Stem Cell, 2015 - Elsevier
Aging is a major risk factor for many human diseases, and in vitro generation of human
neurons is an attractive approach for modeling aging-related brain disorders. However …

Directly Reprogrammed Human Neurons Retain Aging-Associated Transcriptomic Signatures and Reveal Age-Related Nucleocytoplasmic Defects

J Mertens, ACM Paquola, M Ku, E Hatch… - Cell stem …, 2015 - pure.johnshopkins.edu
Aging is a major risk factor for many human diseases, and in vitro generation of human
neurons is an attractive approach for modeling aging-related brain disorders. However …
[HTML] nih.gov

[HTML][HTML] Directly Reprogrammed Human Neurons Retain Aging-Associated Transcriptomic Signatures and Reveal Age-Related Nucleocytoplasmic Defects

J Mertens, ACM Paquola, M Ku, E Hatch, L Böhnke… - Cell stem …, 2015 - ncbi.nlm.nih.gov
Aging is a major risk factor for many human diseases, and in vitro generation of human
neurons is an attractive approach for modeling aging-related brain disorders. However …

Directly Reprogrammed Human Neurons Retain Aging-Associated Transcriptomic Signatures and Reveal Age-Related Nucleocytoplasmic Defects

J Mertens, ACM Paquola, M Ku, E Hatch, L Böhnke… - Cell Stem Cell, 2015 - infona.pl
Aging is a major risk factor for many human diseases, and in vitro generation of human
neurons is an attractive approach for modeling aging-related brain disorders. However …

Directly Reprogrammed Human Neurons Retain Aging-Associated Transcriptomic Signatures and Reveal Age-Related Nucleocytoplasmic Defects.

J Mertens, ACM Paquola, M Ku, E Hatch, L Böhnke… - Cell Stem …, 2015 - europepmc.org
Aging is a major risk factor for many human diseases, and in vitro generation of human
neurons is an attractive approach for modeling aging-related brain disorders. However …