Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Dina A Faddah"'
Autor:
Allen Wang, Joshua Chiou, Olivier B Poirion, Justin Buchanan, Michael J Valdez, Jamie M Verheyden, Xiaomeng Hou, Parul Kudtarkar, Sharvari Narendra, Jacklyn M Newsome, Minzhe Guo, Dina A Faddah, Kai Zhang, Randee E Young, Justinn Barr, Eniko Sajti, Ravi Misra, Heidie Huyck, Lisa Rogers, Cory Poole, Jeffery A Whitsett, Gloria Pryhuber, Yan Xu, Kyle J Gaulton, Sebastian Preissl, Xin Sun, NHLBI LungMap Consortium
Publikováno v:
eLife, Vol 9 (2020)
Respiratory failure associated with COVID-19 has placed focus on the lungs. Here, we present single-nucleus accessible chromatin profiles of 90,980 nuclei and matched single-nucleus transcriptomes of 46,500 nuclei in non-diseased lungs from donors of
Externí odkaz:
https://doaj.org/article/a3ede76a7aec424cbe10045fed11ea98
Autor:
Dina A Faddah, Eric W Ganko, Caroline McCoach, Joseph K Pickrell, Sean E Hanlon, Frederick G Mann, Joanna O Mieczkowska, Corbin D Jones, Jason D Lieb, Todd J Vision
Publikováno v:
PLoS Genetics, Vol 5, Iss 6, p e1000502 (2009)
High-throughput techniques for detecting DNA polymorphisms generally do not identify changes in which the genomic position of a sequence, but not its copy number, varies among individuals. To explore such balanced structural polymorphisms, we used ar
Externí odkaz:
https://doaj.org/article/7883736c185f4c3f9945529f3c23b193
Autor:
Rachel Lasry, Noam Maoz, Albert W. Cheng, Nataly Yom Tov, Elisabeth Kulenkampff, Meir Azagury, Hui Yang, Cora Ople, Styliani Markoulaki, Dina A. Faddah, Kirill Makedonski, Ofra Sabbag, Rudolf Jaenisch, Yosef Buganim
A complete knockout (KO) of a single key pluripotency gene has been shown to drastically affect embryonic stem cell (ESC) function and epigenetic reprogramming. However, knockin (KI)/KO of a reporter gene only in one of two alleles in a single plurip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf279f3ce01365409347813a3802c36f
https://doi.org/10.1101/2022.05.18.492474
https://doi.org/10.1101/2022.05.18.492474
Autor:
Gloria S. Pryhuber, Cory Poole, Sharvari Narendra, Olivier Poirion, Jacklyn M Newsome, Minzhe Guo, Dina A. Faddah, Parul Kudtarkar, Allen Wang, Xiaomeng Hou, Heidie Huyck, Jamie M. Verheyden, Randee E. Young, Ravi S. Misra, Xin Sun, Justin Buchanan, Joshua Chiou, Eniko Sajti, Lisa Rogers, Kyle J. Gaulton, Yan Xu, Kai Zhang, Sebastian Preissl, JA Whitsett, Justinn Barr, Michael J Valdez
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63f210ea57a7c117b41d32c584938487
https://doi.org/10.7554/elife.62522.sa2
https://doi.org/10.7554/elife.62522.sa2
Publikováno v:
PMC
The homeodomain transcription factor Nanog is a central part of the core pluripotency transcriptional network and plays a critical role in embryonic stem cell (ESC) self-renewal. Several reports have suggested that Nanog expression is allelically reg
Autor:
Sandy Klemm, Kibibi Ganz, Yosef Buganim, Elena Itskovich, Alexander van Oudenaarden, Styliani Markoulaki, Dina A. Faddah, Albert W. Cheng, Rudolf Jaenisch
Publikováno v:
Cell, 150(6), 1209-1222. Elsevier B.V.
SummaryDuring cellular reprogramming, only a small fraction of cells become induced pluripotent stem cells (iPSCs). Previous analyses of gene expression during reprogramming were based on populations of cells, impeding single-cell level identificatio
Autor:
Urraca Tavarez, Hong San, Karen N. Conneely, Michelle Olive, Michael R. Erdos, Brian C. Capell, Elizabeth G. Nabel, Francis S. Collins, Renu Virmani, Xiaoyan Chen, Santhi K. Ganesh, Kan Cao, Frank D. Kolodgie, Dina A. Faddah, Xuan Qu, Hedwig Avallone
Publikováno v:
Proceedings of the National Academy of Sciences. 105:15902-15907
Hutchinson-Gilford progeria syndrome (HGPS) is the most dramatic form of human premature aging. Death occurs at a mean age of 13 years, usually from heart attack or stroke. Almost all cases of HGPS are caused by a de novo point mutation in the lamin
Autor:
Renu Virmani, Thomas N. Wight, Leslie B. Gordon, Stacie Perkins, Jun Cheng, Francis S. Collins, Frank D. Kolodgie, Michelle Olive, Michael R. Erdos, Maria Eriksson, Hong San, Xuan Qu, Elizabeth G. Nabel, Santhi K. Ganesh, Hedwig Avallone, Dina A. Faddah, Ingrid A. Harten, Renee Varga, Brian C. Capell
Publikováno v:
Proceedings of the National Academy of Sciences. 103:3250-3255
Children with Hutchinson–Gilford progeria syndrome (HGPS) suffer from dramatic acceleration of some symptoms associated with normal aging, most notably cardiovascular disease that eventually leads to death from myocardial infarction and/or stroke u
Autor:
Haoyi Wang, Benjamin E. Powell, Meelad M. Dawlaty, Ana C. D’Alessio, Richard A. Young, Maya Mitalipova, Nathanael S. Gray, Dina A. Faddah, Thorold W. Theunissen, Dorothea Maetzel, Zi Peng Fan, Jessica Reddy, Kibibi Ganz, Qing Gao, Sumeth Imsoonthornruksa, Linyu Shi, Rudolf Jaenisch, Tenzin Lungjangwa, Yonatan Stelzer, Jianming Zhang, Sudharshan Rangarajan
Publikováno v:
Cell Stem Cell
Summary Embryonic stem cells (ESCs) of mice and humans have distinct molecular and biological characteristics, raising the question of whether an earlier, “naive” state of pluripotency may exist in humans. Here we took a systematic approach to id
Autor:
Alexander van Oudenaarden, Dina A. Faddah, Kay Wiebrands, Rudolf Jaenisch, Sandy Klemm, Dylan Mooijman, Stefan Semrau
Publikováno v:
Nature Methods, 11(5), 549-51. Nature Publishing Group
We have developed a quantitative technique for sorting cells on the basis of endogenous RNA abundance, with a molecular resolution of 10-20 transcripts. We demonstrate efficient and unbiased RNA extraction from transcriptionally sorted cells and repo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9905c6b1ffec714489512d8101240c5b
https://pure.knaw.nl/portal/en/publications/59fa3ea2-0d2b-4cb6-83de-76257c808a01
https://pure.knaw.nl/portal/en/publications/59fa3ea2-0d2b-4cb6-83de-76257c808a01