Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Nathanel Eafergan"'
Autor:
Yi Kuang, Ohad Golan, Kristina Preusse, Brittany Cain, Collin J Christensen, Joseph Salomone, Ian Campbell, FearGod V Okwubido-Williams, Matthew R Hass, Zhenyu Yuan, Nathanel Eafergan, Kenneth H Moberg, Rhett A Kovall, Raphael Kopan, David Sprinzak, Brian Gebelein
Publikováno v:
eLife, Vol 9 (2020)
Notch pathway haploinsufficiency can cause severe developmental syndromes with highly variable penetrance. Currently, we have a limited mechanistic understanding of phenotype variability due to gene dosage. Here, we unexpectedly found that inserting
Externí odkaz:
https://doaj.org/article/d503de51d4de46d4b3e298e0644a7d3d
Autor:
Brian Gebelein, Zhenyu Yuan, Yi Kuang, Raphael Kopan, Matthew R. Hass, FearGod V Okwubido-Williams, Ohad Golan, Kristina Preusse, Joseph Salomone, Collin J Christensen, Brittany Cain, Rhett A. Kovall, David Sprinzak, Ian Campbell, Kenneth H. Moberg, Nathanel Eafergan
Publikováno v:
eLife, Vol 9 (2020)
Notch pathway haploinsufficiency can cause severe developmental syndromes with highly variable penetrance. Currently, we have a limited mechanistic understanding of phenotype variability due to gene dosage. Here, we unexpectedly found that inserting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::830b6f447d0e1bd3898e0fdaa1f85633
https://doi.org/10.7554/elife.53659
https://doi.org/10.7554/elife.53659
Autor:
Yi Kuang, Kristina Preusse, Matthew R. Hass, Ohad Golan, Ian Campbell, Zhenyu Yuan, David Sprinzak, Rhett A. Kovall, Raphael Kopan, Brittany Cain, Collin J Christensen, Brian Gebelein, Kenneth H. Moberg, FearGod V Okwubido-Williams, Nathanel Eafergan, Joseph Salomone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d808fd3b59b5e4b091bd358f10b40808
https://doi.org/10.7554/elife.53659.sa2
https://doi.org/10.7554/elife.53659.sa2
Autor:
Yi, Kuang, Ohad, Golan, Kristina, Preusse, Brittany, Cain, Collin J, Christensen, Joseph, Salomone, Ian, Campbell, FearGod V, Okwubido-Williams, Matthew R, Hass, Zhenyu, Yuan, Nathanel, Eafergan, Kenneth H, Moberg, Rhett A, Kovall, Raphael, Kopan, David, Sprinzak, Brian, Gebelein
Publikováno v:
eLife
Notch pathway haploinsufficiency can cause severe developmental syndromes with highly variable penetrance. Currently, we have a limited mechanistic understanding of phenotype variability due to gene dosage. Here, we unexpectedly found that inserting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::46a87967f57a71a7155d5e1569dca511
https://pubmed.ncbi.nlm.nih.gov/32297857
https://pubmed.ncbi.nlm.nih.gov/32297857