Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Julien Yockell-Lelièvre"'
Autor:
Adam Pietrobon, Julien Yockell‐Lelièvre, Nicole Melong, Laura J. Smith, Sean P. Delaney, Nadine Azzam, Chang Xue, Nishanth Merwin, Eric Lian, Alberto Camacho‐Magallanes, Carole Doré, Gabriel Musso, Lisa M. Julian, Arnold S. Kristof, Roger Y. Tam, Jason N. Berman, Molly S. Shoichet, William L. Stanford
Publikováno v:
Advanced Science, Vol 10, Iss 26, Pp n/a-n/a (2023)
Abstract Lymphangioleiomyomatosis (LAM) is a rare disease involving cystic lung destruction by invasive LAM cells. These cells harbor loss‐of‐function mutations in TSC2, conferring hyperactive mTORC1 signaling. Here, tissue engineering tools are
Externí odkaz:
https://doaj.org/article/a106fabeaeb643adbc219e24ad198f59
Autor:
Mehdi Benlarbi, Geneviève Laroche, Corby Fink, Kathy Fu, Rory P. Mulloy, Alexandra Phan, Ardeshir Ariana, Corina M. Stewart, Jérémie Prévost, Guillaume Beaudoin-Bussières, Redaet Daniel, Yuxia Bo, Omar El Ferri, Julien Yockell-Lelièvre, William L. Stanford, Patrick M. Giguère, Samira Mubareka, Andrés Finzi, Gregory A. Dekaban, Jimmy D. Dikeakos, Marceline Côté
Publikováno v:
iScience, Vol 25, Iss 11, Pp 105316- (2022)
Summary: The severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) spike glycoprotein (S) binds to angiotensin-converting enzyme 2 (ACE2) to mediate membrane fusion via two distinct pathways: 1) a surface, serine protease-dependent or 2) an en
Externí odkaz:
https://doaj.org/article/b5326a00cdee4b078296e90acdff771f
Publikováno v:
Cell Reports, Vol 40, Iss 1, Pp 111048- (2022)
Summary: Tuberous sclerosis complex (TSC) is a multisystem tumor-forming disorder caused by loss of TSC1 or TSC2. Renal manifestations predominately include cysts and angiomyolipomas. Despite a well-described monogenic etiology, the cellular pathogen
Externí odkaz:
https://doaj.org/article/f0004fe5c5dd472186c75770328808a9
Autor:
Richard L. Carpenedo, Sarah Y. Kwon, R. Matthew Tanner, Julien Yockell-Lelièvre, Chandarong Choey, Carole Doré, Mirabelle Ho, Duncan J. Stewart, Theodore J. Perkins, William L. Stanford
Publikováno v:
Stem Cell Reports, Vol 13, Iss 6, Pp 1111-1125 (2019)
Summary: Human pluripotent stem cells (hPSCs) are an essential cell source in tissue engineering, studies of development, and disease modeling. Efficient, broadly amenable protocols for rapid lineage induction of hPSCs are of great interest in the st
Externí odkaz:
https://doaj.org/article/d8a294f5ae494883a11b6954ed5ccb71
Autor:
William L. Stanford, Caryn Y. Ito, Mitchell Sabloff, Theodore J. Perkins, F. Jeffrey Dilworth, Alexander J. Ruthenburg, Elham Sabri, Adrian T. Grzybowski, Yuefeng Li, Joel P. Howard, Safwat T. Khan, Hannah L. Battaion, Julien Yockell-Lelièvre, Christopher J. Porter, Janet L. Manias Rothberg, Christopher Cafariello, Hani Jrade, Harinad B. Maganti
Supplementary figures and legends
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::768a48405a5ec3f531527029e18918fb
https://doi.org/10.1158/2159-8290.22531762.v1
https://doi.org/10.1158/2159-8290.22531762.v1
Autor:
William L. Stanford, Caryn Y. Ito, Mitchell Sabloff, Theodore J. Perkins, F. Jeffrey Dilworth, Alexander J. Ruthenburg, Elham Sabri, Adrian T. Grzybowski, Yuefeng Li, Joel P. Howard, Safwat T. Khan, Hannah L. Battaion, Julien Yockell-Lelièvre, Christopher J. Porter, Janet L. Manias Rothberg, Christopher Cafariello, Hani Jrade, Harinad B. Maganti
Extended Material and Methods
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac72e4f80651b083344b03a2662fac9b
https://doi.org/10.1158/2159-8290.22531774
https://doi.org/10.1158/2159-8290.22531774
Autor:
William L. Stanford, Caryn Y. Ito, Mitchell Sabloff, Theodore J. Perkins, F. Jeffrey Dilworth, Alexander J. Ruthenburg, Elham Sabri, Adrian T. Grzybowski, Yuefeng Li, Joel P. Howard, Safwat T. Khan, Hannah L. Battaion, Julien Yockell-Lelièvre, Christopher J. Porter, Janet L. Manias Rothberg, Christopher Cafariello, Hani Jrade, Harinad B. Maganti
Supplementary Tables 1-2, 4-6, 9-11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1033bcb83d10321319d09903e0a236f7
https://doi.org/10.1158/2159-8290.22531771
https://doi.org/10.1158/2159-8290.22531771
Autor:
William L. Stanford, Caryn Y. Ito, Mitchell Sabloff, Theodore J. Perkins, F. Jeffrey Dilworth, Alexander J. Ruthenburg, Elham Sabri, Adrian T. Grzybowski, Yuefeng Li, Joel P. Howard, Safwat T. Khan, Hannah L. Battaion, Julien Yockell-Lelièvre, Christopher J. Porter, Janet L. Manias Rothberg, Christopher Cafariello, Hani Jrade, Harinad B. Maganti
Supplementary Tables 3, 7-8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f1bb0f9ee0c5eb3f4e21766fecb3b18
https://doi.org/10.1158/2159-8290.22531768
https://doi.org/10.1158/2159-8290.22531768
Autor:
William L. Stanford, Arnold S. Kristof, Joel Moss, Thomas N. Darling, David J. Kwiatkowski, Elizabeth P. Henske, Mary-Ellen Harper, Molly S. Shoichet, Fiona McMurray, Krinio Giannikou, Roger Y. Tam, Julien Yockell-Lelièvre, Carole Doré, Alexander A. Goldberg, Ying Wang, Sean P. Delaney, Lisa M. Julian
Lymphangioleiomyomatosis (LAM) is a progressive destructive neoplasm of the lung associated with inactivating mutations in the TSC1 or TSC2 tumor suppressor genes. Cell or animal models that accurately reflect the pathology of LAM have been challengi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d8ab7f18f8b3d005ebe6781b8fa443f
https://doi.org/10.1158/0008-5472.c.6509205
https://doi.org/10.1158/0008-5472.c.6509205
Autor:
William L. Stanford, Arnold S. Kristof, Joel Moss, Thomas N. Darling, David J. Kwiatkowski, Elizabeth P. Henske, Mary-Ellen Harper, Molly S. Shoichet, Fiona McMurray, Krinio Giannikou, Roger Y. Tam, Julien Yockell-Lelièvre, Carole Doré, Alexander A. Goldberg, Ying Wang, Sean P. Delaney, Lisa M. Julian
This file contains the full descriptive legends for Supplementary Figures S1-S7.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1548f6bcaee4445974e4de36e929f399
https://doi.org/10.1158/0008-5472.22415232.v1
https://doi.org/10.1158/0008-5472.22415232.v1