Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Julia G. Bindman"'
Autor:
Bernadette Y. Hsu, Julia G. Bindman, Andrew A. Grimm, Robert F. Schwabe, Holger Willenbring, Milad Rezvani, Regina Español-Suñer, Dirk Grimm, Ellen Wiedtke, Carlos U. Corvera, Syed Naqvi, Y Malato, Eike Kienle, Laure Dumont
Publikováno v:
Cell Stem Cell. 18:809-816
Liver fibrosis, a form of scarring, develops in chronic liver diseases when hepatocyte regeneration cannot compensate for hepatocyte death. Initially, collagen produced by myofibroblasts (MFs) functions to maintain the integrity of the liver, but exc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::caff4589ed17c8a0983d6dda006bfead
https://doi.org/10.1016/j.stem.2016.05.005
https://doi.org/10.1016/j.stem.2016.05.005
Autor:
Christiane Hammerschmidt-Kamper, Lars Kaderali, Julia M. Sattler, Franziska Hentzschel, Julia G. Bindman, Dirk Grimm, Y Malato, Kirsten Heiss, Kathleen Börner, Ann-Kristin Mueller, Holger Willenbring, Bettina Knapp, Mirco Castoldi
Publikováno v:
Mol. Ther. 22, 2130-2141 (2014)
Molecular therapy : the journal of the American Society of Gene Therapy, vol 22, iss 12
Molecular therapy : the journal of the American Society of Gene Therapy, vol 22, iss 12
Malaria, caused by protozoan Plasmodium parasites, remains a prevalent infectious human disease due to the lack of an efficient and safe vaccine. This is directly related to the persisting gaps in our understanding of the parasite's interactions with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d0a2b78f9411df0b95b4d0a8740292a
https://doi.org/10.1038/mt.2014.172
https://doi.org/10.1038/mt.2014.172
Autor:
Djahida Bedja, Nuria Amat-Alarcon, Norimichi Koitabashi, Eiki Takimoto, Elizabeth E. Gerber, Elena Gallo MacFarlane, Julia G. Bindman, Varun Nagpal, Dong I. Lee, Christopher Schiefer, Rahul Chaudhary, Guangshuo Zhu, Peter P. Rainer, Karen L. Miller, David A. Kass, Rosanne Rouf, Harry C. Dietz, Loretha Myers, Daniel P. Judge
Publikováno v:
JCI insight. 2(15)
Among children with the most severe presentation of Marfan syndrome (MFS), an inherited disorder of connective tissue caused by a deficiency of extracellular fibrillin-1, heart failure is the leading cause of death. Here, we show that, while MFS mice
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50a2522581bb9b3ee2452ace613725c2
https://pubmed.ncbi.nlm.nih.gov/28768908
https://pubmed.ncbi.nlm.nih.gov/28768908