Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Eliza J, Ferrari"'
Autor:
Joanna A. Korecka, Sebastien Talbot, Teresia M. Osborn, Sherida M. de Leeuw, Simon A. Levy, Eliza J. Ferrari, Alyssa Moskites, Elise Atkinson, Francine M. Jodelka, Anthony J. Hinrich, Michelle L. Hastings, Clifford J. Woolf, Penelope J. Hallett, Ole Isacson
Publikováno v:
Stem Cell Reports, Vol 12, Iss 1, Pp 29-41 (2019)
Summary: The Parkinson disease (PD) genetic LRRK2 gain-of-function mutations may relate to the ER pathological changes seen in PD patients at postmortem. Human induced pluripotent stem cell (iPSC)-derived neurons with the PD pathogenic LRRK2 G2019S m
Externí odkaz:
https://doaj.org/article/872a0bc4898b44ba96fb040e2470c7bb
Publikováno v:
Neurobiology of Disease, Vol 120, Iss , Pp 1-11 (2018)
GPNMB is a glycoprotein observed upon tissue damage and inflammation and is associated with astrocytes, microglia, and macrophages. Gene variations in GPNMB are linked with Parkinson's disease (PD) risk, and changes in protein levels of GPNMB have be
Externí odkaz:
https://doaj.org/article/e45ebeff7e3043fdb4b68922daac954b
Autor:
Lucas M. Harrison, Eliza J. Ferrari, Denzil P. Mathew, Christopher A. Derderian, Rami R. Hallac
Publikováno v:
The Cleft Palate Craniofacial Journal. :105566562311768
Objective Unilateral lambdoid synostosis (ULS) is characterized by occipital flattening, mastoid bulging, and contralateral parietal bossing. Anterior craniofacial features are less well-defined. This study utilizes volumetric, craniometric, and comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6cc8aff39071d0cdf389d9cd3ca22a1
https://doi.org/10.1177/10556656231176876
https://doi.org/10.1177/10556656231176876
Autor:
Ole Isacson, Anthony J. Hinrich, Simon A. Levy, Elise Atkinson, Sherida M. de Leeuw, Eliza J. Ferrari, Alyssa Moskites, Sébastien Talbot, Clifford J. Woolf, Penelope J. Hallett, Teresia Osborn, Joanna A. Korecka, Francine M. Jodelka, Michelle L. Hastings
Publikováno v:
Stem Cell Reports, Vol 12, Iss 1, Pp 29-41 (2019)
Summary: The Parkinson disease (PD) genetic LRRK2 gain-of-function mutations may relate to the ER pathological changes seen in PD patients at postmortem. Human induced pluripotent stem cell (iPSC)-derived neurons with the PD pathogenic LRRK2 G2019S m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f993e77d09a81f7c9f359c3ea4c53bf5
http://www.sciencedirect.com/science/article/pii/S2213671118304909
http://www.sciencedirect.com/science/article/pii/S2213671118304909
Autor:
Joanna A, Korecka, Sebastien, Talbot, Teresia M, Osborn, Sherida M, de Leeuw, Simon A, Levy, Eliza J, Ferrari, Alyssa, Moskites, Elise, Atkinson, Francine M, Jodelka, Anthony J, Hinrich, Michelle L, Hastings, Clifford J, Woolf, Penelope J, Hallett, Ole, Isacson
Publikováno v:
Stem Cell Reports
Summary The Parkinson disease (PD) genetic LRRK2 gain-of-function mutations may relate to the ER pathological changes seen in PD patients at postmortem. Human induced pluripotent stem cell (iPSC)-derived neurons with the PD pathogenic LRRK2 G2019S mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::73d3f53cb076d0d3c3693e4544876483
https://pubmed.ncbi.nlm.nih.gov/30595548
https://pubmed.ncbi.nlm.nih.gov/30595548
Publikováno v:
Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology. 31
Hereditary multiple exostoses (HME) is a genetic condition characterized by the development of multiple osteochondromas during childhood and adolescence. On rare occasions, these bony tumors can be associated with vascular injury, most commonly invol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c78c7258b7d24f94cb40b7ed2cbbdcd0
https://pubmed.ncbi.nlm.nih.gov/28818770
https://pubmed.ncbi.nlm.nih.gov/28818770