Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Julie Nouet"'
Autor:
Yoshifumi Kobayashi, Julie Nouet, Erdenechimeg Baljinnyam, Zain Siddiqui, Daniel H. Fine, Diego Fraidenraich, Vivek A. Kumar, Emi Shimizu
Publikováno v:
Bioactive Materials, Vol 14, Iss , Pp 290-301 (2022)
The dental pulp has irreplaceable roles in maintaining healthy teeth and its regeneration is a primary aim of regenerative endodontics. This study aimed to replicate the characteristics of dental pulp tissue by using cranial neural crest (CNC)-like c
Externí odkaz:
https://doaj.org/article/78fc7143d0d846f7aaa2c85075b8bdf4
Autor:
Eric Himelman, Julie Nouet, Mauricio A. Lillo, Alexander Chong, Delong Zhou, Xander H. T. Wehrens, George G. Rodney, Lai-Hua Xie, Natalia Shirokova, Jorge E. Contreras, Diego Fraidenraich
Publikováno v:
American Journal of Physiology-Heart and Circulatory Physiology. 323:H983-H995
Dilated cardiomyopathy is the leading cause of death in Duchenne muscular dystrophy (DMD), an inherited degenerative disease of the cardiac and skeletal muscle caused by absence of the protein dystrophin. We showed one hallmark of DMD cardiomyopathy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a86255591c808805041d03090769303
https://doi.org/10.1152/ajpheart.00179.2022
https://doi.org/10.1152/ajpheart.00179.2022
Autor:
Eric Himelman, Julie Nouet, Mauricio A. Lillo, Alexander Chong, Xander H.T. Wehrens, George G. Rodney, Lai-Hua Xie, Natalia Shirokova, Jorge E. Contreras, Diego Fraidenraich
Dilated cardiomyopathy is the leading cause of death in Duchenne muscular dystrophy (DMD) patients due to advancements in skeletal muscle therapies yet limited presence of cardiac treatments. The phosphorylation status of gap junction protein Connexi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73f953eceef23b02dbe1e5d0f08be8e4
https://doi.org/10.1101/2022.03.29.486276
https://doi.org/10.1101/2022.03.29.486276
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-11 (2020)
Scientific Reports
Scientific Reports
Duchenne muscular dystrophy (DMD) is a severe X-linked neuromuscular disorder that affects males. However, 8% of female carriers are symptomatic and underrepresented in research due to the lack of animal models. We generated a symptomatic mouse model
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9436721c17035881d4f199d910b761fc
http://link.springer.com/article/10.1038/s41598-020-62844-9
http://link.springer.com/article/10.1038/s41598-020-62844-9
Autor:
Emi Shimizu, Vivek A. Kumar, Diego Fraidenraich, Julie Nouet, Yoshifumi Kobayashi, Erdenechimeg Baljinnyam, Zain Siddiqui, Daniel H. Fine
Publikováno v:
Bioactive materials. 14
The dental pulp has irreplaceable roles in maintaining healthy teeth and its regeneration is a primary aim of regenerative endodontics. This study aimed to replicate the characteristics of dental pulp tissue by using cranial neural crest (CNC)-like c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0ee81b374f53e381c49f215254b40ea
https://pubmed.ncbi.nlm.nih.gov/35310357
https://pubmed.ncbi.nlm.nih.gov/35310357
Publikováno v:
Circulation Research. 127
Duchenne muscular dystrophy (DMD) and its associated cardiomyopathy manifest in 8-10% of all female carriers however research remains male-centric. Although underrepresented, symptomatic females face the risk of cardiac, respiratory, and skeletal mus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45367f1ca73a14050f75adcfa971d0c8
https://doi.org/10.1161/res.127.suppl_1.478
https://doi.org/10.1161/res.127.suppl_1.478
Autor:
Mauricio A. Lillo, J. Patrick Gonzalez, Lai-Hua Xie, Qingshi Zhao, Natalia Shirokova, Tong Liu, Jorge E. Contreras, Julie Nouet, Eric Himelman, Hong Li, Paul D. Lampe, Xander H.T. Wehrens, Glenn I. Fishman, Diego Fraidenraich
Publikováno v:
The Journal of clinical investigation, vol 130, iss 4
Aberrant expression of the cardiac gap junction protein connexin-43 (Cx43) has been suggested as playing a role in the development of cardiac disease in the mdx mouse model of Duchenne muscular dystrophy (DMD); however, a mechanistic understanding of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::651f0e462d44d753cec3337bdb21eeb3
https://escholarship.org/uc/item/9rb0m8s6
https://escholarship.org/uc/item/9rb0m8s6
Autor:
Myriam A. Badr, Jayalakshmi Ramachandran, J. Patrick Gonzalez, Nadezhda Fefelova, Julie Nouet, Diego Fraidenraich, Lai-Hua Xie, Natalia Shirokova, Jorge E. Contreras, Chifei Kang, Eric Himelman
Publikováno v:
Neuromuscular disorders : NMD. 28(4)
Duchenne muscular dystrophy (DMD) associated cardiomyopathy remains incurable. Connexin 43 (Cx43) is upregulated and remodeled in the hearts of mdx mice, a mouse model of DMD. Hearts from Wild Type, mdx, and mdx:Cx43(+/-) mice were studied before (4-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16e5d8412a98741087162aa68ce5d8e1
https://pubmed.ncbi.nlm.nih.gov/29477453
https://pubmed.ncbi.nlm.nih.gov/29477453