Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Nina Movsesyan"'
Autor:
Raymond Y. Wang, Kyle D. Rudser, Donald R. Dengel, Nicholas Evanoff, Julia Steinberger, Nina Movsesyan, Robert Garrett, Katherine Christensen, Deborah Boylan, Stephen R. Braddock, Marwan Shinawi, Qi Gan, Adriana M. Montaño
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Abstract Background Cardiovascular disease frequently causes morbidity and mortality in mucopolysaccharidoses (MPS); however, cardiovascular anatomy and dysfunction in MPS IVA (Morquio A disease) is not well described. Consequently, the study aimed t
Externí odkaz:
https://doaj.org/article/86c21a6f386d4ecdb984bab4aa309028
Publikováno v:
Wellcome Open Research, Vol 2 (2017)
In this case series, we demonstrate that Ursodeoxycholic acid (UDCA) improves liver dysfunction in Niemann-Pick type C (NPC) and may restore a suppressed cytochrome p450 system. NPC disease is a progressive neurodegenerative lysosomal storage disease
Externí odkaz:
https://doaj.org/article/fbc598971e374eafa6a45bce90c960d0
Autor:
Nina Movsesyan, Anahit Ghochikyan, Mikayel Mkrtichyan, Irina Petrushina, Hayk Davtyan, Purevdorj B Olkhanud, Elizabeth Head, Arya Biragyn, David H Cribbs, Michael G Agadjanyan
Publikováno v:
PLoS ONE, Vol 3, Iss 5, p e2124 (2008)
The development of a safe and effective AD vaccine requires a delicate balance between providing an adequate anti-Abeta antibody response sufficient to provide therapeutic benefit, while eliminating an adverse T cell-mediated proinflammatory autoimmu
Externí odkaz:
https://doaj.org/article/308a349322b74c7faeaebd492671e2c9
Autor:
Rohini Sidhu, An Ngoc Dang Do, Charles Marques Lourenço, Forbes D. Porter, Raymond Y. Wang, Daniel S. Ory, Xuntian Jiang, Roberto Giugliani, Janine Reunert, Elizabeth Berry-Kravis, Ellen Plummer, Pamela Kell, Nicole Y. Farhat, Jean E. Schaffer, Nina Movsesyan, Dennis J. Dietzen, Thorsten Marquardt
Publikováno v:
Molecular genetics and metabolism, vol 131, iss 4
Mol Genet Metab
Mol Genet Metab
Niemann-Pick disease type C (NPC) is a neurodegenerative disease in which mutation of NPC1 or NPC2 gene leads to lysosomal accumulation of unesterified cholesterol and sphingolipids. Diagnosis of NPC disease is challenging due to non-specific early s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1daa242a612423896105e7fe9b5c50d8
https://doi.org/10.1016/j.ymgme.2020.11.005
https://doi.org/10.1016/j.ymgme.2020.11.005
Autor:
Yelena Aghajanova, Margarita Hovhannisyan, Nina Alchujyan, Arthur Melkonyan, Vanuhi Shaboyan, Nina Movsesyan, Grigory Minasyan, Guevork Kevorkian
Publikováno v:
Endocrine research. 46(4)
Background: Sexual dimorphism in specific biochemical pathways and immune response, underlies the heterogeneity of type 1 diabetes mellitus (T1DM) and affects the outcome of immunotherapy. Arginase...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d8281b9513e26c8ccc9d655f0c991a0
https://pubmed.ncbi.nlm.nih.gov/33944639
https://pubmed.ncbi.nlm.nih.gov/33944639
Autor:
Marwan Shinawi, Donald R. Dengel, Julia Steinberger, Adriana M. Montaño, Raymond Y. Wang, Kyle Rudser, Stephen R. Braddock, Nina Movsesyan, Qi Gan, Katherine M. Christensen, Nicholas G. Evanoff, Deborah Boylan, Robert Garrett
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Orphanet journal of rare diseases, vol 15, iss 1
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Orphanet journal of rare diseases, vol 15, iss 1
Background Cardiovascular disease frequently causes morbidity and mortality in mucopolysaccharidoses (MPS); however, cardiovascular anatomy and dysfunction in MPS IVA (Morquio A disease) is not well described. Consequently, the study aimed to compare
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50656f1dbaf192ca5cc4c2ef985095cf
http://europepmc.org/articles/PMC7079365
http://europepmc.org/articles/PMC7079365
Autor:
Nina Movsesyan, Bryan Pukenas, Shih-hsin Kan, Yoonjin Cho, Paulo Falabella, Igor Nestrasil, Marie-Laure Nevoret, Raymond Y. Wang, Mery Taylor, Tammam Beydoun, Winnie Stockton
Publikováno v:
Molecular Genetics and Metabolism. 132:S110
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20122776a315f66dfe211db4faeda4f0
https://doi.org/10.1016/j.ymgme.2020.12.270
https://doi.org/10.1016/j.ymgme.2020.12.270
Publikováno v:
Journal of Intellectual Disability Research. 59:1071-1079
HHS Public Access Author manuscript Author Manuscript J Intellect Disabil Res. Author manuscript; available in PMC 2016 November 01. Published in final edited form as: J Intellect Disabil Res. 2015 November ; 59(11): 1071–1079. doi:10.1111/jir.1220
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af84d5acfa277822609b420b65281332
https://doi.org/10.1111/jir.12200
https://doi.org/10.1111/jir.12200
Publikováno v:
Wellcome Open Research
In this case series, we demonstrate that Ursodeoxycholic acid (UDCA) improves liver dysfunction in Niemann-Pick type C (NPC) and may restore a suppressed cytochrome p450 system. NPC disease is a progressive neurodegenerative lysosomal storage disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf8a082fa1b4109cba266b995ca6bad7
https://escholarship.org/uc/item/53m1c4jr
https://escholarship.org/uc/item/53m1c4jr
Publikováno v:
Molecular Genetics and Metabolism. 123:S141-S142
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de172ed50cbc7bef0cde2905af5b5f7d
https://doi.org/10.1016/j.ymgme.2017.12.390
https://doi.org/10.1016/j.ymgme.2017.12.390