Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Susan, Sobolov"'
Autor:
Jason Valent, Michaela Liedtke, Jeffrey Zonder, John Silowsky, Michael Kurman, Eileen Daniel, Janet Jobes, Mark Harnett, Amit Bhattacharyya, Candida Cristina Quarta, Julia Catini, Jessica Raviwong, Michael Spector, Susan Sobolov
Publikováno v:
Journal of the American College of Cardiology. 79:305
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee3332b370c05e26b8efe23d02a3c7f7
https://doi.org/10.1016/s0735-1097(22)01296-7
https://doi.org/10.1016/s0735-1097(22)01296-7
Autor:
Lucy S. Jun, Nanda Balasubramanian, Lin Lin, Susan Sobolov, Xiang Gao, Bjorn L. Miliard, Jian-Ping Tang, Melissa A. Lasaro, Michael R. Hodges, John M. Burke, Joshua F. Apgar, Kevin J. Moore, Anna Katharina Wilkins, Pratap Singh
Publikováno v:
CPT: Pharmacometrics & Systems Pharmacology. 7:404-412
Crigler-Najjar syndrome type 1 (CN1) is an autosomal recessive disease caused by a marked decrease in uridine-diphosphate-glucuronosyltransferase (UGT1A1) enzyme activity. Delivery of hUGT1A1-modRNA (a modified messenger RNA encoding for UGT1A1) as a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e596ac0f011b45481ac39b69d38242d
https://doi.org/10.1002/psp4.12301
https://doi.org/10.1002/psp4.12301
Autor:
Joshua F, Apgar, Jian-Ping, Tang, Pratap, Singh, Nanda, Balasubramanian, John, Burke, Michael R, Hodges, Melissa A, Lasaro, Lin, Lin, Bjorn L, Millard, Kristi, Moore, Lucy S, Jun, Susan, Sobolov, Anna Katharina, Wilkins, Xiang, Gao
Publikováno v:
CPT: Pharmacometrics & Systems Pharmacology
Crigler‐Najjar syndrome type 1 (CN1) is an autosomal recessive disease caused by a marked decrease in uridine‐diphosphate‐glucuronosyltransferase (UGT1A1) enzyme activity. Delivery of hUGT1A1‐modRNA (a modified messenger RNA encoding for UGT1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::b6259f975f70e47c83e009e9a153a9d8
http://europepmc.org/articles/PMC6391595
http://europepmc.org/articles/PMC6391595
Autor:
Anjli Kukreja, Angel L. Pey, Susan Sobolov, Jian-Ping Tang, Xiang Gao, Melissa A. Lasaro, Eduardo Salido, Romesh R. Subramanian, Christian Cobaugh, Cristina Martin-Higueras, Chris Forbes
Publikováno v:
Nucleic acid therapeutics. 29(2)
Primary Hyperoxaluria Type 1 (PH1) is an autosomal recessive disorder of glyoxylate metabolism. Loss of alanine glyoxylate aminotransferase (AGT) function to convert intermediate metabolite glyoxylate to glycine causes the accumulation and reduction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c334bb65fe3806467b5a3378eb18e6e9
https://pubmed.ncbi.nlm.nih.gov/30676254
https://pubmed.ncbi.nlm.nih.gov/30676254