Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Nancy, Keller"'
Autor:
Nancy Keller, Julian Midgley, Ehtesham Khalid, Harry Lesmana, Georgie Mathew, Christine Mincham, Norbert Teig, Zubair Khan, Indu Khosla, Sam Mehr, Tulay Guran, Kathrin Buder, Hong Xu, Khalid Alhasan, Gonul Buyukyilmaz, Nicole Weaver, Julie D. Saba
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-17 (2024)
Abstract Background Sphingosine-1-phosphate lyase insufficiency syndrome (SPLIS) is a recently recognized inborn error of metabolism associated with steroid-resistant nephrotic syndrome as well as adrenal insufficiency and immunological, neurological
Externí odkaz:
https://doaj.org/article/001681b6efb54f18aee01a6b8c1590c9
Autor:
Piming Zhao, Gizachew B. Tassew, Joanna Y. Lee, Babak Oskouian, Denise P. Muñoz, Jeffrey B. Hodgin, Gordon L. Watson, Felicia Tang, Jen-Yeu Wang, Jinghui Luo, Yingbao Yang, Sarah King, Ronald M. Krauss, Nancy Keller, Julie D. Saba
Publikováno v:
JCI Insight, Vol 6, Iss 8 (2021)
Sphingosine-1-phosphate lyase insufficiency syndrome (SPLIS) is a rare metabolic disorder caused by inactivating mutations in sphingosine-1-phosphate lyase 1 (SGPL1), which is required for the final step of sphingolipid metabolism. SPLIS features inc
Externí odkaz:
https://doaj.org/article/9c9d0a0bbea44c69ba3c08fe8f691e88
Autor:
Claudio Costantini, Marina M. Bellet, Giorgia Renga, Claudia Stincardini, Monica Borghi, Marilena Pariano, Barbara Cellini, Nancy Keller, Luigina Romani, Teresa Zelante
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Externí odkaz:
https://doaj.org/article/635f34d2e1434f9680ad75373a9996f6
Publikováno v:
ACS Chemical Biology. 17:2828-2835
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c5d77c0585a73cd18b98e639a6b74f7
https://doi.org/10.1021/acschembio.2c00456
https://doi.org/10.1021/acschembio.2c00456
Autor:
Enzo Acerbi, Marcela Hortova-Kohoutkova, Tsokyi Choera, Nancy Keller, Jan Fric, Fabio Stella, Luigina Romani, Teresa Zelante
Publikováno v:
Journal of Fungi, Vol 6, Iss 3, p 108 (2020)
Systems biology approaches are extensively used to model and reverse-engineer gene regulatory networks from experimental data. Indoleamine 2,3-dioxygenases (IDOs)—belonging in the heme dioxygenase family—degrade l-tryptophan to kynurenines. These
Externí odkaz:
https://doaj.org/article/c345c60e28544d8c9035afc0cde4f62f
Publikováno v:
Frontiers in Plant Science, Vol 9 (2018)
The mycotoxin patulin is produced in colonized tissue by Penicillium expansum during storage of apples and is significantly affected by environmental factors that contribute to its accumulation. Few reports have, however, examined the effect of natur
Externí odkaz:
https://doaj.org/article/f9fbdb472e0645bd9167e9d13ed87207
Publikováno v:
PLoS pathogens. 18(3)
Invasive aspergillosis is a common opportunistic infection, causing >50% mortality in infected immunocompromised patients. The specific molecular mechanisms of the innate immune system that prevent pathogenesis of invasive aspergillosis in immunocomp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6bfe0a3b0c9ba9f15e13971c8448abc
https://pubmed.ncbi.nlm.nih.gov/35333905
https://pubmed.ncbi.nlm.nih.gov/35333905
Publikováno v:
Bio-Protocol, Vol 5, Iss 23 (2015)
Filamentous fungi and bacteria form mixed-species biofilms in nature and diverse clinical contexts (Frey-Klett et al., 2011; Peleg et al., 2010). The interactions between fungi and bacteria, often mediated by secreted metabolites, have important rami
Externí odkaz:
https://doaj.org/article/e946b104adcd49528ec821ec34d84db4
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 34:3833-3837
To evaluate if the implementation of five protocols aimed at reducing the preterm birth rate were associated with a decrease in incidence of PTBs at an academic center.This is an observational study of women with singleton gestations delivered at TJU
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::760216b6a570c110909d25c46ade1ca2
https://doi.org/10.1080/14767058.2019.1698029
https://doi.org/10.1080/14767058.2019.1698029
Publikováno v:
Cell biochemistry and biophysics. 79(3)
Sphingosine-1-phosphate lyase insufficiency syndrome (SPLIS) is a rare metabolic disorder caused by a deficiency in sphingosine-1-phosphate lyase (SPL), the final enzyme in the sphingolipid degradative pathway. Inactivating mutations of SGPL1-the gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d61db1f1694339c8751d1027d816f2a1
https://pubmed.ncbi.nlm.nih.gov/34133011
https://pubmed.ncbi.nlm.nih.gov/34133011