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pro vyhledávání: '"T. Burlingame"'
Akademický článek
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Autor:
Wang, Boyuan1,2 (AUTHOR), Mao, Jiale3 (AUTHOR), Ma, Yihan1 (AUTHOR), Ke, Ming4 (AUTHOR), Zhao, Wei1 (AUTHOR), Butt, Usman Dawood1 (AUTHOR), Liu, Shuang3 (AUTHOR), Zhang, Xiaoqin3 (AUTHOR) 382149034@qq.com, Zhang, Zunjing3 (AUTHOR) 382149034@qq.com
Publikováno v:
Natural Product Communications. Nov2024, Vol. 19 Issue 11, p1-13. 13p.
Autor:
Kaatje Meeuws, Cary O. Harding, Piero Rinaldo, T. Burlingame, Melanie B. Gillingham, Dietrich Matern, William E. Connor
Publikováno v:
Molecular Genetics and Metabolism. 79:114-123
Current dietary therapy for long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency consists of fasting avoidance, and limiting long-chain fatty acid (LCFA) intake. This study reports the relationship of dietary i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d4f10d0c1fd0de84700515d8a8e07d5
https://doi.org/10.1016/s1096-7192(03)00073-8
https://doi.org/10.1016/s1096-7192(03)00073-8
Autor:
José Manuel Fernández-Cañón, K. Michael Gibson, Manfred W. Baetscher, T. Burlingame, Milton J. Finegold, Markus Grompe
Publikováno v:
Molecular and Cellular Biology. 22:4943-4951
In mammals, the catabolic pathway of phenylalanine and tyrosine is found in liver (hepatocytes) and kidney (proximal tubular cells). There are well-described human diseases associated with deficiencies of all enzymes in this pathway except for maleyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7353c505c204f3041feeed8f20f4a50a
https://doi.org/10.1128/mcb.22.13.4943-4951.2002
https://doi.org/10.1128/mcb.22.13.4943-4951.2002
Autor:
W. S. Guerand, Markus Grompe, T. Burlingame, Cornelis Jakobs, Henry Senephansiri, D. S. M. Schor, Teodoro Bottiglieri, Maneesh Gupta, Boris M. Hogema, K. M. Gibson, O. C. Snead, Wolfgang Froestl, H. Bartels
Publikováno v:
Journal of Neurochemistry. 81:71-79
Metabolite profiling in succinate semialdehyde dehydrogenase (SSADH; Aldh5a1–/–) deficient mice previously revealed elevated γ-hydroxybutyrate (GHB) and total GABA in urine and total brain and liver extracts. In this study, we extend our metabol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43c9b9319f5a95d3b66c02f7d88af0b7
https://doi.org/10.1046/j.1471-4159.2002.00784.x
https://doi.org/10.1046/j.1471-4159.2002.00784.x
Autor:
G.S. Tint, Robert D. Steiner, Kevin P. Battaile, William E. Connor, Megumi Honda, Akira Honda, Don S. Lin, S. J. Hayflick, Gerald Salen, Sharon Ginat, K. M. Gibson, T. Burlingame, Leesa M. Linck
Publikováno v:
Prenatal Diagnosis. 20:238-240
Smith–Lemli–Opitz syndrome (SLOS), an autosomal recessive condition with multiple malformations, mental retardation, and growth failure, results from markedly reduced activity of the final enzyme in the cholesterol biosynthetic pathway, 7-dehydro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::430f2047fba1fea6f3f691ea93e43414
https://doi.org/10.1002/(sici)1097-0223(200003)20:3<238::aid-pd792>3.0.co
https://doi.org/10.1002/(sici)1097-0223(200003)20:3<238::aid-pd792>3.0.co
Autor:
Melissa Taylor, Markus Grompe, Wolfgang Froestl, Maneesh Gupta, Cornelis Jakobs, Boris M. Hogema, Ramon Diaz-Arrastia, Teodoro Bottiglieri, O. Carter Snead, T. Burlingame, Henry Senephansiri, K. Michael Gibson, Ruud B.H. Schutgens
Publikováno v:
Nature genetics. 29(2)
Succinate semialdehyde dehydrogenase (ALDH5A1, encoding SSADH deficiency is a defect of 4-aminobutyric acid (GABA) degradation that manifests in humans as 4-hydroxybutyric (gamma-hydroxybutyric, GHB) aciduria. It is characterized by a non-specific ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::710f116d52c167be77b0a0613f0a833d
https://pubmed.ncbi.nlm.nih.gov/11544478
https://pubmed.ncbi.nlm.nih.gov/11544478
Autor:
L M, Linck, S J, Hayflick, D S, Lin, K P, Battaile, S, Ginat, T, Burlingame, K M, Gibson, M, Honda, A, Honda, G, Salen, G S, Tint, W E, Connor, R D, Steiner
Publikováno v:
Prenatal diagnosis. 20(3)
Smith-Lemli-Opitz syndrome (SLOS), an autosomal recessive condition with multiple malformations, mental retardation, and growth failure, results from markedly reduced activity of the final enzyme in the cholesterol biosynthetic pathway, 7-dehydrochol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::40418e63a539039c7965adafce705bca
https://pubmed.ncbi.nlm.nih.gov/10719329
https://pubmed.ncbi.nlm.nih.gov/10719329
Autor:
Kemmerer, Pascal (AUTHOR), Maier, Lena (AUTHOR), Singer, Susanne (AUTHOR), Reuter, Katrin (AUTHOR), Engesser, Deborah (AUTHOR)
Publikováno v:
Gruppenpsychotherapie und Gruppendynamik: Beiträge zur Sozialpsychologie und therapeutischen Praxis. Jun2024, Vol. 60 Issue 2, p115-129. 15p.
Autor:
Motoziuk, Liudmyla1 luynik29@gmail.com, Chorna, Nataliia1 natali_chorna@ukr.net, Lukashuk, Maryna1 maryna.luk@gmail.com, Vlasov, Volodymyr2 gelvetic.vv@gmail.com, Sobkova, Svitlana3 si.sobkova@gmail.com
Publikováno v:
Revista de la Universidad del Zulia. may-ago2024, Vol. 15 Issue 43, p44-60. 17p.