Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Propionyl coenzyme-A carboxylase"'
Autor:
Koeberl D; Duke University School of Medicine, Durham, NC, USA., Schulze A; Hospital for Sick Children and University of Toronto, Toronto, Ontario, Canada., Sondheimer N; Hospital for Sick Children and University of Toronto, Toronto, Ontario, Canada., Lipshutz GS; University of California at Los Angeles (UCLA), Los Angeles, CA, USA., Geberhiwot T; University of Birmingham, Birmingham, UK., Li L; Moderna, Inc., Cambridge, MA, USA., Saini R; Moderna, Inc., Cambridge, MA, USA., Luo J; Moderna, Inc., Cambridge, MA, USA., Sikirica V; Moderna, Inc., Cambridge, MA, USA., Jin L; Moderna, Inc., Cambridge, MA, USA., Liang M; Moderna, Inc., Cambridge, MA, USA., Leuchars M; Moderna, Inc., Cambridge, MA, USA., Grunewald S; Great Ormond Street Hospital for Children and Institute for Child Health, NIHR Biomedical Research Centre, London, UK. Stephanie.Grunewald@gosh.nhs.uk.
Publikováno v:
Nature [Nature] 2024 Apr; Vol. 628 (8009), pp. 872-877. Date of Electronic Publication: 2024 Apr 03.
Autor:
Bhatnagar S; National Institute of Immunology, JNU Campus, Aruna Asaf Ali Marg, New Delhi, 110067, India., Sadhukhan D; National Institute of Immunology, JNU Campus, Aruna Asaf Ali Marg, New Delhi, 110067, India., Sundd M; National Institute of Immunology, JNU Campus, Aruna Asaf Ali Marg, New Delhi, 110067, India. monicasundd@nii.ac.in.
Publikováno v:
Biomolecular NMR assignments [Biomol NMR Assign] 2024 Dec; Vol. 18 (2), pp. 309-314. Date of Electronic Publication: 2024 Sep 23.
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 8, Iss C, Pp 51-60 (2016)
Propionic acidemia (PA) is a life-threatening disease caused by the deficiency of a mitochondrial biotin-dependent enzyme known as propionyl coenzyme-A carboxylase (PCC). This enzyme is responsible for degrading the metabolic intermediate, propionyl
Externí odkaz:
https://doaj.org/article/1744eef3ac67426d8bb113eb2aedbb41
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 8, Iss C, Pp 51-60 (2016)
Molecular Genetics and Metabolism Reports, Vol 8, Iss C, Pp 51-60 (2016)
Propionic acidemia (PA) is a life-threatening disease caused by the deficiency of a mitochondrial biotin-dependent enzyme known as propionyl coenzyme-A carboxylase (PCC). This enzyme is responsible for degrading the metabolic intermediate, propionyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e15ebddabdbb1647cd372be6e0f565d
http://europepmc.org/articles/PMC4968140
http://europepmc.org/articles/PMC4968140
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Autor:
Grünert Sarah C, Müllerleile Stephanie, De Silva Linda, Barth Michael, Walter Melanie, Walter Kerstin, Meissner Thomas, Lindner Martin, Ensenauer Regina, Santer René, Bodamer Olaf A, Baumgartner Matthias R, Brunner-Krainz Michaela, Karall Daniela, Haase Claudia, Knerr Ina, Marquardt Thorsten, Hennermann Julia B, Steinfeld Robert, Beblo Skadi, Koch Hans-Georg, Konstantopoulou Vassiliki, Scholl-Bürgi Sabine, van Teeffelen-Heithoff Agnes, Suormala Terttu, Sperl Wolfgang, Kraus Jan P, Superti-Furga Andrea, Schwab Karl Otfried, Sass Jörn Oliver
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 8, Iss 1, p 6 (2013)
Abstract Background Propionic acidemia is an inherited disorder caused by deficiency of propionyl-CoA carboxylase. Although it is one of the most frequent organic acidurias, information on the outcome of affected individuals is still limited. Study d
Externí odkaz:
https://doaj.org/article/218c67c71a224b6abe087e07048905d0
Publikováno v:
Molecular and Cellular Biology. 38
Propionic acidemia is caused by a deficiency of the enzyme propionyl coenzyme A carboxylase (PCC) located in the mitochondrial matrix. Cell-penetrating peptides, including transactivator of transcription (TAT), offer a potential to deliver a cargo in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::585b052b98ea949e82c390a91f5c3bac
https://doi.org/10.1128/mcb.00491-17
https://doi.org/10.1128/mcb.00491-17
Autor:
Go Tajima, Kazunori Kimura, Yuji Hotta, Tetsuya Ito, Yoshihiro Kawade, Yasuhiro Maeda, Tomoya Kataoka, Yoriko Watanabe, Kana Gotoh, Naruji Sugiyama, Yoko Nakajima
Publikováno v:
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 1046
Propionic acidemia (PA) is an inherited metabolic disease caused by low activity of propionyl coenzyme A (CoA) carboxylase (PCC), which metabolizes propionyl-CoA into methylmalonyl-CoA. Although many patients with PA have been identified by tandem ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6216987402fa7dc8cd390e55174ba18
https://pubmed.ncbi.nlm.nih.gov/28189105
https://pubmed.ncbi.nlm.nih.gov/28189105
Publikováno v:
The Journal of Microbiology. 49:407-412
Acyl-CoA carboxylases (ACC) are involved in important primary or secondary metabolic pathways such as fatty acid and/or polyketides synthesis. In the 62 kb fragment of pccB gene locus of Streptomyces toxytricini producing a pancreatic inhibitor lipst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7926f7c79b2f4aff909facbe162297e4
https://doi.org/10.1007/s12275-011-1122-1
https://doi.org/10.1007/s12275-011-1122-1
Autor:
Ines Ben Khemis, Martine Raes, Neila Hamza, Chantal Cahu, Patrick Kestemont, Mohamed Mhetli, Marc Dieu, Frédéric Silvestre
Publikováno v:
Comparative Biochemistry and Physiology-Part D: Genomics and Proteomics
Comparative Biochemistry and Physiology-Part D: Genomics and Proteomics, Elsevier, 2010, 5 (2), pp.130-137. ⟨10.1016/j.cbd.2010.03.005⟩
Comparative Biochemistry And Physiology D-genomics & Proteomics (1744-117X) (Elsevier Science Inc), 2010-06, Vol. 5, N. 2, P. 130-137
Comparative Biochemistry and Physiology-Part D: Genomics and Proteomics, Elsevier, 2010, 5 (2), pp.130-137. ⟨10.1016/j.cbd.2010.03.005⟩
Comparative Biochemistry And Physiology D-genomics & Proteomics (1744-117X) (Elsevier Science Inc), 2010-06, Vol. 5, N. 2, P. 130-137
International audience; A comparative proteomic approach was used to assess the protein expression profile in the liver of 34 days old pikeperch larvae fed from day 10 post hatching, with three isoproteic and isolipidic formulated diets varying by th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6233722ebabf7d081a3d3f926e501943
https://doi.org/10.1016/j.cbd.2010.03.005
https://doi.org/10.1016/j.cbd.2010.03.005