ウロポルフィリノーゲンIII合成酵素
WordNet
- the 9th letter of the Roman alphabet (同)i
PrepTutorEJDIC
- 『私は』私が
- iodineの化学記号
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English Journal
- CRISPR-Cas9 genome editing induces megabase-scale chromosomal truncations.
- Cullot G, Boutin J, Toutain J, Prat F, Pennamen P, Rooryck C, Teichmann M, Rousseau E, Lamrissi-Garcia I, Guyonnet-Duperat V, Bibeyran A, Lalanne M, Prouzet-Mauléon V, Turcq B, Ged C, Blouin JM, Richard E, Dabernat S, Moreau-Gaudry F, Bedel A.
- Nature communications. 2019 03;10(1)1136.
- CRISPR-Cas9 is a promising technology for genome editing. Here we use Cas9 nuclease-induced double-strand break DNA (DSB) at the UROS locus to model and correct congenital erythropoietic porphyria. We demonstrate that homology-directed repair is rare compared with NHEJ pathway leading to on-target i
- PMID 30850590
- Ranking Enzyme Structures in the PDB by Bound Ligand Similarity to Biological Substrates.
- Tyzack JD, Fernando L, Ribeiro AJM, Borkakoti N, Thornton JM.
- Structure (London, England : 1993). 2018 04;26(4)565-571.e3.
- There are numerous applications that use the structures of protein-ligand complexes from the PDB, such as 3D pharmacophore identification, virtual screening, and fragment-based drug design. The structures underlying these applications are potentially much more informative if they contain biologicall
- PMID 29551288
- [Congenital erythropoietic porphyria: case report and management recommendations].
- Salomone B C, Ogueta C I, Reyes V C, Durán S G, Aguirre N, Wietstruck A.
- Archivos argentinos de pediatria. 2018 Apr;116(2)e300-e302.
- Congenital erythropoietic porphyria is an extremely rare, autosomal recessive, non-acute cutaneous porphyria, caused by uroporphyrinogen III synthase deficiency, codificated by UROS gene on the chromosome 10q26.2. Porphyrins deposit in cornea, bones and teeth. The first symptoms could be manifested
- PMID 29557620
★リンクテーブル★
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- 英
- uroporphyrinogen III synthetase, UROS
- 関
- ウロポルフィリノーゲンIII
[★]
- 関
- ligase、synthase
[★]
[★]
[★]
ウロ・ルフィリノーゲン
- 同
- uroporphyrinogens