例句與造句

1. The calculated molecular weight of the ACAD9 is 68.8 kDa.
2. A few cases specific to ACAD9 have been reported.
3. ACAD9 is part of the mitochondrial complex I assembly ( MCIA ) complex.
4. It has been observed that ACAD9 can catalyze acyl-CoAs with very long chains.
5. Mutations in the ACAD9 gene are associated with Mitochondrial Complex I Deficiency, which is autosomal recessive.
6. It's difficult to find acad9 in a sentence. 用acad9造句挺難的
7. The complex comprises at least TMEM126B, NDUFAF1, ECSIT, and ACAD9, which interacts directly with NDUFAF1 and ECSIT.
8. The ACAD9 gene contains an open reading frame of 1866 base pairs; this gene encodes a protein with 621 amino acid residues.
9. The ACAD9 enzyme catalyzes a crucial step in fatty acid beta-oxidation by forming a C2-C3 trans-double bond in the fatty acid.
10. The specific activity of ACAD9 towards palmitoyl-CoA ( C16 : 0 ) is three times higher than that towards stearoyl-CoA ( C18 : 0 ).
11. Complex I deficiency with autosomal recessive inheritance results from mutation in nuclear-encoded subunit genes, including NDUFV1, NDUFV2, NDUFS1, NDUFS2, NDUFS3, NDUFS6, NDUFS7, NDUFS8, NDUFA2, NDUFA11, NDUFAF3, NDUFAF10, NDUFB3, NDUFB9, ACAD9, FOXRED1, and MTFMT.
12. Complex I deficiency with autosomal recessive inheritance results from mutation in nuclear-encoded subunit genes, including NDUFV1, NDUFV2, NDUFS1, NDUFS2, NDUFS3, NDUFS4, NDUFS7, NDUFS8, NDUFA2, NDUFA11, NDUFAF3, NDUFAF10, NDUFB3, NDUFB9, ACAD9, FOXRED1, and MTFMT.
13. Alignment of the ACAD9 protein sequence with that of other human ACAD proteins showed that ACAD-9 protein displays 46 27 % identity, and 56 38 % similarity with the eight members of the ACAD family, including ACADVL, ACADS, ACADM, ACADL, IVD, GCD, ACADSB, and ACD8.
14. In contrast with ACADVL, ACAD9 is also involved in assembly of the oxidative phosphorylation complex I . ACAD9 binds complex I assembly factors NDUFAF1 and Ecsit and is specifically required for the assembly of complex I . Furthermore, ACAD9 mutations result in complex I deficiency and not in disturbed long-chain fatty acid oxidation.
15. In contrast with ACADVL, ACAD9 is also involved in assembly of the oxidative phosphorylation complex I . ACAD9 binds complex I assembly factors NDUFAF1 and Ecsit and is specifically required for the assembly of complex I . Furthermore, ACAD9 mutations result in complex I deficiency and not in disturbed long-chain fatty acid oxidation.
16. In contrast with ACADVL, ACAD9 is also involved in assembly of the oxidative phosphorylation complex I . ACAD9 binds complex I assembly factors NDUFAF1 and Ecsit and is specifically required for the assembly of complex I . Furthermore, ACAD9 mutations result in complex I deficiency and not in disturbed long-chain fatty acid oxidation.