Native conformations of human complement components C3 and C4 show different dependencies on thioester formation (1998)
- Authors:
- USP affiliated authors: ISAAC, LOURDES - ICB ; FARAH, SHAKER CHUCK - IQ
- Unidades: ICB; IQ
- DOI: 10.1042/bj3290705
- Assunto: IMUNOLOGIA
- Language: Inglês
- Source:
- Título do periódico: Biochemical Journal
- Volume/Número/Paginação/Ano: v. 329, p. 705-712, 1998
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: green
-
ABNT
ISAAC, Lourdes et al. Native conformations of human complement components C3 and C4 show different dependencies on thioester formation. Biochemical Journal, v. 329, p. 705-712, 1998Tradução . . Disponível em: https://doi.org/10.1042/bj3290705. Acesso em: 21 maio 2024. -
APA
Isaac, L., Aivazian, D., Taniguchi-Sidle, A., Ebanks, R. O., Farah, C. S., Florido, M. P. C., et al. (1998). Native conformations of human complement components C3 and C4 show different dependencies on thioester formation. Biochemical Journal, 329, 705-712. doi:10.1042/bj3290705 -
NLM
Isaac L, Aivazian D, Taniguchi-Sidle A, Ebanks RO, Farah CS, Florido MPC, Pangburn MK, Isenman DE. Native conformations of human complement components C3 and C4 show different dependencies on thioester formation [Internet]. Biochemical Journal. 1998 ; 329 705-712.[citado 2024 maio 21 ] Available from: https://doi.org/10.1042/bj3290705 -
Vancouver
Isaac L, Aivazian D, Taniguchi-Sidle A, Ebanks RO, Farah CS, Florido MPC, Pangburn MK, Isenman DE. Native conformations of human complement components C3 and C4 show different dependencies on thioester formation [Internet]. Biochemical Journal. 1998 ; 329 705-712.[citado 2024 maio 21 ] Available from: https://doi.org/10.1042/bj3290705 - C1s deficiency associated with systemic lupus erythematosus highlights alternative splicing of anormal C1s gene
- Homozygous hereditary C3 deficiency due to a premature stop codon
- C1s deficiency associated with systemic lupus erythematosus highlights alternative splicing of normal C1s gene
- Combined PCR/gapped-duplex method for site-directed mutagenesis
- Skipping of exon 30 in C5 gene results in complete human C5 deficiency and demonstrates the importance of C5d and CUB domains for stability
- Stability of troponin I and T investigated by a hydrophobic fluorescent probe
- A tropomyosin mutant containing a intrinsic fluorescent probe may be used to study head-to-tail interaction thermodynamics
- Structural genomics of the phytopathogen Xanthomonas axonopodis pv citri
- Ca2+-induced rolling of tropomyosin in muscle thin filaments - The alpha- and beta-band hypothesis revisited
- A specific C-terminal deletion in tropomyosin results in a stronger head-to-tail interaction and increased polymerization
Informações sobre o DOI: 10.1042/bj3290705 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas