C1S

Complement component 1, s subcomponent, also known as C1S, is a human gene. [cite web | title = Entrez Gene: C1S Complement component 1, s subcomponent| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=716| accessdate = ]

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References

Further reading

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*cite journal | author=Luo C, Thielens NM, Gagnon J, "et al." |title=Recombinant human complement subcomponent C1s lacking beta-hydroxyasparagine, sialic acid, and one of its two carbohydrate chains still reassembles with C1q and C1r to form a functional C1 complex. |journal=Biochemistry |volume=31 |issue= 17 |pages= 4254–62 |year= 1992 |pmid= 1533159 |doi=
*cite journal | author=Illy C, Thielens NM, Gagnon J, Arlaud GJ |title=Effect of lactoperoxidase-catalyzed iodination on the Ca(2+)-dependent interactions of human C1s. Location of the iodination sites. |journal=Biochemistry |volume=30 |issue= 29 |pages= 7135–41 |year= 1991 |pmid= 1854725 |doi=
*cite journal | author=Hess D, Schaller J, Rickli EE |title=Identification of the disulfide bonds of human complement C1s. |journal=Biochemistry |volume=30 |issue= 11 |pages= 2827–33 |year= 1991 |pmid= 2007122 |doi=
*cite journal | author=Thielens NM, Van Dorsselaer A, Gagnon J, Arlaud GJ |title=Chemical and functional characterization of a fragment of C1-s containing the epidermal growth factor homology region. |journal=Biochemistry |volume=29 |issue= 14 |pages= 3570–8 |year= 1990 |pmid= 2141278 |doi=
*cite journal | author=Busby TF, Ingham KC |title=NH2-terminal calcium-binding domain of human complement C1s- mediates the interaction of C1r- with C1q. |journal=Biochemistry |volume=29 |issue= 19 |pages= 4613–8 |year= 1990 |pmid= 2372546 |doi=
*cite journal | author=Kusumoto H, Hirosawa S, Salier JP, "et al." |title=Human genes for complement components C1r and C1s in a close tail-to-tail arrangement. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=85 |issue= 19 |pages= 7307–11 |year= 1988 |pmid= 2459702 |doi=
*cite journal | author=Katz Y, Strunk RC |title=Synthesis and regulation of C1 inhibitor in human skin fibroblasts. |journal=J. Immunol. |volume=142 |issue= 6 |pages= 2041–5 |year= 1989 |pmid= 2537870 |doi=
*cite journal | author=Tosi M, Duponchel C, Meo T, Couture-Tosi E |title=Complement genes C1r and C1s feature an intronless serine protease domain closely related to haptoglobin. |journal=J. Mol. Biol. |volume=208 |issue= 4 |pages= 709–14 |year= 1989 |pmid= 2553984 |doi=
*cite journal | author=Tosi M, Duponchel C, Meo T, Julier C |title=Complete cDNA sequence of human complement Cls and close physical linkage of the homologous genes Cls and Clr. |journal=Biochemistry |volume=26 |issue= 26 |pages= 8516–24 |year= 1988 |pmid= 2831944 |doi=
*cite journal | author=Nguyen VC, Tosi M, Gross MS, "et al." |title=Assignment of the complement serine protease genes C1r and C1s to chromosome 12 region 12p13. |journal=Hum. Genet. |volume=78 |issue= 4 |pages= 363–8 |year= 1988 |pmid= 2834284 |doi=
*cite journal | author=Spycher SE, Nick H, Rickli EE |title=Human complement component C1s. Partial sequence determination of the heavy chain and identification of the peptide bond cleaved during activation. |journal=Eur. J. Biochem. |volume=156 |issue= 1 |pages= 49–57 |year= 1986 |pmid= 3007145 |doi=
*cite journal | author=Mackinnon CM, Carter PE, Smyth SJ, "et al." |title=Molecular cloning of cDNA for human complement component C1s. The complete amino acid sequence. |journal=Eur. J. Biochem. |volume=169 |issue= 3 |pages= 547–53 |year= 1988 |pmid= 3500856 |doi=
*cite journal | author=Kauffman D, Hofmann T, Bennick A, Keller P |title=Basic proline-rich proteins from human parotid saliva: complete covalent structures of proteins IB-1 and IB-6. |journal=Biochemistry |volume=25 |issue= 9 |pages= 2387–92 |year= 1986 |pmid= 3521730 |doi=
*cite journal | author=Bock SC, Skriver K, Nielsen E, "et al." |title=Human C1 inhibitor: primary structure, cDNA cloning, and chromosomal localization. |journal=Biochemistry |volume=25 |issue= 15 |pages= 4292–301 |year= 1986 |pmid= 3756141 |doi=
*cite journal | author=Carter PE, Dunbar B, Fothergill JE |title=The serine proteinase chain of human complement component C1s. Cyanogen bromide cleavage and N-terminal sequences of the fragments. |journal=Biochem. J. |volume=215 |issue= 3 |pages= 565–71 |year= 1984 |pmid= 6362661 |doi=
*cite journal | author=Nilsson T, Sjöholm I, Wiman B |title=Structural and circular-dichroism studies on the interaction between human C1-esterase inhibitor and C1s. |journal=Biochem. J. |volume=213 |issue= 3 |pages= 617–24 |year= 1983 |pmid= 6604523 |doi=
*cite journal | author=Rossi V, Gaboriaud C, Lacroix M, "et al." |title=Structure of the catalytic region of human complement protease C1s: study by chemical cross-linking and three-dimensional homology modeling. |journal=Biochemistry |volume=34 |issue= 22 |pages= 7311–21 |year= 1995 |pmid= 7779774 |doi=
*cite journal | author=Bersch B, Hernandez JF, Marion D, Arlaud GJ |title=Solution structure of the epidermal growth factor (EGF)-like module of human complement protease C1r, an atypical member of the EGF family. |journal=Biochemistry |volume=37 |issue= 5 |pages= 1204–14 |year= 1998 |pmid= 9477945 |doi= 10.1021/bi971851v
*cite journal | author=Endo Y, Takahashi M, Nakao M, "et al." |title=Two lineages of mannose-binding lectin-associated serine protease (MASP) in vertebrates. |journal=J. Immunol. |volume=161 |issue= 9 |pages= 4924–30 |year= 1998 |pmid= 9794427 |doi=
*cite journal | author=Inoue N, Saito T, Masuda R, "et al." |title=Selective complement C1s deficiency caused by homozygous four-base deletion in the C1s gene. |journal=Hum. Genet. |volume=103 |issue= 4 |pages= 415–8 |year= 1998 |pmid= 9856483 |doi=

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