Literature for peptidase M12.235: ADAMTS10 peptidase

Summary Gene structure Alignment Tree Sequences Sequence features Distribution Literature

(References are filtered for relevance to Mutation. To remove the filter click here. See explanation.)

    2011
  1. Kuchtey,J., Olson,L.M., Rinkoski,T., Mackay,E.O., Iverson,T.M., Gelatt,K.N., Haines,J.L. and Kuchtey,R.W.
    Mapping of the disease locus and identification of ADAMTS10 as a candidate gene in a canine model of primary open angle glaucoma
    PLoS Genet7, e1001306-e1001306. PubMed  Europe PubMed DOI  M
  2. Kutz,W.E., Wang,L.W., Bader,H.L., Majors,A.K., Iwata,K., Traboulsi,E.I., Sakai,L.Y., Keene,D.R. and Apte,S.S.
    ADAMTS10 protein interacts with fibrillin-1 and promotes its deposition in extracellular matrix of cultured fibroblasts
    J Biol Chem286, 17156-17167. PubMed  Europe PubMed DOI  M
  3. 2009
  4. Morales,J., Al-Sharif,L., Khalil,D.S., Shinwari,J.M., Bavi,P., Al-Mahrouqi,R.A., Al-Rajhi,A., Alkuraya,F.S., Meyer,B.F. and Al Tassan,N.
    Homozygous mutations in ADAMTS10 and ADAMTS17 cause lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature
    Am J Hum Genet85, 558-568. PubMed  Europe PubMed DOI  M
  5. 2008
  6. Kutz,W.E., Wang,L.W., Dagoneau,N., Odrcic,K.J., Cormier-Daire,V., Traboulsi,E.I. and Apte,S.S.
    Functional analysis of an ADAMTS10 signal peptide mutation in Weill-Marchesani syndrome demonstrates a long-range effect on secretion of the full-length enzyme
    Hum Mutat29, 1425-1434. PubMed  Europe PubMed DOI  M