Literature for peptidase M12.235: ADAMTS10 peptidase

(Topics flags: M Mutation, I Inhibitor, V Review. To select only the references relevant to a single topic, click the link above. See explanation.)

2025
1. Taye,N., Karoulias,S.Z., Balic,Z., Wang,L.W., Willard,B.B., Martin,D., Richard,D., Okamoto,A.S., Capellini,T.D., Apte,S.S. and Hubmacher,D.
   Combined ADAMTS10 and ADAMTS17 inactivation exacerbates bone shortening and skin phenotypes
   Life Sci Alliance (2025) 8 PubMed  Europe PubMed DOI  PMC  EPMC
2021
2. Al Motawa,M.N.A., Al Shehri,M.S.S., Al Buali,M.J. and Al Agnam,A.A.M.
   Weill-Marchesani Syndrome, a Rare Presentation of Severe Short Stature with Review of the Literature
   Am J Case Rep (2021) 22, e930824-e930824. PubMed  Europe PubMed DOI  PMC  EPMC
2020
3. Satz-Jacobowitz,B. and Hubmacher,D.
   The quest for substrates and binding partners: A critical barrier for understanding the role of ADAMTS proteases in musculoskeletal development and disease
   Dev Dyn (2020) 250, 8-26. PubMed  Europe PubMed DOI  V
2015
4. Dubail,J. and Apte,S.S.
   Insights on ADAMTS proteases and ADAMTS-like proteins from mammalian genetics
   Matrix Biol (2015) 44-46, 24-37. PubMed  Europe PubMed DOI
2012
5. Apte,S.S.
   ADAMTS10
   [ISSN:978-0-12-407744-7] (2012) 3, 1191-1194. DOI
2011
6. 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 Genet (2011) 7, e1001306-e1001306. PubMed  Europe PubMed DOI  PMC  EPMC  M
7. 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 Chem (2011) 286, 17156-17167. PubMed  Europe PubMed DOI  M
2009
8. 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 Genet (2009) 85, 558-568. PubMed  Europe PubMed DOI  PMC  EPMC  M
2008
9. 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 Mutat (2008) 29, 1425-1434. PubMed  Europe PubMed DOI  M
2004
10. Dagoneau,N., Benoist-Lasselin,C., Huber,C., Faivre,L., Megarbane,A., AlSwaid,A., Dollfus,H., Alembik,Y., Munnich,A., Legeai-Mallet,L. and Cormier-Daire,V.
    ADAMTS10 mutations in autosomal recessive Weill-Marchesani syndrome
    Am J Hum Genet (2004) 75, 801-806. PubMed  Europe PubMed DOI  PMC  EPMC
11. [YEAR:7-9-2004]Somerville,R.P., Jungers,K.A. and Apte,S.S.
    Discovery and characterization of a novel, widely expressed metalloprotease, ADAMTS10, and its proteolytic activation
    J Biol Chem (7-9-2004) 279, 51208-51217. PubMed  Europe PubMed DOI  I