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.)

2021
1. 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 Rep22, e930824-e930824. PubMed  Europe PubMed DOI
2020
2. 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 Dyn250, 8-26. PubMed  Europe PubMed DOI  V
2015
3. Dubail,J. and Apte,S.S.
   Insights on ADAMTS proteases and ADAMTS-like proteins from mammalian genetics
   Matrix Biol44-46, 24-37. PubMed  Europe PubMed DOI
2012
4. Apte,S.S.
   ADAMTS10
   [ISSN:978-0-12-407744-7]3, 1191-1194. DOI
2011
5. 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
6. 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
2009
7. 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
2008
8. 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
2004
9. 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 Genet75, 801-806. PubMed  Europe PubMed DOI
10. [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 Chem279, 51208-51217. PubMed  Europe PubMed DOI  I