Kollagen-Typ 9α3 (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Kollagen-Typ 9α3" in German language version.

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doi.org

  • Lisa A. Neuhold, Loran Killar, Weiguang Zhao, Mei-Li A. Sung, Linda Warber, John Kulik, William Wu, C. Billinghurst, T. Meijers, A. Robin Poole, Philip Babij, Louis J. DeGennaro: Postnatal expression in hyaline cartilage of constitutively active human collagenase-3 (MMP-13) induces osteoarthritis in mice. In: J Clin Invest. 107. Jahrgang, Nr. 1, Januar 2001, S. 24–44, doi:10.1172/JCI10564, PMC 198546 (freier Volltext).
  • Tushar N. Rathod, Ajay S. Chandanwale, Shubhangi Gujrathi, Vinayak Patil, Shital A. Chavan, Munjal N. Shah: Association between single nucleotide polymorphism in collagen IX and intervertebral disc disease in the Indian population. In: Indian J Orthop. 46. Jahrgang, Nr. 4, Juli 2012, S. 420–426, doi:10.4103/0019-5413.97261, PMC 3421932 (freier Volltext).

nih.gov

ncbi.nlm.nih.gov

  • Lisa A. Neuhold, Loran Killar, Weiguang Zhao, Mei-Li A. Sung, Linda Warber, John Kulik, William Wu, C. Billinghurst, T. Meijers, A. Robin Poole, Philip Babij, Louis J. DeGennaro: Postnatal expression in hyaline cartilage of constitutively active human collagenase-3 (MMP-13) induces osteoarthritis in mice. In: J Clin Invest. 107. Jahrgang, Nr. 1, Januar 2001, S. 24–44, doi:10.1172/JCI10564, PMC 198546 (freier Volltext).
  • Michael D. Briggs, Michael J. Wright, Geert R. Mortier: Multiple Epiphyseal Dysplasia, Autosomal Dominant. In: GeneReviews. 8. Januar 2013, PMID 20301302.
  • Tushar N. Rathod, Ajay S. Chandanwale, Shubhangi Gujrathi, Vinayak Patil, Shital A. Chavan, Munjal N. Shah: Association between single nucleotide polymorphism in collagen IX and intervertebral disc disease in the Indian population. In: Indian J Orthop. 46. Jahrgang, Nr. 4, Juli 2012, S. 420–426, doi:10.4103/0019-5413.97261, PMC 3421932 (freier Volltext).

s3.amazonaws.com

  • Faletra F, D’Adamo AP, Bruno I, Athanasakis E, Biskup S, Esposito L, Gasparini P.: Autosomal Recessive Stickler Syndrome Due to a Loss of Function Mutation in the COL9A3 Gene. In: Am J Met Genet Part A. 2014, S. 42–47 (amazonaws.com [PDF]).