Kollagen-Typ 13α1 (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Kollagen-Typ 13α1" in German language version.

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doi.org

  • Hongmin Tu, Takako Sasaki, Anne Snellman, Walter Göhring, Paivi Pirilä, Rupert Timpl, Taina Pihlajaniemi: The type XIII collagen ectodomain is a 150-nm rod and capable of binding to fibronectin, nidogen-2, perlecan, and heparin. In: J Biol Chem. 277. Jahrgang, Nr. 25, 21. Juni 2002, S. 23092–23099, doi:10.1074/jbc.M107583200, PMID 11956183.
  • C. V. Logan, J. Cossins, P. M. Rodríguez Cruz, D. A. Parry, S. Maxwell, P. Martínez-Martínez, J. Riepsaame, Z. A. Abdelhamed, A. V. Lake, M. Moran, S. Robb, G. Chow, C. Sewry, P. M. Hopkins, E. Sheridan, S. Jayawant, J. Palace, C. A. Johnson, D. Beeson: Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain. In: Am J Hum Genet. 97. Jahrgang, Nr. 6, 3. Dezember 2015, S. 878–885, doi:10.1016/j.ajhg.2015.10.017, PMID 26626625, PMC 4678414 (freier Volltext).
  • Naga Chalasani, Xiuqing Guo, Rohit Loomba, Mark O. Goodarzi, Talin Haritunians, Soonil Kwon, Jinrui Cui, Kent D. Taylor, Laura Wilson, Oscar W. Cummings, Yii-Der Ida Chen, Jerome I. Rotter: Genome-Wide Association Study Identifies Variants Associated with Histologic Features of Nonalcoholic Fatty Liver Disease. In: Gastroenterology. 139. Jahrgang, Nr. 5, 1. November 2011, S. 1567–1576, doi:10.1053/j.gastro.2010.07.057, PMID 26626625, PMC 2967576 (freier Volltext).

nih.gov

ncbi.nlm.nih.gov

  • Hongmin Tu, Takako Sasaki, Anne Snellman, Walter Göhring, Paivi Pirilä, Rupert Timpl, Taina Pihlajaniemi: The type XIII collagen ectodomain is a 150-nm rod and capable of binding to fibronectin, nidogen-2, perlecan, and heparin. In: J Biol Chem. 277. Jahrgang, Nr. 25, 21. Juni 2002, S. 23092–23099, doi:10.1074/jbc.M107583200, PMID 11956183.
  • C. V. Logan, J. Cossins, P. M. Rodríguez Cruz, D. A. Parry, S. Maxwell, P. Martínez-Martínez, J. Riepsaame, Z. A. Abdelhamed, A. V. Lake, M. Moran, S. Robb, G. Chow, C. Sewry, P. M. Hopkins, E. Sheridan, S. Jayawant, J. Palace, C. A. Johnson, D. Beeson: Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain. In: Am J Hum Genet. 97. Jahrgang, Nr. 6, 3. Dezember 2015, S. 878–885, doi:10.1016/j.ajhg.2015.10.017, PMID 26626625, PMC 4678414 (freier Volltext).
  • Naga Chalasani, Xiuqing Guo, Rohit Loomba, Mark O. Goodarzi, Talin Haritunians, Soonil Kwon, Jinrui Cui, Kent D. Taylor, Laura Wilson, Oscar W. Cummings, Yii-Der Ida Chen, Jerome I. Rotter: Genome-Wide Association Study Identifies Variants Associated with Histologic Features of Nonalcoholic Fatty Liver Disease. In: Gastroenterology. 139. Jahrgang, Nr. 5, 1. November 2011, S. 1567–1576, doi:10.1053/j.gastro.2010.07.057, PMID 26626625, PMC 2967576 (freier Volltext).