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Fibrillin (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Fibrillin" in German language version.

refsWebsite
Global rank German rank
10zdb-katalog.de
123rd place
6th place
10nih.gov
4th place
7th place
8doi.org
2nd place
3rd place
1biochemj.org
low place
low place

biochemj.org (Global: low place; German: low place)

doi.org (Global: 2nd place; German: 3rd place)

  • C. M. Kielty, C. Baldock, D. Lee, M. J. Rock, J. L. Ashworth, C. A. Shuttleworth: Fibrillin: from microfibril assembly to biomechanical function. In: Philosophical Transactions of the Royal Society B: Biological Sciences. Band 357, Nr. 1418, 2002, ISSN 0962-8436, S. 207–217, doi:10.1098/rstb.2001.1029, PMID 11911778, PMC 1692929 (freier Volltext).
  • T. Massam-Wu, M. Chiu, R. Choudhury, S. S. Chaudhry, A. K. Baldwin, A. McGovern, C. Baldock, C. A. Shuttleworth, C. M. Kielty: Assembly of fibrillin microfibrils governs extracellular deposition of latent TGFβ. In: Journal of Cell Science. Band 123, Nr. 17, 2010, ISSN 0021-9533, S. 3006–3018, doi:10.1242/jcs.073437, PMID 20699357.
  • Ian Robertson, Sacha Jensen, Penny Handford: TB domain proteins: evolutionary insights into the multifaceted roles of fibrillins and LTBPs. In: Biochemical Journal. Band 433, Nr. 2, 2011, ISSN 0264-6021, S. 263–276, doi:10.1042/BJ20101320, PMID 21175431 (biochemj.org).
  • J. G. Buchan, D. M. Alvarado, G. E. Haller, C Cruchaga, M. B. Harms, T Zhang, M. C. Willing, D. K. Grange, A. C. Braverman, N. H. Miller, J. A. Morcuende, N. L. Tang, T. P. Lam, B. K. Ng, J. C. Cheng, M. B. Dobbs, C. A. Gurnett: Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis. In: Human Molecular Genetics. Band 23, Nr. 19, 2014, ISSN 1460-2083, S. 5271–5282, doi:10.1093/hmg/ddu224, PMID 24833718, PMC 4159151 (freier Volltext).
  • Alan E. Guttmacher, Harry C. Dietz: New therapeutic approaches to mendelian disorders. In: The New England Journal of Medicine. Band 363, Nr. 9, August 2010, ISSN 1533-4406, S. 852–863, doi:10.1056/NEJMra0907180, PMID 20818846.
  • Y. von Kodolitsch: Perspectives on the revised Ghent criteria for the diagnosis of Marfan syndrome. In: The Application of Clinical Genetics. Band 8, 2015, ISSN 1178-704X, S. 137–155, doi:10.2147/TACG.S60472, PMID 26124674, PMC 4476478 (freier Volltext).
  • G. M. Corson, N. L. Charbonneau, D. R. Keene, L. Y. Sakai: Differential expression of fibrillin-3 adds to microfibril variety in human and avian, but not rodent, connective tissues. In: Genomics. Band 83, Nr. 3, März 2004, ISSN 0888-7543, S. 461–472, doi:10.1016/j.ygeno.2003.08.023, PMID 14962672.
  • John M. Gansner, Erik C. Madsen, Robert P. Mecham, Jonathan D. Gitlin: Essential role for fibrillin-2 in zebrafish notochord and vascular morphogenesis. In: Developmental Dynamics. An Official Publication of the American Association of Anatomists. Band 237, Nr. 10, Oktober 2008, ISSN 1058-8388, S. 2844–2861, doi:10.1002/dvdy.21705, PMID 18816837, PMC 3081706 (freier Volltext).

nih.gov (Global: 4th place; German: 7th place)

ncbi.nlm.nih.gov

  • C. M. Kielty, C. Baldock, D. Lee, M. J. Rock, J. L. Ashworth, C. A. Shuttleworth: Fibrillin: from microfibril assembly to biomechanical function. In: Philosophical Transactions of the Royal Society B: Biological Sciences. Band 357, Nr. 1418, 2002, ISSN 0962-8436, S. 207–217, doi:10.1098/rstb.2001.1029, PMID 11911778, PMC 1692929 (freier Volltext).
  • T. Massam-Wu, M. Chiu, R. Choudhury, S. S. Chaudhry, A. K. Baldwin, A. McGovern, C. Baldock, C. A. Shuttleworth, C. M. Kielty: Assembly of fibrillin microfibrils governs extracellular deposition of latent TGFβ. In: Journal of Cell Science. Band 123, Nr. 17, 2010, ISSN 0021-9533, S. 3006–3018, doi:10.1242/jcs.073437, PMID 20699357.
  • Ian Robertson, Sacha Jensen, Penny Handford: TB domain proteins: evolutionary insights into the multifaceted roles of fibrillins and LTBPs. In: Biochemical Journal. Band 433, Nr. 2, 2011, ISSN 0264-6021, S. 263–276, doi:10.1042/BJ20101320, PMID 21175431 (biochemj.org).
  • J. G. Buchan, D. M. Alvarado, G. E. Haller, C Cruchaga, M. B. Harms, T Zhang, M. C. Willing, D. K. Grange, A. C. Braverman, N. H. Miller, J. A. Morcuende, N. L. Tang, T. P. Lam, B. K. Ng, J. C. Cheng, M. B. Dobbs, C. A. Gurnett: Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis. In: Human Molecular Genetics. Band 23, Nr. 19, 2014, ISSN 1460-2083, S. 5271–5282, doi:10.1093/hmg/ddu224, PMID 24833718, PMC 4159151 (freier Volltext).
  • L. Y. Sakai: Fibrillin, a new 350-kD glycoprotein, is a component of extracellular microfibrils. In: The Journal of Cell Biology. Band 103, Nr. 6, Dezember 1986, ISSN 0021-9525, S. 2499–2509, PMID 3536967, PMC 2114568 (freier Volltext).
  • Alan E. Guttmacher, Harry C. Dietz: New therapeutic approaches to mendelian disorders. In: The New England Journal of Medicine. Band 363, Nr. 9, August 2010, ISSN 1533-4406, S. 852–863, doi:10.1056/NEJMra0907180, PMID 20818846.
  • Y. von Kodolitsch: Perspectives on the revised Ghent criteria for the diagnosis of Marfan syndrome. In: The Application of Clinical Genetics. Band 8, 2015, ISSN 1178-704X, S. 137–155, doi:10.2147/TACG.S60472, PMID 26124674, PMC 4476478 (freier Volltext).
  • H. Zhang, S. D. Apfelroth, W. Hu; E. C. Davis, C. Sanguineti, J. Bonadio, R. P. Mecham, F. Ramirez: Structure and expression of fibrillin-2, a novel microfibrillar component preferentially located in elastic matrices. In: The Journal of Cell Biology. Band 124, Nr. 5, 1994, ISSN 0021-9525, S. 855–863, PMID 8120105, PMC 2119952 (freier Volltext).
  • G. M. Corson, N. L. Charbonneau, D. R. Keene, L. Y. Sakai: Differential expression of fibrillin-3 adds to microfibril variety in human and avian, but not rodent, connective tissues. In: Genomics. Band 83, Nr. 3, März 2004, ISSN 0888-7543, S. 461–472, doi:10.1016/j.ygeno.2003.08.023, PMID 14962672.
  • John M. Gansner, Erik C. Madsen, Robert P. Mecham, Jonathan D. Gitlin: Essential role for fibrillin-2 in zebrafish notochord and vascular morphogenesis. In: Developmental Dynamics. An Official Publication of the American Association of Anatomists. Band 237, Nr. 10, Oktober 2008, ISSN 1058-8388, S. 2844–2861, doi:10.1002/dvdy.21705, PMID 18816837, PMC 3081706 (freier Volltext).

zdb-katalog.de (Global: 123rd place; German: 6th place)

  • C. M. Kielty, C. Baldock, D. Lee, M. J. Rock, J. L. Ashworth, C. A. Shuttleworth: Fibrillin: from microfibril assembly to biomechanical function. In: Philosophical Transactions of the Royal Society B: Biological Sciences. Band 357, Nr. 1418, 2002, ISSN 0962-8436, S. 207–217, doi:10.1098/rstb.2001.1029, PMID 11911778, PMC 1692929 (freier Volltext).
  • T. Massam-Wu, M. Chiu, R. Choudhury, S. S. Chaudhry, A. K. Baldwin, A. McGovern, C. Baldock, C. A. Shuttleworth, C. M. Kielty: Assembly of fibrillin microfibrils governs extracellular deposition of latent TGFβ. In: Journal of Cell Science. Band 123, Nr. 17, 2010, ISSN 0021-9533, S. 3006–3018, doi:10.1242/jcs.073437, PMID 20699357.
  • Ian Robertson, Sacha Jensen, Penny Handford: TB domain proteins: evolutionary insights into the multifaceted roles of fibrillins and LTBPs. In: Biochemical Journal. Band 433, Nr. 2, 2011, ISSN 0264-6021, S. 263–276, doi:10.1042/BJ20101320, PMID 21175431 (biochemj.org).
  • J. G. Buchan, D. M. Alvarado, G. E. Haller, C Cruchaga, M. B. Harms, T Zhang, M. C. Willing, D. K. Grange, A. C. Braverman, N. H. Miller, J. A. Morcuende, N. L. Tang, T. P. Lam, B. K. Ng, J. C. Cheng, M. B. Dobbs, C. A. Gurnett: Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis. In: Human Molecular Genetics. Band 23, Nr. 19, 2014, ISSN 1460-2083, S. 5271–5282, doi:10.1093/hmg/ddu224, PMID 24833718, PMC 4159151 (freier Volltext).
  • L. Y. Sakai: Fibrillin, a new 350-kD glycoprotein, is a component of extracellular microfibrils. In: The Journal of Cell Biology. Band 103, Nr. 6, Dezember 1986, ISSN 0021-9525, S. 2499–2509, PMID 3536967, PMC 2114568 (freier Volltext).
  • Alan E. Guttmacher, Harry C. Dietz: New therapeutic approaches to mendelian disorders. In: The New England Journal of Medicine. Band 363, Nr. 9, August 2010, ISSN 1533-4406, S. 852–863, doi:10.1056/NEJMra0907180, PMID 20818846.
  • Y. von Kodolitsch: Perspectives on the revised Ghent criteria for the diagnosis of Marfan syndrome. In: The Application of Clinical Genetics. Band 8, 2015, ISSN 1178-704X, S. 137–155, doi:10.2147/TACG.S60472, PMID 26124674, PMC 4476478 (freier Volltext).
  • H. Zhang, S. D. Apfelroth, W. Hu; E. C. Davis, C. Sanguineti, J. Bonadio, R. P. Mecham, F. Ramirez: Structure and expression of fibrillin-2, a novel microfibrillar component preferentially located in elastic matrices. In: The Journal of Cell Biology. Band 124, Nr. 5, 1994, ISSN 0021-9525, S. 855–863, PMID 8120105, PMC 2119952 (freier Volltext).
  • G. M. Corson, N. L. Charbonneau, D. R. Keene, L. Y. Sakai: Differential expression of fibrillin-3 adds to microfibril variety in human and avian, but not rodent, connective tissues. In: Genomics. Band 83, Nr. 3, März 2004, ISSN 0888-7543, S. 461–472, doi:10.1016/j.ygeno.2003.08.023, PMID 14962672.
  • John M. Gansner, Erik C. Madsen, Robert P. Mecham, Jonathan D. Gitlin: Essential role for fibrillin-2 in zebrafish notochord and vascular morphogenesis. In: Developmental Dynamics. An Official Publication of the American Association of Anatomists. Band 237, Nr. 10, Oktober 2008, ISSN 1058-8388, S. 2844–2861, doi:10.1002/dvdy.21705, PMID 18816837, PMC 3081706 (freier Volltext).