Von Willebrandův faktor (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Von Willebrandův faktor" in Czech language version.

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11nih.gov

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ahajournals.org

stroke.ahajournals.org

High von Willebrand factor levels increase the risk of first ischemic stroke: influence of ADAMTS13, inflammation, and genetic variability. Stroke. 2006, roč. 37, čís. 11, s. 2672–7. Dostupné online. DOI 10.1161/01.STR.0000244767.39962.f7. PMID 16990571.

doi.org

dx.doi.org

Sadler JE. Biochemistry and genetics of von Willebrand factor. Annu. Rev. Biochem.. 1998, roč. 67, s. 395–424. DOI 10.1146/annurev.biochem.67.1.395. PMID 9759493.
Massimo Franchini, Franco Capra, Giovanni Targher, Martina Montagnana and Giuseppe Lippi. Relationship between ABO blood group and von Willebrand factor levels: from biology to clinical implications. Thrombosis Journal. 2007, roč. 5, čís. 14. DOI 10.1186/1477-9560-5-14.
Zheng X, Chung D, Takayama TK, Majerus EM, Sadler JE, Fujikawa K. Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura.. J Biol Chem.. 2001, roč. 276, s. 41059–41063. [http:// Dostupné online]. DOI 10.1074/jbc.C100515200. PMID 11557746.
Levy GG, Nichols WC, Lian EC, Foroud T, McClintick JN, McGee BM, Yang AY, Siemieniak DR, Stark KR, Gruppo R, Sarode R, Shurin SB, Chandrasekaran V, Stabler SP, Sabio H, Bouhassira EE, Upshaw JD Jr, Ginsburg D, Tsai HM. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura.. Nature. 2001, roč. 413, s. 488–494. [http:// Dostupné online]. DOI 10.1038/35097008. PMID 11586351.
Levy GG, Motto DG, Ginsburg D. ADAMTS13 turns 3. Blood. 2005, roč. 106, čís. 1, s. 11–7. Dostupné v archivu pořízeném dne 24-08-2010. DOI 10.1182/blood-2004-10-4097. PMID 15774620.
Sadler JE, Budde U, Eikenboom JC, et al.. Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor. J. Thromb. Haemost.. 2006, roč. 4, čís. 10, s. 2103–14. Dostupné online. DOI 10.1111/j.1538-7836.2006.02146.x. PMID 16889557.
Vincentelli A, Susen S, Le Tourneau T, et al.. Acquired von Willebrand syndrome in aortic stenosis. N. Engl. J. Med.. 2003, roč. 349, čís. 4, s. 343–9. Dostupné online. DOI 10.1056/NEJMoa022831. PMID 12878741. Archivováno 21. 2. 2010 na Wayback Machine.
Moake JL. von Willebrand factor, ADAMTS-13, and thrombotic thrombocytopenic purpura. Semin. Hematol.. 2004, roč. 41, čís. 1, s. 4–14. DOI 10.1053/j.seminhematol.2003.10.003. PMID 14727254.
High von Willebrand factor levels increase the risk of first ischemic stroke: influence of ADAMTS13, inflammation, and genetic variability. Stroke. 2006, roč. 37, čís. 11, s. 2672–7. Dostupné online. DOI 10.1161/01.STR.0000244767.39962.f7. PMID 16990571.
von Willebrand EA. Hereditär pseudohemofili. Fin Läkaresällsk Handl. 1926, roč. 68, s. 87–112. Reprodukován v Von Willebrand EA. Hereditary pseudohaemophilia. Haemophilia. 1999, roč. 5, čís. 3, s. 223–31; discussion 222. DOI 10.1046/j.1365-2516.1999.00302.x. PMID 10444294.

doi.org

Sadler JE, Budde U, Eikenboom JC, et al.. Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor. J. Thromb. Haemost.. 2006, roč. 4, čís. 10, s. 2103–14. Dostupné online. DOI 10.1111/j.1538-7836.2006.02146.x. PMID 16889557.

jbc.org

Sodetz JM, Paulson JC, McKee PA. Carbohydrate composition and identification of blood group A, B, and H oligosaccharide structures on human factor VIII/von Willebrand factor. J Biol Chem. 1979, roč. 254, čís. 21, s. 10754–10760. Dostupné online. PMID 315409.

nejm.org

content.nejm.org

Vincentelli A, Susen S, Le Tourneau T, et al.. Acquired von Willebrand syndrome in aortic stenosis. N. Engl. J. Med.. 2003, roč. 349, čís. 4, s. 343–9. Dostupné online. DOI 10.1056/NEJMoa022831. PMID 12878741. Archivováno 21. 2. 2010 na Wayback Machine.

nih.gov

ncbi.nlm.nih.gov

Sadler JE. Biochemistry and genetics of von Willebrand factor. Annu. Rev. Biochem.. 1998, roč. 67, s. 395–424. DOI 10.1146/annurev.biochem.67.1.395. PMID 9759493.
PARETI, F I. Isolation and characterization of a collagen binding domain in human von Willebrand factor. J. Biol. Chem.. Nov. 1986, roč. 261, čís. 32, s. 15310-5. ISSN 0021-9258. PMID 3490481.
Sodetz JM, Paulson JC, McKee PA. Carbohydrate composition and identification of blood group A, B, and H oligosaccharide structures on human factor VIII/von Willebrand factor. J Biol Chem. 1979, roč. 254, čís. 21, s. 10754–10760. Dostupné online. PMID 315409.
Zheng X, Chung D, Takayama TK, Majerus EM, Sadler JE, Fujikawa K. Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura.. J Biol Chem.. 2001, roč. 276, s. 41059–41063. [http:// Dostupné online]. DOI 10.1074/jbc.C100515200. PMID 11557746.
Levy GG, Nichols WC, Lian EC, Foroud T, McClintick JN, McGee BM, Yang AY, Siemieniak DR, Stark KR, Gruppo R, Sarode R, Shurin SB, Chandrasekaran V, Stabler SP, Sabio H, Bouhassira EE, Upshaw JD Jr, Ginsburg D, Tsai HM. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura.. Nature. 2001, roč. 413, s. 488–494. [http:// Dostupné online]. DOI 10.1038/35097008. PMID 11586351.
Levy GG, Motto DG, Ginsburg D. ADAMTS13 turns 3. Blood. 2005, roč. 106, čís. 1, s. 11–7. Dostupné v archivu pořízeném dne 24-08-2010. DOI 10.1182/blood-2004-10-4097. PMID 15774620.
Sadler JE, Budde U, Eikenboom JC, et al.. Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor. J. Thromb. Haemost.. 2006, roč. 4, čís. 10, s. 2103–14. Dostupné online. DOI 10.1111/j.1538-7836.2006.02146.x. PMID 16889557.
Vincentelli A, Susen S, Le Tourneau T, et al.. Acquired von Willebrand syndrome in aortic stenosis. N. Engl. J. Med.. 2003, roč. 349, čís. 4, s. 343–9. Dostupné online. DOI 10.1056/NEJMoa022831. PMID 12878741. Archivováno 21. 2. 2010 na Wayback Machine.
Moake JL. von Willebrand factor, ADAMTS-13, and thrombotic thrombocytopenic purpura. Semin. Hematol.. 2004, roč. 41, čís. 1, s. 4–14. DOI 10.1053/j.seminhematol.2003.10.003. PMID 14727254.
High von Willebrand factor levels increase the risk of first ischemic stroke: influence of ADAMTS13, inflammation, and genetic variability. Stroke. 2006, roč. 37, čís. 11, s. 2672–7. Dostupné online. DOI 10.1161/01.STR.0000244767.39962.f7. PMID 16990571.
von Willebrand EA. Hereditär pseudohemofili. Fin Läkaresällsk Handl. 1926, roč. 68, s. 87–112. Reprodukován v Von Willebrand EA. Hereditary pseudohaemophilia. Haemophilia. 1999, roč. 5, čís. 3, s. 223–31; discussion 222. DOI 10.1046/j.1365-2516.1999.00302.x. PMID 10444294.

web.archive.org

Levy GG, Motto DG, Ginsburg D. ADAMTS13 turns 3. Blood. 2005, roč. 106, čís. 1, s. 11–7. Dostupné v archivu pořízeném dne 24-08-2010. DOI 10.1182/blood-2004-10-4097. PMID 15774620.
Vincentelli A, Susen S, Le Tourneau T, et al.. Acquired von Willebrand syndrome in aortic stenosis. N. Engl. J. Med.. 2003, roč. 349, čís. 4, s. 343–9. Dostupné online. DOI 10.1056/NEJMoa022831. PMID 12878741. Archivováno 21. 2. 2010 na Wayback Machine.

worldcat.org

PARETI, F I. Isolation and characterization of a collagen binding domain in human von Willebrand factor. J. Biol. Chem.. Nov. 1986, roč. 261, čís. 32, s. 15310-5. ISSN 0021-9258. PMID 3490481.