Fibrinogeeni (Finnish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Fibrinogeeni" in Finnish language version.

refsWebsite

Global rank Finnish rank

7nih.gov

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12^th place

6doi.org

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10^th place

6worldcat.org

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9^th place

1nature.com

234^th place

201^st place

1wiley.com

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1ashpublications.org

low place

ashpublications.org

AV Cooper, KF Standeven, RA Ariëns: Fibrinogen gamma-chain splice variant gamma' alters fibrin formation and structure. Blood, 2003, 102. vsk, nro 2, s. 535–540. PubMed:12663453 doi:10.1182/blood-2002-10-3150 ISSN 0006-4971 Artikkelin verkkoversio.

doi.org

dx.doi.org

Y Jiang, RF Doolittle: The evolution of vertebrate blood coagulation as viewed from a comparison of puffer fish and sea squirt genomes. Proceedings of the National Academy of Sciences of the United States of America, 2003, 100. vsk, nro 13, s. 7527–7532. PubMed:12808152 doi:10.1073/pnas.0932632100 ISSN 0027-8424 Artikkelin verkkoversio.
S Spena et al: Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen A α -chain gene. European Journal of Human Genetics, 2004, 12. vsk, nro 11, s. 891–898. doi:10.1038/sj.ejhg.5201207 ISSN 1476-5438 Artikkelin verkkoversio.
GL Tiscia, M Margaglione: Human fibrinogen: molecular and genetic aspects of congenital disorders. International Journal of Molecular Sciences, 2018, 19. vsk, nro 6. PubMed:29844251 doi:10.3390/ijms19061597 ISSN 1422-0067 Artikkelin verkkoversio.
MW Mosesson: Fibrinogen and fibrin structure and functions. Journal of Thrombosis and Haemostasis, 2005, 3. vsk, nro 8, s. 1894–1904. doi:10.1111/j.1538-7836.2005.01365.x ISSN 1538-7836 Artikkelin verkkoversio.
AV Cooper, KF Standeven, RA Ariëns: Fibrinogen gamma-chain splice variant gamma' alters fibrin formation and structure. Blood, 2003, 102. vsk, nro 2, s. 535–540. PubMed:12663453 doi:10.1182/blood-2002-10-3150 ISSN 0006-4971 Artikkelin verkkoversio.
JW Weisel, RI Litvinov: Fibrin formation, structure and properties. Sub-cellular biochemistry, 2017, 82. vsk, s. 405–456. PubMed:28101869 doi:10.1007/978-3-319-49674-0_13 ISSN 0306-0225 Artikkelin verkkoversio.

nature.com

S Spena et al: Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen A α -chain gene. European Journal of Human Genetics, 2004, 12. vsk, nro 11, s. 891–898. doi:10.1038/sj.ejhg.5201207 ISSN 1476-5438 Artikkelin verkkoversio.

nih.gov

pubmed.ncbi.nlm.nih.gov

Y Jiang, RF Doolittle: The evolution of vertebrate blood coagulation as viewed from a comparison of puffer fish and sea squirt genomes. Proceedings of the National Academy of Sciences of the United States of America, 2003, 100. vsk, nro 13, s. 7527–7532. PubMed:12808152 doi:10.1073/pnas.0932632100 ISSN 0027-8424 Artikkelin verkkoversio.
GL Tiscia, M Margaglione: Human fibrinogen: molecular and genetic aspects of congenital disorders. International Journal of Molecular Sciences, 2018, 19. vsk, nro 6. PubMed:29844251 doi:10.3390/ijms19061597 ISSN 1422-0067 Artikkelin verkkoversio.
AV Cooper, KF Standeven, RA Ariëns: Fibrinogen gamma-chain splice variant gamma' alters fibrin formation and structure. Blood, 2003, 102. vsk, nro 2, s. 535–540. PubMed:12663453 doi:10.1182/blood-2002-10-3150 ISSN 0006-4971 Artikkelin verkkoversio.
JW Weisel, RI Litvinov: Fibrin formation, structure and properties. Sub-cellular biochemistry, 2017, 82. vsk, s. 405–456. PubMed:28101869 doi:10.1007/978-3-319-49674-0_13 ISSN 0306-0225 Artikkelin verkkoversio.

ncbi.nlm.nih.gov

Y Jiang, RF Doolittle: The evolution of vertebrate blood coagulation as viewed from a comparison of puffer fish and sea squirt genomes. Proceedings of the National Academy of Sciences of the United States of America, 2003, 100. vsk, nro 13, s. 7527–7532. PubMed:12808152 doi:10.1073/pnas.0932632100 ISSN 0027-8424 Artikkelin verkkoversio.
GL Tiscia, M Margaglione: Human fibrinogen: molecular and genetic aspects of congenital disorders. International Journal of Molecular Sciences, 2018, 19. vsk, nro 6. PubMed:29844251 doi:10.3390/ijms19061597 ISSN 1422-0067 Artikkelin verkkoversio.
JW Weisel, RI Litvinov: Fibrin formation, structure and properties. Sub-cellular biochemistry, 2017, 82. vsk, s. 405–456. PubMed:28101869 doi:10.1007/978-3-319-49674-0_13 ISSN 0306-0225 Artikkelin verkkoversio.

wiley.com

onlinelibrary.wiley.com

MW Mosesson: Fibrinogen and fibrin structure and functions. Journal of Thrombosis and Haemostasis, 2005, 3. vsk, nro 8, s. 1894–1904. doi:10.1111/j.1538-7836.2005.01365.x ISSN 1538-7836 Artikkelin verkkoversio.

worldcat.org

Y Jiang, RF Doolittle: The evolution of vertebrate blood coagulation as viewed from a comparison of puffer fish and sea squirt genomes. Proceedings of the National Academy of Sciences of the United States of America, 2003, 100. vsk, nro 13, s. 7527–7532. PubMed:12808152 doi:10.1073/pnas.0932632100 ISSN 0027-8424 Artikkelin verkkoversio.
S Spena et al: Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen A α -chain gene. European Journal of Human Genetics, 2004, 12. vsk, nro 11, s. 891–898. doi:10.1038/sj.ejhg.5201207 ISSN 1476-5438 Artikkelin verkkoversio.
GL Tiscia, M Margaglione: Human fibrinogen: molecular and genetic aspects of congenital disorders. International Journal of Molecular Sciences, 2018, 19. vsk, nro 6. PubMed:29844251 doi:10.3390/ijms19061597 ISSN 1422-0067 Artikkelin verkkoversio.
MW Mosesson: Fibrinogen and fibrin structure and functions. Journal of Thrombosis and Haemostasis, 2005, 3. vsk, nro 8, s. 1894–1904. doi:10.1111/j.1538-7836.2005.01365.x ISSN 1538-7836 Artikkelin verkkoversio.
AV Cooper, KF Standeven, RA Ariëns: Fibrinogen gamma-chain splice variant gamma' alters fibrin formation and structure. Blood, 2003, 102. vsk, nro 2, s. 535–540. PubMed:12663453 doi:10.1182/blood-2002-10-3150 ISSN 0006-4971 Artikkelin verkkoversio.
JW Weisel, RI Litvinov: Fibrin formation, structure and properties. Sub-cellular biochemistry, 2017, 82. vsk, s. 405–456. PubMed:28101869 doi:10.1007/978-3-319-49674-0_13 ISSN 0306-0225 Artikkelin verkkoversio.