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M Vikkula

Showing results (11-20 of 57) with videos related to

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Annals of Medicine|April 1, 1994
Type II collagen mutations in rare and common cartilage diseasesM Vikkula, M Metsäranta, L Ala-Kokko
Actas Dermo-Sifiliograficas|August 13, 2013
Capillary malformation-arteriovenous malformation syndrome: a report of 2 cases, diagnostic criteria, and managementA Català, E Roé, M Vikkula, et al.
Thrombosis Research|April 1, 2015
Overrepresentation of missense mutations in mild hemophilia A patients from Belgium: founder effect or independent occurrence?N Lannoy, C Lambert, M Vikkula, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|September 22, 2001
Molecular genetics of vascular malformationsM Vikkula, L M Boon, J B Mulliken
Critical Reviews in Oncology/Hematology|November 19, 2018
Prevalence of pathogenic variants and variants of unknown significance in patients at high risk of breast cancer: A systematic review and meta-analysis of gene-panel dataC van Marcke, A Collard, M Vikkula, et al.
Trends in Cardiovascular Medicine|February 28, 2004
Molecular basis of vascular anomaliesM Vikkula, L M Boon, J B Mulliken, et al.
American Journal of Human Genetics|June 17, 2000
Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinaseA Irrthum, M J Karkkainen, K Devriendt, et al.
Molecular Syndromology|June 27, 2013
Variable Somatic TIE2 Mutations in Half of Sporadic Venous MalformationsJ Soblet, N Limaye, M Uebelhoer, et al.
Oncogene|February 2, 1999
Endothelial receptor tyrosine kinases activate the STAT signaling pathway: mutant Tie-2 causing venous malformations signals a distinct STAT activation responseE I Korpelainen, M Kärkkäinen, Y Gunji, et al.
Neuropathology and Applied Neurobiology|September 26, 2003
Tumour necrosis and microvascular proliferation are associated with 9p deletion and CDKN2A alterations in 1p/19q-deleted oligodendrogliomasC Godfraind, E Rousseau, M-M Ruchoux, et al.
Pageof 6

Showing results (11-20 of 57) with videos related to

Sort By:
Pageof 6
Annals of Medicine|April 1, 1994
Type II collagen mutations in rare and common cartilage diseasesM Vikkula, M Metsäranta, L Ala-Kokko
Actas Dermo-Sifiliograficas|August 13, 2013
Capillary malformation-arteriovenous malformation syndrome: a report of 2 cases, diagnostic criteria, and managementA Català, E Roé, M Vikkula, et al.
Thrombosis Research|April 1, 2015
Overrepresentation of missense mutations in mild hemophilia A patients from Belgium: founder effect or independent occurrence?N Lannoy, C Lambert, M Vikkula, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|September 22, 2001
Molecular genetics of vascular malformationsM Vikkula, L M Boon, J B Mulliken
Critical Reviews in Oncology/Hematology|November 19, 2018
Prevalence of pathogenic variants and variants of unknown significance in patients at high risk of breast cancer: A systematic review and meta-analysis of gene-panel dataC van Marcke, A Collard, M Vikkula, et al.
Trends in Cardiovascular Medicine|February 28, 2004
Molecular basis of vascular anomaliesM Vikkula, L M Boon, J B Mulliken, et al.
American Journal of Human Genetics|June 17, 2000
Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinaseA Irrthum, M J Karkkainen, K Devriendt, et al.
Molecular Syndromology|June 27, 2013
Variable Somatic TIE2 Mutations in Half of Sporadic Venous MalformationsJ Soblet, N Limaye, M Uebelhoer, et al.
Oncogene|February 2, 1999
Endothelial receptor tyrosine kinases activate the STAT signaling pathway: mutant Tie-2 causing venous malformations signals a distinct STAT activation responseE I Korpelainen, M Kärkkäinen, Y Gunji, et al.
Neuropathology and Applied Neurobiology|September 26, 2003
Tumour necrosis and microvascular proliferation are associated with 9p deletion and CDKN2A alterations in 1p/19q-deleted oligodendrogliomasC Godfraind, E Rousseau, M-M Ruchoux, et al.
Pageof 6