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Anne C Goodeve

Showing results (11-20 of 29) with videos related to

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Haematologica|July 2, 2013
Specific and global coagulation assays in the diagnosis of discrepant mild hemophilia AAnnette E Bowyer, Joost J Van Veen, Anne C Goodeve, et al.
British Journal of Haematology|November 18, 2003
c-FMS mutational analysis in acute myeloid leukaemiaFaisel M Abu-Duhier, Anne C Goodeve, Giu A Wilson, et al.
Haematologica|February 3, 2004
Second hit mutations in the RTK/RAS signaling pathway in acute myeloid leukemia with inv(16)Peter J M Valk, David T Bowen, Marion E Frew, et al.
Immunology Letters|December 17, 2009
Tribbles-1 and -2 are tumour suppressors, down-regulated in human acute myeloid leukaemiaDaniel C Gilby, Hye Youn Sung, Peter R Winship, et al.
Blood|July 5, 2002
FLT3 internal tandem duplication mutations are rare in agnogenic myeloid metaplasiaFaisal M Abu-Duhier, Anne C Goodeve, Gill A Wilson, et al.
Blood|June 7, 2003
Analysis of intracellular storage and regulated secretion of 3 von Willebrand disease-causing variants of von Willebrand factorGrégoire Michaux, Lindsay J Hewlett, Sarah L Messenger, et al.
British Journal of Haematology|February 13, 2003
Mutational analysis of class III receptor tyrosine kinases (C-KIT, C-FMS, FLT3) in idiopathic myelofibrosisFaisel M Abu-Duhier, Anne C Goodeve, Rory S Care, et al.
Haematologica|September 21, 2010
Polymorphic variation within the VWF gene contributes to the failure to detect mutations in patients historically diagnosed with type 1 von Willebrand disease from the MCMDM-1VWD cohortDaniel J Hampshire, George J Burghel, Jenny Goudemand, et al.
Blood|February 25, 2009
Identification and characterization of a novel P2Y 12 variant in a patient diagnosed with type 1 von Willebrand disease in the European MCMDM-1VWD studyMartina E Daly, Ban B Dawood, William A Lester, et al.
Journal of Thrombosis and Haemostasis : JTH|June 11, 2019
Curated disease-causing genes for bleeding, thrombotic, and platelet disorders: Communication from the SSC of the ISTHKaryn Megy, Kate Downes, Ilenia Simeoni, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Haematologica|July 2, 2013
Specific and global coagulation assays in the diagnosis of discrepant mild hemophilia AAnnette E Bowyer, Joost J Van Veen, Anne C Goodeve, et al.
British Journal of Haematology|November 18, 2003
c-FMS mutational analysis in acute myeloid leukaemiaFaisel M Abu-Duhier, Anne C Goodeve, Giu A Wilson, et al.
Haematologica|February 3, 2004
Second hit mutations in the RTK/RAS signaling pathway in acute myeloid leukemia with inv(16)Peter J M Valk, David T Bowen, Marion E Frew, et al.
Immunology Letters|December 17, 2009
Tribbles-1 and -2 are tumour suppressors, down-regulated in human acute myeloid leukaemiaDaniel C Gilby, Hye Youn Sung, Peter R Winship, et al.
Blood|July 5, 2002
FLT3 internal tandem duplication mutations are rare in agnogenic myeloid metaplasiaFaisal M Abu-Duhier, Anne C Goodeve, Gill A Wilson, et al.
Blood|June 7, 2003
Analysis of intracellular storage and regulated secretion of 3 von Willebrand disease-causing variants of von Willebrand factorGrégoire Michaux, Lindsay J Hewlett, Sarah L Messenger, et al.
British Journal of Haematology|February 13, 2003
Mutational analysis of class III receptor tyrosine kinases (C-KIT, C-FMS, FLT3) in idiopathic myelofibrosisFaisel M Abu-Duhier, Anne C Goodeve, Rory S Care, et al.
Haematologica|September 21, 2010
Polymorphic variation within the VWF gene contributes to the failure to detect mutations in patients historically diagnosed with type 1 von Willebrand disease from the MCMDM-1VWD cohortDaniel J Hampshire, George J Burghel, Jenny Goudemand, et al.
Blood|February 25, 2009
Identification and characterization of a novel P2Y 12 variant in a patient diagnosed with type 1 von Willebrand disease in the European MCMDM-1VWD studyMartina E Daly, Ban B Dawood, William A Lester, et al.
Journal of Thrombosis and Haemostasis : JTH|June 11, 2019
Curated disease-causing genes for bleeding, thrombotic, and platelet disorders: Communication from the SSC of the ISTHKaryn Megy, Kate Downes, Ilenia Simeoni, et al.
Pageof 3