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Anne C Goodeve

Showing results (21-30 of 29) with videos related to

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Plos One|December 3, 2015
Identification and Characterization of Novel Variations in Platelet G-Protein Coupled Receptor (GPCR) Genes in Patients Historically Diagnosed with Type 1 von Willebrand DiseaseJacqueline Stockley, Shaista P Nisar, Vincenzo C Leo, et al.
Blood Advances|July 8, 2018
The common <i>VWF</i> single nucleotide variants c.2365A>G and c.2385T>C modify VWF biosynthesis and clearanceAhmad H Mufti, Kenichi Ogiwara, Laura L Swystun, et al.
British Journal of Haematology|June 5, 2003
Incidence and prognosis of c-KIT and FLT3 mutations in core binding factor (CBF) acute myeloid leukaemiasRory S Care, Peter J M Valk, Anne C Goodeve, et al.
Haematologica|September 26, 2008
Methylation of the suppressor of cytokine signaling 3 gene (SOCS3) in myeloproliferative disordersNasios Fourouclas, Juan Li, Daniel C Gilby, et al.
Thrombosis and Haemostasis|May 25, 2013
Identification and characterisation of mutations associated with von Willebrand disease in a Turkish patient cohortDaniel J Hampshire, Adel M Abuzenadah, Ashley Cartwright, et al.
International Journal of Neonatal Screening|December 18, 2019
Next Generation Sequencing in Newborn Screening in the United Kingdom National Health ServiceJulia C van Campen, Elizabeth S A Sollars, Rebecca C Thomas, et al.
Blood Advances|July 2, 2020
Characterization of large in-frame von Willebrand factor deletions highlights differing pathogenic mechanismsAshley Cartwright, Simon J Webster, Annika de Jong, et al.
Blood|February 11, 2016
Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United StatesVeronica H Flood, Pamela A Christopherson, Joan Cox Gill, et al.
Blood|April 17, 2016
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disordersIlenia Simeoni, Jonathan C Stephens, Fengyuan Hu, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Plos One|December 3, 2015
Identification and Characterization of Novel Variations in Platelet G-Protein Coupled Receptor (GPCR) Genes in Patients Historically Diagnosed with Type 1 von Willebrand DiseaseJacqueline Stockley, Shaista P Nisar, Vincenzo C Leo, et al.
Blood Advances|July 8, 2018
The common <i>VWF</i> single nucleotide variants c.2365A>G and c.2385T>C modify VWF biosynthesis and clearanceAhmad H Mufti, Kenichi Ogiwara, Laura L Swystun, et al.
British Journal of Haematology|June 5, 2003
Incidence and prognosis of c-KIT and FLT3 mutations in core binding factor (CBF) acute myeloid leukaemiasRory S Care, Peter J M Valk, Anne C Goodeve, et al.
Haematologica|September 26, 2008
Methylation of the suppressor of cytokine signaling 3 gene (SOCS3) in myeloproliferative disordersNasios Fourouclas, Juan Li, Daniel C Gilby, et al.
Thrombosis and Haemostasis|May 25, 2013
Identification and characterisation of mutations associated with von Willebrand disease in a Turkish patient cohortDaniel J Hampshire, Adel M Abuzenadah, Ashley Cartwright, et al.
International Journal of Neonatal Screening|December 18, 2019
Next Generation Sequencing in Newborn Screening in the United Kingdom National Health ServiceJulia C van Campen, Elizabeth S A Sollars, Rebecca C Thomas, et al.
Blood Advances|July 2, 2020
Characterization of large in-frame von Willebrand factor deletions highlights differing pathogenic mechanismsAshley Cartwright, Simon J Webster, Annika de Jong, et al.
Blood|February 11, 2016
Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United StatesVeronica H Flood, Pamela A Christopherson, Joan Cox Gill, et al.
Blood|April 17, 2016
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disordersIlenia Simeoni, Jonathan C Stephens, Fengyuan Hu, et al.
Pageof 3