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Ernest Turro

Showing results (21-30 of 81) with videos related to

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Blood Advances|March 10, 2020
Monoallelic loss-of-function THPO variants cause heritable thrombocytopeniaNaomi Cornish, M Riyaad Aungraheeta, Lucy FitzGibbon, et al.
JIMD Reports|June 27, 2019
A novel missense variant in <i>SLC18A2</i> causes recessive brain monoamine vesicular transport disease and absent serotonin in plateletsManisha Padmakumar, Jaak Jaeken, Vincent Ramaekers, et al.
Nucleic Acids Research|August 24, 2021
MitoPhen database: a human phenotype ontology-based approach to identify mitochondrial DNA diseasesThiloka E Ratnaike, Daniel Greene, Wei Wei, et al.
Genome Biology|January 1, 2020
mRNA structural elements immediately upstream of the start codon dictate dependence upon eIF4A helicase activityJoseph A Waldron, David C Tack, Laura E Ritchey, et al.
Blood|July 21, 2016
Altered fibrinolysis in autosomal dominant thrombomodulin-associated coagulopathyKate Burley, Claire S Whyte, Sarah K Westbury, et al.
Blood|August 30, 2023
A signature of platelet reactivity in CBC scattergrams reveals genetic predictors of thrombotic disease riskHippolyte Verdier, Patrick Thomas, Joana Batista, et al.
Journal of Thrombosis and Haemostasis : JTH|July 8, 2020
A new pedigree with thrombomodulin-associated coagulopathy in which delayed fibrinolysis is partially attenuated by co-inherited TAFI deficiencySarah K Westbury, Claire S Whyte, Jonathan Stephens, et al.
Nature Communications|April 10, 2020
Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humansWei Wei, Alistair T Pagnamenta, Nicholas Gleadall, et al.
Nature Communications|July 24, 2020
Author Correction: Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humansWei Wei, Alistair T Pagnamenta, Nicholas Gleadall, et al.
Breast Cancer Research : BCR|January 8, 2021
NRG1 fusions in breast cancerKaren D Howarth, Tashfina Mirza, Susanna L Cooke, et al.
Pageof 9

Showing results (21-30 of 81) with videos related to

Sort By:
Pageof 9
Blood Advances|March 10, 2020
Monoallelic loss-of-function THPO variants cause heritable thrombocytopeniaNaomi Cornish, M Riyaad Aungraheeta, Lucy FitzGibbon, et al.
JIMD Reports|June 27, 2019
A novel missense variant in <i>SLC18A2</i> causes recessive brain monoamine vesicular transport disease and absent serotonin in plateletsManisha Padmakumar, Jaak Jaeken, Vincent Ramaekers, et al.
Nucleic Acids Research|August 24, 2021
MitoPhen database: a human phenotype ontology-based approach to identify mitochondrial DNA diseasesThiloka E Ratnaike, Daniel Greene, Wei Wei, et al.
Genome Biology|January 1, 2020
mRNA structural elements immediately upstream of the start codon dictate dependence upon eIF4A helicase activityJoseph A Waldron, David C Tack, Laura E Ritchey, et al.
Blood|July 21, 2016
Altered fibrinolysis in autosomal dominant thrombomodulin-associated coagulopathyKate Burley, Claire S Whyte, Sarah K Westbury, et al.
Blood|August 30, 2023
A signature of platelet reactivity in CBC scattergrams reveals genetic predictors of thrombotic disease riskHippolyte Verdier, Patrick Thomas, Joana Batista, et al.
Journal of Thrombosis and Haemostasis : JTH|July 8, 2020
A new pedigree with thrombomodulin-associated coagulopathy in which delayed fibrinolysis is partially attenuated by co-inherited TAFI deficiencySarah K Westbury, Claire S Whyte, Jonathan Stephens, et al.
Nature Communications|April 10, 2020
Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humansWei Wei, Alistair T Pagnamenta, Nicholas Gleadall, et al.
Nature Communications|July 24, 2020
Author Correction: Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humansWei Wei, Alistair T Pagnamenta, Nicholas Gleadall, et al.
Breast Cancer Research : BCR|January 8, 2021
NRG1 fusions in breast cancerKaren D Howarth, Tashfina Mirza, Susanna L Cooke, et al.
Pageof 9