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Timothy J Satchwell

Showing results (21-30 of 33) with videos related to

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Haematologica|October 19, 2019
PIEZO1 gain-of-function mutations delay reticulocyte maturation in hereditary xerocytosisPedro L Moura, Bethan R Hawley, Johannes G G Dobbe, et al.
Blood Advances|June 25, 2024
Complete absence of GLUT1 does not impair human terminal erythroid differentiationCatarina Martins Freire, Nadine R King, Monika Dzieciatkowska, et al.
Haematologica|August 5, 2018
Non-muscle myosin II drives vesicle loss during human reticulocyte maturationPedro L Moura, Bethan R Hawley, Tosti J Mankelow, et al.
Blood Advances|September 12, 2019
Reticulocyte and red blood cell deformation triggers specific phosphorylation eventsPedro L Moura, Maria A Lizarralde Iragorri, Olivier Français, et al.
Nucleic Acids Research|February 27, 2024
An engineered baculoviral protein and DNA co-delivery system for CRISPR-based mammalian genome editingJulien Capin, Alexandra Harrison, Renata A Raele, et al.
Haematologica|August 13, 2013
Characteristic phenotypes associated with congenital dyserythropoietic anemia (type II) manifest at different stages of erythropoiesisTimothy J Satchwell, Stephanie Pellegrin, Paola Bianchi, et al.
Nature Communications|March 15, 2017
An immortalized adult human erythroid line facilitates sustainable and scalable generation of functional red cellsKongtana Trakarnsanga, Rebecca E Griffiths, Marieangela C Wilson, et al.
British Journal of Haematology|July 7, 2020
Rapid diagnosis of hereditary haemolytic anaemias using automated rheoscopy and supervised machine learningPedro L Moura, Johannes G G Dobbe, Geert J Streekstra, et al.
Blood|August 19, 2024
Deletions in the MAL gene result in loss of Mal protein, defining the rare inherited AnWj-negative blood group phenotypeLouise A Tilley, Vanja Karamatic Crew, Tosti J Mankelow, et al.
Journal of the American Society of Nephrology : JASN|June 26, 2010
Anion exchanger 1 interacts with nephrin in podocytesFiona Wu, Moin A Saleem, Nicole B Kampik, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Haematologica|October 19, 2019
PIEZO1 gain-of-function mutations delay reticulocyte maturation in hereditary xerocytosisPedro L Moura, Bethan R Hawley, Johannes G G Dobbe, et al.
Blood Advances|June 25, 2024
Complete absence of GLUT1 does not impair human terminal erythroid differentiationCatarina Martins Freire, Nadine R King, Monika Dzieciatkowska, et al.
Haematologica|August 5, 2018
Non-muscle myosin II drives vesicle loss during human reticulocyte maturationPedro L Moura, Bethan R Hawley, Tosti J Mankelow, et al.
Blood Advances|September 12, 2019
Reticulocyte and red blood cell deformation triggers specific phosphorylation eventsPedro L Moura, Maria A Lizarralde Iragorri, Olivier Français, et al.
Nucleic Acids Research|February 27, 2024
An engineered baculoviral protein and DNA co-delivery system for CRISPR-based mammalian genome editingJulien Capin, Alexandra Harrison, Renata A Raele, et al.
Haematologica|August 13, 2013
Characteristic phenotypes associated with congenital dyserythropoietic anemia (type II) manifest at different stages of erythropoiesisTimothy J Satchwell, Stephanie Pellegrin, Paola Bianchi, et al.
Nature Communications|March 15, 2017
An immortalized adult human erythroid line facilitates sustainable and scalable generation of functional red cellsKongtana Trakarnsanga, Rebecca E Griffiths, Marieangela C Wilson, et al.
British Journal of Haematology|July 7, 2020
Rapid diagnosis of hereditary haemolytic anaemias using automated rheoscopy and supervised machine learningPedro L Moura, Johannes G G Dobbe, Geert J Streekstra, et al.
Blood|August 19, 2024
Deletions in the MAL gene result in loss of Mal protein, defining the rare inherited AnWj-negative blood group phenotypeLouise A Tilley, Vanja Karamatic Crew, Tosti J Mankelow, et al.
Journal of the American Society of Nephrology : JASN|June 26, 2010
Anion exchanger 1 interacts with nephrin in podocytesFiona Wu, Moin A Saleem, Nicole B Kampik, et al.
Pageof 4