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BMC Medical Genetics|April 29, 2011
Evidence of association with type 1 diabetes in the SLC11A1 gene regionJennie H M Yang, Kate Downes, Joanna M M Howson, et al.Journal of Thrombosis and Haemostasis : JTH|October 20, 2020
Clinical management, ethics and informed consent related to multi-gene panel-based high throughput sequencing testing for platelet disorders: Communication from the SSC of the ISTHKate Downes, Pascal Borry, Katrin Ericson, et al.Plos One|September 17, 2010
Reduced expression of IFIH1 is protective for type 1 diabetesKate Downes, Marcin Pekalski, Karen L Angus, et al.Platelets|February 22, 2021
A novel RUNX1 exon 3 - 7 deletion causing a familial platelet disorderIbrahim Almazni, Pavel Chudakou, Alison Dawson-Meadows, et al.Blood Advances|January 26, 2021
Elevated levels of tissue factor pathway inhibitor in patients with mild to moderate bleeding tendencyDino Mehic, Alexander Tolios, Stefanie Hofer, et al.Journal of Thrombosis and Haemostasis : JTH|August 12, 2021
Current practice and registration patterns among United Kingdom Haemophilia Centre Doctors' Organisation centers for patients with unclassified bleeding disordersWill Thomas, Kate Downes, Gillian Evans, et al.Scientific Reports|August 15, 2018
TNFR2 ligation in human T regulatory cells enhances IL2-induced cell proliferation through the non-canonical NF-κB pathwayJun Wang, Ricardo Ferreira, Wanhua Lu, et al.Diabetes|October 26, 2011
FUT2 nonsecretor status links type 1 diabetes susceptibility and resistance to infectionDeborah J Smyth, Jason D Cooper, Joanna M M Howson, et al.Human Molecular Genetics|October 19, 2020
Unravelling the disease mechanism for TSPYL1 deficiencyGunnar Buyse, Michela Di Michele, Anouck Wijgaerts, 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.Pageof 9