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Lest we forget. Illuminating lived experience of the Covid-19 pandemic and lockdown

Social science & medicine (1982), 2023-09, Vol.332, p.116080-116080, Article 116080

2023

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The mutational spectrum of type 1 von Willebrand disease: results from a Canadian cohort study

Blood, 2007-01, Vol.109 (1), p.145-154

2007

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Medicalisation of vaping in the UK? E-cigarette users’ perspectives on the merging of commercial and medical routes to vaping

Perspectives in public health, 2023-08, p.17579139231185481-17579139231185481

2023

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The genetics of Canadian type 3 von Willebrand disease: further evidence for co‐dominant inheritance of mutant alleles

Journal of thrombosis and haemostasis, 2013-03, Vol.11 (3), p.512-520

2013

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Abnormal von Willebrand factor secretion, factor VIII stabilization and thrombus dynamics in type 2N von Willebrand disease mice

Journal of thrombosis and haemostasis, 2017-08, Vol.15 (8), p.1607-1619

2017

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Chronic rhinosinusitis: patient experiences of primary and secondary care - a qualitative study

Clinical otolaryngology, 2016-02, Vol.41 (1), p.8-14

2016

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Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian Type 1 VWD Study

Journal of thrombosis and haemostasis, 2006-04, Vol.4 (4), p.783-792

2006

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Influence of a GT repeat element on shear stress responsiveness of the VWF gene promoter

Journal of thrombosis and haemostasis, 2008-07, Vol.6 (7), p.1183-1190

2008

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The Experience of Long-Term Opiate Maintenance Treatment and Reported Barriers to Recovery: A Qualitative Systematic Review

European addiction research, 2013-01, Vol.19 (6), p.287-298

2013

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Challenges in defining type 2M von Willebrand disease: results from a Canadian cohort study

Journal of thrombosis and haemostasis, 2007-09, Vol.5 (9), p.1914-1922

2007

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The effect of exercise on von Willebrand factor and ADAMTS‐13 in individuals with type 1 and type 2B von Willebrand disease

Journal of thrombosis and haemostasis, 2008-01, Vol.6 (1), p.90-96

2008

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Expanded phenotype–genotype correlations in a pediatric population with type 1 von Willebrand disease

Journal of thrombosis and haemostasis, 2011-09, Vol.9 (9), p.1752-1760

2011

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The endothelial lectin clearance receptor CLEC4M binds and internalizes factor VIII in a VWF‐dependent and independent manner

Journal of thrombosis and haemostasis, 2019-04, Vol.17 (4), p.681-694

2019

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PB0815 Involvement of the Nuclear Protein, TC2N, in Regulating VWF Levels in Endothelial Cells

Research and practice in thrombosis and haemostasis, 2023-10, Vol.7, p.101538, Article 101538

2023

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The scavenger receptor SCARA5 is an endocytic receptor for von Willebrand factor expressed by littoral cells in the human spleen

Journal of thrombosis and haemostasis, 2019-08, Vol.17 (8), p.1384-1396

2019

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Role of the Liver-Enriched Transcription Factor Hepatocyte Nuclear Factor 1 in Transcriptional Regulation of the Factor VIII Gene

Molecular and cellular biology, 1996-05, Vol.16 (5), p.1936-1945

1996

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Perception of need and barriers to access: the mental health needs of young people attending a Youth Offending Team in the UK

Health & social care in the community, 2011-07, Vol.19 (4), p.420-428

2011

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Identification and functional characterization of a novel 27-bp deletion in the macroglycopeptide-coding region of the GPIBA gene resulting in platelet-type von Willebrand disease

Blood, 2005-06, Vol.105 (11), p.4330-4336

2005

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Four groups of illicit substance users amongst the adult 'hidden' non-problematic community

Drugs : education, prevention & policy, 2005-08, Vol.12 (4), p.279-290

Notley, Caitlin

2005

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The Factor VIII Acute Phase Response Requires the Participation of NFκB and C/EBP

Thrombosis and haemostasis, 2000, Vol.84 (8), p.216-222

2000

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Systemic delivery of an adenoviral vector encoding canine factor VIII results in short-term phenotypic correction, inhibitor development, and biphasic liver toxicity in hemophilia A dogs

Blood, 2001-01, Vol.97 (1), p.107-113

2001

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Aberrant splicing and premature termination of transcription of the FVIII gene as a cause of severe canine hemophilia A: similarities with the intron 22 inversion mutation in human hemophilia

Thrombosis and haemostasis, 2002-04, Vol.87 (4), p.659-665

2002

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Scavenger receptor class A member 5 (SCARA5) binds and internalizes VWF in vitro : a novel candidate VWF clearance receptor

JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2015, Vol.13, p.222

2015

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The impact of offering a relatives’ clinic on the satisfaction of the next-of-kin of Critical Care patients—A prospective time-interrupted trial

Intensive & critical care nursing, 2008-04, Vol.24 (2), p.122-129

2008

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Cell type–specific regulation of von Willebrand factor expression by the E4BP4 transcriptional repressor

Blood, 2005-02, Vol.105 (4), p.1531-1539

2005

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Lest we forget. Illuminating lived experience of the Covid-19 pandemic and lockdown

The mutational spectrum of type 1 von Willebrand disease: results from a Canadian cohort study

Medicalisation of vaping in the UK? E-cigarette users’ perspectives on the merging of commercial and medical routes to vaping

The genetics of Canadian type 3 von Willebrand disease: further evidence for co‐dominant inheritance of mutant alleles

Abnormal von Willebrand factor secretion, factor VIII stabilization and thrombus dynamics in type 2N von Willebrand disease mice

Chronic rhinosinusitis: patient experiences of primary and secondary care - a qualitative study

Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian Type 1 VWD Study

Influence of a GT repeat element on shear stress responsiveness of the VWF gene promoter

The Experience of Long-Term Opiate Maintenance Treatment and Reported Barriers to Recovery: A Qualitative Systematic Review

Challenges in defining type 2M von Willebrand disease: results from a Canadian cohort study

The effect of exercise on von Willebrand factor and ADAMTS‐13 in individuals with type 1 and type 2B von Willebrand disease

Expanded phenotype–genotype correlations in a pediatric population with type 1 von Willebrand disease

The endothelial lectin clearance receptor CLEC4M binds and internalizes factor VIII in a VWF‐dependent and independent manner

PB0815 Involvement of the Nuclear Protein, TC2N, in Regulating VWF Levels in Endothelial Cells

The scavenger receptor SCARA5 is an endocytic receptor for von Willebrand factor expressed by littoral cells in the human spleen

Role of the Liver-Enriched Transcription Factor Hepatocyte Nuclear Factor 1 in Transcriptional Regulation of the Factor VIII Gene

Perception of need and barriers to access: the mental health needs of young people attending a Youth Offending Team in the UK

Identification and functional characterization of a novel 27-bp deletion in the macroglycopeptide-coding region of the GPIBA gene resulting in platelet-type von Willebrand disease

Four groups of illicit substance users amongst the adult 'hidden' non-problematic community

The Factor VIII Acute Phase Response Requires the Participation of NFκB and C/EBP

Systemic delivery of an adenoviral vector encoding canine factor VIII results in short-term phenotypic correction, inhibitor development, and biphasic liver toxicity in hemophilia A dogs

Aberrant splicing and premature termination of transcription of the FVIII gene as a cause of severe canine hemophilia A: similarities with the intron 22 inversion mutation in human hemophilia

Scavenger receptor class A member 5 (SCARA5) binds and internalizes VWF in vitro : a novel candidate VWF clearance receptor

The impact of offering a relatives’ clinic on the satisfaction of the next-of-kin of Critical Care patients—A prospective time-interrupted trial

Cell type–specific regulation of von Willebrand factor expression by the E4BP4 transcriptional repressor

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