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Endothelial Injury and Glycocalyx Degradation in Critically Ill Coronavirus Disease 2019 Patients: Implications for Microvascular Platelet Aggregation

Critical care explorations, 2020-09, Vol.2 (9), p.e0194-e0194

2020

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Burden of disease of type 2 diabetes mellitus: cost of illness and quality of life estimated using the Maastricht Study

Diabetic medicine, 2020-10, Vol.37 (10), p.1759-1765

2020

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Liver-directed gene therapy results in long-term correction of progressive familial intrahepatic cholestasis type 3 in mice

Journal of hepatology, 2019-07, Vol.71 (1), p.153-162

2019

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Gene Therapy for Progressive Familial Intrahepatic Cholestasis: Current Progress and Future Prospects

International journal of molecular sciences, 2020-12, Vol.22 (1), p.273

2020

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Prevalence and Relevance of Pre-Existing Anti-Adeno-Associated Virus Immunity in the Context of Gene Therapy for Crigler-Najjar Syndrome

Human gene therapy, 2019-10, Vol.30 (10), p.1297-1305

2019

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Knowledge translation tools to guide care of non-intubated patients with acute respiratory illness during the COVID-19 Pandemic

Critical care (London, England), 2021-01, Vol.25 (1), p.22-22, Article 22

2021

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The P4-ATPase ATP9A is a novel determinant of exosome release

PloS one, 2019-04, Vol.14 (4), p.e0213069-e0213069

2019

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Identification and quantification of defective virus genomes in high throughput sequencing data using DVG-profiler, a novel post-sequence alignment processing algorithm

PloS one, 2019-05, Vol.14 (5), p.e0216944-e0216944

2019

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Long-Read High-Throughput Sequencing (HTS) Revealed That the Sf-Rhabdovirus X+ Genome Contains a 3.7 kb Internal Duplication

Viruses, 2023-09, Vol.15 (10), p.1998

2023

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Kinome capture sequencing of high-grade serous ovarian carcinoma reveals novel mutations in the JAK3 gene

PloS one, 2020-07, Vol.15 (7), p.e0235766

2020

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Low efficacy of recombinant SV40 in Ugt1a1-/- mice with severe inherited hyperbilirubinemia

PloS one, 2021-01, Vol.16 (4), p.e0250605-e0250605

2021

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Effects of Arachidonic Acid and Its Metabolites on Functional Beta-Cell Mass

Metabolites, 2022-04, Vol.12 (4), p.342

2022

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Management of necrotizing pneumonia and pulmonary gangrene: a case series and review of the literature

Canadian respiratory journal, 2014, Vol.21 (4), p.239-245

2014

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Ins1-Cre and Ins1-CreER Gene Replacement Alleles Are Susceptible To Silencing By DNA Hypermethylation

Endocrinology (Philadelphia), 2020-08, Vol.161 (8)

2020

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The PROMIZING trial enrollment algorithm for early identification of patients ready for unassisted breathing

Critical care (London, England), 2022-06, Vol.26 (1), p.1-188, Article 188

2022

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Association of Endogenous Erythropoietin Levels and Iron Status With Cognitive Functioning in the General Population

Frontiers in aging neuroscience, 2022-04, Vol.14, p.862856-862856

2022

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The wide spectrum of multidrug resistance 3 deficiency: From neonatal cholestasis to cirrhosis of adulthood

Gastroenterology (New York, N.Y. 1943), 2001-05, Vol.120 (6), p.1448-1458

2001

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A novel UGT1A1 gene mutation causing severe unconjugated hyperbilirubinemia: a case report

BMC pediatrics, 2019-05, Vol.19 (1), p.173-173, Article 173

2019

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De Novo Donor‐Specific HLA Antibody Formation in Two Patients With Crigler‐Najjar Syndrome Type I Following Human Hepatocyte Transplantation With Partial Hepatectomy Preconditioning

American journal of transplantation, 2016-03, Vol.16 (3), p.1021-1030

2016

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Preclinical Development of an AAV8-hUGT1A1 Vector for the Treatment of Crigler-Najjar Syndrome

Molecular therapy. Methods & clinical development, 2019-03, Vol.12, p.157-174

2019

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The Genetic Basis of the Reduced Expression of Bilirubin UDP-Glucuronosyltransferase 1 in Gilbert's Syndrome

The New England journal of medicine, 1995-11, Vol.333 (18), p.1171-1175

1995

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Biliverdin Reductase inhibitors did not improve severe unconjugated hyperbilirubinemia in vivo

Scientific reports, 2017-05, Vol.7 (1), p.1646-9, Article 1646

2017

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Pancreatic islet beta cell-specific deletion of G6pc2 reduces fasting blood glucose

Journal of molecular endocrinology, 2020-05, Vol.64 (4), p.235-248

2020

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Maternal and neonatal outcomes in women with severe early onset pre‐eclampsia before 26 weeks of gestation, a case series

BJOG : an international journal of obstetrics and gynaecology, 2017-08, Vol.124 (9), p.1440-1447

2017

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Life-threatening bronchiolitis related to electronic cigarette use in a Canadian youth

Canadian Medical Association journal (CMAJ), 2019-12, Vol.191 (48), p.E1321-E1331

2019

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Endothelial Injury and Glycocalyx Degradation in Critically Ill Coronavirus Disease 2019 Patients: Implications for Microvascular Platelet Aggregation

Burden of disease of type 2 diabetes mellitus: cost of illness and quality of life estimated using the Maastricht Study

Liver-directed gene therapy results in long-term correction of progressive familial intrahepatic cholestasis type 3 in mice

Gene Therapy for Progressive Familial Intrahepatic Cholestasis: Current Progress and Future Prospects

Prevalence and Relevance of Pre-Existing Anti-Adeno-Associated Virus Immunity in the Context of Gene Therapy for Crigler-Najjar Syndrome

Knowledge translation tools to guide care of non-intubated patients with acute respiratory illness during the COVID-19 Pandemic

The P4-ATPase ATP9A is a novel determinant of exosome release

Identification and quantification of defective virus genomes in high throughput sequencing data using DVG-profiler, a novel post-sequence alignment processing algorithm

Long-Read High-Throughput Sequencing (HTS) Revealed That the Sf-Rhabdovirus X+ Genome Contains a 3.7 kb Internal Duplication

Kinome capture sequencing of high-grade serous ovarian carcinoma reveals novel mutations in the JAK3 gene

Low efficacy of recombinant SV40 in Ugt1a1-/- mice with severe inherited hyperbilirubinemia

Effects of Arachidonic Acid and Its Metabolites on Functional Beta-Cell Mass

Management of necrotizing pneumonia and pulmonary gangrene: a case series and review of the literature

Ins1-Cre and Ins1-CreER Gene Replacement Alleles Are Susceptible To Silencing By DNA Hypermethylation

The PROMIZING trial enrollment algorithm for early identification of patients ready for unassisted breathing

Association of Endogenous Erythropoietin Levels and Iron Status With Cognitive Functioning in the General Population

The wide spectrum of multidrug resistance 3 deficiency: From neonatal cholestasis to cirrhosis of adulthood

A novel UGT1A1 gene mutation causing severe unconjugated hyperbilirubinemia: a case report

De Novo Donor‐Specific HLA Antibody Formation in Two Patients With Crigler‐Najjar Syndrome Type I Following Human Hepatocyte Transplantation With Partial Hepatectomy Preconditioning

Preclinical Development of an AAV8-hUGT1A1 Vector for the Treatment of Crigler-Najjar Syndrome

The Genetic Basis of the Reduced Expression of Bilirubin UDP-Glucuronosyltransferase 1 in Gilbert's Syndrome

Biliverdin Reductase inhibitors did not improve severe unconjugated hyperbilirubinemia in vivo

Pancreatic islet beta cell-specific deletion of G6pc2 reduces fasting blood glucose

Maternal and neonatal outcomes in women with severe early onset pre‐eclampsia before 26 weeks of gestation, a case series

Life-threatening bronchiolitis related to electronic cigarette use in a Canadian youth

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