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Premature Atherosclerosis in Patients with Familial Chylomicronemia Caused by Mutations in the Lipoprotein Lipase Gene

The New England journal of medicine, 1996-09, Vol.335 (12), p.848-854

1996

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High-resolution analysis of genomic alterations and human papillomavirus integration in anal intraepithelial neoplasia

Journal of acquired immune deficiency syndromes (1999), 2005-10, Vol.40 (2), p.182-189

2005

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Mutations in the gene for lipoprotein lipase. A cause for low HDL cholesterol levels in individuals heterozygous for familial hypercholesterolemia

Arteriosclerosis, thrombosis, and vascular biology, 1995-10, Vol.15 (10), p.1704-1712

1995

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The asn9 variant of lipoprotein lipase is associated with the - 93G promoter mutation and an increased risk of coronary artery disease

Clinical genetics, 1998, Vol.53 (1), p.27-33

1998

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Challenging the Paradigm: EGFR wild-type benefit from an EGFR inhibitor in NSCLC

Cancer treatment and research communications, 2017, Vol.11, p.10-16

2017

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Two common mutations (D9N, N291S) in lipoprotein lipase: a cumulative analysis of their influence on plasma lipids and lipoproteins in men and women

Clinical genetics, 1999-10, Vol.56 (4), p.297-305

1999

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Ethnic variation and in vivo effects of the -93t-->g promoter variant in the lipoprotein lipase gene

Arteriosclerosis, thrombosis, and vascular biology, 1997-11, Vol.17 (11), p.2672-2678

1997

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Common sequence variants of lipoprotein lipase: standardized studies of in vitro expression and catalytic function

Biochimica et biophysica acta, 1996-07, Vol.1302 (2), p.159-166

1996

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Identification and the relationship between mutations in the lipoprotein lipase gene, dyslipidemia and coronary heart disease

Gagne, S Eric

1999

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A frequently occurring mutation in the lipoprotein lipase gene (Asn291Ser) results in altered postprandial chylomicron triglyceride and retinyl palmitate response in normolipidemic carriers

Journal of lipid research, 1996-08, Vol.37 (8), p.1675-1684

1996

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The Asn9 variant of lipoprotein lipase is associated with the - 93G promoter mutation and an increased risk of coronary artery disease

Clinical genetics, 1998-01, Vol.53 (1), p.27-33

1998

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Management of Malignant Melanoma: Best Practices

Journal of cutaneous medicine and surgery, 2009-03, Vol.13 (2), p.55-73

2009

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Effect of eprosartan-based antihypertensive therapy on coronary heart disease risk assessed by Framingham methodology in Canadian patients: results of the POWER survey

Vascular health and risk management, 2014-01, Vol.10 (default), p.63-74

2014

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Simvastatin with or without Ezetimibe in Familial Hypercholesterolemia

The New England journal of medicine, 2008-04, Vol.358 (14), p.1431-1443

2008

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Variations in Patients' Perceptions and Use of Generic Drugs: Results of a National Survey

Journal of general internal medicine : JGIM, 2016-06, Vol.31 (6), p.609-614

2016

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BANYAN. XI. The BANYAN Σ Multivariate Bayesian Algorithm to Identify Members of Young Associations with 150 pc

Astrophysical journal. Letters, 2018-03, Vol.856 (1), p.23

2018

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Outcomes of the Latarjet Procedure Versus Free Bone Block Procedures for Anterior Shoulder Instability: A Systematic Review and Meta-analysis

The American journal of sports medicine, 2021-03, Vol.49 (3), p.805-816

2021

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Ultrahigh‐performance liquid chromatography–tandem mass spectrometry quantitation of o‐cresol in hydrolyzed human urine to assess toluene exposure

Rapid communications in mass spectrometry, 2023-08, Vol.37 (16), p.e9595-n/a

2023

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Return to Work After Primary Rotator Cuff Repair: A Systematic Review and Meta-analysis

The American journal of sports medicine, 2021-07, Vol.49 (8), p.2238-2247

2021

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Physicians' Trust in the FDA's Use of Product-Specific Pathways for Generic Drug Approval

PloS one, 2016-10, Vol.11 (10), p.e0163339-e0163339

2016

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Volans-Carina: A New 90 Myr Old Stellar Association at 85 pc

The Astrophysical journal, 2018-10, Vol.865 (2), p.136

2018

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Prevalence and Predictors of Generic Drug Skepticism Among Physicians: Results of a National Survey

JAMA internal medicine, 2016-06, Vol.176 (6), p.845

2016

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Outcomes are comparable using free bone block autografts versus allografts for the management of anterior shoulder instability with glenoid bone loss: a systematic review and meta-analysis of “The Non-Latarjet”

Knee surgery, sports traumatology, arthroscopy : official journal of the ESSKA, 2021-07, Vol.29 (7), p.2159-2174

2021

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Explainable artificial intelligence models for predicting risk of suicide using health administrative data in Quebec

PloS one, 2024-04, Vol.19 (4), p.e0301117-e0301117

2024

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3172 – SINGLE-CELL TRANSCRIPTOMICS REVEAL PERTURBATIONS IN HEMATOPOIETIC LINEAGE MATURATION DRIVEN BY TRISOMY 21 AND GATA1S

Experimental hematology, 2024-08, Vol.137, p.104492, Article 104492

2024

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Premature Atherosclerosis in Patients with Familial Chylomicronemia Caused by Mutations in the Lipoprotein Lipase Gene

High-resolution analysis of genomic alterations and human papillomavirus integration in anal intraepithelial neoplasia

Mutations in the gene for lipoprotein lipase. A cause for low HDL cholesterol levels in individuals heterozygous for familial hypercholesterolemia

The asn9 variant of lipoprotein lipase is associated with the - 93G promoter mutation and an increased risk of coronary artery disease

Challenging the Paradigm: EGFR wild-type benefit from an EGFR inhibitor in NSCLC

Two common mutations (D9N, N291S) in lipoprotein lipase: a cumulative analysis of their influence on plasma lipids and lipoproteins in men and women

Ethnic variation and in vivo effects of the -93t-->g promoter variant in the lipoprotein lipase gene

Common sequence variants of lipoprotein lipase: standardized studies of in vitro expression and catalytic function

Identification and the relationship between mutations in the lipoprotein lipase gene, dyslipidemia and coronary heart disease

A frequently occurring mutation in the lipoprotein lipase gene (Asn291Ser) results in altered postprandial chylomicron triglyceride and retinyl palmitate response in normolipidemic carriers

The Asn9 variant of lipoprotein lipase is associated with the - 93G promoter mutation and an increased risk of coronary artery disease

Management of Malignant Melanoma: Best Practices

Effect of eprosartan-based antihypertensive therapy on coronary heart disease risk assessed by Framingham methodology in Canadian patients: results of the POWER survey

Simvastatin with or without Ezetimibe in Familial Hypercholesterolemia

Variations in Patients' Perceptions and Use of Generic Drugs: Results of a National Survey

BANYAN. XI. The BANYAN Σ Multivariate Bayesian Algorithm to Identify Members of Young Associations with 150 pc

Outcomes of the Latarjet Procedure Versus Free Bone Block Procedures for Anterior Shoulder Instability: A Systematic Review and Meta-analysis

Ultrahigh‐performance liquid chromatography–tandem mass spectrometry quantitation of o‐cresol in hydrolyzed human urine to assess toluene exposure

Return to Work After Primary Rotator Cuff Repair: A Systematic Review and Meta-analysis

Physicians' Trust in the FDA's Use of Product-Specific Pathways for Generic Drug Approval

Volans-Carina: A New 90 Myr Old Stellar Association at 85 pc

Prevalence and Predictors of Generic Drug Skepticism Among Physicians: Results of a National Survey

Outcomes are comparable using free bone block autografts versus allografts for the management of anterior shoulder instability with glenoid bone loss: a systematic review and meta-analysis of “The Non-Latarjet”

Explainable artificial intelligence models for predicting risk of suicide using health administrative data in Quebec

3172 – SINGLE-CELL TRANSCRIPTOMICS REVEAL PERTURBATIONS IN HEMATOPOIETIC LINEAGE MATURATION DRIVEN BY TRISOMY 21 AND GATA1S

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