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Glucose-6-phosphate dehydrogenase deficiency: a historical perspective

Blood, 2008-01, Vol.111 (1), p.16-24

Beutler, Ernest

2008

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The definition of anemia: what is the lower limit of normal of the blood hemoglobin concentration?

Blood, 2006-03, Vol.107 (5), p.1747-1750

2006

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PGK deficiency

British journal of haematology, 2007-01, Vol.136 (1), p.3-11

Beutler, Ernest

2007

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Lysosomal storage diseases: Natural history and ethical and economic aspects

Molecular genetics and metabolism, 2006-07, Vol.88 (3), p.208-215

Beutler, Ernest

2006

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Hemochromatosis: genetics and pathophysiology

Annual review of medicine, 2006-01, Vol.57 (1), p.331-347

Beutler, Ernest

2006

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Bone Morphogenetic Proteins 2, 4, and 9 Stimulate Murine Hepcidin 1 Expression Independently of Hfe, Transferrin Receptor 2 (Tfr2), and IL-6

Proceedings of the National Academy of Sciences - PNAS, 2006-07, Vol.103 (27), p.10289-10293

2006

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Serine Protease TMPRSS6 Is Required to Sense Iron Deficiency

Science (American Association for the Advancement of Science), 2008-05, Vol.320 (5879), p.1088-1092

2008

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Gaucher disease: multiple lessons from a single gene disorder

Acta pædiatrica (Oslo), 2006-04, Vol.95, p.103-109

Beutler, Ernest

2006

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The global prevalence of glucose-6-phosphate dehydrogenase deficiency: A systematic review and meta-analysis

Blood cells, molecules, & diseases, 2009-05, Vol.42 (3), p.267-278

2009

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Regulation of hepcidin and iron-overload disease

Annual review of pathology, 2009-02, Vol.4 (1), p.489-515

2009

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Regulation of Hepcidin Transcription by Interleukin-1 and Interleukin-6

Proceedings of the National Academy of Sciences - PNAS, 2005-02, Vol.102 (6), p.1906-1910

2005

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Two BMP responsive elements, STAT, and bZIP/HNF4/COUP motifs of the hepcidin promoter are critical for BMP, SMAD1, and HJV responsiveness

Blood, 2009-01, Vol.113 (3), p.688-695

2009

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The IL-6- and Lipopolysaccharide-Induced Transcription of Hepcidin in HFE-, Transferrin Receptor 2-, and β2-Microglobulin-Deficient Hepatocytes

Proceedings of the National Academy of Sciences - PNAS, 2004-06, Vol.101 (25), p.9263-9265

2004

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Enzyme replacement in Gaucher disease

PLoS medicine, 2004-11, Vol.1 (2), p.e21

Beutler, Ernest

2004

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Racial Variability in the UDP-Glucuronosyltransferase 1 (UGT1A1) Promoter: A Balanced Polymorphism for Regulation of Bilirubin Metabolism?

Proceedings of the National Academy of Sciences - PNAS, 1998-07, Vol.95 (14), p.8170-8174

1998

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Glucose-6-phosphate dehydrogenase deficiency and antimalarial drug development

The American journal of tropical medicine and hygiene, 2007-10, Vol.77 (4), p.779-789

2007

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Penetrance of 845G→A (C282Y) HFE hereditary haemochromatosis mutation in the USA

The Lancet (British edition), 2002-01, Vol.359 (9302), p.211-218

2002

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Chemical Chaperones Increase the Cellular Activity of N370S β-Glucosidase: A Therapeutic Strategy for Gaucher Disease

Proceedings of the National Academy of Sciences - PNAS, 2002-11, Vol.99 (24), p.15428-15433

2002

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Hematologically important mutations: Gaucher disease

Blood cells, molecules, & diseases, 2005-11, Vol.35 (3), p.355-364

2005

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A Missense Mutation in Human Fatty Acid Amide Hydrolase Associated with Problem Drug Use

Proceedings of the National Academy of Sciences - PNAS, 2002-06, Vol.99 (12), p.8394-8399

2002

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Reduced endocannabinoid immune modulation by a common cannabinoid 2 (CB2) receptor gene polymorphism: possible risk for autoimmune disorders

Journal of leukocyte biology, 2005-07, Vol.78 (1), p.231-238

2005

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Hematologically Important Mutations: Glucose-6-phosphate Dehydrogenase

Blood cells, molecules, & diseases, 2002-03, Vol.28 (2), p.93-103

2002

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Genetic abnormalities and juvenile hemochromatosis: mutations of the HJV gene encoding hemojuvelin

Blood, 2004-06, Vol.103 (12), p.4669-4671

2004

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Population-Based Sample Reveals Gene–Gender Interactions in Blood Pressure in White Americans

Hypertension (Dallas, Tex. 1979), 2007-01, Vol.49 (1), p.96-106

2007

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Phosphatidylserine Exposure and Red Cell Viability in Red Cell Aging and in Hemolytic Anemia

Proceedings of the National Academy of Sciences - PNAS, 1998-03, Vol.95 (6), p.3077-3081

1998

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Glucose-6-phosphate dehydrogenase deficiency: a historical perspective

The definition of anemia: what is the lower limit of normal of the blood hemoglobin concentration?

PGK deficiency

Lysosomal storage diseases: Natural history and ethical and economic aspects

Hemochromatosis: genetics and pathophysiology

Bone Morphogenetic Proteins 2, 4, and 9 Stimulate Murine Hepcidin 1 Expression Independently of Hfe, Transferrin Receptor 2 (Tfr2), and IL-6

Serine Protease TMPRSS6 Is Required to Sense Iron Deficiency

Gaucher disease: multiple lessons from a single gene disorder

The global prevalence of glucose-6-phosphate dehydrogenase deficiency: A systematic review and meta-analysis

Regulation of hepcidin and iron-overload disease

Regulation of Hepcidin Transcription by Interleukin-1 and Interleukin-6

Two BMP responsive elements, STAT, and bZIP/HNF4/COUP motifs of the hepcidin promoter are critical for BMP, SMAD1, and HJV responsiveness

The IL-6- and Lipopolysaccharide-Induced Transcription of Hepcidin in HFE-, Transferrin Receptor 2-, and β2-Microglobulin-Deficient Hepatocytes

Enzyme replacement in Gaucher disease

Racial Variability in the UDP-Glucuronosyltransferase 1 (UGT1A1) Promoter: A Balanced Polymorphism for Regulation of Bilirubin Metabolism?

Glucose-6-phosphate dehydrogenase deficiency and antimalarial drug development

Penetrance of 845G→A (C282Y) HFE hereditary haemochromatosis mutation in the USA

Chemical Chaperones Increase the Cellular Activity of N370S β-Glucosidase: A Therapeutic Strategy for Gaucher Disease

Hematologically important mutations: Gaucher disease

A Missense Mutation in Human Fatty Acid Amide Hydrolase Associated with Problem Drug Use

Reduced endocannabinoid immune modulation by a common cannabinoid 2 (CB2) receptor gene polymorphism: possible risk for autoimmune disorders

Hematologically Important Mutations: Glucose-6-phosphate Dehydrogenase

Genetic abnormalities and juvenile hemochromatosis: mutations of the HJV gene encoding hemojuvelin

Population-Based Sample Reveals Gene–Gender Interactions in Blood Pressure in White Americans

Phosphatidylserine Exposure and Red Cell Viability in Red Cell Aging and in Hemolytic Anemia

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