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The association of coeliac disease and microscopic colitis: a large population‐based study

Alimentary pharmacology & therapeutics, 2011-06, Vol.33 (12), p.1340-1349

2011

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The rising incidence of eosinophilic oesophagitis is associated with increasing biopsy rates: a population-based study

Alimentary pharmacology & therapeutics, 2012-11, Vol.36 (10), p.950-958

2012

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Mesalazine (5‐aminosalicylic acid) alters faecal bacterial profiles, but not mucosal proteolytic activity in diarrhoea‐predominant irritable bowel syndrome

Alimentary pharmacology & therapeutics, 2011-08, Vol.34 (3), p.374-383

2011

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Microcytic anaemia mice have a mutation in Nramp2 , a candidate iron transporter gene

Nature genetics, 1997-08, Vol.16 (4), p.383-386

1997

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Increasing incidence rates, distribution and histological characteristics of primary gastrointestinal non-Hodgkin lymphoma in a North American population

Canadian journal of gastroenterology, 2012-07, Vol.26 (7), p.452-456

2012

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Transferrin receptor is necessary for development of erythrocytes and the nervous system

Nature genetics, 1999-04, Vol.21 (4), p.396-399

1999

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Disorders of Iron Metabolism

The New England journal of medicine, 1999-12, Vol.341 (26), p.1986-1995

Andrews, Nancy C

1999

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The Maf transcription factors: regulators of differentiation

Trends in Biochemical Sciences, 1997-11, Vol.22 (11), p.437-441

1997

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Balancing Acts: Molecular Control of Mammalian Iron Metabolism

Cell, 2004-04, Vol.117 (3), p.285-297

2004

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Gastrointestinal Symptoms in Parkinson Disease: Clinical Aspects and Management

Canadian journal of neurological sciences, 2011-07, Vol.38 (4), p.557-564

2011

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A rapid micropreparation technique for extraction of DNA-binding proteins from limiting numbers of mammalian cells

Nucleic acids research, 1991-05, Vol.19 (9), p.2499-2499

1991

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The C282Y Mutation Causing Hereditary Hemochromatosis Does Not Produce a Null Allele

Blood, 1999-07, Vol.94 (1), p.9-11

1999

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Iron homeostasis: insights from genetics and animal models

Nature reviews. Genetics, 2000-12, Vol.1 (3), p.208-217

Andrews, Nancy C

2000

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Toward modulation of the endocannabinoid system for treatment of gastrointestinal disease: FAAHster but not “higher”

Neurogastroenterology and motility, 2014-04, Vol.26 (4), p.447-454

2014

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The Ubiquitous Subunit of Erythroid Transcription Factor NF-E2 is a Small Basic-Leucine Zipper Protein Related to the v-maf Oncogene

Proceedings of the National Academy of Sciences - PNAS, 1993-12, Vol.90 (24), p.11488-11492

1993

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The Nramp2/DMT1 iron transporter is induced in the duodenum of microcytic anemia mk mice but is not properly targeted to the intestinal brush border

Blood, 2000-12, Vol.96 (12), p.3964-3970

2000

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Expression of the DMT1 (NRAMP2/DCT1) iron transporter in mice with genetic iron overload disorders

Blood, 2001-02, Vol.97 (4), p.1138-1140

2001

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Regulatory defects in liver and intestine implicate abnormal hepcidin and Cybrd1 expression in mouse hemochromatosis

Nature genetics, 2003-05, Vol.34 (1), p.102-107

2003

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Mining Copper Transport Genes

Proceedings of the National Academy of Sciences - PNAS, 2001-06, Vol.98 (12), p.6543-6545

Andrews, Nancy C.

2001

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Constitutive hepcidin expression prevents iron overload in a mouse model of hemochromatosis

Nature genetics, 2003-05, Vol.34 (1), p.97-101

2003

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p63, a p53 Homolog at 3q27–29, Encodes Multiple Products with Transactivating, Death-Inducing, and Dominant-Negative Activities

Molecular cell, 1998-09, Vol.2 (3), p.305-316

1998

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Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene

The Journal of clinical investigation, 2001-08, Vol.108 (4), p.619

2001

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The role of the endocannabinoid system in the pathophysiology and treatment of irritable bowel syndrome

Neurogastroenterology and motility, 2008-08, Vol.20 (8), p.857-868

2008

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Laparoscopic Heller's myotomy or botulinum toxin injection for management of esophageal achalasia : Patient choice and treatment outcomes

Surgical endoscopy, 1999-08, Vol.13 (8), p.742-746

1999

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Purification of the human NF-E2 complex: cDNA cloning of the hematopoietic cell-specific subunit and evidence for an associated partner

Molecular and Cellular Biology, 1993-09, Vol.13 (9), p.5604-5612

1993

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The association of coeliac disease and microscopic colitis: a large population‐based study

The rising incidence of eosinophilic oesophagitis is associated with increasing biopsy rates: a population-based study

Mesalazine (5‐aminosalicylic acid) alters faecal bacterial profiles, but not mucosal proteolytic activity in diarrhoea‐predominant irritable bowel syndrome

Microcytic anaemia mice have a mutation in Nramp2 , a candidate iron transporter gene

Increasing incidence rates, distribution and histological characteristics of primary gastrointestinal non-Hodgkin lymphoma in a North American population

Transferrin receptor is necessary for development of erythrocytes and the nervous system

Disorders of Iron Metabolism

The Maf transcription factors: regulators of differentiation

Balancing Acts: Molecular Control of Mammalian Iron Metabolism

Gastrointestinal Symptoms in Parkinson Disease: Clinical Aspects and Management

A rapid micropreparation technique for extraction of DNA-binding proteins from limiting numbers of mammalian cells

The C282Y Mutation Causing Hereditary Hemochromatosis Does Not Produce a Null Allele

Iron homeostasis: insights from genetics and animal models

Toward modulation of the endocannabinoid system for treatment of gastrointestinal disease: FAAHster but not “higher”

The Ubiquitous Subunit of Erythroid Transcription Factor NF-E2 is a Small Basic-Leucine Zipper Protein Related to the v-maf Oncogene

The Nramp2/DMT1 iron transporter is induced in the duodenum of microcytic anemia mk mice but is not properly targeted to the intestinal brush border

Expression of the DMT1 (NRAMP2/DCT1) iron transporter in mice with genetic iron overload disorders

Regulatory defects in liver and intestine implicate abnormal hepcidin and Cybrd1 expression in mouse hemochromatosis

Mining Copper Transport Genes

Constitutive hepcidin expression prevents iron overload in a mouse model of hemochromatosis

p63, a p53 Homolog at 3q27–29, Encodes Multiple Products with Transactivating, Death-Inducing, and Dominant-Negative Activities

Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene

The role of the endocannabinoid system in the pathophysiology and treatment of irritable bowel syndrome

Laparoscopic Heller's myotomy or botulinum toxin injection for management of esophageal achalasia : Patient choice and treatment outcomes

Purification of the human NF-E2 complex: cDNA cloning of the hematopoietic cell-specific subunit and evidence for an associated partner

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