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α-Amylase: an enzyme specificity found in various families of glycoside hydrolases

Cellular and molecular life sciences : CMLS, 2014-04, Vol.71 (7), p.1149-1170

2014

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A new clan of CBM families based on bioinformatics of starch‐binding domains from families CBM20 and CBM21

The FEBS journal, 2005-11, Vol.272 (21), p.5497-5513

2005

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The starch‐binding domain family CBM41—An in silico analysis of evolutionary relationships

Proteins, structure, function, and bioinformatics, 2017-08, Vol.85 (8), p.1480-1492

2017

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Relation between domain evolution, specificity, and taxonomy of the α‐amylase family members containing a C‐terminal starch‐binding domain

European journal of biochemistry, 2003-02, Vol.270 (4), p.635-645

2003

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[alpha]-Amylase: an enzyme specificity found in various families of glycoside hydrolases

Cellular and molecular life sciences : CMLS, 2014-04, Vol.71 (7), p.1149

2014

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In the clinic. Migraine

Annals of internal medicine, 2013-11, Vol.159 (9), p.ITC5

MacGregor, E Ann

2013

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Possible structure and active site residues of starch, glycogen, and sucrose synthases

Journal of Protein Chemistry, 2002-05, Vol.21 (4), p.297-306

MacGregor, E Ann

2002

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Relationship of sequence and structure to specificity in the α-amylase family of enzymes

Biochimica et Biophysica Acta (BBA)/Protein Structure and Molecular Enzymology, 2001-03, Vol.1546 (1), p.1-20

2001

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Substrate Binding and Catalytic Mechanism of a Barley β-d-Glucosidase/(1,4)-β-d-Glucan Exohydrolase

The Journal of biological chemistry, 1998-05, Vol.273 (18), p.11134-11143

1998

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Starch- and glycogen-debranching and branching enzymes: prediction of structural features of the catalytic (beta/alpha)8-barrel domain and evolutionary relationship to other amylolytic enzymes

Journal of protein chemistry, 1993-12, Vol.12 (6), p.791-805

1993

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Relationships Between Structure and Activity in the α-Amylase Family of Starch-metabolising Enzymes

Starch - Stärke, 1993, Vol.45 (7), p.232-237

MacGregor, E. Ann

1993

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Substrate Binding and Catalytic Mechanism of a Barley Î²-d-Glucosidase/(1,4)-Î²-d-Glucan Exohydrolase

The Journal of biological chemistry, 1998-05, Vol.273 (18), p.11134

1998

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24-Hour Urinary Sodium and Potassium Excretion and Cardiovascular Risk

The New England journal of medicine, 2022-01, Vol.386 (3), p.252-263

2022

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Selection of Optimal Adjuvant Chemotherapy and Targeted Therapy for Early Breast Cancer: ASCO Clinical Practice Guideline Focused Update

Journal of clinical oncology, 2018-08, Vol.36 (23), p.2433-2443

2018

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Homelessness, unstable housing, and risk of HIV and hepatitis C virus acquisition among people who inject drugs: a systematic review and meta-analysis

The Lancet. Public health, 2021-05, Vol.6 (5), p.e309-e323

2021

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Evidence of NLRP3-inflammasome activation in rheumatoid arthritis (RA); genetic variants within the NLRP3-inflammasome complex in relation to susceptibility to RA and response to anti-TNF treatment

Annals of the rheumatic diseases, 2014-06, Vol.73 (6), p.1202-1210

2014

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Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

Nature genetics, 2013-03, Vol.45 (3), p.314-318

2013

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Genome‐wide association study of genetic predictors of anti–tumor necrosis factor treatment efficacy in rheumatoid arthritis identifies associations with polymorphisms at seven loci

Arthritis & rheumatology (Hoboken, N.J.), 2011-03, Vol.63 (3), p.645-653

2011

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Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis

Human molecular genetics, 2013-02, Vol.22 (4), p.832-841

2013

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An Automated, Highly Selective Reaction Monitoring Instrument Using Molecular Rotational Resonance Spectroscopy

Precision Chemistry, 2024-02, Vol.2 (2), p.57-62

2024

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Genetic variants at CD28 , PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk

Nature genetics, 2009-12, Vol.41 (12), p.1313-1318

2009

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Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases

Nature communications, 2019-09, Vol.10 (1), p.4219-10, Article 4219

2019

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Hemophilia prophylaxis adherence and bleeding using a tailored, frequency‐escalated approach: The Canadian Hemophilia Primary Prophylaxis Study

Research and practice in thrombosis and haemostasis, 2020-02, Vol.4 (2), p.318-325

2020

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PADI4 genotype is not associated with rheumatoid arthritis in a large UK Caucasian Population

Annals of the rheumatic diseases, 2010-04, Vol.69 (4), p.666-ard

2010

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The Role of KRAS rs61764370 in Invasive Epithelial Ovarian Cancer: Implications for Clinical Testing

Clinical cancer research, 2011-06, Vol.17 (11), p.3742-3750

2011

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α-Amylase: an enzyme specificity found in various families of glycoside hydrolases

A new clan of CBM families based on bioinformatics of starch‐binding domains from families CBM20 and CBM21

The starch‐binding domain family CBM41—An in silico analysis of evolutionary relationships

Relation between domain evolution, specificity, and taxonomy of the α‐amylase family members containing a C‐terminal starch‐binding domain

[alpha]-Amylase: an enzyme specificity found in various families of glycoside hydrolases

In the clinic. Migraine

Possible structure and active site residues of starch, glycogen, and sucrose synthases

Relationship of sequence and structure to specificity in the α-amylase family of enzymes

Substrate Binding and Catalytic Mechanism of a Barley β-d-Glucosidase/(1,4)-β-d-Glucan Exohydrolase

Starch- and glycogen-debranching and branching enzymes: prediction of structural features of the catalytic (beta/alpha)8-barrel domain and evolutionary relationship to other amylolytic enzymes

Relationships Between Structure and Activity in the α-Amylase Family of Starch-metabolising Enzymes

Substrate Binding and Catalytic Mechanism of a Barley Î²-d-Glucosidase/(1,4)-Î²-d-Glucan Exohydrolase

24-Hour Urinary Sodium and Potassium Excretion and Cardiovascular Risk

Selection of Optimal Adjuvant Chemotherapy and Targeted Therapy for Early Breast Cancer: ASCO Clinical Practice Guideline Focused Update

Homelessness, unstable housing, and risk of HIV and hepatitis C virus acquisition among people who inject drugs: a systematic review and meta-analysis

Evidence of NLRP3-inflammasome activation in rheumatoid arthritis (RA); genetic variants within the NLRP3-inflammasome complex in relation to susceptibility to RA and response to anti-TNF treatment

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

Genome‐wide association study of genetic predictors of anti–tumor necrosis factor treatment efficacy in rheumatoid arthritis identifies associations with polymorphisms at seven loci

Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis

An Automated, Highly Selective Reaction Monitoring Instrument Using Molecular Rotational Resonance Spectroscopy

Genetic variants at CD28 , PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk

Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases

Hemophilia prophylaxis adherence and bleeding using a tailored, frequency‐escalated approach: The Canadian Hemophilia Primary Prophylaxis Study

PADI4 genotype is not associated with rheumatoid arthritis in a large UK Caucasian Population

The Role of KRAS rs61764370 in Invasive Epithelial Ovarian Cancer: Implications for Clinical Testing

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