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Attitude Change in Competitive Framing Environments? Open-/Closed-Mindedness, Framing Effects, and Climate Change

Journal of communication, 2013-08, Vol.63 (4), p.766-785

2013

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Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta

Journal of medical genetics, 2004-07, Vol.41 (7), p.545-549

2004

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Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy

Journal of medical genetics, 2002-12, Vol.39 (12), p.882-892

2002

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MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta

Journal of medical genetics, 2005-03, Vol.42 (3), p.271-275

2005

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Functional and clinical consequences of Fc receptor polymorphic and copy number variants

Clinical and experimental immunology, 2009-08, Vol.157 (2), p.244-254

2009

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Overlapping DSPP Mutations Cause Dentin Dysplasia and Dentinogenesis Imperfecta

Journal of dental research, 2008-12, Vol.87 (12), p.1108-1111

2008

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Genetic studies of craniofacial anomalies: clinical implications and applications

Orthodontics & craniofacial research, 2009-08, Vol.12 (3), p.212-220

2009

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Phagocytosis of opsonized apoptotic cells: roles for ‘old‐fashioned’ receptors for antibody and complement

Clinical and experimental immunology, 2004-02, Vol.135 (2), p.181-185

2004

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Phenotypic Variation in FAM83H-associated Amelogenesis Imperfecta

Journal of dental research, 2009-04, Vol.88 (4), p.356-360

2009

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MMP20 Active-site Mutation in Hypomaturation Amelogenesis Imperfecta

Journal of dental research, 2005-11, Vol.84 (11), p.1031-1035

2005

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Phenotype of ENAM Mutations is Dosage-dependent

Journal of dental research, 2005-11, Vol.84 (11), p.1036-1041

2005

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Early clinical experiences with nintedanib in three UK tertiary interstitial lung disease centres

Clinical and translational medicine, 2017-11, Vol.6 (1), p.1-9

2017

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Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects

Journal of medical genetics, 2003-12, Vol.40 (12), p.900-906

2003

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The Effect of Diets on Milk Production and Composition, and on Lactation Curves in Pastured Dairy Goats

Journal of dairy science, 2005-07, Vol.88 (7), p.2604-2615

2005

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Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin C

Journal of medical genetics, 2000-02, Vol.37 (2), p.88-94

2000

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Climate-smart sustainable agriculture in low-to-intermediate shade agroforests

Nature sustainability, 2018-05, Vol.1 (5), p.234-239

2018

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Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndrome

Journal of medical genetics, 1999-12, Vol.36 (12), p.881-887

1999

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Relationship of Phenotype and Genotype in X-Linked Amelogenesis Imperfecta

Connective tissue research, 2003, Vol.44 (1), p.72-78

2003

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Evaluation of human leukocyte N-formylpeptide receptor (FPR1) SNPs in aggressive periodontitis patients

Genes and immunity, 2003-01, Vol.4 (1), p.22-29

2003

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The effect of grazing forage containing condensed tannins on gastro-intestinal parasite infection and milk composition in Angora does

Veterinary parasitology, 2005-06, Vol.130 (1), p.105-113

2005

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Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta

Clinical genetics, 2009-04, Vol.75 (4), p.401-404

2009

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Molecular characterization of the surface of apoptotic neutrophils: implications for functional downregulation and recognition by phagocytes

Cell death and differentiation, 2000-05, Vol.7 (5), p.493-503

2000

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ASAS Centennial Paper: Impact of animal science research on United States goat production and predictions for the future

Journal of animal science, 2009-01, Vol.87 (1), p.400-418

2009

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Identification of cathepsin C mutations in ethnically diverse Papillon-Lefèvre syndrome patients

Journal of medical genetics, 2000-12, Vol.37 (12), p.927-932

2000

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Growth and slaughter traits of Boer x Spanish, Boer x Angora, and Spanish goats consuming a concentrate-based diet

Journal of animal science, 2001-06, Vol.79 (6), p.1423

2001

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Attitude Change in Competitive Framing Environments? Open-/Closed-Mindedness, Framing Effects, and Climate Change

Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta

Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy

MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta

Functional and clinical consequences of Fc receptor polymorphic and copy number variants

Overlapping DSPP Mutations Cause Dentin Dysplasia and Dentinogenesis Imperfecta

Genetic studies of craniofacial anomalies: clinical implications and applications

Phagocytosis of opsonized apoptotic cells: roles for ‘old‐fashioned’ receptors for antibody and complement

Phenotypic Variation in FAM83H-associated Amelogenesis Imperfecta

MMP20 Active-site Mutation in Hypomaturation Amelogenesis Imperfecta

Phenotype of ENAM Mutations is Dosage-dependent

Early clinical experiences with nintedanib in three UK tertiary interstitial lung disease centres

Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects

The Effect of Diets on Milk Production and Composition, and on Lactation Curves in Pastured Dairy Goats

Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin C

Climate-smart sustainable agriculture in low-to-intermediate shade agroforests

Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndrome

Relationship of Phenotype and Genotype in X-Linked Amelogenesis Imperfecta

Evaluation of human leukocyte N-formylpeptide receptor (FPR1) SNPs in aggressive periodontitis patients

The effect of grazing forage containing condensed tannins on gastro-intestinal parasite infection and milk composition in Angora does

Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta

Molecular characterization of the surface of apoptotic neutrophils: implications for functional downregulation and recognition by phagocytes

ASAS Centennial Paper: Impact of animal science research on United States goat production and predictions for the future

Identification of cathepsin C mutations in ethnically diverse Papillon-Lefèvre syndrome patients

Growth and slaughter traits of Boer x Spanish, Boer x Angora, and Spanish goats consuming a concentrate-based diet

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