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Laminar flow substantially affects the morphology and functional phenotype of glomerular endothelial cells

PloS one, 2021-05, Vol.16 (5), p.e0251129-e0251129

2021

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A Putative Role for TRPC6 in Immune-Mediated Kidney Injury

International journal of molecular sciences, 2023-11, Vol.24 (22), p.16419

2023

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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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Identification of parotid salivary biomarkers in Sjögren's syndrome by surface-enhanced laser desorption/ionization time-of-flight mass spectrometry and two-dimensional difference gel electrophoresis

Rheumatology (Oxford, England), 2006-09, Vol.45 (9), p.1077-1086

2006

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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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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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Microbial Risk Indicators of Early Childhood Caries

Journal of Clinical Microbiology, 2005-11, Vol.43 (11), p.5753-5759

2005

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Co-Culture of Glomerular Endothelial Cells and Podocytes in a Custom-Designed Glomerulus-on-a-Chip Model Improves the Filtration Barrier Integrity and Affects the Glomerular Cell Phenotype

Biosensors (Basel), 2023-03, Vol.13 (3), p.339

2023

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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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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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Phenotypic Variation in FAM83H-associated Amelogenesis Imperfecta

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

2009

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Cytokine profiles in the joint depend on pathology, but are different between synovial fluid, cartilage tissue and cultured chondrocytes

Arthritis research & therapy, 2014-09, Vol.16 (5), p.441-441, Article 441

2014

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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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A fluorescent, paramagnetic and PEGylated gold/silica nanoparticle for MRI, CT and fluorescence imaging

Contrast media and molecular imaging, 2010-07, Vol.5 (4), p.231-236

2010

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Microradian X-ray diffraction in colloidal photonic crystals

Journal of applied crystallography, 2006-04, Vol.39 (2), p.137-144

2006

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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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case of familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic features

Osteoporosis international, 2009-07, Vol.20 (7), p.1273-1278

2009

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Longitudinal Analysis of Heritability for Dental Caries Traits

Journal of dental research, 2005-11, Vol.84 (11), p.1047-1051

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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Oral and dental phenotype of dyskeratosis congenita

Oral diseases, 2008-07, Vol.14 (5), p.419-427

2008

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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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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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Growth factor-induced osteogenesis in a novel radiolucent bone chamber

European cells & materials, 2015-01, Vol.29, p.35-41; discussion 41

2015

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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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Laminar flow substantially affects the morphology and functional phenotype of glomerular endothelial cells

A Putative Role for TRPC6 in Immune-Mediated Kidney Injury

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

Identification of parotid salivary biomarkers in Sjögren's syndrome by surface-enhanced laser desorption/ionization time-of-flight mass spectrometry and two-dimensional difference gel electrophoresis

MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta

Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta

Microbial Risk Indicators of Early Childhood Caries

Co-Culture of Glomerular Endothelial Cells and Podocytes in a Custom-Designed Glomerulus-on-a-Chip Model Improves the Filtration Barrier Integrity and Affects the Glomerular Cell Phenotype

Overlapping DSPP Mutations Cause Dentin Dysplasia and Dentinogenesis Imperfecta

Genetic studies of craniofacial anomalies: clinical implications and applications

MMP20 Active-site Mutation in Hypomaturation Amelogenesis Imperfecta

Phenotypic Variation in FAM83H-associated Amelogenesis Imperfecta

Cytokine profiles in the joint depend on pathology, but are different between synovial fluid, cartilage tissue and cultured chondrocytes

Phenotype of ENAM Mutations is Dosage-dependent

A fluorescent, paramagnetic and PEGylated gold/silica nanoparticle for MRI, CT and fluorescence imaging

Microradian X-ray diffraction in colloidal photonic crystals

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

case of familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic features

Longitudinal Analysis of Heritability for Dental Caries Traits

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

Oral and dental phenotype of dyskeratosis congenita

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

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

Growth factor-induced osteogenesis in a novel radiolucent bone chamber

Relationship of Phenotype and Genotype in X-Linked Amelogenesis Imperfecta

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