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IRF6 mutation screening in non-syndromic orofacial clefting: analysis of 1521 families

Clinical genetics, 2016-07, Vol.90 (1), p.28-34

2016

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Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation

Journal of medical genetics, 2008-02, Vol.45 (2), p.81-86

2008

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The Many Faces and Factors of Orofacial Clefts

Human molecular genetics, 1999-01, Vol.8 (10), p.1853-1859

1999

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Face Forward: Gene Variants, Pathways, and Therapies for Craniofacial Anomalies

Journal of dental research, 2017-10, Vol.96 (11), p.1181-1183

2017

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Full Spectrum of Postnatal Tooth Phenotypes in a Novel Irf6 Cleft Lip Model

Journal of dental research, 2016-10, Vol.95 (11), p.1265-1273

2016

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IRF6 and SPRY4 Signaling Interact in Periderm Development

Journal of dental research, 2017-10, Vol.96 (11), p.1306-1313

2017

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Variable Airway Responsiveness to Inhaled Lipopolysaccharide

American journal of respiratory and critical care medicine, 1999-07, Vol.160 (1), p.297-303

1999

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Improved cytotoxic T-lymphocyte immune responses to a tumor antigen by vaccines co-expressing the SLAM-associated adaptor EAT-2

Cancer gene therapy, 2013-10, Vol.20 (10), p.564-575

2013

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TLR4 mutations are associated with endotoxin hyporesponsiveness in humans

Nature genetics, 2000-06, Vol.25 (2), p.187-191

2000

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Discovery of Five Conserved β-Defensin Gene Clusters Using a Computational Search Strategy

Proceedings of the National Academy of Sciences - PNAS, 2002-02, Vol.99 (4), p.2129-2133

2002

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A novel epithelial-expressed ETS gene, ELF3: human and murine cDNA sequences, murine genomic organization, human mapping to 1q32.2 and expression in tissues and cancer

Oncogene, 1997-11, Vol.15 (20), p.2449-2462

1997

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Refinement of the Van der Woude Gene Location and Construction of a 3.5-Mb YAC Contig and STS Map Spanning the Critical Region in 1q32–q41

Genomics (San Diego, Calif.), 1996-09, Vol.36 (3), p.507-514

1996

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Discovery of new human beta-defensins using a genomics-based approach

Gene, 2001-01, Vol.263 (1-2), p.211-218

2001

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Mutations in IRF6 do not cause Bartsocas-Papas syndrome in a family with two affected sibs

American journal of medical genetics, 2004-08, Vol.128A (4), p.431-433

2004

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Linkage of Infantile Bartter Syndrome with Sensorineural Deafness to Chromosome 1p

American journal of human genetics, 1998-02, Vol.62 (2), p.355-361

1998

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Osteocalcin: Genetic and Physical Mapping of the Human Gene BGLAP and Its Potential Role in Postmenopausal Osteoporosis

Genomics (San Diego, Calif.), 1999-09, Vol.60 (2), p.210-217

1999

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Structure and mapping of the human β-defensin HBD-2 gene and its expression at sites of inflammation

Gene, 1998-11, Vol.222 (2), p.237-244

1998

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Altered GABAergic function accompanies hippocampal degeneration in mice lacking ClC-3 voltage-gated chloride channels

Brain research, 2002-12, Vol.958 (2), p.227-250

2002

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Ontogeny of CLCN3 Chloride Channel Gene Expression in Human Pulmonary Epithelium

American journal of respiratory cell and molecular biology, 2001-04, Vol.24 (4), p.376-381

2001

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Optimized conditions for cloning PCR products into an XcmI T-vector

BioTechniques, 1997, Vol.22 (1), p.40-44

1997

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Dominant Mutations in GRHL3 Cause Van der Woude Syndrome and Disrupt Oral Periderm Development

American journal of human genetics, 2014-01, Vol.94 (1), p.23-32

2014

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recA protein-promoted ATP hydrolysis occurs throughout recA nucleoprotein filaments

The Journal of biological chemistry, 1987-03, Vol.262 (9), p.4011-4016

1987

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Comparative analysis of IRF6 variants in families with Van der Woude syndrome and popliteal pterygium syndrome using public whole-exome databases

Genetics in medicine, 2013-05, Vol.15 (5), p.338-344

2013

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Differential gene expression and regulation of renal angiotensin II receptor subtypes (AT1 and AT2) during fetal life in sheep

Pediatric research, 1995-12, Vol.38 (6), p.896-904

1995

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An etiologic regulatory mutation in IRF6 with loss- and gain-of-function effects

Human molecular genetics, 2014-05, Vol.23 (10), p.2711-2720

2014

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IRF6 mutation screening in non-syndromic orofacial clefting: analysis of 1521 families

Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation

The Many Faces and Factors of Orofacial Clefts

Face Forward: Gene Variants, Pathways, and Therapies for Craniofacial Anomalies

Full Spectrum of Postnatal Tooth Phenotypes in a Novel Irf6 Cleft Lip Model

IRF6 and SPRY4 Signaling Interact in Periderm Development

Variable Airway Responsiveness to Inhaled Lipopolysaccharide

Improved cytotoxic T-lymphocyte immune responses to a tumor antigen by vaccines co-expressing the SLAM-associated adaptor EAT-2

TLR4 mutations are associated with endotoxin hyporesponsiveness in humans

Discovery of Five Conserved β-Defensin Gene Clusters Using a Computational Search Strategy

A novel epithelial-expressed ETS gene, ELF3: human and murine cDNA sequences, murine genomic organization, human mapping to 1q32.2 and expression in tissues and cancer

Refinement of the Van der Woude Gene Location and Construction of a 3.5-Mb YAC Contig and STS Map Spanning the Critical Region in 1q32–q41

Discovery of new human beta-defensins using a genomics-based approach

Mutations in IRF6 do not cause Bartsocas-Papas syndrome in a family with two affected sibs

Linkage of Infantile Bartter Syndrome with Sensorineural Deafness to Chromosome 1p

Osteocalcin: Genetic and Physical Mapping of the Human Gene BGLAP and Its Potential Role in Postmenopausal Osteoporosis

Structure and mapping of the human β-defensin HBD-2 gene and its expression at sites of inflammation

Altered GABAergic function accompanies hippocampal degeneration in mice lacking ClC-3 voltage-gated chloride channels

Ontogeny of CLCN3 Chloride Channel Gene Expression in Human Pulmonary Epithelium

Optimized conditions for cloning PCR products into an XcmI T-vector

Dominant Mutations in GRHL3 Cause Van der Woude Syndrome and Disrupt Oral Periderm Development

recA protein-promoted ATP hydrolysis occurs throughout recA nucleoprotein filaments

Comparative analysis of IRF6 variants in families with Van der Woude syndrome and popliteal pterygium syndrome using public whole-exome databases

Differential gene expression and regulation of renal angiotensin II receptor subtypes (AT1 and AT2) during fetal life in sheep

An etiologic regulatory mutation in IRF6 with loss- and gain-of-function effects

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