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RNA Technology to Regenerate and Repair Alveolar Bone Defects

Journal of dental research, 2024-06, Vol.103 (6), p.622-630

2024

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Candidate Gene Analyses of Skeletal Variation in Malocclusion

Journal of dental research, 2015-07, Vol.94 (7), p.913-920

2015

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Epigenetic Regulation of Ameloblast Differentiation by HMGN Proteins

Journal of dental research, 2024-01, Vol.103 (1), p.51-61

2024

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Inhibition of the miR-17-92 Cluster Separates Stages of Palatogenesis

Journal of dental research, 2017-10, Vol.96 (11), p.1257-1264

2017

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Sox2 Controls Periderm and Rugae Development to Inhibit Oral Adhesions

Journal of dental research, 2020-11, Vol.99 (12), p.1397-1405

2020

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MicroRNAs Play a Critical Role in Tooth Development

Journal of dental research, 2010-08, Vol.89 (8), p.779-784

2010

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Differentiation of human dental stem cells reveals a role for microRNA-218

Journal of periodontal research, 2014-02, Vol.49 (1), p.110-120

2014

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A new plasmid-based microRNA inhibitor system that inhibits microRNA families in transgenic mice and cells: a potential new therapeutic reagent

Gene therapy, 2016-07, Vol.23 (7), p.634-634

2016

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TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome

Human molecular genetics, 2015-04, Vol.24 (8), p.2330-2348

2015

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CACNA1S mutation‐associated dental anomalies: A calcium channelopathy

Oral diseases, 2024-04, Vol.30 (3), p.1350-1359

2024

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A new plasmid-based microRNA inhibitor system that inhibits microRNA families in transgenic mice and cells: a potential new therapeutic reagent

Gene therapy, 2016-06, Vol.23 (6), p.527-542

2016

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Rieger syndrome: a clinical, molecular, and biochemical analysis

Cellular and molecular life sciences : CMLS, 2000-10, Vol.57 (11), p.1652-1666

2000

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Presence of negative and positive cis-acting RNA splicing elements within and flanking the first tat coding exon of human immunodeficiency virus type 1

Molecular and Cellular Biology, 1994-06, Vol.14 (6), p.3960-3970

1994

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Bone marrow cells produce a novel TSHβ splice variant that is upregulated in the thyroid following systemic virus infection

Genes and immunity, 2009-01, Vol.10 (1), p.18-26

2009

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Presence of exon splicing silencers within human immunodeficiency virus type 1 tat exon 2 and tat-rev exon 3: evidence for inhibition mediated by cellular factors

Molecular and Cellular Biology, 1995-08, Vol.15 (8), p.4606-4615

1995

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Splicing efficiency of human immunodeficiency virus type 1 tat RNA is determined by both a suboptimal 3' splice site and a 10 nucleotide exon splicing silencer element located within tat exon 2

Nucleic acids research, 1997-02, Vol.25 (4), p.861-867

1997

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Antagonistic Regulation of Dlx2 Expression by PITX2 and Msx2: Implications for Tooth Development

Gene expression, 2001-01, Vol.9 (6), p.265-281

2001

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Multifunctional Role of the Pitx2 Homeodomain Protein C-Terminal Tail

Molecular and Cellular Biology, 1999-10, Vol.19 (10), p.7001-7010

1999

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PITX2 Regulates Procollagen Lysyl Hydroxylase (PLOD) Gene Expression: Implications for the Pathology of Rieger Syndrome

The Journal of cell biology, 2001-02, Vol.152 (3), p.545-552

2001

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The molecular basis of Rieger syndrome. Analysis of Pitx2 homeodomain protein activities

The Journal of biological chemistry, 1998-08, Vol.273 (32), p.20066-20072

1998

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Identification of a Dominant Negative Homeodomain Mutation in Rieger Syndrome

The Journal of biological chemistry, 2001-06, Vol.276 (25), p.23034-23041

2001

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Short-chain acyl-coenzyme A dehydrogenase deficiency: clinical and biochemical studies in two patients

The Journal of clinical investigation, 1987-05, Vol.79 (5), p.1303-1308

1987

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Chromatin-associated HMG-17 is a major regulator of homeodomain transcription factor activity modulated by Wnt/ -catenin signaling

Nucleic acids research, 2007-11, Vol.36 (2), p.462-476

2007

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The hinge deletion allelic variant of porcine IgA results from a mutation at the splice acceptor site in the first C alpha intron

The Journal of immunology (1950), 1995-04, Vol.154 (8), p.3836-3842

1995

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The multiple acyl-coenzyme A dehydrogenation disorders, glutaric aciduria type II and ethylmalonic-adipic aciduria: mitochondrial fatty acid oxidation, acyl-coenzyme A dehydrogenase, and electron transfer flavoprotein activities in fibroblasts

The Journal of clinical investigation, 1986-07, Vol.78 (1), p.205-213

1986

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RNA Technology to Regenerate and Repair Alveolar Bone Defects

Candidate Gene Analyses of Skeletal Variation in Malocclusion

Epigenetic Regulation of Ameloblast Differentiation by HMGN Proteins

Inhibition of the miR-17-92 Cluster Separates Stages of Palatogenesis

Sox2 Controls Periderm and Rugae Development to Inhibit Oral Adhesions

MicroRNAs Play a Critical Role in Tooth Development

Differentiation of human dental stem cells reveals a role for microRNA-218

A new plasmid-based microRNA inhibitor system that inhibits microRNA families in transgenic mice and cells: a potential new therapeutic reagent

TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome

CACNA1S mutation‐associated dental anomalies: A calcium channelopathy

A new plasmid-based microRNA inhibitor system that inhibits microRNA families in transgenic mice and cells: a potential new therapeutic reagent

Rieger syndrome: a clinical, molecular, and biochemical analysis

Presence of negative and positive cis-acting RNA splicing elements within and flanking the first tat coding exon of human immunodeficiency virus type 1

Bone marrow cells produce a novel TSHβ splice variant that is upregulated in the thyroid following systemic virus infection

Presence of exon splicing silencers within human immunodeficiency virus type 1 tat exon 2 and tat-rev exon 3: evidence for inhibition mediated by cellular factors

Splicing efficiency of human immunodeficiency virus type 1 tat RNA is determined by both a suboptimal 3' splice site and a 10 nucleotide exon splicing silencer element located within tat exon 2

Antagonistic Regulation of Dlx2 Expression by PITX2 and Msx2: Implications for Tooth Development

Multifunctional Role of the Pitx2 Homeodomain Protein C-Terminal Tail

PITX2 Regulates Procollagen Lysyl Hydroxylase (PLOD) Gene Expression: Implications for the Pathology of Rieger Syndrome

The molecular basis of Rieger syndrome. Analysis of Pitx2 homeodomain protein activities

Identification of a Dominant Negative Homeodomain Mutation in Rieger Syndrome

Short-chain acyl-coenzyme A dehydrogenase deficiency: clinical and biochemical studies in two patients

Chromatin-associated HMG-17 is a major regulator of homeodomain transcription factor activity modulated by Wnt/ -catenin signaling

The hinge deletion allelic variant of porcine IgA results from a mutation at the splice acceptor site in the first C alpha intron

The multiple acyl-coenzyme A dehydrogenation disorders, glutaric aciduria type II and ethylmalonic-adipic aciduria: mitochondrial fatty acid oxidation, acyl-coenzyme A dehydrogenase, and electron transfer flavoprotein activities in fibroblasts

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