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Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines

Molecular genetics and metabolism, 2016-03, Vol.117 (3), p.313-321

2016

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Genome-wide analysis of miRNA and mRNA transcriptomes during amelogenesis

BMC genomics, 2014-11, Vol.15 (1), p.998-998

2014

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Clinical diagnosis of metabolic disorders using untargeted metabolomic profiling and disease-specific networks learned from profiling data

Scientific reports, 2022-04, Vol.12 (1), p.6556-6556, Article 6556

2022

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Modulation of noncanonical TGF-β signaling prevents cleft palate in Tgfbr2 mutant mice

The Journal of clinical investigation, 2012-03, Vol.122 (3), p.873-885

2012

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The Circadian Clock Modulates Enamel Development

Journal of biological rhythms, 2012-06, Vol.27 (3), p.237-245

2012

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Zellweger spectrum disorder patient–derived fibroblasts with the PEX1‐Gly843Asp allele recover peroxisome functions in response to flavonoids

Journal of cellular biochemistry, 2019-03, Vol.120 (3), p.3243-3258

2019

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A TGFβ-Smad4-Fgf6 signaling cascade controls myogenic differentiation and myoblast fusion during tongue development

Development (Cambridge), 2012-05, Vol.139 (9), p.1640-1650

2012

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Identification of novel candidate genes involved in mineralization of dental enamel by genome-wide transcript profiling

Journal of cellular physiology, 2012-05, Vol.227 (5), p.2264-2275

2012

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MiR-153 Regulates Amelogenesis by Targeting Endocytotic and Endosomal/lysosomal Pathways–Novel Insight into the Origins of Enamel Pathologies

Scientific reports, 2017-03, Vol.7 (1), p.44118-44118, Article 44118

2017

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AAV-mediated PEX1 gene augmentation improves visual function in the PEX1-Gly844Asp mouse model for mild Zellweger spectrum disorder

Molecular therapy. Methods & clinical development, 2021-12, Vol.23, p.225-240

2021

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Fibroblast Growth Factor 9 (FGF9)-Pituitary Homeobox 2 (PITX2) Pathway Mediates Transforming Growth Factor β (TGFβ) Signaling to Regulate Cell Proliferation in Palatal Mesenchyme during Mouse Palatogenesis

The Journal of biological chemistry, 2012-01, Vol.287 (4), p.2353-2363

2012

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mtDNA depletion confers specific gene expression profiles in human cells grown in culture and in xenograft

BMC genomics, 2008-11, Vol.9 (1), p.521-521, Article 521

2008

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Synthesis and anticancer properties of water-soluble zinc ionophores

Cancer research (Chicago, Ill.), 2008-07, Vol.68 (13), p.5318-5325

2008

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Identification of candidate downstream targets of TGFβ signaling during palate development by genome-wide transcript profiling

Journal of cellular biochemistry, 2013-04, Vol.114 (4), p.796-807

2013

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The Pex1-G844D mouse: A model for mild human Zellweger spectrum disorder

Molecular genetics and metabolism, 2014-04, Vol.111 (4), p.522-532

2014

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A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population

BMC medical genetics, 2012-08, Vol.13 (1), p.72-72, Article 72

2012

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X-linked adrenoleukodystrophy in a chimpanzee due to an ABCD1 mutation reported in multiple unrelated humans

Molecular genetics and metabolism, 2017-11, Vol.122 (3), p.130-133

2017

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Resequencing and mutational analysis using oligonucleotide microarrays

Nature genetics, 1999-01, Vol.21 (1 Suppl), p.42-47

Hacia, J G

1999

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Accelerated evolution of the ASPM gene controlling brain size begins prior to human brain expansion

PLoS biology, 2004-05, Vol.2 (5), p.E126-0653

2004

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Mutation and Genomic Deletion Status of ataxia telangiectasia mutated (ATM) and p53 Confer Specific Gene Expression Profiles in Mantle Cell Lymphoma

Proceedings of the National Academy of Sciences - PNAS, 2006-02, Vol.103 (7), p.2352-2357

2006

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Nonsense suppressor therapies rescue peroxisome lipid metabolism and assembly in cells from patients with specific PEX gene mutations

Journal of cellular biochemistry, 2011-05, Vol.112 (5), p.1250-1258

2011

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Novel Gene Expression Signature Predictive of Clinical Recurrence After Radical Prostatectomy in Early Stage Prostate Cancer Patients

The Prostate, 2016-10, Vol.76 (14), p.1239-1256

2016

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Gene-expression analysis of early- and late-maturation-stage rat enamel organ

European journal of oral sciences, 2011-12, Vol.119 (s1), p.149-157

2011

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Human and great ape red blood cells differ in plasmalogen levels and composition

Lipids in health and disease, 2011-06, Vol.10 (1), p.101-101, Article 101

2011

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Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines

Genome-wide analysis of miRNA and mRNA transcriptomes during amelogenesis

Clinical diagnosis of metabolic disorders using untargeted metabolomic profiling and disease-specific networks learned from profiling data

Modulation of noncanonical TGF-β signaling prevents cleft palate in Tgfbr2 mutant mice

The Circadian Clock Modulates Enamel Development

FaceBase 3: analytical tools and FAIR resources for craniofacial and dental research

Zellweger spectrum disorder patient–derived fibroblasts with the PEX1‐Gly843Asp allele recover peroxisome functions in response to flavonoids

A TGFβ-Smad4-Fgf6 signaling cascade controls myogenic differentiation and myoblast fusion during tongue development

Identification of novel candidate genes involved in mineralization of dental enamel by genome-wide transcript profiling

MiR-153 Regulates Amelogenesis by Targeting Endocytotic and Endosomal/lysosomal Pathways–Novel Insight into the Origins of Enamel Pathologies

AAV-mediated PEX1 gene augmentation improves visual function in the PEX1-Gly844Asp mouse model for mild Zellweger spectrum disorder

Fibroblast Growth Factor 9 (FGF9)-Pituitary Homeobox 2 (PITX2) Pathway Mediates Transforming Growth Factor β (TGFβ) Signaling to Regulate Cell Proliferation in Palatal Mesenchyme during Mouse Palatogenesis

mtDNA depletion confers specific gene expression profiles in human cells grown in culture and in xenograft

Synthesis and anticancer properties of water-soluble zinc ionophores

Identification of candidate downstream targets of TGFβ signaling during palate development by genome-wide transcript profiling

The Pex1-G844D mouse: A model for mild human Zellweger spectrum disorder

A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population

X-linked adrenoleukodystrophy in a chimpanzee due to an ABCD1 mutation reported in multiple unrelated humans

Resequencing and mutational analysis using oligonucleotide microarrays

Accelerated evolution of the ASPM gene controlling brain size begins prior to human brain expansion

Mutation and Genomic Deletion Status of ataxia telangiectasia mutated (ATM) and p53 Confer Specific Gene Expression Profiles in Mantle Cell Lymphoma

Nonsense suppressor therapies rescue peroxisome lipid metabolism and assembly in cells from patients with specific PEX gene mutations

Novel Gene Expression Signature Predictive of Clinical Recurrence After Radical Prostatectomy in Early Stage Prostate Cancer Patients

Gene-expression analysis of early- and late-maturation-stage rat enamel organ

Human and great ape red blood cells differ in plasmalogen levels and composition

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