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Mechanistic Insights into Axenfeld–Rieger Syndrome from Zebrafish foxc1 and pitx2 Mutants

International journal of molecular sciences, 2021-09, Vol.22 (18), p.10001

French, Curtis R.

2021

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Pleiotropy in FOXC1-attributable phenotypes involves altered ciliation and cilia-dependent signaling

Scientific reports, 2024-08, Vol.14 (1), p.20278-16, Article 20278

2024

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foxc1 is required for embryonic head vascular smooth muscle differentiation in zebrafish

Developmental biology, 2019-09, Vol.453 (1), p.34-47

2019

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Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease

The Journal of clinical investigation, 2014-11, Vol.124 (11), p.4877-4881

2014

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Phytocannabinoids Reduce Seizures in Larval Zebrafish and Affect Endocannabinoid Gene Expression

Biomolecules (Basel, Switzerland), 2023-09, Vol.13 (9), p.1398

2023

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Gdf6a is required for the initiation of dorsal–ventral retinal patterning and lens development

Developmental biology, 2009-09, Vol.333 (1), p.37-47

2009

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Contribution of growth differentiation factor 6-dependent cell survival to early-onset retinal dystrophies

Human molecular genetics, 2013-04, Vol.22 (7), p.1432-1442

2013

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GDF6, a Novel Locus for a Spectrum of Ocular Developmental Anomalies

American journal of human genetics, 2007-02, Vol.80 (2), p.306-315

2007

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Meis1 specifies positional information in the retina and tectum to organize the zebrafish visual system

Neural development, 2010-09, Vol.5 (1), p.22-22, Article 22

2010

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Aberrant forebrain signaling during early development underlies the generation of holoprosencephaly and coloboma

Biochimica et biophysica acta, 2011-03, Vol.1812 (3), p.390-401

2011

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Loss of foxc1 in zebrafish reduces optic nerve size and cell number in the retinal ganglion cell layer

Vision research (Oxford), 2019-03, Vol.156, p.66-72

2019

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Protein fucosylation is required for Notch dependent vascular integrity in zebrafish

Developmental biology, 2021-12, Vol.480, p.62-68

2021

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Expression of three P4-phospholipid flippases—atp11a, atp11b, and atp11c in zebrafish (Danio rerio)

Gene Expression Patterns, 2020-06, Vol.36, p.119115-119115, Article 119115

2020

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Comparison of multifrequency bioelectrical impedance analysis with dual-energy X-ray absorptiometry for assessment of percentage body fat in a large, healthy population

The American journal of clinical nutrition, 2005, Vol.81 (1), p.74-78

2005

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Mutation of foxl1 Results in Reduced Cartilage Markers in a Zebrafish Model of Otosclerosis

Genes, 2022-06, Vol.13 (7), p.1107

2022

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Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies

Human molecular genetics, 2010-01, Vol.19 (2), p.287-298

2010

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Pbx homeodomain proteins pattern both the zebrafish retina and tectum

BMC developmental biology, 2007-07, Vol.7 (1), p.85-85, Article 85

2007

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Apoptotic and proliferative defects characterize ocular development in a microphthalmic BMP model

Investigative ophthalmology & visual science, 2013-07, Vol.54 (7), p.4636-4647

2013

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The Axenfeld-Rieger Syndrome Gene FOXC1 Contributes to Left-Right Patterning

Genes, 2021-01, Vol.12 (2), p.170

2021

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Molecular mechanisms regulating ocular apoptosis in zebrafish gdf6a mutants

Investigative ophthalmology & visual science, 2013-08, Vol.54 (8), p.5871-5879

2013

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Changes in the transcriptome of abdominal subcutaneous adipose tissue in response to short-term overfeeding in lean and obese men

The American journal of clinical nutrition, 2009-01, Vol.89 (1), p.407-415

2009

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A pathogenic deletion in Forkhead Box L1 gene

Human genetics, 2022-04, Vol.141 (3-4), p.965

2022

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Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes

Human molecular genetics, 2009-03, Vol.18 (6), p.1110-1121

2009

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Mechanistic Insights into Axenfeld–Rieger Syndrome from Zebrafish foxc1 and pitx2 Mutants

Pleiotropy in FOXC1-attributable phenotypes involves altered ciliation and cilia-dependent signaling

foxc1 is required for embryonic head vascular smooth muscle differentiation in zebrafish

Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease

Phytocannabinoids Reduce Seizures in Larval Zebrafish and Affect Endocannabinoid Gene Expression

Gdf6a is required for the initiation of dorsal–ventral retinal patterning and lens development

Contribution of growth differentiation factor 6-dependent cell survival to early-onset retinal dystrophies

GDF6, a Novel Locus for a Spectrum of Ocular Developmental Anomalies

Meis1 specifies positional information in the retina and tectum to organize the zebrafish visual system

Aberrant forebrain signaling during early development underlies the generation of holoprosencephaly and coloboma

Loss of foxc1 in zebrafish reduces optic nerve size and cell number in the retinal ganglion cell layer

Protein fucosylation is required for Notch dependent vascular integrity in zebrafish

Expression of three P4-phospholipid flippases—atp11a, atp11b, and atp11c in zebrafish (Danio rerio)

Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene

A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene

Comparison of multifrequency bioelectrical impedance analysis with dual-energy X-ray absorptiometry for assessment of percentage body fat in a large, healthy population

Mutation of foxl1 Results in Reduced Cartilage Markers in a Zebrafish Model of Otosclerosis

Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies

Pbx homeodomain proteins pattern both the zebrafish retina and tectum

Apoptotic and proliferative defects characterize ocular development in a microphthalmic BMP model

The Axenfeld-Rieger Syndrome Gene FOXC1 Contributes to Left-Right Patterning

Molecular mechanisms regulating ocular apoptosis in zebrafish gdf6a mutants

Changes in the transcriptome of abdominal subcutaneous adipose tissue in response to short-term overfeeding in lean and obese men

A pathogenic deletion in Forkhead Box L1 gene

Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes

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