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Notch Signaling in Skeletal Development, Homeostasis and Pathogenesis

Biomolecules (Basel, Switzerland), 2020-02, Vol.10 (2), p.332

2020

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TGFβ and BMP Dependent Cell Fate Changes Due to Loss of Filamin B Produces Disc Degeneration and Progressive Vertebral Fusions

PLoS genetics, 2016-03, Vol.12 (3), p.e1005936-e1005936

2016

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Systematic evaluation of factors influencing ChIP-seq fidelity

Nature methods, 2012-06, Vol.9 (6), p.609

2012

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The inositol phosphatase SHIP2 enables sustained ERK activation downstream of FGF receptors by recruiting Src kinases

Science signaling, 2018-09, Vol.11 (548)

2018

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Intervertebral disc degeneration is rescued by TGFβ/BMP signaling modulation in an ex vivo filamin B mouse model

Bone research, 2022-04, Vol.10 (1), p.37-37

2022

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Altered Sox9 and FGF signaling gene expression in Aga2 OI mice negatively affects linear growth

JCI insight, 2023-11, Vol.8 (21)

2023

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Skeletal diseases caused by mutations in PTH1R show aberrant differentiation of skeletal progenitors due to dysregulation of DEPTOR

Frontiers in cell and developmental biology, 2023-01, Vol.10, p.963389-963389

2023

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Biallelic mutations in LAMA5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasia

EBioMedicine, 2020-12, Vol.62, p.103075-103075, Article 103075

2020

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Loss of the long form of Plod2 phenocopies contractures of Bruck syndrome - osteogenesis imperfecta

Journal of bone and mineral research, 2024-08

2024

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Fracture Healing in Collagen‐Related Preclinical Models of Osteogenesis Imperfecta

Journal of bone and mineral research, 2020-06, Vol.35 (6), p.1132-1148

2020

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4‐PBA Treatment Improves Bone Phenotypes in the Aga2 Mouse Model of Osteogenesis Imperfecta

Journal of bone and mineral research, 2022-04, Vol.37 (4), p.675-686

2022

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Fibroblast growth factor receptor influences primary cilium length through an interaction with intestinal cell kinase

Proceedings of the National Academy of Sciences - PNAS, 2019-03, Vol.116 (10), p.4316-4325

2019

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Interpopulation hybridization results in widespread viability selection across the genome in Tigriopus californicus

BMC genetics, 2011-06, Vol.12, p.54

2011

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A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosis

Scientific reports, 2017-02, Vol.7 (1), p.41803-41803, Article 41803

2017

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Intervertebral disc degeneration is rescued by TGFβ/BMP signaling modulation in an ex vivo filamin B mouse model

骨研究（英文版）, 2022, Vol.10 (3), p.524-535

2022

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ER stress reduction by 4-PBA treatment improves bone phenotypes in the Aga2 mouse model of osteogenesis imperfecta

Bone Reports, 2022-05, Vol.16, p.101495, Article 101495

2022

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Diverse patterns of genomic targeting by transcriptional regulators in Drosophila melanogaster

Genome research, 2014-07, Vol.24 (7), p.1224

2014

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Discovering the Pathophysiology and Molecular Origins of Spondylocarpotarsal Synostosis Syndrome Using a Murine Model

Zieba, Jennifer

2016

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TGF[beta] and BMP Dependent Cell Fate Changes Due to Loss of Filamin B Produces Disc Degeneration and Progressive Vertebral Fusions

PLoS genetics, 2016-03, Vol.12 (3)

2016

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TGF square and BMP Dependent Cell Fate Changes Due to Loss of Filamin B Produces Disc Degeneration and Progressive Vertebral Fusions

PLoS genetics, 2016-03, Vol.12 (3)

2016

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A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGF[beta] signaling and cause autosomal dominant spondylocarpotarsal synostosis

Scientific reports, 2017-02, Vol.7, p.41803

2017

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A global-scale screening of non-native aquatic organisms to identify potentially invasive species under current and future climate conditions

The Science of the total environment, 2021-09, Vol.788, p.147868-147868, Article 147868

2021

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Notch Signaling in Skeletal Development, Homeostasis and Pathogenesis

TGFβ and BMP Dependent Cell Fate Changes Due to Loss of Filamin B Produces Disc Degeneration and Progressive Vertebral Fusions

Systematic evaluation of factors influencing ChIP-seq fidelity

The inositol phosphatase SHIP2 enables sustained ERK activation downstream of FGF receptors by recruiting Src kinases

Intervertebral disc degeneration is rescued by TGFβ/BMP signaling modulation in an ex vivo filamin B mouse model

Altered Sox9 and FGF signaling gene expression in Aga2 OI mice negatively affects linear growth

Skeletal diseases caused by mutations in PTH1R show aberrant differentiation of skeletal progenitors due to dysregulation of DEPTOR

Biallelic mutations in LAMA5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasia

Loss of the long form of Plod2 phenocopies contractures of Bruck syndrome - osteogenesis imperfecta

Fracture Healing in Collagen‐Related Preclinical Models of Osteogenesis Imperfecta

4‐PBA Treatment Improves Bone Phenotypes in the Aga2 Mouse Model of Osteogenesis Imperfecta

A cis-regulatory map of the Drosophila genome

Fibroblast growth factor receptor influences primary cilium length through an interaction with intestinal cell kinase

Interpopulation hybridization results in widespread viability selection across the genome in Tigriopus californicus

A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosis

Intervertebral disc degeneration is rescued by TGFβ/BMP signaling modulation in an ex vivo filamin B mouse model

ER stress reduction by 4-PBA treatment improves bone phenotypes in the Aga2 mouse model of osteogenesis imperfecta

Diverse patterns of genomic targeting by transcriptional regulators in Drosophila melanogaster

Discovering the Pathophysiology and Molecular Origins of Spondylocarpotarsal Synostosis Syndrome Using a Murine Model

TGF[beta] and BMP Dependent Cell Fate Changes Due to Loss of Filamin B Produces Disc Degeneration and Progressive Vertebral Fusions

TGF square and BMP Dependent Cell Fate Changes Due to Loss of Filamin B Produces Disc Degeneration and Progressive Vertebral Fusions

A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGF[beta] signaling and cause autosomal dominant spondylocarpotarsal synostosis

A global-scale screening of non-native aquatic organisms to identify potentially invasive species under current and future climate conditions

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