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Single-Cell Mass Spectrometry for Discovery Proteomics: Quantifying Translational Cell Heterogeneity in the 16-Cell Frog (Xenopus) Embryo

Angewandte Chemie (International ed.), 2016-02, Vol.55 (7), p.2454-2458

International ed. in English, 2016

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Single-cell mass spectrometry reveals small molecules that affect cell fates in the 16-cell embryo

Proceedings of the National Academy of Sciences - PNAS, 2015-05, Vol.112 (21), p.6545-6550

2015

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Microsampling Capillary Electrophoresis Mass Spectrometry Enables Single-Cell Proteomics in Complex Tissues: Developing Cell Clones in Live Xenopus laevis and Zebrafish Embryos

Analytical chemistry (Washington), 2019-04, Vol.91 (7), p.4797-4805

2019

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In Situ Microprobe Single-Cell Capillary Electrophoresis Mass Spectrometry: Metabolic Reorganization in Single Differentiating Cells in the Live Vertebrate (Xenopus laevis) Embryo

Analytical chemistry (Washington), 2017-07, Vol.89 (13), p.7069-7076

2017

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Xenopus: From Basic Biology to Disease Models in the Genomic Era

1, 2022

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Normal Table of Xenopus development: a new graphical resource

Development (Cambridge), 2022-07, Vol.149 (14)

2022

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Using Xenopus to understand human disease and developmental disorders

Genesis (New York, N.Y. : 2000), 2017-01, Vol.55 (1-2), p.np-n/a

2017

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Microinjection of mRNAs and Oligonucleotides

Cold Spring Harbor protocols, 2018-12, Vol.2018 (12), p.pdb.prot097261

Moody, Sally A.

2018

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Six1 and Irx1 have reciprocal interactions during cranial placode and otic vesicle formation

Developmental biology, 2019-02, Vol.446 (1), p.68-79

2019

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Contribute to special issues in developmental biology

Developmental biology, 2024-11, Vol.515, p.59-59

Moody, Sally A.

2024

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Yes-associated protein 65 (YAP) expands neural progenitors and regulates Pax3 expression in the neural plate border zone

PloS one, 2011-06, Vol.6 (6), p.e20309-e20309

2011

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Meet the new Special Content Editor

Developmental biology, 2024-02, Vol.506, p.95-95

Moody, Sally A

2024

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Six1 proteins with human branchio-oto-renal mutations differentially affect cranial gene expression and otic development

Disease models & mechanisms, 2020-03, Vol.13 (3)

2020

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Proteomic Characterization of the Neural Ectoderm Fated Cell Clones in the Xenopus laevis Embryo by High-Resolution Mass Spectrometry

ACS chemical neuroscience, 2018-08, Vol.9 (8), p.2064-2073

2018

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Subcellular metabolite and lipid analysis of Xenopus laevis eggs by LAESI mass spectrometry

PloS one, 2014-12, Vol.9 (12), p.e115173-e115173

2014

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Time-resolved quantitative proteomic analysis of the developing Xenopus otic vesicle reveals putative congenital hearing loss candidates

iScience, 2023-09, Vol.26 (9), p.107665-107665, Article 107665

2023

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Metabolic comparison of dorsal versus ventral cells directly in the live 8-cell frog embryo by microprobe single-cell CE-ESI-MS

Analytical methods, 2017-09, Vol.9 (34), p.4964-497

2017

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Selective disruption of trigeminal sensory neurogenesis and differentiation in a mouse model of 22q11.2 deletion syndrome

Disease models & mechanisms, 2022-02, Vol.15 (2)

2022

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Early neural ectodermal genes are activated by siamois and twin during blastula stages

Genesis (New York, N.Y. : 2000), 2015-05, Vol.53 (5), p.308-320

2015

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Advances in Understanding the Pathogenesis of Craniofacial Birth Defects

Journal of developmental biology, 2022-07, Vol.10 (3), p.27

2022

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Mutations in SIX1 Associated with Branchio-oto-Renal Syndrome (BOR) Differentially Affect Otic Expression of Putative Target Genes

Journal of developmental biology, 2021-06, Vol.9 (3), p.25

2021

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Six1 promotes a placodal fate within the lateral neurogenic ectoderm by functioning as both a transcriptional activator and repressor

Development (Cambridge), 2004-12, Vol.131 (23), p.5871-5881

2004

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Foxd4 is essential for establishing neural cell fate and for neuronal differentiation

Genesis (New York, N.Y. : 2000), 2017-06, Vol.55 (6), p.n/a

2017

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Zmym4 is required for early cranial gene expression and craniofacial cartilage formation

Frontiers in cell and developmental biology, 2023-10, Vol.11, p.1274788-1274788

2023

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Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome

Disease models & mechanisms, 2014-02, Vol.7 (2), p.245-257

2014

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Single-Cell Mass Spectrometry for Discovery Proteomics: Quantifying Translational Cell Heterogeneity in the 16-Cell Frog (Xenopus) Embryo

Single-cell mass spectrometry reveals small molecules that affect cell fates in the 16-cell embryo

Microsampling Capillary Electrophoresis Mass Spectrometry Enables Single-Cell Proteomics in Complex Tissues: Developing Cell Clones in Live Xenopus laevis and Zebrafish Embryos

In Situ Microprobe Single-Cell Capillary Electrophoresis Mass Spectrometry: Metabolic Reorganization in Single Differentiating Cells in the Live Vertebrate (Xenopus laevis) Embryo

Xenopus: From Basic Biology to Disease Models in the Genomic Era

Normal Table of Xenopus development: a new graphical resource

Using Xenopus to understand human disease and developmental disorders

Microinjection of mRNAs and Oligonucleotides

Six1 and Irx1 have reciprocal interactions during cranial placode and otic vesicle formation

Contribute to special issues in developmental biology

Yes-associated protein 65 (YAP) expands neural progenitors and regulates Pax3 expression in the neural plate border zone

Meet the new Special Content Editor

Six1 proteins with human branchio-oto-renal mutations differentially affect cranial gene expression and otic development

Proteomic Characterization of the Neural Ectoderm Fated Cell Clones in the Xenopus laevis Embryo by High-Resolution Mass Spectrometry

Subcellular metabolite and lipid analysis of Xenopus laevis eggs by LAESI mass spectrometry

Time-resolved quantitative proteomic analysis of the developing Xenopus otic vesicle reveals putative congenital hearing loss candidates

Metabolic comparison of dorsal versus ventral cells directly in the live 8-cell frog embryo by microprobe single-cell CE-ESI-MS

Selective disruption of trigeminal sensory neurogenesis and differentiation in a mouse model of 22q11.2 deletion syndrome

Early neural ectodermal genes are activated by siamois and twin during blastula stages

Advances in Understanding the Pathogenesis of Craniofacial Birth Defects

Mutations in SIX1 Associated with Branchio-oto-Renal Syndrome (BOR) Differentially Affect Otic Expression of Putative Target Genes

Six1 promotes a placodal fate within the lateral neurogenic ectoderm by functioning as both a transcriptional activator and repressor

Foxd4 is essential for establishing neural cell fate and for neuronal differentiation

Zmym4 is required for early cranial gene expression and craniofacial cartilage formation

Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome

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