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CRISPRscan: designing highly efficient sgRNAs for CRISPR-Cas9 targeting in vivo

Nature methods, 2015-10, Vol.12 (10), p.982-988

2015

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Mink1 regulates spemann organizer cell fate in the xenopus gastrula via Hmga2

Developmental biology, 2023-03, Vol.495, p.42-53

2023

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Congenital Heart Disease Genetics Uncovers Context-Dependent Organization and Function of Nucleoporins at Cilia

Developmental cell, 2016-09, Vol.38 (5), p.478-492

2016

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CRISPR-Cpf1 mediates efficient homology-directed repair and temperature-controlled genome editing

Nature communications, 2017-12, Vol.8 (1), p.2024-9, Article 2024

2017

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Expanding EMC foldopathies: Topogenesis deficits alter the neural crest

Genesis (New York, N.Y. : 2000), 2023-09, Vol.61 (5), p.e23520-e23520

2023

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Genes and mechanisms of heterotaxy: patients drive the search

Current opinion in genetics & development, 2019-06, Vol.56, p.34-40

2019

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Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation

Nature genetics, 2014-10, Vol.46 (10), p.1135-1139

2014

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Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development

Cell reports (Cambridge), 2016-01, Vol.14 (3), p.632-647

2016

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CRISPR/Cas9: An inexpensive, efficient loss of function tool to screen human disease genes in Xenopus

Developmental biology, 2015-12, Vol.408 (2), p.196-204

2015

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Xenopus as a platform for discovery of genes relevant to human disease

Current topics in developmental biology, 2021, Vol.145, p.277-312

2021

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Nucleoporin NUP205 plays a critical role in cilia and congenital disease

Developmental biology, 2021-01, Vol.469, p.46-53

2021

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The dishevelled associated activator of morphogenesis protein 2 (Daam2) regulates neural tube closure

Developmental dynamics, 2024-06

2024

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The ribosome biogenesis factor Nol11 is required for optimal rDNA transcription and craniofacial development in Xenopus

PLoS genetics, 2015-03, Vol.11 (3), p.e1005018-e1005018

2015

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Codon identity regulates mRNA stability and translation efficiency during the maternal-to-zygotic transition

The EMBO journal, 2016-10, Vol.35 (19), p.2087-2103

2016

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The heterotaxy gene GALNT11 glycosylates Notch to orchestrate cilia type and laterality

Nature (London), 2013-12, Vol.504 (7480), p.456-459

2013

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Paired Box 9 (PAX9), the RNA polymerase II transcription factor, regulates human ribosome biogenesis and craniofacial development

PLoS genetics, 2020-08, Vol.16 (8), p.e1008967-e1008967

2020

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WDR5 Stabilizes Actin Architecture to Promote Multiciliated Cell Formation

Developmental cell, 2018-09, Vol.46 (5), p.595-610.e3

2018

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WDR5 regulates left-right patterning via chromatin-dependent and -independent functions

Development (Cambridge), 2018-12, Vol.145 (23)

2018

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Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning

Proceedings of the National Academy of Sciences - PNAS, 2011-02, Vol.108 (7), p.2915-2920

2011

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Challenges and opportunities at the interface of birth defects, human genetics and developmental biology

Development (Cambridge), 2020-11, Vol.147 (21)

2020

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Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR

Nature communications, 2022-11, Vol.13 (1), p.6681-17, Article 6681

2022

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Xenopus as a model organism for birth defects—Congenital heart disease and heterotaxy

Seminars in cell & developmental biology, 2016-03, Vol.51, p.73-79

2016

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RAPGEF5 Regulates Nuclear Translocation of β-Catenin

Developmental cell, 2018-01, Vol.44 (2), p.248-260.e4

2018

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A chromosome-scale genome assembly and dense genetic map for Xenopus tropicalis

Developmental biology, 2019-08, Vol.452 (1), p.8-20

2019

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Obtaining Xenopus tropicalis Embryos by In Vitro Fertilization

Cold Spring Harbor protocols, 2022-04, Vol.2022 (4), p.Pdb.prot106351

2022

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CRISPRscan: designing highly efficient sgRNAs for CRISPR-Cas9 targeting in vivo

Mink1 regulates spemann organizer cell fate in the xenopus gastrula via Hmga2

Congenital Heart Disease Genetics Uncovers Context-Dependent Organization and Function of Nucleoporins at Cilia

CRISPR-Cpf1 mediates efficient homology-directed repair and temperature-controlled genome editing

Expanding EMC foldopathies: Topogenesis deficits alter the neural crest

Genes and mechanisms of heterotaxy: patients drive the search

Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation

Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development

CRISPR/Cas9: An inexpensive, efficient loss of function tool to screen human disease genes in Xenopus

Xenopus as a platform for discovery of genes relevant to human disease

Nucleoporin NUP205 plays a critical role in cilia and congenital disease

The dishevelled associated activator of morphogenesis protein 2 (Daam2) regulates neural tube closure

The ribosome biogenesis factor Nol11 is required for optimal rDNA transcription and craniofacial development in Xenopus

Codon identity regulates mRNA stability and translation efficiency during the maternal-to-zygotic transition

The heterotaxy gene GALNT11 glycosylates Notch to orchestrate cilia type and laterality

Paired Box 9 (PAX9), the RNA polymerase II transcription factor, regulates human ribosome biogenesis and craniofacial development

WDR5 Stabilizes Actin Architecture to Promote Multiciliated Cell Formation

WDR5 regulates left-right patterning via chromatin-dependent and -independent functions

Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning

Challenges and opportunities at the interface of birth defects, human genetics and developmental biology

Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR

Xenopus as a model organism for birth defects—Congenital heart disease and heterotaxy

RAPGEF5 Regulates Nuclear Translocation of β-Catenin

A chromosome-scale genome assembly and dense genetic map for Xenopus tropicalis

Obtaining Xenopus tropicalis Embryos by In Vitro Fertilization

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