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Discovery and characterization of anti-cancer peptides from a random peptide library

PloS one, 2024-02, Vol.19 (2), p.e0293072-e0293072

2024

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Novel Cell-Penetrating Peptides Derived From Scaffold-Attachment- Factor A Inhibits Cancer Cell Proliferation and Survival

Frontiers in oncology, 2021-03, Vol.11, p.621825-621825

2021

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Mesodermal Nkx2.5 is necessary and sufficient for early second heart field development

Developmental biology, 2014-06, Vol.390 (1), p.68-79

2014

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TBX3 regulates splicing in vivo: a novel molecular mechanism for Ulnar-mammary syndrome

PLoS genetics, 2014-03, Vol.10 (3), p.e1004247-e1004247

2014

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Lethal arrhythmias in Tbx3-deficient mice reveal extreme dosage sensitivity of cardiac conduction system function and homeostasis

Proceedings of the National Academy of Sciences - PNAS, 2012-01, Vol.109 (3), p.665-666

2012

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Coordinated control of senescence by lncRNA and a novel T-box3 co-repressor complex

eLife, 2014-05, Vol.3

2014

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Role of Mesodermal FGF8 and FGF10 Overlaps in the Development of the Arterial Pole of the Heart and Pharyngeal Arch Arteries

Circulation research, 2010-02, Vol.106 (3), p.495-503

2010

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TBX3 is dynamically expressed in pancreatic organogenesis and fine-tunes regeneration

BMC biology, 2023-03, Vol.21 (1), p.55-55, Article 55

2023

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Required, tissue-specific roles for Fgf8 in outflow tract formation and remodeling

Development (Cambridge), 2006-06, Vol.133 (12), p.2419-2433

2006

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Mouse TBX3 mutants suggest novel molecular mechanisms for Ulnar-mammary syndrome

PloS one, 2013-07, Vol.8 (7), p.e67841-e67841

2013

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Myocardial wall stiffening in a mouse model of persistent truncus arteriosus

PloS one, 2017-09, Vol.12 (9), p.e0184678-e0184678

2017

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An FGF autocrine loop initiated in second heart field mesoderm regulates morphogenesis at the arterial pole of the heart

Development (Cambridge), 2008-11, Vol.135 (21), p.3599-3610

2008

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Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm

Development (Cambridge), 2009-09, Vol.136 (18), p.3173-3183

2009

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Essential Roles of Androgen Signaling in Wolffian Duct Stabilization and Epididymal Cell Differentiation

Endocrinology (Philadelphia), 2011-04, Vol.152 (4), p.1640-1651

2011

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The roles of Fgf4 and Fgf8 in limb bud initiation and outgrowth

Developmental biology, 2004-09, Vol.273 (2), p.361-372

2004

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Complex functional redundancy of Tbx2 and Tbx3 in mouse limb development

Developmental dynamics, 2022-09, Vol.251 (9), p.1613-1627

2022

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FGF8 initiates inner ear induction in chick and mouse

Genes & development, 2005-03, Vol.19 (5), p.603-613

2005

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Development of a subset of forelimb muscles and their attachment sites requires the ulnar-mammary syndrome gene Tbx3

Disease models & mechanisms, 2016-11, Vol.9 (11), p.1257-1269

2016

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T-box3 is a ciliary protein and regulates stability of the Gli3 transcription factor to control digit number

eLife, 2016-04, Vol.5

2016

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An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome

Development (Cambridge), 2002-10, Vol.129 (19), p.4591-4603

2002

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Fgf8 is required for outgrowth and patterning of the limbs

Nature genetics, 2000-12, Vol.26 (4), p.455-459

2000

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Ablation of specific expression domains reveals discrete functions of ectoderm- and endoderm-derived FGF8 during cardiovascular and pharyngeal development

Development (Cambridge), 2003-12, Vol.130 (25), p.6361-6374

2003

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System for tamoxifen‐inducible expression of cre‐recombinase from the Foxa2 locus in mice

Developmental dynamics, 2008-02, Vol.237 (2), p.447-453

2008

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Disruption of G-protein γ5 subtype causes embryonic lethality in mice

PloS one, 2014-03, Vol.9 (3), p.e90970-e90970

2014

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Crkl Deficiency Disrupts Fgf8 Signaling in a Mouse Model of 22q11 Deletion Syndromes

Developmental cell, 2006, Vol.10 (1), p.71-80

2006

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Discovery and characterization of anti-cancer peptides from a random peptide library

Novel Cell-Penetrating Peptides Derived From Scaffold-Attachment- Factor A Inhibits Cancer Cell Proliferation and Survival

Mesodermal Nkx2.5 is necessary and sufficient for early second heart field development

TBX3 regulates splicing in vivo: a novel molecular mechanism for Ulnar-mammary syndrome

Lethal arrhythmias in Tbx3-deficient mice reveal extreme dosage sensitivity of cardiac conduction system function and homeostasis

Coordinated control of senescence by lncRNA and a novel T-box3 co-repressor complex

Role of Mesodermal FGF8 and FGF10 Overlaps in the Development of the Arterial Pole of the Heart and Pharyngeal Arch Arteries

TBX3 is dynamically expressed in pancreatic organogenesis and fine-tunes regeneration

Required, tissue-specific roles for Fgf8 in outflow tract formation and remodeling

Mouse TBX3 mutants suggest novel molecular mechanisms for Ulnar-mammary syndrome

Myocardial wall stiffening in a mouse model of persistent truncus arteriosus

An FGF autocrine loop initiated in second heart field mesoderm regulates morphogenesis at the arterial pole of the heart

Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm

Essential Roles of Androgen Signaling in Wolffian Duct Stabilization and Epididymal Cell Differentiation

The roles of Fgf4 and Fgf8 in limb bud initiation and outgrowth

Complex functional redundancy of Tbx2 and Tbx3 in mouse limb development

FGF8 initiates inner ear induction in chick and mouse

Development of a subset of forelimb muscles and their attachment sites requires the ulnar-mammary syndrome gene Tbx3

T-box3 is a ciliary protein and regulates stability of the Gli3 transcription factor to control digit number

An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome

Fgf8 is required for outgrowth and patterning of the limbs

Ablation of specific expression domains reveals discrete functions of ectoderm- and endoderm-derived FGF8 during cardiovascular and pharyngeal development

System for tamoxifen‐inducible expression of cre‐recombinase from the Foxa2 locus in mice

Disruption of G-protein γ5 subtype causes embryonic lethality in mice

Crkl Deficiency Disrupts Fgf8 Signaling in a Mouse Model of 22q11 Deletion Syndromes

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