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Germline Chd8 haploinsufficiency alters brain development in mouse

Nature neuroscience, 2017-08, Vol.20 (8), p.1062

2017

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Beyond autophagy: a novel role for autism-linked Wdfy3 in brain mitophagy

Scientific reports, 2018-07, Vol.8 (1), p.11348-19, Article 11348

2018

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Neural crest-derived mesenchymal cells require Wnt signaling for their development and drive invagination of the telencephalic midline

PloS one, 2014-02, Vol.9 (2), p.e86025

2014

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A genome-wide CRISPR screen identifies WDFY3 as a regulator of macrophage efferocytosis

Nature communications, 2022-12, Vol.13 (1), p.7929-19, Article 7929

2022

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Deficient or Excess Folic Acid Supply During Pregnancy Alter Cortical Neurodevelopment in Mouse Offspring

Cerebral cortex (New York, N.Y. 1991), 2021-01, Vol.31 (1), p.635-649

2021

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Loss of Wdfy3 in mice alters cerebral cortical neurogenesis reflecting aspects of the autism pathology

Nature communications, 2014-09, Vol.5 (1), p.4692-4692, Article 4692

2014

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Wdfy3 regulates glycophagy, mitophagy, and synaptic plasticity

Journal of cerebral blood flow and metabolism, 2021-12, Vol.41 (12), p.3213-3231

2021

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Prenatal Neurogenesis in Autism Spectrum Disorders

Frontiers in chemistry, 2016-03, Vol.4, p.12-12

2016

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Retinoic Acid from the Meninges Regulates Cortical Neuron Generation

Cell, 2009-10, Vol.139 (3), p.597-609

2009

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Lipid-based DNA/siRNA transfection agents disrupt neuronal bioenergetics and mitophagy

Biochemical journal, 2017-12, Vol.474 (23), p.3887-3902

2017

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Prenatal folic acid and vitamin B12 imbalance alter neuronal morphology and synaptic density in the mouse neocortex

Communications biology, 2023-11, Vol.6 (1), p.1133-1133, Article 1133

2023

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Correction: WDFY3 mutation alters laminar position and morphology of cortical neurons

Molecular autism, 2023-01, Vol.14 (1), p.4-4, Article 4

2023

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WDFY3 mutation alters laminar position and morphology of cortical neurons

Molecular autism, 2022-06, Vol.13 (1), p.27-27, Article 27

2022

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The emerging roles of ribosome biogenesis in craniofacial development

Frontiers in physiology, 2014, Vol.5, p.26-26

2014

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Editorial: Autophagy in Mammalian Development and Differentiation

Frontiers in cell and developmental biology, 2021-07, Vol.9, p.722821-722821

2021

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Maternal exposure to carbamazepine at environmental concentrations can cross intestinal and placental barriers

Biochemical and biophysical research communications, 2016-05, Vol.474 (2), p.291-295

2016

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Extracellular Engrailed Participates in the Topographic Guidance of Retinal Axons In Vivo

Neuron (Cambridge, Mass.), 2009-11, Vol.64 (3), p.355-366

2009

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Corrigendum to “Autophagy-linked FYVE containing protein WDFY3 interacts with TRAF6 and modulates RANKL-induced osteoclastogenesis” [J. Autoimmun. 73C (2016) 73–84]

Journal of autoimmunity, 2017-11, Vol.84, p.132-132

2017

Volltextzugriff (PDF)

A mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial clefting

PloS one, 2013-07, Vol.8 (7), p.e69333

2013

Volltextzugriff (PDF)

Cortical Dysplasia and Skull Defects in Mice with a Foxc1 Allele Reveal the Role of Meningeal Differentiation in Regulating Cortical Development

Proceedings of the National Academy of Sciences - PNAS, 2007-08, Vol.104 (35), p.14002-14007

2007

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Pak1ip1 Loss-of-Function Leads to Cell Cycle Arrest, Loss of Neural Crest Cells, and Craniofacial Abnormalities

Frontiers in cell and developmental biology, 2020-09, Vol.8, p.510063-510063

2020

Volltextzugriff (PDF)

A focused and efficient genetic screening strategy in the mouse: identification of mutations that disrupt cortical development

PLoS biology, 2004-08, Vol.2 (8), p.E219

2004

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Meningeal defects alter the tangential migration of cortical interneurons in Foxc1hith/hith mice

Neural development, 2012-01, Vol.7 (1), p.2-2

2012

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A role for the EphA family in the topographic targeting of vomeronasal axons

Development (Cambridge), 2001-03, Vol.128 (6), p.895-906

2001

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EphA-Ephrin-A-Mediated β Cell Communication Regulates Insulin Secretion from Pancreatic Islets

Cell, 2007-04, Vol.129 (2), p.359-370

2007

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Germline Chd8 haploinsufficiency alters brain development in mouse

Beyond autophagy: a novel role for autism-linked Wdfy3 in brain mitophagy

Neural crest-derived mesenchymal cells require Wnt signaling for their development and drive invagination of the telencephalic midline

A genome-wide CRISPR screen identifies WDFY3 as a regulator of macrophage efferocytosis

Deficient or Excess Folic Acid Supply During Pregnancy Alter Cortical Neurodevelopment in Mouse Offspring

Loss of Wdfy3 in mice alters cerebral cortical neurogenesis reflecting aspects of the autism pathology

Wdfy3 regulates glycophagy, mitophagy, and synaptic plasticity

Prenatal Neurogenesis in Autism Spectrum Disorders

Retinoic Acid from the Meninges Regulates Cortical Neuron Generation

Lipid-based DNA/siRNA transfection agents disrupt neuronal bioenergetics and mitophagy

Prenatal folic acid and vitamin B12 imbalance alter neuronal morphology and synaptic density in the mouse neocortex

Correction: WDFY3 mutation alters laminar position and morphology of cortical neurons

WDFY3 mutation alters laminar position and morphology of cortical neurons

The emerging roles of ribosome biogenesis in craniofacial development

Editorial: Autophagy in Mammalian Development and Differentiation

Maternal exposure to carbamazepine at environmental concentrations can cross intestinal and placental barriers

Extracellular Engrailed Participates in the Topographic Guidance of Retinal Axons In Vivo

Corrigendum to “Autophagy-linked FYVE containing protein WDFY3 interacts with TRAF6 and modulates RANKL-induced osteoclastogenesis” [J. Autoimmun. 73C (2016) 73–84]

A mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial clefting

Cortical Dysplasia and Skull Defects in Mice with a Foxc1 Allele Reveal the Role of Meningeal Differentiation in Regulating Cortical Development

Pak1ip1 Loss-of-Function Leads to Cell Cycle Arrest, Loss of Neural Crest Cells, and Craniofacial Abnormalities

A focused and efficient genetic screening strategy in the mouse: identification of mutations that disrupt cortical development

Meningeal defects alter the tangential migration of cortical interneurons in Foxc1hith/hith mice

A role for the EphA family in the topographic targeting of vomeronasal axons

EphA-Ephrin-A-Mediated β Cell Communication Regulates Insulin Secretion from Pancreatic Islets

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