UB Paderborn / Katalog / Suche / in CDI

Hectd1 regulates intracellular localization and secretion of Hsp90 to control cellular behavior of the cranial mesenchyme

The Journal of cell biology, 2012-03, Vol.196 (6), p.789-800

2012

Link zum Volltext

Verfügbarkeit prüfen

The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation

Nature genetics, 2011-01, Vol.43 (1), p.79-84

2011

Link zum Volltext

Verfügbarkeit prüfen

The visceral yolk sac endoderm provides for absorption of nutrients to the embryo during neurulation

Birth defects research. A Clinical and molecular teratology, 2010-08, Vol.88 (8), p.593-600

2010

Link zum Volltext

Verfügbarkeit prüfen

p38 and a p38-Interacting Protein Are Critical for Downregulation of E-Cadherin during Mouse Gastrulation

Cell, 2006-06, Vol.125 (5), p.957-969

2006

Link zum Volltext

Verfügbarkeit prüfen

Persistent Feeding and Swallowing Deficits in a Mouse Model of 22q11.2 Deletion Syndrome

Frontiers in neurology, 2020-01, Vol.11, p.4-4

2020

Link zum Volltext

Verfügbarkeit prüfen

Model organisms and mechanisms of gene–environment interactions in structural birth defects

Genesis (New York, N.Y. : 2000), 2021-11, Vol.59 (11), p.e23461-n/a

Zohn, Irene E.

2021

Link zum Volltext

Verfügbarkeit prüfen

Hsp90 and complex birth defects: A plausible mechanism for the interaction of genes and environment

Neuroscience letters, 2020-01, Vol.716, p.134680-134680, Article 134680

Zohn, Irene E.

2020

Link zum Volltext

Verfügbarkeit prüfen

The ubiquitin ligase HECTD1 promotes retinoic acid signaling required for development of the aortic arch

Disease models & mechanisms, 2019-01, Vol.12 (1)

2019

Link zum Volltext

Verfügbarkeit prüfen

Parental obesity-induced changes in developmental programming

Frontiers in cell and developmental biology, 2022-10, Vol.10, p.918080-918080

2022

Link zum Volltext

Verfügbarkeit prüfen

The iron exporter ferroportin 1 is essential for development of the mouse embryo, forebrain patterning and neural tube closure

Development (Cambridge), 2010-09, Vol.137 (18), p.3079-3088

2010

Link zum Volltext

Verfügbarkeit prüfen

Identification and functional analysis of rare HECTD1 missense variants in human neural tube defects

Human genetics, 2024-03, Vol.143 (3), p.263-277

2024

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

The Hectd1 ubiquitin ligase is required for development of the head mesenchyme and neural tube closure

Developmental biology, 2007-06, Vol.306 (1), p.208-221

2007

Link zum Volltext

Verfügbarkeit prüfen

Mouse Models of Neural Tube Defects

Advances in experimental medicine and biology, 2020, Vol.1236, p.39-64

Zohn, Irene E.

2020

Link zum Volltext

Verfügbarkeit prüfen

ALDH1A2‐related disorder: A new genetic syndrome due to alteration of the retinoic acid pathway

American journal of medical genetics. Part A, 2023-01, Vol.191 (1), p.90-99

2023

Link zum Volltext

Verfügbarkeit prüfen

Reduced maternal vitamin A status increases the incidence of normal aortic arch variants

Genesis (New York, N.Y. : 2000), 2019-11, Vol.57 (11-12), p.e23343-n/a

2019

Link zum Volltext

Verfügbarkeit prüfen

Reduced maternal vitamin A status increases the incidence of normal aortic arch variants

Genesis (New York, N.Y. : 2000), 2019-07, Vol.57 (7-8), p.e23326-n/a

2019

Link zum Volltext

Verfügbarkeit prüfen

Hard to swallow: Developmental biological insights into pediatric dysphagia

Developmental biology, 2016-01, Vol.409 (2), p.329-342

2016

Link zum Volltext

Verfügbarkeit prüfen

Mouse as a model for multifactorial inheritance of neural tube defects

Birth defects research. Part C. Embryo today, 2012-06, Vol.96 (2), p.193-205

Zohn, Irene E.

2012

Link zum Volltext

Verfügbarkeit prüfen

Using genomewide mutagenesis screens to identify the genes required for neural tube closure in the mouse

Birth defects research. A Clinical and molecular teratology, 2005-09, Vol.73 (9), p.583-590

2005

Link zum Volltext

Verfügbarkeit prüfen

Supt20 is required for development of the axial skeleton

Developmental biology, 2017-01, Vol.421 (2), p.245-257

2017

Link zum Volltext

Verfügbarkeit prüfen

Variations in maternal vitamin A intake modifies phenotypes in a mouse model of 22q11.2 deletion syndrome

Birth defects research, 2020-10, Vol.112 (16), p.1194-1208

2020

Link zum Volltext

Verfügbarkeit prüfen

HectD1 E3 Ligase Modifies Adenomatous Polyposis Coli (APC) with Polyubiquitin to Promote the APC-Axin Interaction

The Journal of biological chemistry, 2013-02, Vol.288 (6), p.3753-3767

2013

Link zum Volltext

Verfügbarkeit prüfen

Hectd1 is required for development of the junctional zone of the placenta

Developmental biology, 2014-08, Vol.392 (2), p.368-380

2014

Link zum Volltext

Verfügbarkeit prüfen

Abnormal labyrinthine zone in the Hectd1 -null placenta

Placenta (Eastbourne), 2016-02, Vol.38, p.16-23

2016

Link zum Volltext

Verfügbarkeit prüfen

Menü

Weitere Dienste

Einstellungen

Hectd1 regulates intracellular localization and secretion of Hsp90 to control cellular behavior of the cranial mesenchyme

The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation

The visceral yolk sac endoderm provides for absorption of nutrients to the embryo during neurulation

p38 and a p38-Interacting Protein Are Critical for Downregulation of E-Cadherin during Mouse Gastrulation

Persistent Feeding and Swallowing Deficits in a Mouse Model of 22q11.2 Deletion Syndrome

Model organisms and mechanisms of gene–environment interactions in structural birth defects

Hsp90 and complex birth defects: A plausible mechanism for the interaction of genes and environment

The ubiquitin ligase HECTD1 promotes retinoic acid signaling required for development of the aortic arch

Parental obesity-induced changes in developmental programming

The iron exporter ferroportin 1 is essential for development of the mouse embryo, forebrain patterning and neural tube closure

Identification and functional analysis of rare HECTD1 missense variants in human neural tube defects

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

The Hectd1 ubiquitin ligase is required for development of the head mesenchyme and neural tube closure

Mouse Models of Neural Tube Defects

ALDH1A2‐related disorder: A new genetic syndrome due to alteration of the retinoic acid pathway

Reduced maternal vitamin A status increases the incidence of normal aortic arch variants

Reduced maternal vitamin A status increases the incidence of normal aortic arch variants

Hard to swallow: Developmental biological insights into pediatric dysphagia

Mouse as a model for multifactorial inheritance of neural tube defects

Using genomewide mutagenesis screens to identify the genes required for neural tube closure in the mouse

Supt20 is required for development of the axial skeleton

Variations in maternal vitamin A intake modifies phenotypes in a mouse model of 22q11.2 deletion syndrome

HectD1 E3 Ligase Modifies Adenomatous Polyposis Coli (APC) with Polyubiquitin to Promote the APC-Axin Interaction

Hectd1 is required for development of the junctional zone of the placenta

Abnormal labyrinthine zone in the Hectd1 -null placenta

Suchergebnisse filtern