Maldevelopment of the submandibular gland in a mouse model of apert syndrome (Q91714629)

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24 April 2020

title

Maldevelopment of the submandibular gland in a mouse model of apert syndrome (English)

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24 April 2020

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24 April 2020

Jumpei Morita

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24 April 2020

Tsukasa Watanabe

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24 April 2020

Kaori Gunjigake

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24 April 2020

Mitsushiro Nakatomi

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24 April 2020

Momotoshi Shiga

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24 April 2020

Kentaro Ono

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24 April 2020

Keiji Moriyama

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24 April 2020

Tatsuo Kawamoto

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24 April 2020

publication date

10 November 2018

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24 April 2020

published in

Developmental Dynamics

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24 April 2020

volume

247

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issue

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24 April 2020

page(s)

1175-1185

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Brain phenotypes in two FGFR2 mouse models for Apert syndrome

24 April 2020

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A Ser250Trp substitution in mouse fibroblast growth factor receptor 2 (Fgfr2) results in craniosynostosis

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Angiopoietins modulate endothelial adaptation, glomerular and podocyte hypertrophy after uninephrectomy

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Early onset of craniosynostosis in an Apert mouse model reveals critical features of this pathology

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Twist1- and Twist2-haploinsufficiency results in reduced bone formation

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FGF10/FGFR2b signaling plays essential roles during in vivo embryonic submandibular salivary gland morphogenesis

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EGFR/HER2 inhibitors effectively reduce the malignant potential of MDR breast cancer evoked by P-gp substrates in vitro and in vivo

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M2 macrophage polarisation is associated with alveolar formation during postnatal lung development

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TMEM16A exacerbates renal injury by activating P38/JNK signaling pathway to promote podocyte apoptosis in diabetic nephropathy mice

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Single-stranded DNA binding protein Ssbp3 induces differentiation of mouse embryonic stem cells into trophoblast-like cells.

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7 January 2021

MiR542-3p Regulates the Epithelial-Mesenchymal Transition by Directly Targeting BMP7 in NRK52e

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7 January 2021

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

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7 January 2021

Salivary Gland Dysplasia in Fgf10 Heterozygous Mice: A New Mouse Model of Xerostomia.

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Regulation of fluid and electrolyte secretion in salivary gland acinar cells

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7 January 2021

Soluble form of FGFR2 with S252W partially prevents craniosynostosis of the apert mouse model.

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7 January 2021

EGF-dependent lobule formation and FGF7-dependent stalk elongation in branching morphogenesis of mouse salivary epithelium in vitro

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7 January 2021

WT1 induction of mitogen-activated protein kinase phosphatase 3 represents a novel mechanism of growth suppression

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7 January 2021

Changes of salivary functions in experimental periodontitis model rats

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7 January 2021

FGF10 acts as a major ligand for FGF receptor 2 IIIb in mouse multi-organ development

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7 January 2021

The Fibroblast Growth Factor signaling pathway

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7 January 2021

Developmental localization of the splicing alternatives of fibroblast growth factor receptor-2 (FGFR2)

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7 January 2021

Salivary gland branching morphogenesis

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7 January 2021

Structural basis for FGF receptor dimerization and activation

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7 January 2021

Laminin alpha5 is necessary for submandibular gland epithelial morphogenesis and influences FGFR expression through beta1 integrin signaling

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7 January 2021

MCSF orchestrates branching morphogenesis in developing submandibular gland tissue.

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7 January 2021

RNA interference and inhibition of MEK-ERK signaling prevent abnormal skeletal phenotypes in a mouse model of craniosynostosis

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7 January 2021

Bile deficiency induces changes in intestinal Cl(-) and HCO3 (-) secretions in mice.

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7 January 2021

FGFR2b signaling regulates ex vivo submandibular gland epithelial cell proliferation and branching morphogenesis.

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7 January 2021

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7 January 2021

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

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7 January 2021

Platelet-derived growth factor receptor regulates salivary gland morphogenesis via fibroblast growth factor expression

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7 January 2021

The study of abnormal bone development in the Apert syndrome Fgfr2+/S252W mouse using a 3D hydrogel culture model

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7 January 2021

A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Identifiers

DOI

10.1002/DVDY.24673

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30251381%20AND%20SRC:MED&resulttype=core&format=json

24 April 2020

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