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Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebs

Data up to Jan 2025

Published2005
Citations157
References14

Total Citations Per Year

Abstract

References (14)

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Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein

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A direct functional link between the multi-PDZ domain protein GRIP1 and the Fraser syndrome protein Fras1

2004 • 142 citations

The extracellular matrix geneFrem1is essential for the normal adhesion of the embryonic epidermis

2004 • 112 citations

Fras1 deficiency results in cryptophthalmos, renal agenesis and blebbed phenotype in mice

2003 • 111 citations

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2002 • 111 citations

Cell-substrate interactions during sea urchin gastrulation: Migrating primary mesenchyme cells interact with and align extracellular matrix fibers that contain ECM3, a molecule with NG2-like and multiple calcium-binding domains

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A mouse model for Fraser syndrome?

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Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebs (2005) – Nature Genetics | Metascience Observatory Explorer