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Receptor tyrosine kinases activate canonical WNT/β-catenin signaling via MAP kinase/LRP6 pathway and direct β-catenin phosphorylation

PloS one, 2012-04, Vol.7 (4), p.e35826-e35826

2012

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Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia

American journal of human genetics, 2003-02, Vol.72 (2), p.408-418

2003

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Mutations in TWIST , a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome

Nature genetics, 1997-01, Vol.15 (1), p.36-41

1997

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GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype

Human mutation, 2009-05, Vol.30 (5), p.724-733

2009

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Characterization of the nucleolar gene product, treacle, in Treacher Collins syndrome

Molecular biology of the cell, 2000-09, Vol.11 (9), p.3061-3071

2000

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TCOF1 Gene Encodes a Putative Nucleolar Phosphoprotein that Exhibits Mutations in Treacher Collins Syndrome throughout its Coding Region

Proceedings of the National Academy of Sciences - PNAS, 1997-04, Vol.94 (7), p.3110-3115

1997

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Oculodentodigital dysplasia connexin43 mutations result in non-functional connexin hemichannels and gap junctions in C6 glioma cells

Journal of cell science, 2006-02, Vol.119 (Pt 3), p.532-541

2006

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Tyrosine-dependent basolateral targeting of human connexin43-eYFP in Madin-Darby canine kidney cells can be disrupted by the oculodentodigital dysplasia mutation L90V

The FEBS journal, 2009-12, Vol.276 (23), p.6992-7005

2009

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Genetic Heterogeneity of Saethre-Chotzen Syndrome, Due to TWIST and FGFR Mutations

American journal of human genetics, 1998-06, Vol.62 (6), p.1370-1380

1998

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Increased risk for developmental delay in Saethre-Chotzen syndrome is associated with TWIST deletions: an improved strategy for TWIST mutation screening

Human genetics, 2003-12, Vol.114 (1), p.68-76

2003

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Genomic Organization, Expression, and Chromosome Location of the Human SNAIL Gene (SNAI1) and a Related Processed Pseudogene (SNAI1P)

Genomics (San Diego, Calif.), 1999-11, Vol.62 (1), p.42-49

1999

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On the mechanism of membrane damage by complement: the effect of length and unsaturation of the acyl chains in liposomal bilayers and the effect of cholesterol concentration in sheep erythrocyte and liposomal membranes

The Journal of immunology (1950), 1978-06, Vol.120 (6), p.1996

1978

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Receptor Tyrosine Kinases Activate Canonical WNT/[beta]-Catenin Signaling via MAP Kinase/LRP6 Pathway and Direct [beta]-Catenin Phosphorylation

PloS one, 2012-04, Vol.7 (4), p.e35826

2012

Volltextzugriff (PDF)

Human SLUG gene organization, expression, and chromosome map location on 8q

Genomics (San Diego, Calif.), 1998-08, Vol.51 (3), p.468-471

1998

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Mouse TCOF1 Is Expressed Widely, Has Motifs Conserved in Nucleolar Phosphoproteins, and Maps to Chromosome 18

Biochemical and biophysical research communications, 1997-09, Vol.238 (1), p.1-6

1997

Volltextzugriff (PDF)

Definition of a lipopolysaccharide-responsive element in the 5'-flanking regions of MuRantes and crg-2

Molecular and Cellular Biology, 1994-05, Vol.14 (5), p.2914-2925

1994

Volltextzugriff (PDF)

HumanSLUGGene Organization, Expression, and Chromosome Map Location on 8q

Genomics (San Diego, Calif.), 1998-08, Vol.51 (3), p.468-471

1998

Volltextzugriff (PDF)

Consequences of Cell Membrane Attack by Complement: Release of Arachidonate and Formation of Inflammatory Derivatives

Proceedings of the National Academy of Sciences - PNAS, 1983-11, Vol.80 (21), p.6647-6651

1983

Volltextzugriff (PDF)

A requirement for membrane-associated phospholipase A2 in platelet cytotoxicity activated by receptors for immunoglobulin G and complement

The Journal of experimental medicine, 1993-04, Vol.177 (4), p.937-947

1993

Volltextzugriff (PDF)

Definition of a Lipopolysaccharide-Responsive Element in the 5′-Flanking Regions of MuRantes and crg-2

Molecular and cellular biology, 1994-05, Vol.14 (5), p.2914-2925

1994

Volltextzugriff (PDF)

Functional Characterization of Connexin43 Mutations Found in Patients With Oculodentodigital Dysplasia

Circulation research, 2005-05, Vol.96 (10), p.e83-e91

2005

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OTX2 mutations contribute to the otocephaly-dysgnathia complex

Journal of medical genetics, 2012-06, Vol.49 (6), p.373-379

2012

Volltextzugriff (PDF)

Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome

Nature genetics, 1996-08, Vol.13 (4), p.492-494

1996

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Receptor tyrosine kinases activate canonical WNT/β-catenin signaling via MAP kinase/LRP6 pathway and direct β-catenin phosphorylation

Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia

Mutations in TWIST , a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome

GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype

Characterization of the nucleolar gene product, treacle, in Treacher Collins syndrome

TCOF1 Gene Encodes a Putative Nucleolar Phosphoprotein that Exhibits Mutations in Treacher Collins Syndrome throughout its Coding Region

Oculodentodigital dysplasia connexin43 mutations result in non-functional connexin hemichannels and gap junctions in C6 glioma cells

Tyrosine-dependent basolateral targeting of human connexin43-eYFP in Madin-Darby canine kidney cells can be disrupted by the oculodentodigital dysplasia mutation L90V

Genetic Heterogeneity of Saethre-Chotzen Syndrome, Due to TWIST and FGFR Mutations

Increased risk for developmental delay in Saethre-Chotzen syndrome is associated with TWIST deletions: an improved strategy for TWIST mutation screening

Genomic Organization, Expression, and Chromosome Location of the Human SNAIL Gene (SNAI1) and a Related Processed Pseudogene (SNAI1P)

On the mechanism of membrane damage by complement: the effect of length and unsaturation of the acyl chains in liposomal bilayers and the effect of cholesterol concentration in sheep erythrocyte and liposomal membranes

Receptor Tyrosine Kinases Activate Canonical WNT/[beta]-Catenin Signaling via MAP Kinase/LRP6 Pathway and Direct [beta]-Catenin Phosphorylation

Human SLUG gene organization, expression, and chromosome map location on 8q

Mouse TCOF1 Is Expressed Widely, Has Motifs Conserved in Nucleolar Phosphoproteins, and Maps to Chromosome 18

Definition of a lipopolysaccharide-responsive element in the 5'-flanking regions of MuRantes and crg-2

HumanSLUGGene Organization, Expression, and Chromosome Map Location on 8q

Consequences of Cell Membrane Attack by Complement: Release of Arachidonate and Formation of Inflammatory Derivatives

A requirement for membrane-associated phospholipase A2 in platelet cytotoxicity activated by receptors for immunoglobulin G and complement

Definition of a Lipopolysaccharide-Responsive Element in the 5′-Flanking Regions of MuRantes and crg-2

Functional Characterization of Connexin43 Mutations Found in Patients With Oculodentodigital Dysplasia

OTX2 mutations contribute to the otocephaly-dysgnathia complex

Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome

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