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Publications by L C Wilson

Mutations in CUL7, OBSL1 and CCDC8 in 3-M Syndrome Lead to Disordered Growth Factor Signalling

Journal of Molecular Endocrinology

Molecular Biology

English

Related publications

Novel CUL7 Biallelic Mutations Alter the Skeletal Phenotype of 3M Syndrome

Human Genome Variation

Molecular Biology

English

Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome

American Journal of Human Genetics

English

Biallelic Mutations in ADPRHL2 , Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome

American Journal of Human Genetics

English

Caveolin-3 T78M and T78K Missense Mutations Lead to Different Phenotypes in Vivo and in Vitro

Laboratory Investigation

Forensic Medicine

Molecular Biology

English

Disordered Structures in Lead-Free Piezoelectrics

Acta Crystallographica Section A: Foundations and Advances

Materials Science

Condensed Matter Physics

Theoretical Chemistry

Structural Biology

Inorganic Chemistry

English

The 3-M Syndrome.

Journal of Medical Genetics

English

Antiapoptotic Signalling by the Insulin-Like Growth Factor I Receptor, Phosphatidylinositol 3-Kinase, and Akt.

Molecular and Cellular Biology

Molecular Biology

English

Grb2 Regulates Stat3 Activation Negatively in Epidermal Growth Factor Signalling

Biochemical Journal

Molecular Biology

English

Activating Transcription Factor 3 Regulates Canonical TGFβ Signalling in Systemic Sclerosis

Annals of the Rheumatic Diseases

Molecular Biology

English