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Publications by Fenella Greig

Characterization of Novel Cathepsin K Mutations in the Pro and Mature Polypeptide Regions Causing Pycnodysostosis

Journal of Clinical Investigation

English

Related publications

Clinical and Animal Research Findings in Pycnodysostosis and Gene Mutations of Cathepsin K From 1996 to 2011

Orphanet Journal of Rare Diseases

English

Linking Osteopetrosis and Pycnodysostosis: Regulation of Cathepsin K Expression by the Microphthalmia Transcription Factor Family

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

English

The Clinical Rehabilitation and Cathepsin K Gene Analysis of a Turkish Family With Pycnodysostosis.

Marmara Dental Journal

English

Characterization of Seven Novel Mutations Causing Factor XI Deficiency

English

Nonclinical and Clinical Pharmacological Characterization of the Potent and Selective Cathepsin K Inhibitor MIV-711

Journal of Translational Medicine

Molecular Biology

English

Immunological Identification and Characterization of a Delayed Rectifier K+ Channel Polypeptide in Rat Brain.

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

English

Investigating Functional Consequences of Novel Disease-Causing Mutations of CLCN7 Gene

Biophysical Journal

English

Crystal Structures of the Novel Cysteine Protease, Cathepsin K, in Complex With the Inhibitor E-64

Acta Crystallographica Section A Foundations of Crystallography

English

Novel Mutations in PRPF31 Causing Retinitis Pigmentosa Identified Using Whole-Exome Sequencing

Investigative Ophthalmology and Visual Science

Molecular Neuroscience

Sensory Systems

English