Rebecca J. Fairclough

Publications by Year

Research Areas

Muscle Physiology and Disorders, Nerve injury and regeneration, Virus-based gene therapy research, Genetic and rare skin diseases., Pancreatic function and diabetes

Most-Cited Works

• → Therapy for Duchenne muscular dystrophy: renewed optimism from genetic approaches(2013)222 cited
• → Daily Treatment with SMTC1100, a Novel Small Molecule Utrophin Upregulator, Dramatically Reduces the Dystrophic Symptoms in the mdx Mouse(2011)172 cited
• → The Secretory Pathway Ca2+/Mn2+-ATPase 2 Is a Golgi-localized Pump with High Affinity for Ca2+ Ions(2005)132 cited
• → Calcium pumps and keratinocytes: lessons from Darier's disease and Hailey-Hailey disease(2004)129 cited
• → Gata3-deficient mice develop parathyroid abnormalities due to dysregulation of the parathyroid-specific transcription factor Gcm2(2010)125 cited
• → Effect of Hailey-Hailey Disease Mutations on the Function of a New Variant of Human Secretory Pathway Ca2+/Mn2+-ATPase (hSPCA1)(2003)104 cited
• → Sarcolemmal nNOS anchoring reveals a qualitative difference between dystrophin and utrophin(2010)97 cited
• → Hailey-Hailey Disease: Molecular and Clinical Characterization of Novel Mutations in the ATP2C1 Gene(2002)92 cited
• → 11β-Hydroxysteroid dehydrogenase type 1 inhibition in idiopathic intracranial hypertension: a double-blind randomized controlled trial(2020)68 cited
• → Progress in therapy for Duchenne muscular dystrophy(2011)63 cited