Rebecca J. Fairclough

Author

University of Oxford ORCID

Also Known As

Fairclough, RJ, R. Fairclough, R.J. Fairclough, Rebecca Fairclough, Rebecca J Fairclough, Rebecca J. Fairclough

Publications

1.5K

Citations

H-Index

Concepts

All Affiliations

University of Oxford Churchill Hospital AstraZeneca (United Kingdom)Oxford Centre for Diabetes, Endocrinology and Metabolism Centre for Human Genetics

About

Rebecca J. Fairclough is an author at University of Oxford specializing in medicine, genetics, and molecular physiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	390
2	Biochemistry	2	2	109
3	Health Sciences	1	1	124
4	Natural Sciences	1	1	12
5	Public Health	1	1	14

Rebecca J. Fairclough

Publications

998

Citations

H-Index

Page 1

	Year	Citations
Daily Treatment with SMTC1100, a Novel Small Molecule Utrophin Upregulator, Dramatically Reduces the Dystrophic Symptoms in the mdx Mouse Jonathon M. Tinsley, Rebecca J. Fairclough, Richard Storer, PLoS ONE	2011	172
The Secretory Pathway Ca2+/Mn2+-ATPase 2 Is a Golgi-localized Pump with High Affinity for Ca2+ Ions Jo Vanoevelen, Leonard Dode, Kurt Van Baelen, Journal of Biological Chemistry	2005	132
Gata3-deficient mice develop parathyroid abnormalities due to dysregulation of the parathyroid-specific transcription factor Gcm2 I. V. Grigorieva, Samantha Mirczuk, Katherine U. Gaynor, Journal of Clinical Investigation Parathyroid AbnormalitiesGeneticsParathyroid DiseaseParathyroid GlandGata3-deficient Mice	2010	124
Effect of Hailey-Hailey Disease Mutations on the Function of a New Variant of Human Secretory Pathway Ca2+/Mn2+-ATPase (hSPCA1) Rebecca J. Fairclough, Leonard Dode, Jo Vanoevelen, Journal of Biological Chemistry	2003	104
Sarcolemmal nNOS anchoring reveals a qualitative difference between dystrophin and utrophin Dejia Li, Akshay Bareja, Luke M. Judge, Journal of Cell Science Muscle FunctionPathologyCytoskeletonCellular PhysiologySkeletal Muscle	2010	97
Hailey-Hailey Disease: Molecular and Clinical Characterization of Novel Mutations in the ATP2C1 Gene Carol Dobson‐Stone, Rebecca J. Fairclough, Eimear Dunne, Journal of Investigative Dermatology Mendelian DisorderAtp2c1 GeneGenetic DisorderGeneticsNovel Mutations	2002	92
11β-Hydroxysteroid dehydrogenase type 1 inhibition in idiopathic intracranial hypertension: a double-blind randomized controlled trial Keira Markey, James Mitchell, Hannah Botfield, Brain Communications	2020	67
11βHSD1 Inhibition with AZD4017 Improves Lipid Profiles and Lean Muscle Mass in Idiopathic Intracranial Hypertension Rowan Hardy, Hannah Botfield, Keira Markey, The Journal of Clinical Endocrinology & Metabolism	2020	58
Hailey–Hailey Disease: Identification of Novel Mutations in ATP2C1 and Effect of Missense Mutation A528P on Protein Expression Levels Rebecca J. Fairclough, Lorne Lonie, Kurt Van Baelen, Journal of Investigative Dermatology Missense Mutation A528pHailey–hailey DiseaseMolecular PhysiologyGenetic DisorderGenetics	2004	51
The replication and stable-inheritance functions of IncP-9 plasmid pM3 The GenBank accession number for the sequence reported in this paper is AF078924. Alicia Greated, Renata Krasowiak, Rebecca J. Fairclough, Microbiology	2000	31

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