Rachel A. Peat

发表

Zoledronic Acid Treatment Results in Retention of Femoral Head Structure After Traumatic Osteonecrosis in Young Wistar Rats

Paul R. Williams, P. Baldock, D. Little, 2003, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Zoledronic acid improves femoral head sphericity in a rat model of perthes disease

M. McDonald, P. Williams, D. Little, 2005, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

Low-Intensity Ultrasound Stimulation in Distraction Osteogenesis in Rabbits

Lynne E Bilston, L. Bilston, M. Uglow, 2003, Clinical orthopaedics and related research.

Variable penetrance of COL6A1 null mutations: Implications for prenatal diagnosis and genetic counselling in Ullrich congenital muscular dystrophy families

K. North, K. Jones, R. Peat, 2007, Neuromuscular Disorders.

Reduced Plasma Membrane Expression of Dysferlin Mutants Is Attributed to Accelerated Endocytosis via a Syntaxin-4-associated Pathway*

K. North, R. Parton, F. Evesson, 2010, The Journal of Biological Chemistry.

Congenital muscular dystrophy type 1D (MDC1D) due to a large intragenic insertion/deletion, involving intron 10 of the LARGE gene

K. Campbell, E. Chouery, A. Mégarbané, 2011, European Journal of Human Genetics.

Collagen VI glycine mutations: Perturbed assembly and a spectrum of clinical severity

K. Mathews, K. North, M. Mörgelin, 2008, Annals of neurology.

Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy.

K. North, N. Goemans, M. Mörgelin, 2004, Human molecular genetics.

Diagnosis and etiology of congenital muscular dystrophy

K. North, A. Compton, D. Burkin, 2008, Neurology.

Identification of a KCNQ1 Polymorphism Acting as a Protective Modifier Against Arrhythmic Risk in Long-QT Syndrome

P. Schwartz, D. Trégouët, W. Shimizu, 2013, Circulation. Cardiovascular genetics.

Collagen VI Microfibril Formation Is Abolished by an α2(VI) von Willebrand Factor Type A Domain Mutation in a Patient with Ullrich Congenital Muscular Dystrophy*

K. North, C. Baldock, J. Bateman, 2010, The Journal of Biological Chemistry.

Molecular consequences of dominant Bethlem myopathy collagen VI mutations

B. Ceulemans, S. Aftimos, M. Hannibal, 2007, Annals of neurology.

R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation.

Michael John Ackerman, Craig T. January, Brian P. Delisle, 2011, Heart rhythm.

Collagen VI Microfibril Formation Is Abolished by an α2(VI) von Willebrand Factor Type A Domain Mutation in a Patient with Ullrich Congenital Muscular Dystrophy*

K. North, C. Baldock, J. Bateman, 2010, The Journal of Biological Chemistry.

Arrhythmic Risk in Long-QT Syndrome Polymorphism Acting as a Protective Modifier Against KCNQ 1 Identification of a

P. Schwartz, D. Trégouët, W. Shimizu, 2013 .

Effect of voluntary physical activity initiated at age 7 months on skeletal hindlimb and cardiac muscle function in mdx mice of both genders

G. Butler-Browne, A. Ferry, O. Agbulut, 2015, Muscle & nerve.