Hayley J. Durling
University of Western Australia(AU)
Publications by Year
Research Areas
Cardiomyopathy and Myosin Studies, Muscle Physiology and Disorders, Nuclear Structure and Function, Cell Adhesion Molecules Research, Cellular Mechanics and Interactions
Most-Cited Works
- → Mutations in the Slow Skeletal Muscle Fiber Myosin Heavy Chain Gene (MYH7) Cause Laing Early-Onset Distal Myopathy (MPD1)(2004)227 cited
- → Muscle disease caused by mutations in the skeletal muscle alpha-actin gene (ACTA1)(2003)214 cited
- → Nemaline Myopathy Caused by Mutations in the Muscle α-Skeletal-Actin Gene(2001)157 cited
- → Actin myopathy with nemaline bodies, intranuclear rods, and a heterozygous mutation in ACTA1 (Asp154Asn)(2004)60 cited
- → De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy(2002)37 cited
- → Nemaline Rods and Complex I Deficiency in Three Infants with Hypotonia, Motor Delay and Failure to Thrive(2004)26 cited
- → Actin-Related Myopathy Without Any Missense Mutation in the ACTA1 Gene(2004)17 cited
- Predominantly upper limb weakness, enlarged cisterna magna, and borderline intelligence in a child with de novo mutation of the skeletal muscle alpha-actin gene.(2005)
- → Patient With Actin Aggregate Myopathy and Not Formerly Identified ACTA1 Mutation Is Heterozygous for the Gly15Arg Mutation of ACTA1, Which Has Previously Been Associated With Actinopathy(2006)7 cited