Sue Shackleton

LMNA, encoding lamin A/C, is mutated in partial lipodystrophy

Sue Shackleton, David J. Lloyd, Stephen N.J. Jackson et al. · Nature Genetics · 2000 · 695 citations

Cell Biology, Lamin A/c, Molecular Biology +1

SUN1 Interacts with Nuclear Lamin A and Cytoplasmic Nesprins To Provide a Physical Connection between the Nuclear Lamina and the Cytoskeleton

Farhana Haque, David J. Lloyd, Dawn T. Smallwood et al. · Molecular and Cellular Biology · 2006 · 499 citations · Full text

Nuclear Structure, Nuclear Lamina, Molecular Biology +19

Mammalian SUN Protein Interaction Networks at the Inner Nuclear Membrane and Their Role in Laminopathy Disease Processes

Farhana Haque, Daniela Mazzeo, Jennifer T. Patel et al. · Journal of Biological Chemistry · 2009 · 280 citations · Full text

Muscular Dystrophy-Associated SUN1 and SUN2 Variants Disrupt Nuclear-Cytoskeletal Connections and Myonuclear Organization

Peter Meinke, Elisabetta Mattioli, Farhana Haque et al. · PLoS Genetics · 2014 · 179 citations · Full text

Genetics, Cytoskeleton, Molecular Genetics +16

Lamin A/C gene: sex-determined expression of mutations in Dunnigan-type familial partial lipodystrophy and absence of coding mutations in congenital and acquired generalized lipoatrophy.

Corinne Vigouroux, Jocelyne Magré, Marie‐Christine Vantyghem et al. · Diabetes · 2000 · 175 citations

Metabolic Syndrome, Typical Fpld, Developmental Biology +14