Juliet A. Ellis

发表

Novartis Foundation (NF) Symposium 264: Nuclear organisation in development and disease” 31 authors of equal ranking.

Juliet A. Ellis, 2005 .

Cell biology: Patches for wounded muscle

Juliet A. Ellis, J. A. Ellis, 2003, Nature.

Emery and Rimoin's principles and practice of medical genetics (3rd edn)

Juliet A. Ellis, Martin Bobrow, M. Bobrow, 1997 .

The spatial organization of human chromosomes within the nuclei of normal and emerin-mutant cells.

Juliet A. Ellis, W. Bickmore, S. Boyle, 2001, Human molecular genetics.

Nesprin-2 is a multi-isomeric protein that binds lamin and emerin at the nuclear envelope and forms a subcellular network in skeletal muscle

Juliet A. Ellis, J. Skepper, P. Weissberg, 2005, Journal of Cell Science.

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

Juliet A. Ellis, C. Shanahan, D. Mazzeo, 2009, The Journal of Biological Chemistry.

Further Characterisation of the Molecular Signature of Quiescent and Activated Mouse Muscle Satellite Cells

Robert B. White, Juliet A. Ellis, V. Gnocchi, 2009, PLoS ONE.

Nesprins: a novel family of spectrin-repeat-containing proteins that localize to the nuclear membrane in multiple tissues.

Juliet A. Ellis, J. Skepper, P. Weissberg, 2001, Journal of cell science.

Nesprin-1 and -2 are involved in the pathogenesis of Emery Dreifuss muscular dystrophy and are critical for nuclear envelope integrity.

Juliet A. Ellis, B. Schlotter-Weigel, J. Skepper, 2007, Human molecular genetics.

Muscular dystrophies, dilated cardiomyopathy, lipodystrophy and neuropathy: the nuclear connection

Juliet A. Ellis, J. A. Ellis, S. Maidment, 2002, Expert Reviews in Molecular Medicine.

Emery-Dreifuss muscular dystrophy at the nuclear envelope: 10 years on

Juliet A. Ellis, J. A. Ellis, 2006, Cellular and Molecular Life Sciences CMLS.

Retinoschisin, the X-linked retinoschisis protein, is a secreted photoreceptor protein, and is expressed and released by Weri-Rb1 cells.

Juliet A. Ellis, D. Farber, J. Yates, 1999, Human molecular genetics.

The cell cycle dependent mislocalisation of emerin may contribute to the Emery-Dreifuss muscular dystrophy phenotype.

Juliet A. Ellis, A. Riddell, J. Kendrick‐Jones, 2002, Journal of cell science.

Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2α.

Juliet A. Ellis, C. Stewart, R. Foisner, 2013, Human molecular genetics.

Aberrant intracellular targeting and cell cycle-dependent phosphorylation of emerin contribute to the Emery-Dreifuss muscular dystrophy phenotype.

Juliet A. Ellis, J. Yates, M. Craxton, 1998, Journal of cell science.

International Workshop : Newborn screening for Duchenne muscular dystrophy 14 – 16 th December , 2012 , Naarden , The Netherlands

Juliet A. Ellis, F. Muntoni, J. A. Ellis, 2013 .

The Emery-Dreifuss muscular dystrophy phenotype arises from aberrant targeting and binding of emerin at the inner nuclear membrane.

Juliet A. Ellis, J. A. Ellis, E. Fairley, 1999, Journal of cell science.

Inhibition of apical but not basolateral endocytosis of ricin and folate in Caco-2 cells by cytochalasin D.

Juliet A. Ellis, J. Luzio, W. Shurety, 1994, Journal of cell science.

Novel LMNA mutations in patients with Emery‐Dreifuss muscular dystrophy and functional characterization of four LMNA mutations

Juliet A. Ellis, J. Mendell, S. Iannaccone, 2011, Human mutation.

Distinct functional domains in nesprin-1alpha and nesprin-2beta bind directly to emerin and both interactions are disrupted in X-linked Emery-Dreifuss muscular dystrophy.

Juliet A. Ellis, C. Shanahan, J. A. Ellis, 2007, Experimental cell research.

Genotype-phenotype analysis in X-linked Emery–Dreifuss muscular dystrophy and identification of a missense mutation associated with a milder phenotype

Juliet A. Ellis, J. Kendrick‐Jones, J. Whittaker, 1999, Neuromuscular Disorders.

Changes at P183 of emerin weaken its protein-protein interactions resulting in X-linked Emery-Dreifuss muscular dystrophy

Juliet A. Ellis, J. Kendrick‐Jones, J. Yates, 1999, Human Genetics.

Lamins A and C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophy.

Susan C. Brown, Juliet A. Ellis, M. Dabauvalle, 2005, European journal of cell biology.

81st ENMC International Workshop: 4th Meeting on Emery–Dreifuss Muscular Dystrophy 7th and 8th July 2000, Naarden, The Netherlands

Juliet A. Ellis, J. A. Ellis, 2001, Neuromuscular Disorders.

The inner nuclear membrane protein Emerin regulates β‐catenin activity by restricting its accumulation in the nucleus

Juliet A. Ellis, H. Clevers, N. Barker, 2006, The EMBO journal.

NEP-A and NEP-B both contribute to nuclear pore formation in Xenopus eggs and oocytes

Juliet A. Ellis, C. Smythe, E. Kiseleva, 2008, Journal of Cell Science.

Does satellite cell dysfunction contribute to disease progression in Emery-Dreifuss muscular dystrophy?

Juliet A. Ellis, V. Gnocchi, P. Zammit, 2008, Biochemical Society transactions.

Nuclear envelope disease and chromatin organization.

Juliet A. Ellis, J. A. Ellis, S. Shackleton, 2011, Biochemical Society transactions.

Identification and Characterization of a Novel Protein (p137) Which Transcytoses Bidirectionally in Caco-2 Cells (*)

Juliet A. Ellis, J. Luzio, J. A. Ellis, 1995, The Journal of Biological Chemistry.

Genotype-phenotype correlations in laminopathies: how does fate translate?

Juliet A. Ellis, V. Gnocchi, P. Zammit, 2010, Biochemical Society transactions.

Identification of an emerin–β-catenin complex in the heart important for intercalated disc architecture and β-catenin localisation

Juliet A. Ellis, E. Ehler, A. Warley, 2010, Cellular and Molecular Life Sciences.

Molecular signatures of Emery-Dreifuss muscular dystrophy.

Juliet A. Ellis, J. A. Ellis, Matthew A. Wheeler, 2008, Biochemical Society transactions.

Ameliorating pathogenesis by removing an exon containing a missense mutation: a potential exon-skipping therapy for laminopathies

Juliet A. Ellis, P. Zammit, J. A. Ellis, 2015, Gene Therapy.

Defects in cell spreading and ERK1/2 activation in fibroblasts with lamin A/C mutations.

Juliet A. Ellis, M. Parsons, J. A. Ellis, 2009, Biochimica et biophysica acta.

The Emery–Dreifuss muscular dystrophy associated‐protein emerin is phosphorylated on serine 49 by protein kinase A

Juliet A. Ellis, C. Tate, J. Kendrick‐Jones, 2006, The FEBS journal.

Two distal mutations in the gene encoding emerin have profoundly different effects on emerin protein expression

Juliet A. Ellis, J. Kendrick‐Jones, J. Yates, 2000, Neuromuscular Disorders.

Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2α.

Juliet A. Ellis, C. Stewart, R. Foisner, 2013, Human molecular genetics.

Uncoordinated Transcription and Compromised Muscle Function in the Lmna-Null Mouse Model of Emery-Dreifuss Muscular Dystrophy

Robert B. White, Juliet A. Ellis, Yin-Biao Sun, 2011, PloS one.

Mapping disease‐related missense mutations in the immunoglobulin‐like fold domain of lamin A/C reveals novel genotype–phenotype associations for laminopathies

Juliet A. Ellis, F. Fraternali, Hui-Chun Lu, 2014, Proteins.