R. Eady

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Preimplantation genetic diagnosis of compound heterozygous mutations leading to ablation of plakophilin‐1 (PKP1) and resulting in skin fragility ectodermal dysplasia syndrome: a case report

J. McGrath, A. Thornhill, A. Handyside, 2000 .

Plectin defects in epidermolysis bullosa simplex with muscular dystrophy

E. Lane, J. R. McMillan, M. Akiyama, 2007, Muscle & nerve.

Genomic organization and amplification of the human keratin 15 and keratin 19 genes.

J. McGrath, N. Whittock, R. Eady, 2000, Biochemical and biophysical research communications.

Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome

E. Lane, J. R. McMillan, J. McGrath, 1997, Nature Genetics.

Gap junction development in the human fetal hair follicle and bulge region

J. R. McMillan, M. Akiyama, H. Shimizu, 2004, The British journal of dermatology.

Epidermolysis bullosa simplex (Dowling-Meara type) is a genetic disease characterized by an abnormal keratin-filament network involving keratins K5 and K14.

E. Lane, A. Ishida-Yamamoto, J. McGrath, 1991, The Journal of investigative dermatology.

Prenatal diagnosis for severe inherited skin disorders: 25 years' experience

K. Nicolaides, C. Rodeck, K. Nicolaides, 2006, The British journal of dermatology.

EEC (Ectrodactyly, Ectodermal dysplasia, Clefting) syndrome: heterozygous mutation in the p63 gene (R279H) and DNA‐based prenatal diagnosis

J. McGrath, C. Willoughby, R. Eady, 2002, The British journal of dermatology.

The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB.

E. Bauer, H. Shimizu, J. Uitto, 2008, Journal of the American Academy of Dermatology.

Epidermolysis Bullosa: Scientific Advances and Therapeutic Challenges

R. Eady, 2001, The Journal of dermatology.

Endothelial cell pathology as a marker for urticarial vasculitis: a light microscopic study

R. Eady, R. Eady, R. Jones, 1984, The British journal of dermatology.

Tn-MUC1 DC Vaccination of Rhesus Macaques and a Phase I/II Trial in Patients with Nonmetastatic Castrate-Resistant Prostate Cancer

J. Gariépy, L. Lacombe, A. Bergeron, 2016, Cancer Immunology Research.

Tn-MUC 1 DC Vaccination of Rhesus Macaques and a Phase I / II Trial in Patients with Non-Metastatic Castrate Resistant Prostate Cancer

J. Gariépy, L. Lacombe, A. Bergeron, 2016 .

Recent advances in the molecular basis of inherited skin diseases.

J. McGrath, R. Eady, 2001, Advances in genetics.

Compound heterozygosity for non-sense and mis-sense mutations in desmoplakin underlies skin fragility/woolly hair syndrome.

J. McGrath, A. Christiano, L. Pulkkinen, 2002, The Journal of investigative dermatology.

Erratum: Haploinsufficiency of desmoplakin causes a striate subtype of palmoplantar keratoderma (Human Molecular Genetics (1999) 8 (143-148))

I. Leigh, K. Mckenna, R. Eady, 1999 .

Bullous pemphigoid and cicatricial pemphigoid autoantibodies react with ultrastructurally separable epitopes on the BP180 ectodomain: evidence that BP180 spans the lamina lucida.

J. R. McMillan, J. Bonnetblanc, R. Eady, 1997, The Journal of investigative dermatology.

Adult-onset Still's disease. Twenty-year followup and further studies of patients with active disease.

G. Hughes, K. Elkon, R. Eady, 1982, Arthritis and rheumatism.

Mast cell population density, blood vessel density and histamine content in normal human skin

T. Marshall, R. Eady, T. Cowen, 1979, The British journal of dermatology.

Production of rabbit antibodies against carboxy-terminal epitopes encoded by bullous pemphigoid cDNA.

H. Shimizu, K. Cehrs, R. Eady, 1990, The Journal of investigative dermatology.

Human dermal microvasculature: II. Enzyme histochemical and cytochemical study

J. C. Higgins, R. Eady, J. C. Higgins, 1981, The British journal of dermatology.

A microscopic study of inflammatory reactions in human skin induced by histamine and compound 48/80.

R. Eady, A. Kennedy, M. James, 1982, The Journal of investigative dermatology.

Novel splice site mutation in keratin 1 underlies mild epidermolytic palmoplantar keratoderma in three kindreds.

D. Kelsell, I. Leigh, C. Munro, 2001, The Journal of investigative dermatology.

Ichthyosis bullosa of Siemens--a disease involving keratin 2e.

E. Lane, I. Leigh, R. Eady, 1994, The Journal of investigative dermatology.

Selective involvement of keratins K1 and K10 in the cytoskeletal abnormality of epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma).

E. Lane, A. Ishida-Yamamoto, J. McGrath, 1992, The Journal of investigative dermatology.

A mutation in the conserved helix termination peptide of keratin 5 in hereditary skin blistering

E. Lane, A. Ishida-Yamamoto, I. Leigh, 1992, Nature.

A keratin 14 ‘knockout’ mutation in recessive epidermolysis bullosa simplex resulting in less severe disease

E. Lane, R. Eady, N. West, 2000, The British journal of dermatology.

Genomic organization and amplification of the human epidermal type II keratin genes K1 and K5.

J. McGrath, N. Whittock, R. Eady, 2000, Biochemical and biophysical research communications.

Homozygous nonsense mutation in helix 2 of K14 causes severe recessive epidermolysis bullosa simplex

E. Lane, J. McGrath, R. Eady, 1998, Human mutation.

Recessive epidermolysis bullosa simplex associated with plectin mutations: infantile respiratory complications in two unrelated cases

E. Lane, J. R. McMillan, J. Uitto, 1997, The British journal of dermatology.

Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome.

J. McGrath, I. Leigh, R. Eady, 2004, The Journal of investigative dermatology.

New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ichthyosis bullosa of Siemens

J. McGrath, N. Whittock, R. Eady, 2001, The British journal of dermatology.

Epidermolysis bullosa simplex (Dowling‐Meara). A clinicopathological review

A. Ishida-Yamamoto, J. McGrath, R. Eady, 1992, The British journal of dermatology.

Keratin 16 and keratin 17 mutations cause pachyonychia congenita

E. Lane, T. Strachan, I. Leigh, 1995, Nature Genetics.

Cold urticaria with vasculitis: report of a case with light and electron microscopic, immunofluorescence and pharmacological studies

R. Eady, A. Black, R. Sibbald, 1981, Clinical and experimental dermatology.

Dissociation of histamine release and clinical improvement following treatment of acquired cold urticaria by prednisone.

R. Eady, A. Black, M. Greaves, 1981, British journal of clinical pharmacology.

The use of silver-enhanced 1-nm gold probes for light and electron microscopic localization of intra- and extracellular antigens in skin.

H. Shimizu, A. Ishida-Yamamoto, R. Eady, 1992, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization.

E. Lane, R. Ray, S. DeArmond, 1996, Genes & development.

Epidermolysis Bullosa: To Split and to Clump

R. Eady, 1992, Pediatric dermatology.

Current Perspectives and Differential Diagnosis in Epidermolysis Bullosa

R. Eady, 1992 .

Genomic amplification of the human plakophilin 1 gene and detection of a new mutation in ectodermal dysplasia/skin fragility syndrome.

J. McGrath, N. Whittock, R. Eady, 2000, The Journal of investigative dermatology.

A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in lethal (Herlitz) junctional epidermolysis bullosa.

J. R. McMillan, J. McGrath, J. Ortonne, 1995, Human molecular genetics.

α6β4 integrin abnormalities in junctional epidermolysis bullosa with pyloric atresia

J. McGrath, R. Eady, J. Mellerio, 2001 .

Morphology of the keratin filament network in palm and sole skin: Evidence for site-dependent features based on stereological analysis

R. Eady, O. Swensson, 1996, Archives of Dermatological Research.

Keratin expression in epidermolysis bullosa simplex (Dowling-Meara).

D. Macdonald, I. Leigh, R. Eady, 1988, Acta dermato-venereologica.

Blistering in keratinocyte cultures: a regular phenomenon associated with differentiation.

R. Eady, S. J. Chapman, 1986, European journal of cell biology.

Epidermolysis bullosa: preliminary observations of blister formation in keratinocyte cultures

I. Leigh, I. Leigh, R. Eady, 1984, The British journal of dermatology.

(8) Epidermolysis bullosa herpetiformis (Dowling‐Meara)

R. Eady, P. Coburn, M. Tidman, 1983 .

(6) Epidermolysis bullosa herpetiformis (Dowling‐Meara)

R. Eady, F. Wojnarowska, M. Tidman, 1983 .

Half‐and‐half cells in lichen planus

R. Eady, T. Cowen, R. Eady, 1978, The British journal of dermatology.

Diagnosis and diagnostic techniques

R. Eady, M. Tidman, 1990 .

Genotype–phenotype correlation in skin fragility‐ectodermal dysplasia syndrome resulting from mutations in plakophilin 1

J. McGrath, R. Eady, T. Hashimoto, 2002, Experimental dermatology.

Genomic organization and amplification of the human plakoglobin gene (JUP)

J. McGrath, N. Whittock, R. Eady, 2000, Experimental dermatology.

Oral and gastrointestinal manifestations of epidermolysis bullosa

J. McGrath, R. Eady, A. O'connor, 1992, The Lancet.

Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

E. Lane, D. Kelsell, J. R. McMillan, 1996, Nature Genetics.

The use of Michel's transport medium for immunofluorescence and immunoelectron microscopy in autoimmune bullous diseases

R. Eady, M. Black, B. Bhogal, 1995, Journal of cutaneous pathology.

Monoclonal antibody GB3 defines a widespread defect of several basement membranes and a keratinocyte dysfunction in patients with lethal junctional epidermolysis bullosa.

J. Ortonne, P. Verrando, R. Eady, 1991, Laboratory investigation; a journal of technical methods and pathology.

A functional "knockout" of human keratin 14.

E. Lane, J. R. McMillan, I. Leigh, 1994, Genes & development.

Familial urticaria pigmentosa with giant mast cell granules. A clinical, light, and electron microscopic study.

R. Eady, M. James, 1981, Archives of dermatology.

Cold urticaria: inhibition of cold-induced histamine release by doxantrazole.

R. Eady, M. Greaves, C. Bentley‐Phillips, 1978, The Journal of investigative dermatology.

INDUCTION OF CUTANEOUS VASCULITIS BY REPEATED COLD CHALLENGE IN COLD URTICARIA

R. Eady, M. Greaves, 1978, The Lancet.

Adenosine triphosphate-evoked vascular changes in human skin: mechanism of action.

G. Burnstock, R. Eady, J. Jorizzo, 1981, European journal of pharmacology.

Comparative mutation detection screening of the type VII collagen gene (COL7A1) using the protein truncation test, fluorescent chemical cleavage of mismatch, and conformation sensitive gel electrophoresis.

C. Mathew, J. McGrath, N. Whittock, 1999, The Journal of investigative dermatology.

Vascular responses of human skin to injection of substance P and mechanism of action.

R. Eady, J. Jorizzo, M. Greaves, 1983, European journal of pharmacology.

The basement membrane. Interface between the epithelium and the dermis: structural features.

R. Eady, 1988, Archives of dermatology.

The permeability of epidermis lacking normal membrane-coating granules: an ultrastructural tracer study of Kyrle-Flegel disease.

R. Eady, C. Squier, R. Hopps, 1978, The Journal of investigative dermatology.

Hemidesmosome ontogeny in digit skin of the human fetus

J. R. McMillan, R. Eady, J. McMillan, 1996, Archives of Dermatological Research.

Allelic heterogeneity of dominant and recessive COL7A1 mutations underlying epidermolysis bullosa pruriginosa.

J. McGrath, R. Eady, J. Mellerio, 1999, The Journal of investigative dermatology.

DISSOCIATIONOFHISTAMINERELEASEAND CLINICAL IMPROVEMENT FOLLOWING TREATMENT OFACQUIRED COLD URTICARIABY PREDNISONE

R. Eady, A. Black, M. Greaves, 1981 .

Treatment of acquired cold urticaria by prednisone: dissociation of histamine release and clinical improvement [proceedings].

R. Eady, G. Sibbald, A. Black, 1980, British journal of clinical pharmacology.

The surgical management of dystrophic epidermolysis bullosa (excluding the hand).

R. Eady, P. Terrill, B. Mayou, 1992, British journal of plastic surgery.

Heparan sulphate proteoglycan and wound healing in skin

J. McGrath, R. Eady, 1997, The Journal of pathology.

Epidermolysis bullosa pruriginosa: dystrophic epidermolysis bullosa with distinctive clinicopathological features

J. McGrath, R. Eady, O. Schofield, 1994, The British journal of dermatology.

Mitten deformity in severe generalized recessive dystrophic epidermolysis bullosa: histological, immunofluorescence, and ultrastructural study

J. McGrath, R. Eady, B. Mayou, 1992, Journal of cutaneous pathology.

Rapid processing of fetal skin for prenatal diagnosis by light and electron microscopy.

K. Nicolaides, C. Rodeck, R. Eady, 1984, Journal of clinical pathology.

Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentition.

J. R. McMillan, J. Uitto, J. McGrath, 1996, The American journal of pathology.

Evaluation of anchoring fibrils and other components of the dermal-epidermal junction in dystrophic epidermolysis bullosa by a quantitative ultrastructural technique.

R. Eady, M. Tidman, 1985, The Journal of investigative dermatology.

A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in Herlitz junctional epidermolysis bullosa: prenatal exclusion in a fetus at risk.

C. Rodeck, J. Uitto, J. McGrath, 1995, Genomics.

Genetic basis of lethal junctional epidermolysis bullosa in an affected fetus: Implications for prenatal diagnosis in one family

C. Rodeck, J. R. McMillan, J. Uitto, 1995, Prenatal diagnosis.

Hemidesmosome heterogeneity in junctional epidermolysis bullosa revealed by morphometric analysis.

R. Eady, M. Tidman, 1986, The Journal of investigative dermatology.

PRENATAL DIAGNOSIS OF EPIDERMOLYSIS BULLOSA LETALIS

C. Rodeck, R. Eady, C. Gosden, 1980, The Lancet.

Epidermolysis bullosa acquisita antigen and the carboxy terminus of type VII collagen have a common immunolocalization to anchoring fibrils and lamina densa of basement membrane

H. Shimizu, I. Leigh, I. Leigh, 1990, The British journal of dermatology.

Elevated blood histamine levels and mast cell degranulation in solar urticaria.

J. Hawk, R. Eady, M. Greaves, 1980, British journal of clinical pharmacology.

A new method for recovery of exudates from normal and inflamed human skin *

R. Eady, M. Greaves, C. Hensby, 1977, Clinical and experimental dermatology.

Desmosomes exhibit site‐specific features in human palm skin

J. McGrath, R. Eady, P. Dopping-Hepenstal, 2003, Experimental dermatology.

Alterations in desmosome size and number coincide with the loss of keratinocyte cohesion in skin with homozygous and heterozygous defects in the desmosomal protein plakophilin 1.

J. R. McMillan, M. Akiyama, H. Shimizu, 2003, The Journal of investigative dermatology.

Mutations in the 180–kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1), in generalized atrophic benign epidermolysis bullosa

J. R. McMillan, J. Uitto, J. McGrath, 1995, Nature Genetics.

Chapter 3 Anatomy and Organization of Human Skin

J. McGrath, R. Eady, F. M. Pope, 2004 .

Psoriasis bullosa acquisita

J. McGrath, R. Eady, T. Hashimoto, 2002, Clinical and experimental dermatology.

Demonstration of intra- and extracellular localization of bullous pemphigoid antigen using cryofixation and freeze substitution for postembedding immunoelectron microscopy

H. Shimizu, R. Eady, A. Kennedy, 2004, Archives of Dermatological Research.

Migratory Erythema and Eosinophilic Cellulitis associated with Nasopharyngeal Carcinoma 1

R. Eady, D. Murray, 1981, Journal of the Royal Society of Medicine.

Efficacy and safety of endoscopic dilation of esophageal strictures in epidermolysis bullosa.

K. N. Williams, R. Eady, L. Doig, 2004, Gastrointestinal endoscopy.

Oesophageal web formation in dystrophic epidermolysis bullosa

R. Eady, R. Marsden, R. Wells, 1988, Clinical and experimental dermatology.

Gross Hyperkeratosis of Palms and Soles, Pemphigoid and Epilepsy

R. Eady, J. Wilkinson, E. Moynahan, 1972, Proceedings of the Royal Society of Medicine.

Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification.

E. Bauer, H. Shimizu, J. Uitto, 2014, Journal of the American Academy of Dermatology.

Anatomy and Organization of Human Skin

J. McGrath, R. Eady, F. M. Pope, 2008 .

Prenatal diagnosis for inherited skin diseases.

J. McGrath, R. Eady, G. Ashton, 2000, Clinics in dermatology.

Dilemmas in distinguishing between dominant and recessive forms of dystrophic epidermolysis bullosa

J. McGrath, R. Eady, J. Mellerio, 2003, The British journal of dermatology.

Cultured keratinocyte allografts and wound healing in severe recessive dystrophic epidermolysis bullosa.

J. McGrath, I. Leigh, R. Eady, 1993, Journal of the American Academy of Dermatology.

Structural variations in anchoring fibrils in dystrophic epidermolysis bullosa: correlation with type VII collagen expression.

J. McGrath, I. Leigh, R. Eady, 1993, The Journal of investigative dermatology.

Epidermolysis bullosa simplex Dowling-Meara: troublesome blistering and pruritus in an adult patient.

J. McGrath, N. Burrows, R. Eady, 1993, Dermatology.

Intracellular expression of type VII collagen during wound healing in severe recessive dystrophic epidermolysis bullosa and normal human skin

J. McGrath, I. Leigh, I. Leigh, 1992, The British journal of dermatology.

GB3 monoclonal antibody for the diagnosis of junctional epidermolysis bullosa: results of a multicenter study.

J. Ortonne, P. Verrando, R. Eady, 1990, Journal of the American Academy of Dermatology.

Type VII collagen is a normal component of epidermal basement membrane, which shows altered expression in recessive dystrophic epidermolysis bullosa.

R. Burgeson, I. Leigh, R. Eady, 1988, The Journal of investigative dermatology.

Babes, blisters and basement membranes: from sticky molecules to epidermolysis bullosa

R. Eady, R. Eady, 1987, Clinical and experimental dermatology.

Identification of an epidermal basement membrane defect in recessive forms of dystrophic epidermolysis bullosa by LH 7:2 monoclonal antibody: use in diagnosis

I. Leigh, R. Eady, P. Purkis, 1986, The British journal of dermatology.

GB3 MONOCLONAL ANTIBODY FOR DIAGNOSIS OF JUNCTIONAL EPIDERMOLYSIS BULLOSA

J. Ortonne, P. Verrando, R. Eady, 1986, The Lancet.

Dystrophic epidermolysis bullosa presenting with congenital localized absence of skin: report of four cases

R. Eady, F. Wojnarowska, R. Wells, 1983, The British journal of dermatology.

Rapid prenatal diagnosis and exclusion of epidermolysis bullosa using novel antibody probes.

R. Eady, A. Heagerty, A. Kennedy, 1986, The Journal of investigative dermatology.

Squamous cell carcinoma as a complication of dystrophic epidermolysis bullosa.

R. Eady, D. Atherton, M. Tidman, 1984, Journal of the Royal Society of Medicine.

Prenatal diagnosis of bullous ichthyosiform erythroderma: detection of tonofilament clumps in fetal epidermal and amniotic fluid cells.

C. Rodeck, R. Eady, F. Bricarelli, 1986, Journal of medical genetics.

Haploinsufficiency of desmoplakin causes a striate subtype of palmoplantar keratoderma.

I. Leigh, K. Mckenna, R. Eady, 1999, Human molecular genetics.

Reduced expression of insulin-like growth factor-binding protein-3 (IGFBP-3) in Squamous cell carcinoma complicating recessive dystrophic epidermolysis bullosa.

J. McGrath, R. Eady, R. Mallipeddi, 2004, The Journal of investigative dermatology.

Three cases of de novo dominant dystrophic epidermolysis bullosa associated with the mutation G2043R in COL7A1

J. McGrath, R. Eady, J. Mellerio, 2001, Clinical and experimental dermatology.

Clinicopathological correlations of compound heterozygous COL7A1 mutations in recessive dystrophic epidermolysis bullosa.

J. Uitto, J. McGrath, A. Christiano, 1996, The Journal of investigative dermatology.

Increased risk of squamous cell carcinoma in junctional epidermolysis bullosa

J. McGrath, R. Eady, R. Mallipeddi, 2004, Journal of the European Academy of Dermatology and Venereology : JEADV.

Detection of a novel basement membrane antigen by GDA‐J/F3 anti‐human sperm fibrous sheath monoclonal antibody

I. Leigh, R. Eady, P. Purkis, 1991, The British journal of dermatology.

An unusual N-terminal deletion of the laminin alpha3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome.

Jonathan E. Moore, J. McGrath, C. Munro, 2003, Human molecular genetics.

Aquagenic pruritus.

R. Eady, A. Black, M. Greaves, 1981, British medical journal.

Melanocyte changes in epidermal hyperplasia--an experimental study.

R. Eady, R. Marks, 1973, British journal of experimental pathology.

Immunohistochemical analysis of the skin in junctional epidermolysis bullosa using laminin 5 chain specific antibodies is of limited value in predicting the underlying gene mutation

R. Burgeson, J. R. McMillan, J. McGrath, 1997, The British journal of dermatology.

Loricrin mutation in Vohwinkel's keratoderma is unique to the variant with ichthyosis.

H. Iizuka, C. Munro, R. Eady, 1997, The Journal of investigative dermatology.

Mutations in ABCA12 underlie the severe congenital skin disease harlequin ichthyosis.

D. Kelsell, E. Sprecher, C. Mein, 2005, American journal of human genetics.

Junctional epidermolysis bullosa

R. Eady, M. Tidman, 1990 .

Hemidesmosomes show abnormal association with the keratin filament network in junctional forms of epidermolysis bullosa.

J. R. McMillan, J. McGrath, R. Eady, 1998, The Journal of investigative dermatology.

The role of immunohistochemistry in the diagnosis of the non-lethal forms of junctional epidermolysis bullosa.

J. McGrath, R. Eady, J. McGrath, 1997, Journal of dermatological science.

First trimester DNA‐based exclusion of recessive dystrophic epidermolysis bullosa from chorionic villus sampling

C. Rodeck, J. Uitto, J. McGrath, 1996, The British journal of dermatology.

Altered laminin 5 expression due to mutations in the gene encoding the beta 3 chain (LAMB3) in generalized atrophic benign epidermolysis bullosa.

J. Uitto, J. McGrath, A. Christiano, 1995, The Journal of investigative dermatology.

Ultrastructural clues to genetic disorders of skin: the dermal-epidermal junction.

J. R. McMillan, J. McGrath, R. Eady, 1994, The Journal of investigative dermatology.

Nicein (BM-600) in junctional epidermolysis bullosa: polyclonal antibodies provide new clues for pathogenic role.

J. Ortonne, P. Verrando, R. Eady, 1993, The Journal of investigative dermatology.

PRENATAL DIAGNOSIS OF JUNCTIONAL EPIDERMOLYSIS BULLOSA

K. Nicolaides, C. Rodeck, R. Eady, 1989, The Lancet.

Monoclonal Antibody Techniques

D. Macdonald, R. Eady, R. Bauer, 1988 .

Rapid prenatal diagnosis of epidermolysis bullosa letalis using GB3 monoclonal antibody

C. Rodeck, J. Ortonne, R. Eady, 1987, The British journal of dermatology.

Abnormal binding of an anti‐amnion antibody to epidermal basement membrane provides a novel diagnostic probe for junctional epidermolysis bullosa

J. Ortonne, R. Eady, B. Hsi, 1985, The British journal of dermatology.

Human monoclonal anti‐basement membrane zone antibodies derived from virally transformed lymphocytes of a patient with bullous pemphigoid recognize epitopes associated with hemidesmosomes

H. Shimizu, T. Nishikawa, R. Eady, 1991, The British journal of dermatology.

Transient bullous dermolysis of the newborn: a disorder of type VII collagen secretion?

J. McGrath, R. Eady, O. Schofield, 1991 .

Transmission electron microscopy for the diagnosis of epidermolysis bullosa.

R. Eady, P. Dopping-Hepenstal, 2010, Dermatologic clinics.

Transmission Microscopy for the Diagnosis of Epidermolysis Bullosa

R. Eady, P. Dopping-Hepenstal, 2010 .

Oesophageal complications in epidermolysis bullosa.

S. Travis, R. P. Thompson, R. Eady, 1991, Gut.

Ultrastructural morphometry of normal human dermal-epidermal junction. The influence of age, sex, and body region on laminar and nonlaminar components.

R. Eady, M. Tidman, 1984, The Journal of investigative dermatology.

Linkage of autosomal dominant dystrophic epidermolysis bullosa in three British families to the marker D3S2 close to the COL7A1 locus.

M. Farrall, I. Leigh, R. Eady, 1992, Journal of medical genetics.

A recurrent laminin 5 mutation in British patients with lethal (Herlitz) junctional epidermolysis bullosa: evidence for a mutational hotspot rather than propagation of an ancestral allele

J. Uitto, J. McGrath, L. Pulkkinen, 1997, The British journal of dermatology.

Compound heterozygosity for nonsense ans missense mutations in the LAMB3 gene in nonlethal junctional epidermolysis bullosa.

J. Uitto, A. Christiano, L. Pulkkinen, 1996, The Journal of investigative dermatology.

(23) Junctional epidermolysis bullosa: a clinicopathological review of 30 patients

R. Eady, O. Schofield, M. Tidman, 1988 .

Non-lethal junctional epidermolysis bullosa in two adult sisters.

R. Eady, S. Bor, A. Heagerty, 1985, Journal of the Royal Society of Medicine.

Moderation of phenotypic severity in dystrophic and junctional forms of epidermolysis bullosa through in-frame skipping of exons containing non-sense or frameshift mutations.

J. R. McMillan, J. McGrath, R. Eady, 1999, The Journal of investigative dermatology.

Discovery of basement membrane zone ultrastructural entities by electron microscopy.

R. Eady, 2008, The Journal of investigative dermatology.

Discovery of Basement Membrane Zone Ultrastructural Entities by Electron Microscopy.

R. Eady, 2008, The Journal of investigative dermatology.

Genetic linkage to the type VII collagen gene (COL7A1) in 26 families with generalised recessive dystrophic epidermolysis bullosa and anchoring fibril abnormalities.

M. Farrall, I. Winship, R. Eady, 1994, Journal of medical genetics.

Prenatal Diagnosis of Genetic Skin Disease

J. McGrath, R. Eady, 2008 .

Prenatal diagnosis of genetic skin disease by fetoscopy and electron microscopy: report on 5 years' experience

K. Nicolaides, C. Rodeck, R. Eady, 1985 .

Mutations in the rod 1A domain of keratins 1 and 10 in bullous congenital ichthyosiform erythroderma (BCIE).

E. Lane, J. R. McMillan, I. Leigh, 1994, The Journal of investigative dermatology.

The pathology of the autologous serum skin test response in chronic urticaria resembles IgE-mediated late-phase reactions.

R. Winkelmann, R. Eady, C. Grattan, 1990, International archives of allergy and applied immunology.

Plasma immunoreactive melanotrophic hormones in patients on maintenance haemodialysis.

J. Moorhead, R. Eady, L. Rees, 1975, British medical journal.

Naevoid Pigmentation with Giant Melanosomes (Two Cases)

R. Eady, K. Grice, G. Sparrow, 1975, Proceedings of the Royal Society of Medicine.

An oculocerebral hypopigmentation syndrome: a case report with clinical, histochemical, and ultrastructural findings.

M. Patton, R. Eady, M. Baraitser, 1987, Journal of medical genetics.

Prenatal diagnosis of oculocutaneous albinism by electron microscopy of fetal skin.

C. Rodeck, A. Garner, R. Eady, 1983, The Journal of investigative dermatology.

A germline mutation in BLOC1S3/reduced pigmentation causes a novel variant of Hermansky-Pudlak syndrome (HPS8).

Colin A. Johnson, S. Watson, R. Trembath, 2006, American journal of human genetics.

Gene targeting at the mouse cytokeratin 10 locus: severe skin fragility and changes of cytokeratin expression in the epidermis

D. Melton, R. Eady, T. Magin, 1996, The Journal of cell biology.

Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratoderma

D. Kelsell, H. Hennies, I. Leigh, 2001, European Journal of Human Genetics.

N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratoderma.

D. Kelsell, I. Leigh, R. Eady, 1999, Human molecular genetics.

Loricrin immunoreactivity in human skin: localization to specific granules (L-granules) in acrosyringia

D. Hohl, D. Roop, H. Iizuka, 1993, Archives of Dermatological Research.

Frameshift mutation in the V2 domain of human keratin 1 results in striate palmoplantar keratoderma.

J. McGrath, N. Whittock, R. Eady, 2002, The Journal of investigative dermatology.

Mutant loricrin is not crosslinked into the cornified cell envelope but is translocated into the nucleus in loricrin keratoderma.

H. Takahashi, S. Nakamura, M. Kinouchi, 2000, The Journal of investigative dermatology.

Immunoelectron microscopic analysis of cornified cell envelope formation in normal and psoriatic epidermis.

F. Watt, D. Hohl, D. Roop, 1996, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Immunoelectron microscopy of skin basement membrane zone antigens: a pre-embedding method using 1-nm immunogold with silver enhancement.

H. Shimizu, J. McGrath, R. Eady, 1994, Acta dermato-venereologica.

Changes in Gap Junction Distribution and Connexin Expression Pattern During Human Fetal Skin Development

J. R. McMillan, M. Akiyama, H. Shimizu, 2002, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1).

M. Ramsay, T. Jenkins, J. McGrath, 2002, Human molecular genetics.

Photochemotherapy (PUVA) in the treatment of urticaria pigmentosa

R. Eady, S. Gatti, S. Bleehen, 1983, The British journal of dermatology.

Lack of plakophilin 1 increases keratinocyte migration and reduces desmosome stability

J. McGrath, I. Leigh, R. Eady, 2003, Journal of Cell Science.

Pseudopyogenic granuloma: the histopathogenesis in the light of ultrastructural studies

R. Eady, T. Cowen, E. WILSON JONES, 1976, The British journal of dermatology.

Identification of a novel mutation R42P in the gap junction protein beta-3 associated with autosomal dominant erythrokeratoderma variabilis.

D. Kelsell, I. Leigh, R. Eady, 1999, The Journal of investigative dermatology.

Sequential reorganization of cornified cell keratin filaments involving filaggrin-mediated compaction and keratin 1 deimination.

Hiroshi Shimizu, Hidetoshi Takahashi, Hajime Iizuka, 2002, The Journal of investigative dermatology.

Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome.

H. Feiler, E. Fuchs, A. Prescott, 2003, American journal of human genetics.

Desmosomal proteins, including desmoglein 3, serve as novel negative markers for epidermal stem cell-containing population of keratinocytes

R. Eady, J. Marshall, I. Hart, 2003, Journal of Cell Science.

A recurrent frameshift mutation in exon 19 of the type VII collagen gene (COL7A1) in Mexican patients with recessive dystrophic epidermolysis bullosa

J. McGrath, R. Eady, J. Mellerio, 1999, Experimental dermatology.

Striate palmoplantar keratoderma resulting from desmoplakin haploinsufficiency.

J. McGrath, N. Whittock, R. Eady, 1999, The Journal of investigative dermatology.

Naevus spilus: a light and electron microscopical study

R. Eady, T. Cowen, 1975 .

Alpha 6 beta 4 integrin abnormalities in junctional epidermolysis bullosa with pyloric atresia.

J. McGrath, R. Eady, J. Mellerio, 2001, The British journal of dermatology.

Pregnancy in epidermolysis bullosa

S. Bewley, J. McGrath, R. Eady, 2003 .

Recurrent mutations in the type VII collagen gene (COL7A1) in patients with recessive dystrophic epidermolysis bullosa.

J. Uitto, J. McGrath, A. Christiano, 1997, The Journal of investigative dermatology.

Common antigen expression between human periderm and other tissues identified by GB1-monoclonal antibody

J. Ortonne, R. Eady, D. Fredj-Reygrobellet, 2004, Archives of Dermatological Research.

A comparison of different lysis buffers to assess allele dropout from single cells for preimplantation genetic diagnosis

J. McGrath, A. Thornhill, A. Handyside, 2001, Prenatal diagnosis.

Cholinergic dermographism

R. Eady, A. Black, M. Greaves, 1986, The British journal of dermatology.

Aquagenic pruritus.

R. Eady, A. Black, M. Greaves, 1981, British medical journal.

Altered distribution of keratinization markers in epidermolytic hyperkeratosis

D. Hohl, D. Roop, H. Iizuka, 2005, Archives of Dermatological Research.

Mutation in DSG1 causing autosomal dominant striate palmoplantar keratoderma

L. Tetley, C. Munro, R. Eady, 2009, The British journal of dermatology.

A Germline Mutation in BLOC 1 S 3 / Reduced Pigmentation Causes a Novel Variant of Hermansky-Pudlak Syndrome ( HPS 8 )

Colin A. Johnson, S. Watson, R. Trembath, 2005 .

Severe palmo-plantar hyperkeratosis in Dowling-Meara epidermolysis bullosa simplex caused by a mutation in the keratin 14 gene (KRT14).

E. Lane, R. Eady, J. Mellerio, 1998, The Journal of investigative dermatology.

Ultrastructural changes resulting from keratin-9 gene mutations in two families with epidermolytic palmoplantar keratoderma.

E. Lane, I. Leigh, M. Shamsher, 1995, The Journal of investigative dermatology.

The first report of familial adult T‐cell leukaemia lymphoma in the United Kingdom

D. Catovsky, E. Matutes, N. Smith, 1995, British journal of haematology.

Cold urticaria and complement C2 deficiency.

R. Eady, M. Greaves, R. Sibbald, 1979, The British journal of dermatology.

Structural and functional properties of the dermoepidermal junction in obligate heterozygotes for recessive forms of epidermolysis bullosa.

R. Eady, M. Tidman, 1986, Archives of dermatology.

Revised classification system for inherited epidermolysis bullosa: Report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa.

E. Bauer, H. Shimizu, J. Uitto, 2000, Journal of the American Academy of Dermatology.

Ulcerative Lichen Planus Associated with Webbing of the Toes

R. Eady, T. Sonnex, B. Mayou, 1986, Journal of the Royal Society of Medicine.

Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa. A consensus report by the Subcommittee on Diagnosis and Classification of the National Epidermolysis Bullosa Registry.

E. Bauer, K. Holbrook, R. Pearson, 1991, Journal of the American Academy of Dermatology.

The gene for Naegeli-Franceschetti-Jadassohn syndrome maps to 17q21.

J. McGrath, N. Whittock, R. Eady, 2000, The Journal of investigative dermatology.

Heparan sulphate proteoglycan and wound healing in skin

J. McGrath, R. Eady, 1997, The Journal of pathology.

E210K mutation in the gene encoding the β3 chain of laminin‐5 (LAMB3) is predictive of a phenotype of generalized atrophic benign epidermolysis bullosa

R. Eady, J. Mellerio, Lake, 1998, The British journal of dermatology.

(37) Non‐lethal junctional epidermolysis bullosa

R. Eady, R. Marsden, M. Tidman, 1985 .

The mast cells distribution and morphology

R. Eady, R. Eady, 1976, Clinical and experimental dermatology.

Epidermal repair in lichen planus: a light and electron microscopical study *

R. Eady, T. Cowen, 1977, Clinical and experimental dermatology.

Summaries of papers

R. Vaughan, R. Eady, S. Challacombe, 1996 .