C. Munro

发表

Molecular genetics of the skin: the implications of understanding.

C. Munro, 2009, Clinical medicine.

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

Yang Liu, Sen Yang, Miao Sun, 2009, Nature Genetics.

Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema

Colin N A Palmer, Robert Gruber, C. Palmer, 2007, Nature Genetics.

Platelet and cardiac function in Darier's disease

T. McDonagh, R. Tait, C. Munro, 2001, Clinical and experimental dermatology.

ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class.

T. Strachan, P. Itin, D. Hohl, 1999, Human molecular genetics.

Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family

D. Kelsell, I. Leigh, C. Munro, 2000, European Journal of Human Genetics.

Genes, growth factors and acanthosis nigricans

G. Bellus, C. Munro, D. Torley, 2002, The British journal of dermatology.

Corrigendum: Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

S. Cichon, M. Nöthen, C. Bodemer, 2009, Nature Genetics.

The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing.

H. Kremer, J. Uitto, J. McGrath, 1999, American journal of human genetics.

Mutations in the SASPase gene (ASPRV1) are not associated with atopic eczema or clinically dry skin

J. Kudoh, C. Munro, A. Irvine, 2012, The Journal of investigative dermatology.

Cutaneous Mycobacterium kansasii infection: case report and review.

C. Munro, N. Levell, S. Pedler, 1995, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Refined genetic mapping of the darier locus to a <1-cM region of chromosome 12q24.1, and construction of a complete, high-resolution P1 artificial chromosome/bacterial artificial chromosome contig of the critical region.

A. Monaco, R. Cox, M. Lathrop, 1998, American journal of human genetics.

Hailey–Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca2+ pump

A. Monaco, H. Lehrach, J. Ramser, 2000 .

Safety and Efficacy of Combined High-Dose Treatment with Calcipotriol Ointment and Solution in Patients with Psoriasis

F. G. Larsen, K. Kragballe, P. V. D. van de Kerkhof, 2002, Dermatology.

Early death from cardiomyopathy in a family with autosomal dominant striate palmoplantar keratoderma and woolly hair associated with a novel insertion mutation in desmoplakin.

D. Kelsell, I. Leigh, C. Munro, 2006, The Journal of investigative dermatology.

Heterozygous null alleles in filaggrin contribute to clinical dry skin in young adults and the elderly.

C. Palmer, C. Munro, W. McLean, 2009, The Journal of investigative dermatology.

Localisation of a gene for Darier's disease.

T. Strachan, J. Rees, C. Munro, 1993, Human molecular genetics.

Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis

J. R. McMillan, J. McGrath, C. Cole, 2015, The British journal of 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.

Pachyonychia congenita type 2: abnormal dentition extending into adulthood

C. Munro, M. Hodgins, M. Zamiri, 2008, The British journal of dermatology.

Pachyonychia congenita: mutations and clinical presentations

C. Munro, 2001, The British journal of dermatology.

A mutation in the mucosal keratin K4 is associated with oral white sponge nevus

E. Lane, C. Munro, W. McLean, 1995, Nature Genetics.

Novel and recurrent mutations in the genes encoding keratins K6a, K16 and K17 in 13 cases of pachyonychia congenita.

G. Melino, A. Verloes, D. Hohl, 2001, The Journal of investigative dermatology.

A mutational hotspot in the 2B domain of human hair basic keratin 6 (hHb6) in monilethrix patients.

A. Messenger, E. Healy, J. Rees, 1998, The Journal of investigative dermatology.

Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: implications for protein structure and clinical phenotype.

D. Parry, A. Messenger, E. Healy, 1999, The Journal of investigative dermatology.

A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13.

E. Healy, J. Rees, C. Munro, 1995, Human molecular genetics.

Novel proline substitution mutations in keratin 16 in two cases of pachyonychia congenita type 1

J. Uitto, C. Coleman, C. Munro, 1999, The British journal of dermatology.

Mutations in keratin K9 in kindreds with epidermolytic palmoplantar keratoderma and epidemiology in Northern Ireland.

J. Uitto, K. Mckenna, C. Munro, 1998, The Journal of investigative dermatology.

Cross‐linked envelopes in nail plate in lamellar ichthyosis

D. Hohl, R. Rice, C. Munro, 2003, The British journal of dermatology.

Keratin 16 and keratin 17 mutations cause pachyonychia congenita

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

Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex.

E. Lane, D. Hohl, I. Leigh, 1997, The Journal of investigative dermatology.

The K veim response: still useful, still a puzzle.

C. Munro, D. Mitchell, 1987, Thorax.

Mutations in AQP5, encoding a water-channel protein, cause autosomal-dominant diffuse nonepidermolytic palmoplantar keratoderma.

D. Kelsell, K. Linton, V. Plagnol, 2013, American journal of human genetics.

Two families with Greither's syndrome caused by a keratin 1 mutation.

E. Lane, C. Munro, N. Wilson, 2005, Journal of the American Academy of Dermatology.

Linear lichen planus related to hepatitis C infection?

C. Munro, C. Jury, 2000, The British journal of dermatology.

The neuropsychiatric phenotype in Darier disease

L. A. Jones, K. Gordon-Smith, C. Munro, 2010, The British journal of dermatology.

Expression of the sarco/endoplasmic reticulum calcium ATPase type 2 and 3 isoforms in normal skin and Darier's disease

C. Munro, M. Hodgins, K. Authi, 2004, The British journal of dermatology.

The unexpectedly rapid response of fungal nail infection to short duration therapy.

C. Munro, S. Shuster, J. Rees, 1992, Acta dermato-venereologica.

Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family

D. Kelsell, I. Leigh, C. Munro, 2000, European Journal of Human Genetics.

Hailey-Hailey disease: identification of novel mutations in ATP2C1 and effect of missense mutation A528P on protein expression levels.

A. Hovnanian, C. Munro, K. Van Baelen, 2004, The Journal of investigative dermatology.

Hailey-Hailey disease: molecular and clinical characterization of novel mutations in the ATP2C1 gene.

A. Monaco, T. Strachan, R. Sudbrak, 2002, The Journal of investigative dermatology.

The route of rapid access of drugs to the distal nail plate.

C. Munro, S. Shuster, 1992, Acta dermato-venereologica.

[Cyclosporin A in atopic dermatitis: therapeutic effect and effect on allergic reactions are dissociated from each other].

C. Munro, S. Shuster, P. Friedmann, 1991, Wiener medizinische Wochenschrift.

Filaggrin null mutations are not a protective factor for acne vulgaris.

M. Tang, E. Lane, J. Common, 2011, The Journal of investigative dermatology.

Disorders of Keratinization

C. Munro, W. McLean, M. Judge, 2008 .

Acne

C. Munro, 1997, Journal of the Royal College of Physicians of London.

Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis

Colin N A Palmer, Ann Sergeant, Hans Bisgaard, 2006, Nature Genetics.

The clinical photography of Herbert Brown: a perspective on early 20th Century dermatology

C. Munro, C S Jury, T W Lucke, 2001, Clinical and experimental dermatology.

The Mode of Action of Cyclosporin

C. Munro, S. Shuster, P. Farr, 1990 .

Clinical and pathological features of pachyonychia congenita.

E. Lane, S. Leachman, S. Florell, 2005, The journal of investigative dermatology. Symposium proceedings.

Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease

N. Craddock, M. O’Donovan, A. Monaco, 1999, Nature Genetics.

Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pump.

A. Monaco, H. Lehrach, J. Ramser, 2000, Human molecular genetics.

The phenotype of Darier's disease: penetrance and expressivity in adults and children

C. Munro, 1992, The British journal of dermatology.

An acantholytic dyskeratotic epidermal naevus with other features of Darier's disease on the same side of the body

C. Munro, N. Cox, N. Cox, 1992, The British journal of dermatology.

Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43.

R. Houlston, M. Murdoch, D. Kelsell, 2001, American journal of human genetics.

Pyoderma gangrenosum associated with Behçet's syndrome--response to thalidomide.

C. Munro, N. Cox, 1988, Clinical and experimental dermatology.

Lichen nitidus presenting as palmoplantar hyperkeratosis and nail dystrophy

C. Munro, N. Cox, J. Marks, 1993, Clinical and experimental dermatology.

A Novel Mutation in the Keratin 13 Gene Causing Oral White Sponge Nevus

G. Melino, A. Terrinoni, C. Munro, 2001, Journal of dental research.

Mapping of the Darier's disease gene by serogenetic markers: results in two large British kindreds.

S. Mastana, C. Munro, S. Papiha, 1992, Annales de genetique.

Cyclosporin A in the treatment of lichen planus.

C. Munro, P. Friedmann, J. Marks, 1989, Archives of dermatology.

Relapse rates in moderately severe chronic psoriasis treated with cyclosporin A

C. Munro, S. Shuster, P. Friedmann, 1989, The British journal of dermatology.

Dermatological conditions of the foot and leg

C. Munro, K. Springett, T. Lucke, 2005 .

A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families.

E. Maestrini, A. Monaco, E. Calzolari, 1999, Human molecular genetics.

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.

Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris

S. Bale, D. Goudie, C. Munro, 2006, Nature Genetics.

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.

Successful treatment with oral alitretinoin in women of childbearing potential with Darier's disease

C. Munro, M. Zamiri, 2013, The British journal of dermatology.

Novel ATP2A2 mutations in a large sample of individuals with Darier disease

D. Grozeva, K. Gordon-Smith, E. Green, 2013, The Journal of dermatology.

Genetic epidemiology of Darier's disease: a population study  in the west of Scotland

C. Munro, S. Tavadia, E. Mortimer, 2002, The British journal of dermatology.

Linkage analyses in British pedigrees suggest a single locus for Darier disease and narrow the location to the interval between D12S105 and D12S129.

J. Weissenbach, R. Kucherlapati, E. Healy, 1994, Genomics.

The incidence and distribution of oral lesions in patients with Darier's disease

C. Munro, R. Macleod, 1991, British dental journal.

Symptomatic and asymptomatic salivary duct abnormalities in Darier's disease: a sialographic study.

C. Munro, R. Macleod, A. M. Adams, 1994, Dento maxillo facial radiology.

Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity

E. Healy, C. Munro, M. Birch-Machin, 1997, The British journal of 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.

Angiolymphoid hyperplasia with eosinophilia: successful treatment with pulsed dye laser using the double pulse technique

C. Munro, G. Gupta, 2000, The British journal of dermatology.

Inherited Acantholytic Disorders

C. Munro, M. Zamiri, 2016 .

Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma

G. Barton, M. Akiyama, H. Shimizu, 2012, Nature Genetics.

Treatment of psoriasis with intermittent short course cyclosporin (Neoral®). A multicentre study

C. Munro, P. Friedmann, M. J. Sumner, 1997, The British journal of dermatology.

Peripheral nerve blockade for biopsy of plantar skin

C. Munro, M. Zamiri, D. Wylie, 2010, The British journal of dermatology.

trans-dominant inhibition of connexin-43 by mutant connexin-26: implications for dominant connexin disorders affecting epidermal differentiation.

A. Taylor, J. Uitto, D. Paul, 2001, Journal of cell science.

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.

Nail and scalp lesions in a man with diabetes insipidus. Langerhans cell histiocytosis (LCH).

C. Munro, R. Morton, 1998, Archives of dermatology.

Severe lichen planus clears with very low‐dose cyclosporin

C. Munro, J. Marks, N. Levell, 1992, The British journal of dermatology.

An open and single-blind comparative assessment of unguentum cocois compound in the treatment of psoriasis of the scalp

C. Munro, C. Darley, B. Monk, 1995 .

Maintenance treatment with cyclosporin in atopic eczema

C. Munro, S. Shuster, P. Friedmann, 1994, The British journal of dermatology.

Systemic lupus erythematosus complicating complement type 2 deficiency: successful treatment with fresh frozen plasma

C. Munro, N. Simpson, J. Cox, 1997, The British journal of dermatology.

Post‐menopausal frontal fibrosing alopecia

C. Munro, G. Dawn, D. Moffat, 2003, Clinical and experimental dermatology.

Remission of ordinary psoriasis following a short clearance course of cyclosporin.

C. Munro, S. Shuster, P. Friedmann, 1995, Acta dermato-venereologica.

Mutation in DSG1 causing autosomal dominant striate palmoplantar keratoderma

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

Blistering, erosions and scarring in a patient on etretinate

C. Munro, B. Ramsay, J. Marks, 1989, The British journal of dermatology.

Multigeminate beard hairs and folliculitis

C. Munro, D. D. de Berker, L. Naysmith, 2001, The British journal of dermatology.

The genetic basis of pachyonychia congenita.

S. Leachman, C. Munro, W. McLean, 2005, The journal of investigative dermatology. Symposium proceedings.

A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.

T. Strachan, J. Rees, C. Munro, 1994, Journal of medical genetics.

An immunohistochemical analysis of human aortic fatty streaks.

J. D. van der Walt, C. Munro, J. M. Munro, 1987, Human pathology.

Novel mutations in the gene encoding secreted lymphocyte antigen-6/urokinase-type plasminogen activator receptor-related protein-1 (SLURP-1) and description of five ancestral haplotypes in patients with Mal de Meleda.

J. Prud'homme, D. Hohl, C. Munro, 2003, The Journal of investigative dermatology.

Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2

Munro, C. S. Coleman, R. Tenconi, 1998, The British journal of dermatology.

Contact Dermatitis In Divers

C. Munro, B. Wood, 2000 .

Erratum: Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis (Nature Genetics (2009) 41 (228-233))

S. Cichon, M. Nöthen, C. Bodemer, 2009 .

Novel ATP2A2 mutations in a large sample of individuals with Darier disease

D. Grozeva, K. Gordon-Smith, E. Green, 2013, The Journal of dermatology.