H. Liao

发表

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.

Analysis of the individual and aggregate genetic contributions of previously identified serine peptidase inhibitor Kazal type 5 (SPINK5), kallikrein-related peptidase 7 (KLK7), and filaggrin (FLG) polymorphisms to eczema risk.

C. Strobl, N. Klopp, T. Illig, 2008, The Journal of allergy and clinical immunology.

Filaggrin mutations are a major predisposing factor in childhood-onset adult-persistent atopic dermatitis

R. Trembath, N. Reynolds, J. Barker, 2006 .

Analysis of the individual and aggregate genetic contributions of previously identified SPINK 5 , KLK 7 and FLG polymorphisms to eczema risk

C. Strobl, N. Klopp, T. Illig, 2015 .

Mechanisms of Chemical Cooperative Carcinogenesis by Epidermal Langerhans Cells

R. Filler, R. Tigelaar, M. Girardi, 2014, The Journal of investigative dermatology.

Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis.

M. Akiyama, H. Shimizu, C. Palmer, 2007, The Journal of allergy and clinical immunology.

Prevalent and rare mutations in the gene encoding filaggrin cause ichthyosis vulgaris and predispose individuals to atopic dermatitis.

D. Goudie, Yiwei Zhao, A. Irvine, 2006, The Journal of investigative dermatology.

Filaggrin null alleles are not associated with psoriasis.

R. McManus, C. Palmer, R. Trembath, 2007, The Journal of investigative dermatology.

Filaggrin Null Alleles Are Not Associated with

R. Trembath, F. Capon, D. Kane, 2007 .

Development of Allele-Specific Therapeutic siRNA in Meesmann Epithelial Corneal Dystrophy

Jonathan E. Moore, A. Irvine, W. McLean, 2011, PloS one.

Recurrent mutation in keratin 17 in a large family with pachyonychia congenita type 2

S. Leachman, H. Liao, F. Smith, 2008, Archives of Dermatological Research.

A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita.

E. Lane, M. Fimiani, S. Leachman, 2007, Journal of dermatological science.

Development of allele-specific therapeutic siRNA for keratin 5 mutations in epidermolysis bullosa simplex.

V. Mcgilligan, C. Moore, Ildikó Szeverényi, 2011, The Journal of investigative dermatology.

Filaggrin mutations are genetic modifying factors exacerbating X-linked ichthyosis.

D. Goudie, W. McLean, G. Graham, 2007, The Journal of investigative dermatology.

Null mutations in the filaggrin gene (FLG) determine major susceptibility to early-onset atopic dermatitis that persists into adulthood.

C. Palmer, R. Trembath, N. Reynolds, 2007, The Journal of investigative dermatology.

Atopic dermatitis and skin disease Filaggrin null mutations and childhood atopic eczema : A population-based case-control study

H. Cordell, C. Relton, I. Wilson, 2022 .

A heterozygous frameshift mutation in the V1 domain of keratin 5 in a family with Dowling-Degos disease.

J. McGrath, Yiwei Zhao, W. McLean, 2007, The Journal of investigative dermatology.

Prevalent and low-frequency null mutations in the filaggrin gene are associated with early-onset and persistent atopic eczema.

H. Cordell, R. Trembath, C. Relton, 2008, The Journal of investigative dermatology.

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.

siRNA silencing of the mutant keratin 12 allele in corneal limbal epithelial cells grown from patients with Meesmann's epithelial corneal dystrophy.

G. Pellegrini, C. Walsh, A. Irvine, 2014, Investigative ophthalmology & visual science.

Allele-specific siRNA silencing for the common keratin 12 founder mutation in Meesmann epithelial corneal dystrophy.

Jonathan E. Moore, W. McLean, C. Moore, 2013, Investigative ophthalmology & visual science.

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

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

Filaggrin haploinsufficiency is highly penetrant and is associated with increased severity of eczema: further delineation of the skin phenotype in a prospective epidemiological study of 792 school children

H. Cordell, C. Relton, N. Reynolds, 2009, The British journal of dermatology.

Filaggrin loss‐of‐function variants are associated with atopic comorbidity in pediatric inflammatory bowel disease

H. Drummond, E. Nimmo, J. Satsangi, 2009, Inflammatory bowel diseases.

Filaggrin null mutations are associated with increased asthma severity in children and young adults.

Colin N A Palmer, C. Palmer, Yiwei Zhao, 2007, The Journal of allergy and clinical immunology.

Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergy

C. Wijmenga, G. Roberts, H. Cordell, 2011, The Journal of allergy and clinical immunology.

Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations.

N. Klopp, T. Illig, J. Ring, 2006, The Journal of allergy and clinical immunology.

The burden of disease associated with filaggrin mutations: a population-based, longitudinal birth cohort study.

M. Pembrey, G. Smith, C. Palmer, 2008, The Journal of allergy and clinical immunology.

The genetic basis of pachyonychia congenita.

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

Filaggrin null mutations are associated with increased asthma exacerbations in children and young adults

B. Lipworth, C. Palmer, S. Mukhopadhyay, 2008, Allergy.

Filaggrin null mutations and childhood atopic eczema: a population-based case-control study.

H. Cordell, Yiwei Zhao, A. Sandilands, 2008, The Journal of allergy and clinical immunology.