T. Techanukul

发表

Loss-of-function FERMT1 mutations in kindler syndrome implicate a role for fermitin family homolog-1 in integrin activation.

J. McGrath, M. Parsons, S. Ussar, 2009, The American journal of pathology.

Rapp–Hodgkin and Hay–Wells ectodermal dysplasia syndromes represent a variable spectrum of the same genetic disorder

J. McGrath, S. Holden, F. Escande, 2010, British Journal of Dermatology.

Revertant mosaicism in recessive dystrophic epidermolysis bullosa.

J. McGrath, J. Mellerio, N. Nagy, 2010, The Journal of investigative dermatology.

HB-EGF induces COL7A1 expression in keratinocytes and fibroblasts: possible mechanism underlying allogeneic fibroblast therapy in recessive dystrophic epidermolysis Bullosa.

J. McGrath, J. Mellerio, N. Nagy, 2011, The Journal of investigative dermatology.

Ectodermal dysplasia‐skin fragility syndrome due to a new homozygous internal deletion mutation in the PKP1 gene

J. McGrath, D. Murrell, C. Chow, 2012, The Australasian journal of dermatology.

Stem cell and tissue engineering in breast reconstruction.

V. Lohsiriwat, T. Techanukul, Tanasit Techanukul, 2014, Gland surgery.

Novel and recurrent FERMT1 gene mutations in Kindler syndrome.

J. McGrath, M. Lens, A. Zlotogorski, 2011, Acta dermato-venereologica.

The molecular skin pathology of familial primary localized cutaneous amyloidosis

J. McGrath, A. South, N. Nagy, 2010, Experimental dermatology.

Molecular basis of EEC (ectrodactyly, ectodermal dysplasia, clefting) syndrome: five new mutations in the DNA‐binding domain of the TP63 gene and genotype–phenotype correlation

J. McGrath, J. Mellerio, D. Coman, 2010, The British journal of dermatology.

Enhancement of the proteomics workflow and application to stem cell characterisation

Tanasit Techanukul, T. Techanukul, Tanasit Techanukul, 2012 .

CE-based sample quality assessment prior to 2-D gel electrophoresis: towards the standardization of gel-based proteomics.

Tanasit Techanukul, Fiona Pereira, Judit M Nagy, 2010, Journal of separation science.

Comparison of two combinations of cyanine dyes for prelabelling and gel electrophoresis

J. Nagy, Amanda Wallington, J. Wheeler, 2009, Proteomics.

Mutations in AEC syndrome skin reveal a role for p63 in basement membrane adhesion, skin barrier integrity and hair follicle biology

J. McGrath, J. Mellerio, C. Pourreyron, 2012, The British journal of dermatology.

Common IL-31 gene haplotype associated with non-atopic eczema is not implicated in epidermolysis bullosa pruriginosa.

J. McGrath, N. Nagy, A. Tanaka, 2010, Acta dermato-venereologica.

Comparison of three commercially available DIGE analysis software packages: minimal user intervention in gel-based proteomics.

Tanasit Techanukul, Yunyi Kang, Judit M Nagy, 2009, Journal of proteome research.