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Wei-Li Di

Research Profile

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Fluorescence Resonance Energy Transfer

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Publications

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Claire A Scott; Shefali Rajpopat; Wei-Li Di
Harlequin ichthyosis: ABCA12 mutations underlie defective lipid transport, reduced protease regulation and skin-barrier dysfunction.
Diana C Blaydon; Matthew A Brooke; Rita M Cabral; Wei-Li Di; John I Harper; Dominic J Abrams; Paolo Biancheri; Keith Lindley; Thomas T MacDonald; Joanne E Martin; Edel A O'Toole; Vincent Plagnol; Franz Ruschendorf; Mark Toynbee; David A van Heel; Tom Vulliamy; Amanda Walne; David P Kelsell
Inflammatory skin and bowel disease linked to ADAM17 deletion.
Wei-Li Di; Yan Gu; John Common; Trond Aasen; Edel A O'Toole; David P Kelsell; Daniel Zicha
Connexin interaction patterns in keratinocytes revealed morphologically and by FRET analysis.

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All Publications

2013: Claire A Scott; Shefali Rajpopat; Wei-Li Di
Harlequin ichthyosis: ABCA12 mutations underlie defective lipid transport, reduced protease regulation and skin-barrier dysfunction.
Cell and tissue research 2013;351(2):281-8.
2011: Diana C Blaydon; Matthew A Brooke; Rita M Cabral; Wei-Li Di; John I Harper; Dominic J Abrams; Paolo Biancheri; Keith Lindley; Thomas T MacDonald; Joanne E Martin; Edel A O'Toole; Vincent Plagnol; Franz Ruschendorf; Mark Toynbee; David A van Heel; Tom Vulliamy; Amanda Walne; David P Kelsell
Inflammatory skin and bowel disease linked to ADAM17 deletion.
The New England journal of medicine 2011;365(16):1502-8.
2005: Wei-Li Di; Yan Gu; John Common; Trond Aasen; Edel A O'Toole; David P Kelsell; Daniel Zicha
Connexin interaction patterns in keratinocytes revealed morphologically and by FRET analysis.
Journal of cell science 2005;118(Pt 7):1505-14.
2004: Y Gu; Wei-Li Di; David P Kelsell; Daniel Zicha
Quantitative fluorescence resonance energy transfer (FRET) measurement with acceptor photobleaching and spectral unmixing.
Journal of microscopy 2004;215(Pt 2):162-73.
2004: John Common; Wei-Li Di; Derek Davies; David P Kelsell
Further evidence for heterozygote advantage of GJB2 deafness mutations: a link with cell survival.
Journal of medical genetics 2004;41(7):573-5.
2004: I Martha Skerrett; Wei-Li Di; Eileen M Kasperek; David P Kelsell; Bruce Nicholson
Aberrant gating, but a normal expression pattern, underlies the recessive phenotype of the deafness mutant Connexin26M34T.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2004;18(7):860-2.
2003: John Common; Wei-Li Di; Derek Davies; Helen Galvin; Irene M Leigh; Edel A O'Toole; David P Kelsell
Cellular mechanisms of mutant connexins in skin disease and hearing loss.
Cell communication & adhesion 2003;10(4-6):347-51.
2002: John Common; David Becker; Wei-Li Di; Irene M Leigh; Edel A O'Toole; David P Kelsell
Functional studies of human skin disease- and deafness-associated connexin 30 mutations.
Biochemical and biophysical research communications 2002;298(5):651-6.
2002: Wei-Li Di; James Monypenny; John Common; C T C Kennedy; Katalin A Holland; Irene M Leigh; Elizabeth L Rugg; Daniel Zicha; David P Kelsell
Defective trafficking and cell death is characteristic of skin disease-associated connexin 31 mutations.
Human molecular genetics 2002;11(17):2005-14.
2002: Irit Gottfried; Meytal Landau; Fabian Glaser; Wei-Li Di; Joseph Ophir; Barukh Mevorah; Nir Ben-Tal; David P Kelsell; Karen B Avraham
A mutation in GJB3 is associated with recessive erythrokeratodermia variabilis (EKV) and leads to defective trafficking of the connexin 31 protein.
Human molecular genetics 2002;11(11):1311-6.
2001: Wei-Li Di; Elizabeth L Rugg; Irene M Leigh; David P Kelsell
Multiple epidermal connexins are expressed in different keratinocyte subpopulations including connexin 31.
The Journal of investigative dermatology 2001;117(4):958-64.
2001: David P Kelsell; Wei-Li Di; MJ Houseman
Connexin mutations in skin disease and hearing loss.
American journal of human genetics 2001;68(3):559-68.
2001: Wei-Li Di; John Common; David P Kelsell
Connexin 26 expression and mutation analysis in epidermal disease.
Cell communication & adhesion 2001;8(4-6):415-8.
2001: MJ Houseman; Lucy A Ellis; Alistair T Pagnamenta; Wei-Li Di; S Rickard; AH Osborn; Hans-Henrik M Dahl; Graham Taylor; Maria Bitner-Glindzicz; W Reardon; Robert F Mueller; David P Kelsell
Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss.
Journal of medical genetics 2001;38(1):20-5.