Keratin 12 missense mutation induces the unfolded protein response and apoptosis in Meesmann epithelial corneal dystrophy.

Tara Moore, Sarah Atkinson, Davide Schiroli, Andrew Nesbit

Research output: Contribution to journal › Article

3 Citations (Scopus)
LanguageEnglish
Pages1176-1191
JournalHuman Molecular Genetics
Volume25
Issue number6
DOIs
Publication statusPublished - 11 Jan 2016

Keywords

  • Meesmann Corneal Dystrophy
  • MECD mouse model

Cite this

Moore, Tara ; Atkinson, Sarah ; Schiroli, Davide ; Nesbit, Andrew. / Keratin 12 missense mutation induces the unfolded protein response and apoptosis in Meesmann epithelial corneal dystrophy. In: Human Molecular Genetics. 2016 ; Vol. 25, No. 6. pp. 1176-1191.
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Moore, T, Atkinson, S, Schiroli, D & Nesbit, A 2016, 'Keratin 12 missense mutation induces the unfolded protein response and apoptosis in Meesmann epithelial corneal dystrophy.', Human Molecular Genetics, vol. 25, no. 6, pp. 1176-1191. https://doi.org/10.1093/hmg/ddw001

Keratin 12 missense mutation induces the unfolded protein response and apoptosis in Meesmann epithelial corneal dystrophy. / Moore, Tara; Atkinson, Sarah; Schiroli, Davide; Nesbit, Andrew.

In: Human Molecular Genetics, Vol. 25, No. 6, 11.01.2016, p. 1176-1191.

Research output: Contribution to journal › Article

TY - JOUR

T1 - Keratin 12 missense mutation induces the unfolded protein response and apoptosis in Meesmann epithelial corneal dystrophy.

AU - Moore, Tara

AU - Atkinson, Sarah

AU - Schiroli, Davide

AU - Nesbit, Andrew

PY - 2016/1/11

Y1 - 2016/1/11

KW - Meesmann Corneal Dystrophy

KW - MECD mouse model

UR - https://pure.ulster.ac.uk/en/publications/keratin-12-missense-mutation-induces-the-unfolded-protein-respons-3

U2 - 10.1093/hmg/ddw001

DO - 10.1093/hmg/ddw001

M3 - Article

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EP - 1191

JO - Human Molecular Genetics

T2 - Human Molecular Genetics

JF - Human Molecular Genetics

SN - 0964-6906

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Moore T, Atkinson S, Schiroli D, Nesbit A. Keratin 12 missense mutation induces the unfolded protein response and apoptosis in Meesmann epithelial corneal dystrophy. Human Molecular Genetics. 2016 Jan 11;25(6):1176-1191. https://doi.org/10.1093/hmg/ddw001

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