Literature DB >> 25234742

Two novel mutations in the LOR gene in three families with loricrin keratoderma.

A Hotz1, E Bourrat, I Hausser, M Haftek, M V da Silva, J Fischer.   

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Year:  2015        PMID： 25234742     DOI： 10.1111/bjd.13414

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN： 0007-0963            Impact factor:   9.302


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  2 in total

1.  Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis.

Authors:  E Pohler; F Cunningham; A Sandilands; C Cole; S Digby; J R McMillan; S Aristodemou; J A McGrath; F J D Smith; W H I McLean; C S Munro; M Zamiri
Journal:  Br J Dermatol       Date:  2015-08-22       Impact factor: 9.302

2.  HNRNPK maintains epidermal progenitor function through transcription of proliferation genes and degrading differentiation promoting mRNAs.

Authors:  Jingting Li; Yifang Chen; Xiaojun Xu; Jackson Jones; Manisha Tiwari; Ji Ling; Ying Wang; Olivier Harismendy; George L Sen
Journal:  Nat Commun       Date:  2019-09-13       Impact factor: 14.919
  2 in total

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