Literature DB >> 29904921

Identification of a novel substitution mutation (R103C) in the rod domain of the keratin 17 gene associated with pachyonychia congenita type 2.

Feras M Ghazawi1, Kimya Hassani-Ardakani1, Lisa Henriques1, Fatemeh Jafarian2.   

Abstract

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Year:  2018        PMID： 29904921     DOI： 10.1111/ijd.14082

Source DB:  PubMed          Journal:  Int J Dermatol        ISSN： 0011-9059            Impact factor:   2.736


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  4 in total

1.  KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies.

Authors:  Mine Koprulu; Muhammad Naeem; Gökhan Nalbant; Rana M Kamran Shabbir; Tariq Mahmood; Zele Huma; Sajid Malik; Aslıhan Tolun
Journal:  Eur J Hum Genet       Date:  2022-06-09       Impact factor: 4.246

2.  Distinctions in the Management, Patient Impact, and Clinical Profiles of Pachyonychia Congenita Subtypes.

Authors:  Albert G Wu; Shari R Lipner
Journal:  Skin Appendage Disord       Date:  2021-02-05

3.  A KRT6A and a Novel KRT16 Gene Mutations in Chinese Patients with Pachyonychia Congenita.

Authors:  Li Gong; Shuping Guo; Detong Wang; Ting Wang; Xiaoli Ren; Yuting Yuan; Hongzhou Cui
Journal:  Int J Gen Med       Date:  2021-03-17

4.  Silencing of keratin 17 by lentivirus-mediated short hairpin RNA inhibits the proliferation of PANC-1 human pancreatic cancer cells.

Authors:  Peng Chen; Zhengchao Shen; Xiaosan Fang; Guannan Wang; Xiaoming Wang; Jun Wang; Shihang Xi
Journal:  Oncol Lett       Date:  2020-03-20       Impact factor: 2.967
  4 in total

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