Literature DB >> 23154628

Genetics of structural hair disorders.

Sivan Harel1, Angela M Christiano.   

Abstract

The identification of causative genes carries the promise of new and innovative therapeutic strategies for both inherited and acquired hair disorders. Moreover, the delineation of the relationships between similar phenotypes, resulting from mutations affecting seemingly distinct regulatory pathways, paves the way to improved diagnosis and treatment. Finally, understanding the biological processes governing HF development and maintenance may have implications for more general disease processes in the skin, such as inflammation and cancer.

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Year:  2012        PMID： 23154628     DOI： 10.1038/skinbio.2012.7

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN： 0022-202X            Impact factor:   8.551


  6 in total

Review 1.  Drug discovery for alopecia: gone today, hair tomorrow.

Authors:  Zenildo Santos; Pinar Avci; Michael R Hamblin
Journal:  Expert Opin Drug Discov       Date:  2015-02-09       Impact factor: 6.098

2.  Hair keratin mutations in tooth enamel increase dental decay risk.

Authors:  Olivier Duverger; Takahiro Ohara; John R Shaffer; Danielle Donahue; Patricia Zerfas; Andrew Dullnig; Christopher Crecelius; Elia Beniash; Mary L Marazita; Maria I Morasso
Journal:  J Clin Invest       Date:  2014-10-27       Impact factor: 14.808

3.  A homozygous missense variant in type I keratin KRT25 causes autosomal recessive woolly hair.

Authors:  Muhammad Ansar; Syed Irfan Raza; Kwanghyuk Lee; Shamim Shahi; Anushree Acharya; Hang Dai; Joshua D Smith; Jay Shendure; Michael J Bamshad; Deborah A Nickerson; Regie Lyn P Santos-Cortez; Wasim Ahmad; Suzanne M Leal
Journal:  J Med Genet       Date:  2015-07-09       Impact factor: 6.318

4.  Somatic HRAS p.G12S mutation causes woolly hair and epidermal nevi.

Authors:  Jonathan L Levinsohn; Joyce Teng; Brittany G Craiglow; Erin C Loring; T Andrew Burrow; Shrikant S Mane; John D Overton; Richard P Lifton; Jennifer M McNiff; Anne W Lucky; Keith A Choate
Journal:  J Invest Dermatol       Date:  2013-10-15       Impact factor: 7.590

5.  Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss.

Authors:  Akira Oka; Atsushi Takagi; Etsuko Komiyama; Nagisa Yoshihara; Shuhei Mano; Kazuyoshi Hosomichi; Shingo Suzuki; Yuko Haida; Nami Motosugi; Tomomi Hatanaka; Minoru Kimura; Mahoko Takahashi Ueda; So Nakagawa; Hiromi Miura; Masato Ohtsuka; Masayuki Tanaka; Tomoyoshi Komiyama; Asako Otomo; Shinji Hadano; Tomotaka Mabuchi; Stephan Beck; Hidetoshi Inoko; Shigaku Ikeda
Journal:  EBioMedicine       Date:  2020-06-21       Impact factor: 8.143

6.  Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75.

Authors:  Ying Liu; Elizabeth R Snedecor; Xu Zhang; Yanfeng Xu; Lan Huang; Evan C Jones; Lianfeng Zhang; Richard A Clark; Dennis R Roop; Chuan Qin; Jiang Chen
Journal:  J Invest Dermatol       Date:  2016-01       Impact factor: 8.551
  6 in total

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