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Links from PubMed

Items: 7

1.

A missense mutation in the type II hair keratin hHb3 is associated with monilethrix.

van Steensel MA, Steijlen PM, Bladergroen RS, Vermeer M, van Geel M.

J Med Genet. 2005 Mar;42(3):e19. No abstract available.

2.

Hair follicle-specific keratins and their diseases.

Schweizer J, Langbein L, Rogers MA, Winter H.

Exp Cell Res. 2007 Jun 10;313(10):2010-20. Epub 2007 Mar 14. Review.

PMID:
17428470
3.

A mutational hotspot in the 2B domain of human hair basic keratin 6 (hHb6) in monilethrix patients.

Korge BP, Healy E, Munro CS, P√ľnter C, Birch-Machin M, Holmes SC, Darlington S, Hamm H, Messenger AG, Rees JL, Traupe H.

J Invest Dermatol. 1998 Nov;111(5):896-9. Review.

4.

Hair shaft abnormalities in localized autosomal recessive hypotrichosis 2 and a review of other non-syndromic human alopecias.

Suga H, Tsunemi Y, Sugaya M, Shinkuma S, Akiyama M, Shimizu H, Sato S.

Acta Derm Venereol. 2011 Jun;91(4):486-8. doi: 10.2340/00015555-1095. Review. No abstract available.

5.

Keratins of the human hair follicle.

Langbein L, Schweizer J.

Int Rev Cytol. 2005;243:1-78. Review.

PMID:
15797458
6.

[Hair and genes: continuing progress].

Dereure O.

Ann Dermatol Venereol. 2010 Aug-Sep;137(8-9):576-7. doi: 10.1016/j.annder.2010.07.003. Epub 2010 Aug 21. Review. French. No abstract available.

PMID:
20804908
7.

Keratotic lesions in epidermolysis bullosa simplex with mottled pigmentation.

Yasukawa K, Sawamura D, Akiyama M, Motoda N, Shimizu H.

J Am Acad Dermatol. 2005 Jan;52(1):172-3. Review. No abstract available.

PMID:
15627110

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