Cited In for PMID: 7508181

Year	Number of Results
1994	4
1996	1
2000	1
2007	1
2010	1
2011	2
2015	2
2019	1
2020	1
2024	0

1

Preferential sites in keratin 10 that are mutated in epidermolytic hyperkeratosis.

Chipev CC, Yang JM, DiGiovanna JJ, Steinert PM, Marekov L, Compton JG, Bale SJ. Chipev CC, et al. Am J Hum Genet. 1994 Feb;54(2):179-90. Am J Hum Genet. 1994. PMID: 7508181 Free PMC article.

2

First Case of KRT2 Epidermolytic Nevus and Novel Clinical and Genetic Findings in 26 Italian Patients with Keratinopathic Ichthyoses.

Diociaiuti A, Castiglia D, Corbeddu M, Rotunno R, Rossi S, Pisaneschi E, Cesario C, Condorelli AG, Zambruno G, El Hachem M. Diociaiuti A, et al. Int J Mol Sci. 2020 Oct 18;21(20):7707. doi: 10.3390/ijms21207707. Int J Mol Sci. 2020. PMID: 33081034 Free PMC article.

3

Epidermolytic hyperkeratosis: clinical update.

Peter Rout D, Nair A, Gupta A, Kumar P. Peter Rout D, et al. Clin Cosmet Investig Dermatol. 2019 May 8;12:333-344. doi: 10.2147/CCID.S166849. eCollection 2019. Clin Cosmet Investig Dermatol. 2019. PMID: 31190940 Free PMC article. Review.

4

Mutations Affecting Keratin 10 Surface-Exposed Residues Highlight the Structural Basis of Phenotypic Variation in Epidermolytic Ichthyosis.

Mirza H, Kumar A, Craiglow BG, Zhou J, Saraceni C, Torbeck R, Ragsdale B, Rehder P, Ranki A, Choate KA. Mirza H, et al. J Invest Dermatol. 2015 Dec;135(12):3041-3050. doi: 10.1038/jid.2015.284. Epub 2015 Jun 15. J Invest Dermatol. 2015. PMID: 26176760 Free article.

5

Emerging roles of sumoylation in the regulation of actin, microtubules, intermediate filaments, and septins.

Alonso A, Greenlee M, Matts J, Kline J, Davis KJ, Miller RK. Alonso A, et al. Cytoskeleton (Hoboken). 2015 Jul;72(7):305-39. doi: 10.1002/cm.21226. Epub 2015 Aug 22. Cytoskeleton (Hoboken). 2015. PMID: 26033929 Free PMC article. Review.

6

Unique amino acid signatures that are evolutionarily conserved distinguish simple-type, epidermal and hair keratins.

Strnad P, Usachov V, Debes C, Gräter F, Parry DA, Omary MB. Strnad P, et al. J Cell Sci. 2011 Dec 15;124(Pt 24):4221-32. doi: 10.1242/jcs.089516. Epub 2012 Jan 3. J Cell Sci. 2011. PMID: 22215855 Free PMC article.

7

Keratin gene mutations in disorders of human skin and its appendages.

Chamcheu JC, Siddiqui IA, Syed DN, Adhami VM, Liovic M, Mukhtar H. Chamcheu JC, et al. Arch Biochem Biophys. 2011 Apr 15;508(2):123-37. doi: 10.1016/j.abb.2010.12.019. Epub 2010 Dec 19. Arch Biochem Biophys. 2011. PMID: 21176769 Free PMC article. Review.

8

Ichthyosis update: towards a function-driven model of pathogenesis of the disorders of cornification and the role of corneocyte proteins in these disorders.

Schmuth M, Gruber R, Elias PM, Williams ML. Schmuth M, et al. Adv Dermatol. 2007;23:231-56. doi: 10.1016/j.yadr.2007.07.011. Adv Dermatol. 2007. PMID: 18159904 Free PMC article. Review.

9

Head and/or CaaX domain deletions of lamin proteins disrupt preformed lamin A and C but not lamin B structure in mammalian cells.

Izumi M, Vaughan OA, Hutchison CJ, Gilbert DM. Izumi M, et al. Mol Biol Cell. 2000 Dec;11(12):4323-37. doi: 10.1091/mbc.11.12.4323. Mol Biol Cell. 2000. PMID: 11102526 Free PMC article.

10

The molecular basis for inherited bullous diseases.

Korge BP, Krieg T. Korge BP, et al. J Mol Med (Berl). 1996 Feb;74(2):59-70. doi: 10.1007/BF00196781. J Mol Med (Berl). 1996. PMID: 8820401 Review.

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