PubMed (GeneRIF) for id: 126410

Year	Number of Results
2011	2
2012	1
2013	1
2015	1
2016	2
2017	1
2018	1
2019	1
2020	2
2021	1
2024	0

1

Impaired production of the skin barrier lipid acylceramide by CYP4F22 ichthyosis mutations.

Nohara T, Ohno Y, Kihara A. Nohara T, et al. J Dermatol Sci. 2021 Jan;101(1):69-71. doi: 10.1016/j.jdermsci.2020.10.003. Epub 2020 Oct 6. J Dermatol Sci. 2021. PMID: 33067036 No abstract available.

2

Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis (ARCI). Study of the CYP4F22 c.1303C>T founder mutation.

Esperón-Moldes U, Ginarte-Val M, Rodríguez-Pazos L, Fachal L, Martín-Santiago A, Vicente A, Jiménez-Gallo D, Guillén-Navarro E, Sampol LM, González-Enseñat MA, Vega A. Esperón-Moldes U, et al. PLoS One. 2020 Feb 18;15(2):e0229025. doi: 10.1371/journal.pone.0229025. eCollection 2020. PLoS One. 2020. PMID: 32069299 Free PMC article.

3

A Tunisian family with a novel mutation in the gene CYP4F22 for lamellar ichthyosis and co-occurrence of hearing loss in a child due to mutation in the SLC26A4 gene.

Sayeb M, Riahi Z, Laroussi N, Bonnet C, Romdhane L, Mkaouar R, Zaouak A, Marrakchi J, Abdessalem G, Messaoud O, Bouchniba O, Ghilane N, Mokni M, Besbes G, Yacoub-Youssef H, Petit C, Abdelhak S. Sayeb M, et al. Int J Dermatol. 2019 Dec;58(12):1439-1443. doi: 10.1111/ijd.14452. Epub 2019 Apr 25. Int J Dermatol. 2019. PMID: 31020658

4

Mutation update for CYP4F22 variants associated with autosomal recessive congenital ichthyosis.

Hotz A, Bourrat E, Küsel J, Oji V, Alter S, Hake L, Korbi M, Ott H, Hausser I, Zimmer AD, Fischer J. Hotz A, et al. Hum Mutat. 2018 Oct;39(10):1305-1313. doi: 10.1002/humu.23594. Epub 2018 Aug 7. Hum Mutat. 2018. PMID: 30011118

5

Two missense mutations in CYP4F22 in autosomal recessive congenital ichthyosis.

Feng C, Wang H, Lee M, Zhao J, Lin Z, Yang Y. Feng C, et al. Clin Exp Dermatol. 2017 Jan;42(1):98-100. doi: 10.1111/ced.12988. Epub 2016 Oct 13. Clin Exp Dermatol. 2017. PMID: 27735052 No abstract available.

6

Two Cases of Autosomal Recessive Congenital Ichthyosis due to CYP4F22 Mutations: Expanding the Genotype of Self-Healing Collodion Baby.

Noguera-Morel L, Feito-Rodríguez M, Maldonado-Cid P, García-Miñáur S, Kamsteeg EJ, González-Sarmiento R, De Lucas-Laguna R, Hernández-Martín A, Torrelo A. Noguera-Morel L, et al. Pediatr Dermatol. 2016 Mar-Apr;33(2):e48-51. doi: 10.1111/pde.12740. Epub 2015 Dec 9. Pediatr Dermatol. 2016. PMID: 26646773

7

Lamellar ichthyosis in a collodion baby caused by CYP4F22 mutations in a non-consanguineous family outside the Mediterranean.

Sugiura K, Takeichi T, Tanahashi K, Ito Y, Kosho T, Saida K, Uhara H, Okuyama R, Akiyama M. Sugiura K, et al. J Dermatol Sci. 2013 Nov;72(2):193-5. doi: 10.1016/j.jdermsci.2013.06.008. Epub 2013 Jun 28. J Dermatol Sci. 2013. PMID: 23871423 No abstract available.

8

CYP4F22 is highly expressed at the site and timing of onset of keratinization during skin development.

Sasaki K, Akiyama M, Yanagi T, Sakai K, Miyamura Y, Sato M, Shimizu H. Sasaki K, et al. J Dermatol Sci. 2012 Feb;65(2):156-8. doi: 10.1016/j.jdermsci.2011.12.006. Epub 2011 Dec 13. J Dermatol Sci. 2012. PMID: 22209317 No abstract available.

9

Finding homes for orphan cytochrome P450s: CYP4V2 and CYP4F22 in disease states.

Kelly EJ, Nakano M, Rohatgi P, Yarov-Yarovoy V, Rettie AE. Kelly EJ, et al. Mol Interv. 2011 Apr;11(2):124-32. doi: 10.1124/mi.11.2.10. Mol Interv. 2011. PMID: 21540472 Free PMC article. Review.

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