202 related articles for article (PubMed ID: 22258272)
1. Ichthyin/NIPAL4 localizes to keratins and desmosomes in epidermis and Ichthyin mutations affect epidermal lipid metabolism.
Dahlqvist J; Westermark GT; Vahlquist A; Dahl N
Arch Dermatol Res; 2012 Jul; 304(5):377-86. PubMed ID: 22258272
[TBL] [Abstract][Full Text] [Related]
2. Interactions between FATP4 and ichthyin in epidermal lipid processing may provide clues to the pathogenesis of autosomal recessive congenital ichthyosis.
Li H; Vahlquist A; Törmä H
J Dermatol Sci; 2013 Mar; 69(3):195-201. PubMed ID: 23290633
[TBL] [Abstract][Full Text] [Related]
3. Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis.
Dahlqvist J; Klar J; Hausser I; Anton-Lamprecht I; Pigg MH; Gedde-Dahl T; Gånemo A; Vahlquist A; Dahl N
J Med Genet; 2007 Oct; 44(10):615-20. PubMed ID: 17557927
[TBL] [Abstract][Full Text] [Related]
4. Autosomal Recessive Congenital Ichthyosis in American Bulldogs Is Associated With NIPAL4 (ICHTHYIN) Deficiency.
Mauldin EA; Wang P; Evans E; Cantner CA; Ferracone JD; Credille KM; Casal ML
Vet Pathol; 2015 Jul; 52(4):654-62. PubMed ID: 25322746
[TBL] [Abstract][Full Text] [Related]
5. The expression of epidermal lipoxygenases and transglutaminase-1 is perturbed by NIPAL4 mutations: indications of a common metabolic pathway essential for skin barrier homeostasis.
Li H; Loriè EP; Fischer J; Vahlquist A; Törmä H
J Invest Dermatol; 2012 Oct; 132(10):2368-2375. PubMed ID: 22622417
[TBL] [Abstract][Full Text] [Related]
6. NIPAL4/ichthyin is expressed in the granular layer of human epidermis and mutated in two Pakistani families with autosomal recessive ichthyosis.
Wajid M; Kurban M; Shimomura Y; Christiano AM
Dermatology; 2010; 220(1):8-14. PubMed ID: 20016120
[TBL] [Abstract][Full Text] [Related]
7. Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)-Deficient Canines.
Mauldin EA; Crumrine D; Casal ML; Jeong S; Opálka L; Vavrova K; Uchida Y; Park K; Craiglow B; Choate KA; Shin KO; Lee YM; Grove GL; Wakefield JS; Khnykin D; Elias PM
Am J Pathol; 2018 Jun; 188(6):1419-1429. PubMed ID: 29548991
[TBL] [Abstract][Full Text] [Related]
8. Decreased Skin Barrier Lipid Acylceramide and Differentiation-Dependent Gene Expression in Ichthyosis Gene Nipal4-Knockout Mice.
Honda Y; Kitamura T; Naganuma T; Abe T; Ohno Y; Sassa T; Kihara A
J Invest Dermatol; 2018 Apr; 138(4):741-749. PubMed ID: 29174370
[TBL] [Abstract][Full Text] [Related]
9. Reduced stratum corneum acylceramides in autosomal recessive congenital ichthyosis with a NIPAL4 mutation.
Murase Y; Takeichi T; Kawamoto A; Tanahashi K; Okuno Y; Takama H; Shimizu E; Ishikawa J; Ogi T; Akiyama M
J Dermatol Sci; 2020 Jan; 97(1):50-56. PubMed ID: 31836270
[TBL] [Abstract][Full Text] [Related]
10. Vitamin C enhances differentiation of a continuous keratinocyte cell line (REK) into epidermis with normal stratum corneum ultrastructure and functional permeability barrier.
Pasonen-Seppänen S; Suhonen TM; Kirjavainen M; Suihko E; Urtti A; Miettinen M; Hyttinen M; Tammi M; Tammi R
Histochem Cell Biol; 2001 Oct; 116(4):287-97. PubMed ID: 11702187
[TBL] [Abstract][Full Text] [Related]
11. Cornified cell envelope proteins and keratins are normally distributed in harlequin ichthyosis.
Akiyama M; Yoneda K; Kim SY; Koyama H; Shimizu H
J Cutan Pathol; 1996 Dec; 23(6):571-5. PubMed ID: 9001990
[TBL] [Abstract][Full Text] [Related]
12. Striate palmoplantar keratoderma arising from desmoplakin and desmoglein 1 mutations is associated with contrasting perturbations of desmosomes and the keratin filament network.
Wan H; Dopping-Hepenstal PJ; Gratian MJ; Stone MG; Zhu G; Purkis PE; South AP; Keane F; Armstrong DK; Buxton RS; McGrath JA; Eady RA
Br J Dermatol; 2004 May; 150(5):878-91. PubMed ID: 15149499
[TBL] [Abstract][Full Text] [Related]
13. Inherited disorders of corneocyte proteins.
Elias PM; Williams ML; Crumrine D; Schmuth M
Curr Probl Dermatol; 2010; 39():98-131. PubMed ID: 20838039
[No Abstract] [Full Text] [Related]
14. The roles of ABCA12 in epidermal lipid barrier formation and keratinocyte differentiation.
Akiyama M
Biochim Biophys Acta; 2014 Mar; 1841(3):435-40. PubMed ID: 23954554
[TBL] [Abstract][Full Text] [Related]
15. Epidermal growth factor and temperature regulate keratinocyte differentiation.
Ponec M; Gibbs S; Weerheim A; Kempenaar J; Mulder A; Mommaas AM
Arch Dermatol Res; 1997 May; 289(6):317-26. PubMed ID: 9209676
[TBL] [Abstract][Full Text] [Related]
16. Diseases of epidermal keratins and their linker proteins.
Uitto J; Richard G; McGrath JA
Exp Cell Res; 2007 Jun; 313(10):1995-2009. PubMed ID: 17531221
[TBL] [Abstract][Full Text] [Related]
17. PNPLA1 defects in patients with autosomal recessive congenital ichthyosis and KO mice sustain PNPLA1 irreplaceable function in epidermal omega-O-acylceramide synthesis and skin permeability barrier.
Pichery M; Huchenq A; Sandhoff R; Severino-Freire M; Zaafouri S; Opálka L; Levade T; Soldan V; Bertrand-Michel J; Lhuillier E; Serre G; Maruani A; Mazereeuw-Hautier J; Jonca N
Hum Mol Genet; 2017 May; 26(10):1787-1800. PubMed ID: 28369476
[TBL] [Abstract][Full Text] [Related]
18. Proteomic analysis of desmosomes reveals novel components required for epidermal integrity.
Badu-Nkansah KA; Lechler T
Mol Biol Cell; 2020 May; 31(11):1140-1153. PubMed ID: 32238101
[TBL] [Abstract][Full Text] [Related]
19. Subcellular distribution of envoplakin and periplakin: insights into their role as precursors of the epidermal cornified envelope.
DiColandrea T; Karashima T; Määttä A; Watt FM
J Cell Biol; 2000 Oct; 151(3):573-86. PubMed ID: 11062259
[TBL] [Abstract][Full Text] [Related]
20. Corneocyte desquamation.
Pierard GE; Goffin V; Hermanns-Le T; Pierard-Franchimont C
Int J Mol Med; 2000 Aug; 6(2):217-21. PubMed ID: 10891569
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
