294 related articles for article (PubMed ID: 32147743)
1. Ichthyosis: A Road Model for Skin Research.
Vahlquist A; Törmä H
Acta Derm Venereol; 2020 Mar; 100(7):adv00097. PubMed ID: 32147743
[TBL] [Abstract][Full Text] [Related]
2. [Epidermal barrier - molecular structure and disorders in selected ichthyoses].
Śniegórska D; Kowalewski C; Wertheim-Tysarowska K
Postepy Biochem; 2016; 62(1):36-45. PubMed ID: 28132443
[TBL] [Abstract][Full Text] [Related]
3. Enlightened therapy of the disorders of cornification.
Williams ML; Elias PM
Clin Dermatol; 2003; 21(4):269-73. PubMed ID: 14572696
[No Abstract] [Full Text] [Related]
4. Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment.
Vahlquist A; Fischer J; Törmä H
Am J Clin Dermatol; 2018 Feb; 19(1):51-66. PubMed ID: 28815464
[TBL] [Abstract][Full Text] [Related]
5. Corneocyte lipid envelope (CLE), the key structure for skin barrier function and ichthyosis pathogenesis.
Akiyama M
J Dermatol Sci; 2017 Oct; 88(1):3-9. PubMed ID: 28623042
[TBL] [Abstract][Full Text] [Related]
6. Pharmacological treatments for cutaneous manifestations of inherited ichthyoses.
Cortés H; Del Prado-Audelo ML; Urbán-Morlán Z; Alcalá-Alcalá S; González-Torres M; Reyes-Hernández OD; González-Del Carmen M; Leyva-Gómez G
Arch Dermatol Res; 2020 May; 312(4):237-248. PubMed ID: 31624898
[TBL] [Abstract][Full Text] [Related]
7. Knockdown of SDR9C7 Impairs Epidermal Barrier Function.
Youssefian L; Niaziorimi F; Saeidian AH; South AP; Khosravi-Bachehmir F; Khodavaisy S; Vahidnezhad H; Uitto J
J Invest Dermatol; 2021 Jul; 141(7):1754-1764.e1. PubMed ID: 33422619
[TBL] [Abstract][Full Text] [Related]
8. Abnormal barrier function in the pathogenesis of ichthyosis: therapeutic implications for lipid metabolic disorders.
Elias PM; Williams ML; Feingold KR
Clin Dermatol; 2012; 30(3):311-22. PubMed ID: 22507046
[TBL] [Abstract][Full Text] [Related]
9. Genetics of Inherited Ichthyoses and Related Diseases.
Fischer J; Bourrat E
Acta Derm Venereol; 2020 Mar; 100(7):adv00096. PubMed ID: 32147747
[TBL] [Abstract][Full Text] [Related]
10. Keratinocytes cultured from subjects with ichthyosis vulgaris are phenotypically abnormal.
Fleckman P; Holbrook KA; Dale BA; Sybert VP
J Invest Dermatol; 1987 May; 88(5):640-5. PubMed ID: 2437218
[TBL] [Abstract][Full Text] [Related]
11. [Functional consequences of cutaneous lipid perturbation].
Humbert P
Pathol Biol (Paris); 2003 Jul; 51(5):271-4. PubMed ID: 14567193
[TBL] [Abstract][Full Text] [Related]
12. [Clinical presentation and etiology of ichthyoses. Overview of the new nomenclature and classification].
Oji V
Hautarzt; 2010 Oct; 61(10):891-902; quiz 903-4. PubMed ID: 20827455
[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. 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]
15. 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]
16. hiPSC-Derived Epidermal Keratinocytes from Ichthyosis Patients Show Altered Expression of Cornification Markers.
Lima Cunha D; Oram A; Gruber R; Plank R; Lingenhel A; Gupta MK; Altmüller J; Nürnberg P; Schmuth M; Zschocke J; Šarić T; Eckl KM; Hennies HC
Int J Mol Sci; 2021 Feb; 22(4):. PubMed ID: 33670118
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Pathophysiologic basis for growth failure in children with ichthyosis: an evaluation of cutaneous ultrastructure, epidermal permeability barrier function, and energy expenditure.
Moskowitz DG; Fowler AJ; Heyman MB; Cohen SP; Crumrine D; Elias PM; Williams ML
J Pediatr; 2004 Jul; 145(1):82-92. PubMed ID: 15238912
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. A spontaneous Fatp4/Scl27a4 splice site mutation in a new murine model for congenital ichthyosis.
Tao J; Koster MI; Harrison W; Moran JL; Beier DR; Roop DR; Overbeek PA
PLoS One; 2012; 7(11):e50634. PubMed ID: 23226340
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
