202 related articles for article (PubMed ID: 22258272)
21. Molecular basis of the skin barrier structures revealed by electron microscopy.
Ishida-Yamamoto A; Igawa S; Kishibe M
Exp Dermatol; 2018 Aug; 27(8):841-846. PubMed ID: 29704884
[TBL] [Abstract][Full Text] [Related]
22. An update on molecular aspects of the non-syndromic ichthyoses.
Akiyama M; Shimizu H
Exp Dermatol; 2008 May; 17(5):373-82. PubMed ID: 18341575
[TBL] [Abstract][Full Text] [Related]
23. Defects in Stratum Corneum Desquamation Are the Predominant Effect of Impaired ABCA12 Function in a Novel Mouse Model of Harlequin Ichthyosis.
Zhang L; Ferreyros M; Feng W; Hupe M; Crumrine DA; Chen J; Elias PM; Holleran WM; Niswander L; Hohl D; Williams T; Torchia EC; Roop DR
PLoS One; 2016; 11(8):e0161465. PubMed ID: 27551807
[TBL] [Abstract][Full Text] [Related]
24. Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans.
Heinz L; Kim GJ; Marrakchi S; Christiansen J; Turki H; Rauschendorf MA; Lathrop M; Hausser I; Zimmer AD; Fischer J
Am J Hum Genet; 2017 Jun; 100(6):926-939. PubMed ID: 28575648
[TBL] [Abstract][Full Text] [Related]
25. 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
Hum Mutat; 2018 Oct; 39(10):1305-1313. PubMed ID: 30011118
[TBL] [Abstract][Full Text] [Related]
26. [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]
27. Genetical, clinical, and functional analysis of a large international cohort of patients with autosomal recessive congenital ichthyosis due to mutations in NIPAL4.
Ballin N; Hotz A; Bourrat E; Küsel J; Oji V; Bouadjar B; Brognoli D; Hickman G; Heinz L; Vabres P; Marrakchi S; Leclerc-Mercier S; Irvine A; Tadini G; Hamm H; Has C; Blume-Peytavi U; Mitter D; Reitenbach M; Hausser I; Zimmer AD; Alter S; Fischer J
Hum Mutat; 2019 Dec; 40(12):2318-2333. PubMed ID: 31347739
[TBL] [Abstract][Full Text] [Related]
28. Patients with congenital ichthyosis and TGM1 mutations overexpress other ARCI genes in the skin: Part of a barrier repair response?
Zhang H; Ericsson M; Weström S; Vahlquist A; Virtanen M; Törmä H
Exp Dermatol; 2019 Oct; 28(10):1164-1171. PubMed ID: 30372788
[TBL] [Abstract][Full Text] [Related]
29. Epidermal barrier in disorders of the skin.
Fartasch M
Microsc Res Tech; 1997 Aug; 38(4):361-72. PubMed ID: 9297686
[TBL] [Abstract][Full Text] [Related]
30. Morphometric analysis of human epidermis treated with testosterone and dehydroepiandrosterone in organ culture.
Tammi R; Santti R
Arch Dermatol Res; 1989; 281(6):417-23. PubMed ID: 2480753
[TBL] [Abstract][Full Text] [Related]
31. Exploration of novel candidate genes involved in epidermal keratinocyte differentiation and skin barrier repair in man.
Zhang H; Weström S; Kappelin P; Virtanen M; Vahlquist A; Törmä H
Differentiation; 2021; 119():19-27. PubMed ID: 34029921
[TBL] [Abstract][Full Text] [Related]
32. NIPAL4 deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy.
Briand A; Cochet-Faivre N; Reyes-Gomez E; Jaraud-Darnault A; Tiret L; Chevallier L
Vet Med Sci; 2019 May; 5(2):112-117. PubMed ID: 30741495
[TBL] [Abstract][Full Text] [Related]
33. Disruption of the suprabasal keratin network by mutation M150T in the helix initiation motif of keratin 10 does not affect cornified cell envelope formation in human epidermis.
Akiyama M; Takizawa Y; Sawamura D; Matsuo I; Shimizu H
Exp Dermatol; 2003 Oct; 12(5):638-45. PubMed ID: 14705805
[TBL] [Abstract][Full Text] [Related]
34. High TMEM45A expression is correlated to epidermal keratinization.
Hayez A; Malaisse J; Roegiers E; Reynier M; Renard C; Haftek M; Geenen V; Serre G; Simon M; de Rouvroit CL; Michiels C; Poumay Y
Exp Dermatol; 2014 May; 23(5):339-44. PubMed ID: 24689342
[TBL] [Abstract][Full Text] [Related]
35. Pathogenesis of abnormal keratinization in ichthyosiform cetrimide dermatitis: an ultrastructural study.
Lee JY
Am J Dermatopathol; 1997 Apr; 19(2):162-7. PubMed ID: 9129701
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Hepatocyte growth factor activator inhibitor type 1 maintains the assembly of keratin into desmosomes in keratinocytes by regulating protease-activated receptor 2-dependent p38 signaling.
Kawaguchi M; Kanemaru A; Sawaguchi A; Yamamoto K; Baba T; Lin CY; Johnson MD; Fukushima T; Kataoka H
Am J Pathol; 2015 Jun; 185(6):1610-23. PubMed ID: 25842366
[TBL] [Abstract][Full Text] [Related]
38. Freeze-fracture cytochemical study of membrane systems in human epidermis using filipin as a probe for cholesterol.
Kitajima Y; Sekiya T; Mori S; Nozawa Y; Yaoita H
J Invest Dermatol; 1985 Feb; 84(2):149-53. PubMed ID: 2578531
[TBL] [Abstract][Full Text] [Related]
39. Functional expression of NF1 tumor suppressor protein: association with keratin intermediate filaments during the early development of human epidermis.
Malminen M; Peltonen S; Koivunen J; Peltonen J
BMC Dermatol; 2002 Aug; 2():10. PubMed ID: 12199909
[TBL] [Abstract][Full Text] [Related]
40. A Defect in NIPAL4 Is Associated with Autosomal Recessive Congenital Ichthyosis in American Bulldogs.
Casal ML; Wang P; Mauldin EA; Lin G; Henthorn PS
PLoS One; 2017; 12(1):e0170708. PubMed ID: 28122049
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
