204 related articles for article (PubMed ID: 25050598)
1. Suppressing AP1 factor signaling in the suprabasal epidermis produces a keratoderma phenotype.
Rorke EA; Adhikary G; Young CA; Roop DR; Eckert RL
J Invest Dermatol; 2015 Jan; 135(1):170-180. PubMed ID: 25050598
[TBL] [Abstract][Full Text] [Related]
2. Vohwinkel syndrome, ichthyosiform variant--by Camisa--case report.
Corte LD; Silva MV; Oliveira CF; Vetoratto G; Steglich RB; Borges J
An Bras Dermatol; 2013; 88(6 Suppl 1):206-8. PubMed ID: 24346921
[TBL] [Abstract][Full Text] [Related]
3. A new variant of Vohwinkel syndrome: a case report.
Seirafi H; Khezri S; Morowati S; Kamyabhesari K; Mirzaeipour M; Khezri F
Dermatol Online J; 2011 Mar; 17(3):3. PubMed ID: 21426869
[TBL] [Abstract][Full Text] [Related]
4. Vohwinkel syndrome with mental retardation.
Mercy P; Singh A; Ghorpade AK; Das MN; Upadhyay A; Keswani N
Indian J Dermatol Venereol Leprol; 2013; 79(5):725. PubMed ID: 23974601
[No Abstract] [Full Text] [Related]
5. Loss of epidermal AP1 transcription factor function reduces filaggrin level, alters chemokine expression and produces an ichthyosis-related phenotype.
Young CA; Rorke EA; Adhikary G; Xu W; Eckert RL
Cell Death Dis; 2017 Jun; 8(6):e2840. PubMed ID: 28569792
[TBL] [Abstract][Full Text] [Related]
6. [Mutation analysis for GJB2 and LOR genes in two patients with Vohwinkel syndrome].
Liu YM; Gao XJ; Tian X; Li XM; Zhang XB
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Apr; 30(2):203-6. PubMed ID: 23568736
[TBL] [Abstract][Full Text] [Related]
7. Abnormal cornified cell envelope formation in mutilating palmoplantar keratoderma unrelated to epidermal differentiation complex.
Akiyama M; Christiano AM; Yoneda K; Shimizu H
J Invest Dermatol; 1998 Jul; 111(1):133-8. PubMed ID: 9665400
[TBL] [Abstract][Full Text] [Related]
8. Loricrin keratoderma: a novel disease entity characterized by nuclear accumulation of mutant loricrin.
Ishida-Yamamoto A
J Dermatol Sci; 2003 Feb; 31(1):3-8. PubMed ID: 12615358
[TBL] [Abstract][Full Text] [Related]
9. Low-dose isotretinoin prevents digital amputation in loricrin keratoderma (Vohwinkel syndrome with ichthyosis).
Nico MMS; Fernandes JD
J Dtsch Dermatol Ges; 2017 Jun; 15(6):665-667. PubMed ID: 28591443
[No Abstract] [Full Text] [Related]
10. A Deletion Mutation of the Connexin 26 (Gjb2) Gene in a Turkish Patient with Vohwinkel Syndrome .
Ozturk S; Can I; Eser B; Yazici H
Genet Couns; 2016; 27(2):187-91. PubMed ID: 29485809
[TBL] [Abstract][Full Text] [Related]
11. A novel missense mutation in GJB2, p.Tyr65His, causes severe Vohwinkel syndrome.
de Zwart-Storm EA; van Geel M; Veysey E; Burge S; Cooper S; Steijlen PM; Martin PE; van Steensel MA
Br J Dermatol; 2011 Jan; 164(1):197-9. PubMed ID: 20854437
[TBL] [Abstract][Full Text] [Related]
12. Vohwinkel syndrome: ichthyosiform variant in a family.
Reinehr CPH; Peruzzo J; Cestari T
An Bras Dermatol; 2018; 93(5):723-725. PubMed ID: 30156625
[TBL] [Abstract][Full Text] [Related]
13. Structural and functional consequences of loricrin mutations in human loricrin keratoderma (Vohwinkel syndrome with ichthyosis).
Schmuth M; Fluhr JW; Crumrine DC; Uchida Y; Hachem JP; Behne M; Moskowitz DG; Christiano AM; Feingold KR; Elias PM
J Invest Dermatol; 2004 Apr; 122(4):909-22. PubMed ID: 15102081
[TBL] [Abstract][Full Text] [Related]
14. G59S mutation in the GJB2 gene in a Chinese family with classic Vohwinkel syndrome.
Xie MX; Yang WP; Luo HJ; Ismail F; Hao YY; Yang JQ
J Dermatol; 2019 Feb; 46(2):154-157. PubMed ID: 30565282
[TBL] [Abstract][Full Text] [Related]
15. AP1 factor inactivation in the suprabasal epidermis causes increased epidermal hyperproliferation and hyperkeratosis but reduced carcinogen-dependent tumor formation.
Rorke EA; Adhikary G; Jans R; Crish JF; Eckert RL
Oncogene; 2010 Nov; 29(44):5873-82. PubMed ID: 20818430
[TBL] [Abstract][Full Text] [Related]
16. Keratins K2 and K10 are essential for the epidermal integrity of plantar skin.
Fischer H; Langbein L; Reichelt J; Buchberger M; Tschachler E; Eckhart L
J Dermatol Sci; 2016 Jan; 81(1):10-6. PubMed ID: 26603179
[TBL] [Abstract][Full Text] [Related]
17. Embryonic AP1 Transcription Factor Deficiency Causes a Collodion Baby-Like Phenotype.
Young CA; Eckert RL; Adhikary G; Crumrine D; Elias PM; Blumenberg M; Rorke EA
J Invest Dermatol; 2017 Sep; 137(9):1868-1877. PubMed ID: 28526300
[TBL] [Abstract][Full Text] [Related]
18. D66H mutation in GJB2 gene in a Chinese family with classical Vohwinkel syndrome.
Qiu Y; Wang Z; Chen N; Song Y; Wang Z; Zhang L
Indian J Dermatol Venereol Leprol; 2012; 78(5):640-2. PubMed ID: 22960825
[No Abstract] [Full Text] [Related]
19. [Vohwinkel syndrome. Hearing loss and keratoderma on the hands and feet].
Dippold S; Butsch F; Schopf R; Keilmann A
HNO; 2013 Jul; 61(7):617-9. PubMed ID: 23247752
[TBL] [Abstract][Full Text] [Related]
20. A novel c.545-546insG mutation in the loricrin gene correlates with a heterogeneous phenotype of loricrin keratoderma.
Song S; Shen C; Song G; Mao X; Yan G; Wang X; Yan M; Zhong N
Br J Dermatol; 2008 Sep; 159(3):714-9. PubMed ID: 18844868
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
