These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

83 related articles for article (PubMed ID: 25644735)

  • 1. Novel TGM5 mutations in acral peeling skin syndrome.
    van der Velden JJ; van Geel M; Nellen RG; Jonkman MF; McGrath JA; Nanda A; Sprecher E; van Steensel MA; McLean WH; Cassidy AJ
    Exp Dermatol; 2015 Apr; 24(4):285-9. PubMed ID: 25644735
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome.
    Cassidy AJ; van Steensel MA; Steijlen PM; van Geel M; van der Velden J; Morley SM; Terrinoni A; Melino G; Candi E; McLean WH
    Am J Hum Genet; 2005 Dec; 77(6):909-17. PubMed ID: 16380904
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Acral peeling skin syndrome resulting from mutations in TGM5.
    Cañueto J; Bueno E; Rodríguez-Diaz E; Vicente-Díaz MA; Álvarez-Cuesta CC; Gonzalvo-Rodríguez P; González-Sarmiento R
    J Eur Acad Dermatol Venereol; 2016 Mar; 30(3):477-80. PubMed ID: 25510201
    [No Abstract]   [Full Text] [Related]  

  • 4. TGM5 mutations impact epidermal differentiation in acral peeling skin syndrome.
    Pigors M; Kiritsi D; Cobzaru C; Schwieger-Briel A; Suárez J; Faletra F; Aho H; Mäkelä L; Kern JS; Bruckner-Tuderman L; Has C
    J Invest Dermatol; 2012 Oct; 132(10):2422-2429. PubMed ID: 22622422
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Under-recognition of acral peeling skin syndrome: 59 new cases with 15 novel mutations.
    Szczecinska W; Nesteruk D; Wertheim-Tysarowska K; Greenblatt DT; Baty D; Browne F; Liu L; Ozoemena L; Terron-Kwiatkowski A; McGrath JA; Mellerio JE; Morton J; Woźniak K; Kowalewski C; Has C; Moss C
    Br J Dermatol; 2014 Nov; 171(5):1206-10. PubMed ID: 24628291
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis.
    Mohamad J; Nanda A; Pavlovsky M; Peled A; Malchin N; Malovitski K; Pramanik R; Weissglas-Volkov D; Shomron N; McGrath J; Sprecher E; Sarig O
    Exp Dermatol; 2020 Aug; 29(8):742-748. PubMed ID: 32618001
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A missense mutation in TGM5 causes acral peeling skin syndrome in a Tunisian family.
    Kharfi M; El Fekih N; Ammar D; Jaafoura H; Schwonbeck S; van Steensel MA; Fazaa B; Kamoun MR; Fischer J
    J Invest Dermatol; 2009 Oct; 129(10):2512-5. PubMed ID: 19440220
    [No Abstract]   [Full Text] [Related]  

  • 8. Acral peeling skin syndrome with TGM5 gene mutations may resemble epidermolysis bullosa simplex in young individuals.
    Kiritsi D; Cosgarea I; Franzke CW; Schumann H; Oji V; Kohlhase J; Bruckner-Tuderman L; Has C
    J Invest Dermatol; 2010 Jun; 130(6):1741-6. PubMed ID: 20164844
    [No Abstract]   [Full Text] [Related]  

  • 9. Acral peeling skin syndrome associated with a novel CSTA gene mutation.
    Muttardi K; Nitoiu D; Kelsell DP; O'Toole EA; Batta K
    Clin Exp Dermatol; 2016 Jun; 41(4):394-8. PubMed ID: 26684698
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Acral peeling skin syndrome: a clinically and genetically heterogeneous disorder.
    Pavlovic S; Krunic AL; Bulj TK; Medenica MM; Fong K; Arita K; McGrath JA
    Pediatr Dermatol; 2012; 29(3):258-63. PubMed ID: 22066523
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Acral peeling skin syndrome resembling epidermolysis bullosa simplex in a 10-month-old boy.
    Kavaklieva S; Yordanova I; Bruckner-Tuderman L; Has C
    Case Rep Dermatol; 2013; 5(2):210-4. PubMed ID: 24019772
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A recurrent mutation in the TGM5 gene in European patients with acral peeling skin syndrome.
    van der Velden JJ; Jonkman MF; McLean WH; Hamm H; Steijlen PM; van Steensel MA; van Geel M
    J Dermatol Sci; 2012 Jan; 65(1):74-6. PubMed ID: 22036214
    [No Abstract]   [Full Text] [Related]  

  • 13. Coincidence of acral peeling skin syndrome and Nagashima-type palmoplantar keratosis in a Japanese pedigree with acral skin peeling.
    Higashino T; Konomi M; Kubo A; Horinosono H; Miura Y
    J Dermatol; 2024 Aug; ():. PubMed ID: 39133571
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hypercalciuria in a child with acral peeling skin syndrome: a case report.
    Gorczyca D; Węgłowska J; Prescha A; Woźniak Z; Nesteruk D; Wertheim-Tysarowska K; Śmigiel R
    Acta Dermatovenerol Croat; 2015; 23(1):59-62. PubMed ID: 25969915
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Acral peeling skin syndrome resulting from a novel homozygous mutation in the CSTA gene-A report of two cases.
    Sarika GM; Ibrahim R; Zlotogorski A; Molho-Pessach V
    Pediatr Dermatol; 2021 Nov; 38(6):1546-1548. PubMed ID: 34713485
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Acral Peeling Skin Syndrome: A Case Report and Literature Review.
    Ruiz Rivero J; Campos Dominguez M; Parra Blanco V; Suárez Fernández R
    Actas Dermosifiliogr; 2016 Oct; 107(8):702-4. PubMed ID: 27206604
    [No Abstract]   [Full Text] [Related]  

  • 17. Acral peeling skin syndrome in two East-African siblings: case report.
    Kiprono SK; Chaula BM; Naafs B; Masenga JE
    BMC Dermatol; 2012 Mar; 12():2. PubMed ID: 22429841
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Peeling skin syndrome: genetic defects in late terminal differentiation of the epidermis.
    Bowden PE
    J Invest Dermatol; 2011 Mar; 131(3):561-4. PubMed ID: 21307953
    [TBL] [Abstract][Full Text] [Related]  

  • 19. SPINK5 and Netherton syndrome: novel mutations, demonstration of missing LEKTI, and differential expression of transglutaminases.
    Raghunath M; Tontsidou L; Oji V; Aufenvenne K; Schürmeyer-Horst F; Jayakumar A; Ständer H; Smolle J; Clayman GL; Traupe H
    J Invest Dermatol; 2004 Sep; 123(3):474-83. PubMed ID: 15304086
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Very mild lamellar ichthyosis with compound heterozygous TGM1 mutations including the novel missense mutation p.Leu693Phe.
    Sugiura K; Suga Y; Akiyama M
    J Dermatol Sci; 2013 Nov; 72(2):197-9. PubMed ID: 23895935
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.