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 *

185 related articles for article (PubMed ID: 24607543)

  • 1. Connexins: sensors of epidermal integrity that are therapeutic targets.
    Martin PE; Easton JA; Hodgins MB; Wright CS
    FEBS Lett; 2014 Apr; 588(8):1304-14. PubMed ID: 24607543
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Disease-linked connexin26 S17F promotes volar skin abnormalities and mild wound healing defects in mice.
    Press E; Alaga KC; Barr K; Shao Q; Bosen F; Willecke K; Laird DW
    Cell Death Dis; 2017 Jun; 8(6):e2845. PubMed ID: 28569788
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Connexin 26 (GJB2) mutations in two Swedish patients with atypical Vohwinkel (mutilating keratoderma plus deafness) and KID syndrome both extensively treated with acitretin.
    Bondeson ML; Nyström AM; Gunnarsson U; Vahlquist A
    Acta Derm Venereol; 2006; 86(6):503-8. PubMed ID: 17106596
    [TBL] [Abstract][Full Text] [Related]  

  • 4. From Hyperactive Connexin26 Hemichannels to Impairments in Epidermal Calcium Gradient and Permeability Barrier in the Keratitis-Ichthyosis-Deafness Syndrome.
    García IE; Bosen F; Mujica P; Pupo A; Flores-Muñoz C; Jara O; González C; Willecke K; Martínez AD
    J Invest Dermatol; 2016 Mar; 136(3):574-583. PubMed ID: 26777423
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel mutation in the connexin 26 gene (GJB2) in a child with clinical and histological features of keratitis-ichthyosis-deafness (KID) syndrome.
    Koppelhus U; Tranebjaerg L; Esberg G; Ramsing M; Lodahl M; Rendtorff ND; Olesen HV; Sommerlund M
    Clin Exp Dermatol; 2011 Mar; 36(2):142-8. PubMed ID: 20846357
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Keratitis-ichthyosis-deafness syndrome-associated Cx26 mutants produce nonfunctional gap junctions but hyperactive hemichannels when co-expressed with wild type Cx43.
    García IE; Maripillán J; Jara O; Ceriani R; Palacios-Muñoz A; Ramachandran J; Olivero P; Perez-Acle T; González C; Sáez JC; Contreras JE; Martínez AD
    J Invest Dermatol; 2015 May; 135(5):1338-1347. PubMed ID: 25625422
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic heterogeneity of KID syndrome: identification of a Cx30 gene (GJB6) mutation in a patient with KID syndrome and congenital atrichia.
    Jan AY; Amin S; Ratajczak P; Richard G; Sybert VP
    J Invest Dermatol; 2004 May; 122(5):1108-13. PubMed ID: 15140211
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Connexin-26 mutations in deafness and skin disease.
    Lee JR; White TW
    Expert Rev Mol Med; 2009 Nov; 11():e35. PubMed ID: 19939300
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Missense mutations in GJB2 encoding connexin-26 cause the ectodermal dysplasia keratitis-ichthyosis-deafness syndrome.
    Richard G; Rouan F; Willoughby CE; Brown N; Chung P; Ryynänen M; Jabs EW; Bale SJ; DiGiovanna JJ; Uitto J; Russell L
    Am J Hum Genet; 2002 May; 70(5):1341-8. PubMed ID: 11912510
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Altered cellular localization and hemichannel activities of KID syndrome associated connexin26 I30N and D50Y mutations.
    Aypek H; Bay V; Meşe G
    BMC Cell Biol; 2016 Feb; 17():5. PubMed ID: 26831144
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Connexin channels in congenital skin disorders.
    Lilly E; Sellitto C; Milstone LM; White TW
    Semin Cell Dev Biol; 2016 Feb; 50():4-12. PubMed ID: 26775130
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel connexin 26 mutation in a patient diagnosed with keratitis-ichthyosis-deafness syndrome.
    van Steensel MA; van Geel M; Nahuys M; Smitt JH; Steijlen PM
    J Invest Dermatol; 2002 Apr; 118(4):724-7. PubMed ID: 11918723
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The Cx26-G45E mutation displays increased hemichannel activity in a mouse model of the lethal form of keratitis-ichthyosis-deafness syndrome.
    Mese G; Sellitto C; Li L; Wang HZ; Valiunas V; Richard G; Brink PR; White TW
    Mol Biol Cell; 2011 Dec; 22(24):4776-86. PubMed ID: 22031297
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Extending the phenotypic spectrum of keratitis-ichthyosis-deafness syndrome: report of a patient with GJB2 (G12R) Connexin 26 mutation and unusual clinical findings.
    Lazic T; Li Q; Frank M; Uitto J; Zhou LH
    Pediatr Dermatol; 2012; 29(3):349-57. PubMed ID: 22011219
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The D50N mutation and syndromic deafness: altered Cx26 hemichannel properties caused by effects on the pore and intersubunit interactions.
    Sanchez HA; Villone K; Srinivas M; Verselis VK
    J Gen Physiol; 2013 Jul; 142(1):3-22. PubMed ID: 23797419
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pathological hemichannels associated with human Cx26 mutations causing Keratitis-Ichthyosis-Deafness syndrome.
    Levit NA; Mese G; Basaly MG; White TW
    Biochim Biophys Acta; 2012 Aug; 1818(8):2014-9. PubMed ID: 21933663
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel connexin 26 gene mutation associated with features of the keratitis-ichthyosis-deafness syndrome and the follicular occlusion triad.
    Montgomery JR; White TW; Martin BL; Turner ML; Holland SM
    J Am Acad Dermatol; 2004 Sep; 51(3):377-82. PubMed ID: 15337980
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Conserved glycine at position 45 of major cochlear connexins constitutes a vital component of the Ca²⁺ sensor for gating of gap junction hemichannels.
    Zhang Y; Hao H
    Biochem Biophys Res Commun; 2013 Jul; 436(3):424-9. PubMed ID: 23756814
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Differential susceptibility of Cx26 mutations associated with epidermal dysplasias to peptidoglycan derived from Staphylococcus aureus and Staphylococcus epidermidis.
    Donnelly S; English G; de Zwart-Storm EA; Lang S; van Steensel MA; Martin PE
    Exp Dermatol; 2012 Aug; 21(8):592-8. PubMed ID: 22643125
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [The perennial problem of keratinisation disorders].
    Dereure O
    Ann Dermatol Venereol; 2013 Mar; 140(3):240-1. PubMed ID: 23466163
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.