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 *

162 related articles for article (PubMed ID: 12711220)

  • 21. A mouse keratin 1 mutation causes dark skin and epidermolytic hyperkeratosis.
    McGowan KA; Aradhya S; Fuchs H; de Angelis MH; Barsh GS
    J Invest Dermatol; 2006 May; 126(5):1013-6. PubMed ID: 16528356
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Keratins and skin disorders.
    Lane EB; McLean WH
    J Pathol; 2004 Nov; 204(4):355-66. PubMed ID: 15495218
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Bullous congenital ichthyosiform erythroderma of Brocq; 2 patients with different phenotype and genotype].
    Lavrijsen AP; Bergman W; Steijlen PM
    Ned Tijdschr Geneeskd; 2001 Aug; 145(31):1527-8. PubMed ID: 11569466
    [No Abstract]   [Full Text] [Related]  

  • 24. A novel substitution in keratin 10 in epidermolytic hyperkeratosis.
    Arin MJ; Longley MA; Anton-Lamprecht I; Kurze G; Huber M; Hohl D; Rothnagel JA; Roop DR
    J Invest Dermatol; 1999 Apr; 112(4):506-8. PubMed ID: 10201536
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Epidermolytic hyperkeratosis and epidermolysis bullosa simplex caused by frameshift mutations altering the v2 tail domains of keratin 1 and keratin 5.
    Sprecher E; Yosipovitch G; Bergman R; Ciubutaro D; Indelman M; Pfendner E; Goh LC; Miller CJ; Uitto J; Richard G
    J Invest Dermatol; 2003 Apr; 120(4):623-6. PubMed ID: 12648226
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Use of laser capture microscopy in the analysis of mouse models of human diseases.
    Arin MJ; Roop DR
    Methods Enzymol; 2002; 356():207-15. PubMed ID: 12418199
    [No Abstract]   [Full Text] [Related]  

  • 28. The keratins and their disorders.
    Rugg EL; Leigh IM
    Am J Med Genet C Semin Med Genet; 2004 Nov; 131C(1):4-11. PubMed ID: 15452838
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The molecular genetics of keratin disorders.
    Smith F
    Am J Clin Dermatol; 2003; 4(5):347-64. PubMed ID: 12688839
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mild recessive epidermolytic hyperkeratosis associated with a novel keratin 10 donor splice-site mutation in a family of Norfolk terrier dogs.
    Credille KM; Barnhart KF; Minor JS; Dunstan RW
    Br J Dermatol; 2005 Jul; 153(1):51-8. PubMed ID: 16029326
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A mutational hot spot in keratin 10 (KRT 10) in patients with epidermolytic hyperkeratosis.
    Rothnagel JA; Fisher MP; Axtell SM; Pittelkow MR; Anton-Lamprecht I; Huber M; Hohl D; Roop DR
    Hum Mol Genet; 1993 Dec; 2(12):2147-50. PubMed ID: 7509230
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Epidermolytic hyperkeratosis.
    Bale SJ; Compton JG; DiGiovanna JJ
    Semin Dermatol; 1993 Sep; 12(3):202-9. PubMed ID: 7692917
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Gene targeting at the mouse cytokeratin 10 locus: severe skin fragility and changes of cytokeratin expression in the epidermis.
    Porter RM; Leitgeb S; Melton DW; Swensson O; Eady RA; Magin TM
    J Cell Biol; 1996 Mar; 132(5):925-36. PubMed ID: 8603923
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Epidermolytic hyperkeratosis: applied molecular genetics.
    DiGiovanna JJ; Bale SJ
    J Invest Dermatol; 1994 Mar; 102(3):390-4. PubMed ID: 7509838
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mutations of keratin 9 in two families with palmoplantar epidermolytic hyperkeratosis.
    Bonifas JM; Matsumura K; Chen MA; Berth-Jones J; Hutchison PE; Zloczower M; Fritsch PO; Epstein EH
    J Invest Dermatol; 1994 Oct; 103(4):474-7. PubMed ID: 7523529
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Molecular genetics of epidermolysis bullosa.
    Epstein EH
    Science; 1992 May; 256(5058):799-804. PubMed ID: 1375393
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Out of balance: consequences of a partial keratin 10 knockout.
    Reichelt J; Bauer C; Porter R; Lane E; Magin V
    J Cell Sci; 1997 Sep; 110 ( Pt 18)():2175-86. PubMed ID: 9378767
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Keratin transgenic and knockout mice: functional analysis and validation of disease-causing mutations.
    Vijayaraj P; Söhl G; Magin TM
    Methods Mol Biol; 2007; 360():203-51. PubMed ID: 17172732
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetic skin disorders of keratin.
    Fuchs E
    J Invest Dermatol; 1992 Dec; 99(6):671-4. PubMed ID: 1281858
    [No Abstract]   [Full Text] [Related]  

  • 40. Perinuclear eosinophilic bands: a clue to keratin gene mutation.
    El Shabrawi-Caelen L; McCalmont TH
    J Cutan Pathol; 2010 Jul; 37(7):718-9. PubMed ID: 20602663
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.