200 related articles for article (PubMed ID: 16250207)
21. A severe case of pachyonychia congenita type I due to a novel proline mutation in keratin 6a.
García-Rio I; Peñas PF; García-Díez A; McLean WH; Smith FJ
Br J Dermatol; 2005 Apr; 152(4):800-2. PubMed ID: 15840119
[No Abstract] [Full Text] [Related]
22. Identification of clinically useful predictive genetic variants in pachyonychia congenita.
Samuelov L; Sarig O; Adir N; Pavlovsky M; Smith FJ; Schwartz J; Hansen CD; Sprecher E
Clin Exp Dermatol; 2021 Jul; 46(5):867-873. PubMed ID: 33486795
[TBL] [Abstract][Full Text] [Related]
23. Identification of a recurrent mutation in keratin 6a in a patient with overlapping clinical features of pachyonychia congenita types 1 and 2.
Ward KM; Cook-Bolden FE; Christiano AM; Celebi JT
Clin Exp Dermatol; 2003 Jul; 28(4):434-6. PubMed ID: 12823309
[TBL] [Abstract][Full Text] [Related]
24. The phenotypic and molecular genetic features of pachyonychia congenita.
McLean WH; Hansen CD; Eliason MJ; Smith FJ
J Invest Dermatol; 2011 May; 131(5):1015-7. PubMed ID: 21430705
[TBL] [Abstract][Full Text] [Related]
25. [Type I pachyonychia congenita (Jadarssohn-Lewandowsky)].
Wimmershoff MB; Stolz W; Schiffner R; Landthaler M
Klin Padiatr; 1999; 211(3):179-83. PubMed ID: 10412130
[TBL] [Abstract][Full Text] [Related]
26. Keratin 17 mutation in pachyonychia congenita type 2 with early onset sebaceous cysts.
Feng YG; Xiao SX; Ren XR; Wang WQ; Liu A; Pan M
Br J Dermatol; 2003 Mar; 148(3):452-5. PubMed ID: 12653736
[TBL] [Abstract][Full Text] [Related]
27. Novel keratin 17 mutations in pachyonychia congenita type 2.
Smith FJ; Coleman CM; Bayoumy NM; Tenconi R; Nelson J; David A; McLean WH
J Invest Dermatol; 2001 May; 116(5):806-8. PubMed ID: 11348474
[TBL] [Abstract][Full Text] [Related]
28. Gene expression profiling in pachyonychia congenita skin.
Cao YA; Hickerson RP; Seegmiller BL; Grapov D; Gross MM; Bessette MR; Phinney BS; Flores MA; Speaker TJ; Vermeulen A; Bravo AA; Bruckner AL; Milstone LM; Schwartz ME; Rice RH; Kaspar RL
J Dermatol Sci; 2015 Mar; 77(3):156-65. PubMed ID: 25656049
[TBL] [Abstract][Full Text] [Related]
29. A new KRT16 mutation associated with a phenotype of pachyonychia congenita.
Paris F; Hurtado C; Azón A; Aguado L; Vizmanos JL
Exp Dermatol; 2013 Dec; 22(12):838-9. PubMed ID: 24118415
[TBL] [Abstract][Full Text] [Related]
30. Genotype‒Structurotype‒Phenotype Correlations in Patients with Pachyonychia Congenita.
Wu TT; Eldirany SA; Bunick CG; Teng JMC
J Invest Dermatol; 2021 Dec; 141(12):2876-2884.e4. PubMed ID: 34116063
[TBL] [Abstract][Full Text] [Related]
31. Identification of sporadic mutations in the helix initiation motif of keratin 6 in two pachyonychia congenita patients: further evidence for a mutational hot spot.
Lin MT; Levy ML; Bowden PE; Magro C; Baden L; Baden HP; Roop DR
Exp Dermatol; 1999 Apr; 8(2):115-9. PubMed ID: 10232401
[TBL] [Abstract][Full Text] [Related]
32. Pachyonychia congenita in pediatric patients: natural history, features, and impact.
Shah S; Boen M; Kenner-Bell B; Schwartz M; Rademaker A; Paller AS
JAMA Dermatol; 2014 Feb; 150(2):146-53. PubMed ID: 24132595
[TBL] [Abstract][Full Text] [Related]
33. Pachyonychia congenita. Immunohistologic findings.
Wollina U; Schaarschmidt H; Fünfstück V; Knopf B
Zentralbl Pathol; 1991; 137(4):372-5. PubMed ID: 1722707
[TBL] [Abstract][Full Text] [Related]
34. Keratin 17 expression in the hard epithelial context of the hair and nail, and its relevance for the pachyonychia congenita phenotype.
McGowan KM; Coulombe PA
J Invest Dermatol; 2000 Jun; 114(6):1101-7. PubMed ID: 10844551
[TBL] [Abstract][Full Text] [Related]
35. A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita.
Liao H; Sayers JM; Wilson NJ; Irvine AD; Mellerio JE; Baselga E; Bayliss SJ; Uliana V; Fimiani M; Lane EB; McLean WH; Leachman SA; Smith FJ
J Dermatol Sci; 2007 Dec; 48(3):199-205. PubMed ID: 17719747
[TBL] [Abstract][Full Text] [Related]
36. Keratins and skin disorders.
Lane EB; McLean WH
J Pathol; 2004 Nov; 204(4):355-66. PubMed ID: 15495218
[TBL] [Abstract][Full Text] [Related]
37. Pure hair-nail ectodermal dysplasia maps to chromosome 12p11.1-q21.1 in a consanguineous Pakistani family.
Naeem M; John P; Ali G; Ahmad W
Clin Exp Dermatol; 2007 Sep; 32(5):502-5. PubMed ID: 17489990
[TBL] [Abstract][Full Text] [Related]
38. [Pachyonychia congenita type 2 due to mutation in the keratin 6b gene].
Toth GG; Van Goor H; McLean WH; Jonkman MF
Ned Tijdschr Geneeskd; 2000 Aug; 144(32):1563-4. PubMed ID: 10979817
[No Abstract] [Full Text] [Related]
39. Overcoming functional redundancy to elicit pachyonychia congenita-like nail lesions in transgenic mice.
Wong P; Domergue R; Coulombe PA
Mol Cell Biol; 2005 Jan; 25(1):197-205. PubMed ID: 15601842
[TBL] [Abstract][Full Text] [Related]
40. [A de nono I462S mutation in the KRT6A gene is associated with pachyonychia congenita type I].
Kang XJ; Sun M; Yang W; Yu M; Ju Q; Lo WH; Xia LQ; Zhang X
Zhonghua Yi Xue Za Zhi; 2004 Aug; 84(16):1344-7. PubMed ID: 15387942
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]