Citations for
1KRT16
Keratin and filaggrin expression in keratoacanthoma.
Ito Y, Kurokawa I, Nishimura K, Hakamada A, Isoda K, Yamanaka K, Tsubura A, Mizutani H.
J Eur Acad Dermatol Venereol 22(3):353-5. Epub 2007 Nov 12. 2008
2KRT6A, KRT16, KRT17
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 48(3):199-205. Epub 2007 Aug 24. 2007
3KRT1, KRT10, KRT12, KRT13, KRT14, KRT14P, KRT15, KRT16, KRT17, KRT17P3, KRT18, KRT18P12, KRT18P16, KRT18P17, KRT18P18, KRT18P19, KRT18P20, KRT18P21, KRT18P22, KRT18P23, KRT18P24, KRT18P25, KRT18P26, KRT18P27, KRT18P28, KRT18P29, KRT18P30, KRT18P31, KRT18P32, KRT18P33, KRT18P34, KRT18P35, KRT18P36, KRT18P37, KRT18P38, KRT18P39, KRT18P40, KRT18P41, KRT18P42, KRT18P43, KRT18P44, KRT18P45, KRT18P46, KRT18P47, KRT18P48, KRT18P49, KRT18P5, KRT18P50, KRT18P8, KRT19, KRT19P1, KRT19P2, KRT19P3, KRT2, KRT20, KRT222, KRT23, KRT24, KRT25, KRT26, KRT27, KRT28, KRT3, KRT31, KRT32, KRT33, KRT33A, KRT34, KRT35, KRT36, KRT37, KRT38, KRT39, KRT4, KRT40, KRT5, KRT6A, KRT6B, KRT6C, KRT7, KRT71, KRT72, KRT73, KRT74, KRT75, KRT76, KRT77, KRT78, KRT79, KRT8, KRT80, KRT81, KRT82, KRT83, KRT84, KRT85, KRT86, KRT8P10, KRT8P13, KRT8P15, KRT8P17, KRT8P18, KRT8P19, KRT8P20, KRT8P21, KRT8P22, KRT8P23, KRT8P24, KRT8P25, KRT8P26, KRT8P27, KRT8P28, KRT8P29, KRT8P30, KRT8P5, KRT8P6, KRT8P7, KRT8P8, KRT8P9, KRT9, KRTAP19-8, KRTAP20-4
New consensus nomenclature for mammalian keratins.
Schweizer J, Bowden PE, Coulombe PA, Langbein L, Lane EB, Magin TM, Maltais L, Omary MB, Parry DA, Rogers MA, Wright MW.
J Cell Biol 174(2):169-74. Epub 2006 Jul 10. 2006
4TCHP, KRT16, KRT18
Identification of trichoplein, a novel keratin filament-binding protein.
Nishizawa M, Izawa I, Inoko A, Hayashi Y, Nagata K, Yokoyama T, Usukura J, Inagaki M.
J Cell Sci 118(Pt 5):1081-90. 2005
5PC112, PC117, PC212, PC217, KRT17, KRT16, KRT6A
Novel and recurrent mutations in the genes encoding keratins K6a, K16 and K17 in 13 cases of pachyonychia congenita.
Terrinoni A, Smith FJ, Didona B, Canzona F, Paradisi M, Huber M, Hohl D, David A, Verloes A, Leigh IM, Munro CS, Melino G, McLean WH.
J Invest Dermatol 117(6):1391-6. 2001
6PC117, KRT16
Delayed-onset pachyonychia congenita associated with a novel mutation in the central 2B domain of keratin 16.
Connors JB, Rahil AK, Smith FJ, McLean WH, Milstone LM.
Br J Dermatol 144(5):1058-62. 2001
7KRT16, NEPPK
A mutation in the V1 domain of K16 is responsible for unilateral palmoplantar verrucous nevus.
Terrinoni A, Puddu P, Didona B, De Laurenzi V, Candi E, Smith FJ, McLean WH, Melino G.
J Invest Dermatol 114(6):1136-40. 2000
8EPPK, KRT16, KRT9, NEPPK, PC117
A mutation in the V1 domain of K16 is responsible for unilateral palmoplantar verrucous nevus.
Terrinoni A, Puddu P, Didona B, De Laurenzi V, Candi E, Smith FJ, McLean WH, Melino G.
J Invest Dermatol 114(6):1136-40. 2000
9KRT1@1, KRT19, KRT15, KRT17, KRT16, KRT14
Close linkage of the two keratin gene clusters in the human genome.
Milisavljevic V, Freedberg IM, Blumenberg M.
Genomics 34(1):134-8. 1996
10KRT16
cDNA cloning and bacterial expression of the human type I keratin 16.
Paladini RD, et al.
Biochem Biophys Res Commun 215 : 517-523. 1995
11NEPPK, KRT16
Novel mutations in keratin 16 gene underly focal non-epidermolytic palmoplantar keratoderma (NEPPK) in two families.
Shamsher MK, Navsaria HA, Stevens HP, Ratnavel RC, Purkis PE, Kelsell DP, McLean WH, Cook LJ, Griffiths WA, Gschmeissner S, et al.
Hum Mol Genet 4(10):1875-81. 1995
12KRT16, PC117, PC217, KRT17
Keratin 16 and keratin 17 mutations cause pachyonychia congenita.
McLean WHI, et al.
Nat Genet 9 : 273-278. 1995
13KRT1@1, KRT1@2, KRT14, KRT16
A group of type I keratin genes on human chromosome 17: characterization and expression.
Rosenberg M, RayChaudhury A, Shows TB, Le Beau MM, Fuchs E.
Mol Cell Biol 8(2):722-36. 1988