Citations for
1CDM1, CDM2, KRT12, KRT13, KRT14, KRT3, KRT5, KTRT4, WHSN1, WHSN2
The molecular basis of human keratin disorders.
Arin MJ.
Hum Genet 125(4):355-73. Epub 2009 Feb 27. Review. 2009
2KRT1, 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
3KRT13, WHSN2
Constitutional mutation of keratin 13 gene in familial white sponge nevus.
Shibuya Y, Zhang J, Yokoo S, Umeda M, Komori T.
Oral Surg Oral Med Oral Pathol Oral Radiol Endod 96(5):561-5. 2003
4KRT13
Stage-specific expression of the intermediate filament protein cytokeratin 13 in luminal epithelial cells of secretory phase human endometrium and peri-implantation stage rabbit endometrium.
Olson GE, Winfrey VP, Blaeuer GL, Palisano JR, NagDas SK.
Biol Reprod 66(4):1006-15. 2002
5KRT13
Isolation, sequence and expression of the gene encoding human keratin 13.
Waseem A, Alam Y, Dogan B, White KN, Leigh IM, Waseem NH.
Gene 215 : 269-279. 1998
6BSCL2,GNG3,KRT13,WHSN2
Keratin 13 point mutation underlies the hereditary mucosal epithelia disorder white sponge nevus.structure and mapping of the G protein gamma 3 subunit gene and a divergently transcribed novel gene,Gng3lg
Richard G, et al.Downes GB et al.
Nat Genet 11 : 453-455. 1995
7KRT13
Chromosomal mapping of human cytokeratin 13 gene (KRT13).
Romano V, et al.
Genomics 14 : 495-497. 1992
8KRT10, KRT13, KRT15
Chromosomal mapping and physical linkage analysis of human acidic cytokeratin genes.
Romano V, et al.
(HGM11) Cytogenet Cell Genet 58 : 2009-2010. 1991