|1.||Coulombe, Pierre A: 3 articles (11/2013 - 02/2003)|
|2.||Rotty, Jeremy D: 2 articles (11/2013 - 04/2012)|
|3.||Bahmanzadeh, Maryam: 1 article (06/2015)|
|4.||Sabbagh, Susan: 1 article (06/2015)|
|5.||Ghadiri, Atta: 1 article (06/2015)|
|6.||Orazizadeh, Mahmoud: 1 article (06/2015)|
|7.||Hashemitabar, Mahmoud: 1 article (06/2015)|
|8.||Amin, Asif: 1 article (01/2015)|
|9.||Wani, Sajad H: 1 article (01/2015)|
|10.||Mir, Masood S: 1 article (01/2015)|
11/01/1998 - "In several families with autosomal dominant monilethrix, the disorder has been linked to the type II keratin gene cluster at chromosome 12q13. "
09/01/1997 - "Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity."
12/01/1995 - "A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13."
04/01/1996 - "This study demonstrates linkage of monilethrix in a pedigree to microsatellite DNA loci mapping to the region on chromosome 12 containing the type II keratin cluster. "
09/01/1997 - "In three British families of monilethrix, linkage has recently been reported to the type II keratin gene cluster at chromosome 12q13, and it has been suggested that the disease is due to a defect in the hard keratins of hair and nail. "
|2.||Ichthyosis Bullosa of Siemens
09/01/1994 - "Linkage analysis pointed to the involvement of a keratin type II gene (12q11-13) in ichthyosis bullosa of Siemens. "
09/01/1994 - "Genetic linkage of the keratin type II gene cluster with ichthyosis bullosa of Siemens and with autosomal dominant ichthyosis exfoliativa."
03/01/1997 - "The corresponding glutamate in keratin 2e was previously reported to be frequently mutated in ichthyosis bullosa of Siemens, suggesting that this highly conserved residue may be a potential mutational hot spot in other type II keratins or nonkeratin intermediate filament proteins."
|3.||Epidermolytic Hyperkeratosis (Bullous Congenital Ichthyosiform Erythroderma)
11/01/1992 - "Linkage of the epidermolytic hyperkeratosis phenotype and the region of the type II keratin gene cluster on chromosome 12."
07/01/1992 - "Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q."
12/01/1994 - "Mutations in type I and type II keratin genes have now been implicated in three different human genetic disorders, epidermolysis bullosa simplex, epidermolytic hyperkeratosis, and epidermolytic palmoplantar keratoderma. "
|4.||Wounds and Injuries (Trauma)
04/30/2012 - "The type II keratins 6a and 6b (K6a and K6b) are among the genes induced early on in wound-proximal keratinocytes and maintained during reepithelialization. "
02/01/2003 - "A conserved aspect of this response is a rapid switch in gene expression whereby the type II keratin 6 (K6) and type I keratins 16 and 17 (K16, K17) are induced in epithelial cells at the wound edge. "
02/01/1991 - "By screening a cDNA expression library from the newt blastema with LP1K, we have identified cDNA clones coding for a type II keratin (NvKII) expressed both in the mesenchyme and the specialized wound epithelium of the blastema. "
|5.||Pachyonychia Congenita (Jadassohn-Lewandowsky Syndrome)
07/01/1995 - "Mutation of a type II keratin gene (K6a) in pachyonychia congenita."
11/26/2013 - "Mutations in the type I keratin 16 (Krt16) and its partner type II keratin 6 (Krt6a, Krt6b) cause pachyonychia congenita (PC), a disorder typified by dystrophic nails, painful hyperkeratotic calluses in glabrous skin, and lesions involving other epithelial appendages. "
|1.||DNA (Deoxyribonucleic Acid)
|2.||Type I Keratins (Type I Keratin)
|4.||Proteins (Proteins, Gene)
|5.||Glutamic Acid (Glutamate)
|6.||Glutathione Transferase (Glutathione S-Transferase)
|7.||Keratin-2 (Keratin 2)
|8.||Keratin-19 (Keratin 19)
|10.||Proteasome Endopeptidase Complex (Proteasome)