|2.||Esophageal Neoplasms (Esophageal Cancer)
|5.||Wounds and Injuries (Trauma)
|1.||Risk, Janet M: 4 articles (01/2012 - 05/2004)|
|2.||McRonald, Fiona E: 4 articles (01/2012 - 05/2004)|
|3.||Field, John K: 3 articles (07/2006 - 05/2004)|
|4.||Kelsell, David P: 2 articles (06/2010 - 05/2004)|
|5.||Liloglou, Triantafillos: 2 articles (07/2006 - 04/2006)|
|6.||Xinarianos, George: 2 articles (07/2006 - 04/2006)|
|7.||Ellis, Anthony: 2 articles (04/2006 - 05/2004)|
|8.||Shaw, Joan M: 2 articles (04/2006 - 05/2004)|
|9.||Rowbottom, Lynn: 2 articles (04/2006 - 05/2004)|
|10.||Langan, Joanne E: 2 articles (04/2006 - 05/2004)|
|1.||Hyperkeratosis of the palms and soles and esophageal papillomasIBA
04/15/2006 - "Tylosis (focal non-epidermolytic palmoplantar keratoderma) is an autosomal dominant skin disorder that is associated with the early onset of squamous cell oesophageal cancer (SCOC) in three families. "
05/01/2004 - "Tylosis (focal non-epidermolytic palmoplantar keratoderma) is associated with the early onset of squamous cell oesophageal cancer in three families. "
01/01/1999 - "Tylosis (focal non-epidermolytic palmoplantar keratoderma; NEPPK) is associated with esophageal cancer in three families, two of which contain six or seven generations. "
04/10/2003 - "Moreover, a locus responsible for hereditary focal non-epidermolytic palmoplantar keratoderma (tylosis oesophageal cancer; TOC), a condition associated with esophageal cancer, has been mapped to the same band. "
04/01/2001 - "Moreover, a genetic locus for hereditary focal non-epidermolytic palmoplantar keratoderma, a condition associated with cancer of the esophagus (TOC; Tylosis with Oesophageal Cancer), lies in the same region. "
01/01/2012 - "Cytoglobin is a candidate for the tylosis with oesophageal cancer gene, and its expression is strongly down-regulated in non-cancerous oesophageal biopsies from patients with TOC compared with normal biopsies. "
07/01/2006 - "One candidate tumour-suppressor gene is cytoglobin (CYGB), which is contained entirely within the 42.5 kb tylosis with oesophageal cancer (TOC) minimal region. "
04/15/2006 - "Down-regulation of the cytoglobin gene, located on 17q25, in tylosis with oesophageal cancer (TOC): evidence for trans-allele repression."
09/01/2009 - "Mutation L437P in the 2B domain of keratin 1 causes diffuse palmoplantar keratoderma in a Chinese pedigree."
01/01/2006 - "A novel mutation and large size polymorphism affecting the V2 domain of keratin 1 in an African-American family with severe, diffuse palmoplantar keratoderma of the ichthyosis hystrix Curth-Macklin type."
|4.||Mal de MeledaIBA
01/01/2015 - "SLURP1 is the causal gene for Mal de Meleda (MDM), an autosomal recessive skin disorder characterized by diffuse palmoplantar keratoderma and transgressive keratosis. "
01/01/2003 - "Mal de Meleda (MDM) or keratosis palmoplantaris transgrediens of Siemens is an autosomal recessive skin disorder characterized by diffuse palmoplantar keratoderma (PPK) and transgressive keratosis with an onset in early infancy. "
11/01/1996 - "Chromosomal localisation of the human envoplakin gene (EVPL) to the region of the tylosis oesophageal cancer gene (TOCG) on 17q25."
04/01/2005 - "Infrequent mutation of the human envoplakin gene is closely linked to the tylosis oesophageal cancer locus in sporadic oesophageal squamous cell carcinomas."
|6.||Keratin-9 (Keratin 9)IBA
|7.||Nonsense Codon (Nonsense Mutation)IBA
|8.||Vitamin A (Retinol)FDA LinkGeneric
11/30/1963 - "SERUM-VITAMIN-A LEVELS IN TWO FAMILIES WITH TYLOSIS."
|10.||Glutamine (L-Glutamine)FDA Link