Oncostatin M Receptor-β Mutations Underlie Familial Primary Localized Cutaneous Amyloidosis
- 1 January 2008
- journal article
- research article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 82 (1), 73-80
- https://doi.org/10.1016/j.ajhg.2007.09.002
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- A Cys634Gly substitution of the RET proto-oncogene in a family with recurrence of multiple endocrine neoplasia type 2A and cutaneous lichen amyloidosisClinical Genetics, 2008
- Genome-wide scan identifies a susceptibility locus for familial primary cutaneous amyloidosis on chromosome 5p13.1-q11.2British Journal of Dermatology, 2006
- Frontiers in pruritus research: scratching the brain for more effective itch therapyJCI Insight, 2006
- Transcriptional responses of human epidermal keratinocytes to Oncostatin-MCytokine, 2005
- Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23British Journal of Dermatology, 2005
- Expression of oncostatin M receptor β in a specific subset of nociceptive sensory neuronsEuropean Journal of Neuroscience, 2003
- Primary Macular Amyloidosis: An Ultrastructural Approach to DiagnosisUltrastructural Pathology, 1999
- Familial primary cutaneous amyloidosisBritish Journal of Dermatology, 1985
- Amyloidogenesis in Organ-Limited Cutaneous Amyloidosis: An Antigenic Identity Between Epidermal Keratin and Skin AmyloidJournal of Investigative Dermatology, 1983
- Histogenesis of Primary Localized Cutaneous Amyloidosis: Sequential Change of Epidermal Keratinocytes to Amyloid via Filamentous DegenerationJournal of Investigative Dermatology, 1979