يعرض 1 - 14 نتائج من 14 نتيجة بحث عن '"Hair cuticle"', وقت الاستعلام: 0.43s تنقيح النتائج
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    وصف الملف: application/pdf

    Relation: Kantaputra, Piranit; Jotikasthira, Dhirawat; Carlson, Bruce; Wongmaneerung, Teerapat; Quarto, Natalina; Khankasikum, Theerapong; Powcharoen, Warit; Intachai, Worrachet; Tripuwabhrut, Kanich (2020). "TRPS1 mutation associated with trichorhinophalangeal syndrome type 1 with 15 supernumerary teeth, hypoplastic mandibular condyles with slender condylar necks and unique hair morphology." The Journal of Dermatology 47(7): 774-778.; https://hdl.handle.net/2027.42/155929; The Journal of Dermatology; Fantauzzo KA, Christiano AM. Trps1 activates a network of secreted Wnt inhibitors and transcription factors crucial to vibrissa follicle morphogenesis. Development 2012; 139: 203 – 214.; Momeni P, Glöckner G, Schmidt O et al. Mutations in a new gene, encoding a zinc‐finger protein, cause Trichorhinophalangeal syndrome type I. Nat Genet 2000; 24: 71 – 74.; Kuna GB, Collipp PJ, Balsam D. Trichorhinophalangeal dysplasia (Giedion syndrome). A case report. Clin Pediatr (Phila) 1978; 17: 96 – 98.; Giedion A, Burdea M, Fruchter Z, Meloni T. Trosc V. Autosomal‐dominant transmission of the Trichorhinophalangeal syndrome. Report of 4 unrelated families, review of 60 cases. Helv Paediatr Acta 1973; 28: 249 – 259.; Malik TH, Shoichet SA, Latham P, Kroll TG, Peters LL, Shivdasani RA. Transcriptional repression and developmental functions of the atypical vertebrate GATA protein TRPS1. EMBO J 2001; 20: 1715 – 1725.; Lüdecke HJ, Schaper J, Meinecke P et al. Genotypic and phenotypic spectrum in Trichorhinophalangeal syndrome types I and III. Am J Hum Genet 2001; 68: 81 – 91.; Chitsazan A, Mukhopadhyay P, Ferguson B, Handoko HY, Walker GJ. Keratinocyte Cytokine Networks Associated with Human Melanocytic Nevus Development. J Invest Dermatol 2019; 139: 177 – 185.; Kato M, Takeda K, Kawamoto Y et al. RET tyrosine kinase enhances hair growth in association with promotion of melanogenesis. Oncogene 2001; 20: 7536 – 7541.; Kiso M, Tanaka S, Saba R et al. The disruption of Sox21‐mediated hair shaft cuticle differentiation causes cyclic alopecia in mice. Proc Natl Acad Sci USA 2009; 106: 9292 – 9297.; Ito T, Shimomura Y, Farooq M, Suzuki N, Sakabe J, Tokura Y. Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells. J Dermatol 2013; 40: 396 – 8.; Kim YJ, Yoon B, Han K, Park BC. Comprehensive Transcriptome Profiling of Balding and Non‐Balding Scalps in Trichorhinophalangeal Syndrome Type I Patient. Ann Dermatol 2017; 29: 597 – 601.; Michikami I, Fukushi T, Honma S et al. Trps1 is necessary for normal temporomandibular joint development. Cell Tissue Res 2012; 348: 131 – 140.; Kunotai W, Ananpornruedee P, Lubinsky M, Pruksametanan A, Kantaputra PN. Making extra teeth: Lessons from a TRPS1 mutation. Am J Med Genet Part A 2017; 173: 99 – 107.; Kantaputra P, Miletich I, Lüdecke HJ et al. Trichorhinophalangeal syndrome with supernumerary teeth. J Dent Res 2008; 87: 1027 – 1031.; Niikawa N, Kamei T. The Sugio‐Kajii syndrome, proposed Trichorhinophalangeal syndrome type III. Am J Med Genet 1986; 24: 759 – 760.

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    المؤلفون: Kuhn, Rachel1,2, Meyer, Wilfried3,1

    المصدر: Zoological Science 27(10):826-829. 2010