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Research 151–180 of 1000+
- Analogs of human genetic skin disease in domesticated animals
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Hair shaft disorders
- A second <i>KRT</i>71 allele in curly coated dogs
- Hair loss in children.
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- The Roles of EDA2R in Ageing and Disease
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Proliferative and Non-Proliferative Lesions of the Rat and Mouse Integument
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- DNA phenotyping: current application in forensic science
- Editor's evaluation: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Use of Induced Pluripotent Stem Cells in Dermatological Research
- Pathophysiology of Alopecia Areata in the Pediatric Patient
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins