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Research 61–90 of 1000+
- A novel EDA variant that causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family
- Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome with Concomitant Lymphopenia: A Novel TP63 Mutation
- Trichothiodystrophy: Review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasias
- SPECIFIC ECTODERMAL ENHANCERS CONTROL THE EXPRESSION OF<i>Hoxc</i>GENES IN DEVELOPING MAMMALIAN INTEGUMENTS
- Tooth, hair and claw: Comparing epithelial stem cell niches of ectodermal appendages
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- Orai1 expression pattern in tooth and craniofacial ectodermal tissues and potential functions during ameloblast differentiation
- 1426 Deletion of hoxc13 in frogs reveals key steps in the molecular evolution of cornified skin appendages
- Altered skin development and impaired proliferative and inflammatory responses in transgenic mice overexpressing the glucocorticoid receptor
- Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin
- Trichoscopy in Hair Shaft Disorders
- Atrichia With Papular Lesions
- <i>WNT10A</i> , dermatology and dentistry
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Genetic Hair Disorders: A Review
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Hair and Nail Relationship
- Genetics of Structural Hair Disorders
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Dermatopathology and molecular genetics
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations
- Congenital atrichia and hypotrichosis
- Small molecules facilitate single factor-mediated sweat gland cell reprogramming
- Hair loss among a group of Egyptian children
- Transcriptional activation of a subset of hair keratin genes by the NF-κB effector p65/RelA