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Research 181–210 of 1000+
- Displasia folicular en un Doberman adulto de capa negra : un caso clínico
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Keratin disorders: from gene to therapy
- Biology and Genetics of Hair
- Role of the Autoimmune Regulator (<i>AIRE</i>) gene in alopecia areata: Strong association of a potentially functional <i>AIRE</i> polymorphism with alopecia universalis
- Myodegeneration in EDA-A2 Transgenic Mice Is Prevented by XEDAR Deficiency
- Epidermal abnormalities and increased malignancy of skin tumors in human epidermal keratin 8‐expressing transgenic mice
- Identification of Ectodysplasin Target Genes Reveals the Involvement of Chemokines in Hair Development
- Expression of <i>Foxi3</i> is regulated by ectodysplasin in skin appendage placodes
- Genetic hair and nail disorders
- Propranolol induced alopecia
- An overview on congenital alopecia in domestic animals
- Becker's nevus associated with chromosomal mosaicism and congenital adrenal hyperplasia
- Ectodysplasin research—Where to next?
- Phenotypic variability associated with<i>WNT10A</i>nonsense mutations
- Squamous epithelial proliferation induced by walleye dermal sarcoma retrovirus cyclin in transgenic mice
- Histological and dermatoscopic description of sphynx cat skin
- XEDAR activates the non-canonical NF-κB pathway
- Orai1 expression pattern in tooth and craniofacial ectodermal tissues and potential functions during ameloblast differentiation
- Suppression of hair follicle development inhibits induction of sonic hedgehog, patched, and patched-2 in hair germs in mice
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Acute sensitivity of the oral mucosa to oncogenic <i>K‐ras</i>
- A new type of pachyonychia congenita.
- Store-operated calcium channels in skin
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- The Tabby (Ta), Tabby-c (Tac), and Tabby-J (TaJ) Mutations, Chromosome X
- Scaling dermatosis in three dogs associated with abnormal sebaceous gland differentiation
- Inherited Disorders of the Hair
- The Roles of EDA2R in Ageing and Disease
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