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Research 271–300 of 1000+
- The Naked (N) Mutation, Chromosome 15
- SPECIFIC ECTODERMAL ENHANCERS CONTROL THE EXPRESSION OF<i>Hoxc</i>GENES IN DEVELOPING MAMMALIAN INTEGUMENTS
- Index
- Hypotrichosis and Alopecia
- Congenital and Hereditary Skin Diseases
- Mutant Cx43 in Skin Differentiation and Disease
- A clinician's approach to canine alopecia
- El teorema del 0,7 o el otro teorema de Pitágoras
- FC‐10 Adult‐onset hair loss in Chesapeake Bay retrievers: a clinical and histological study
- N02. Hair and Nails
- Displasia folicular en un Doberman adulto de capa negra : un caso clínico
- Epidermal abnormalities and increased malignancy of skin tumors in human epidermal keratin 8‐expressing transgenic mice
- Propranolol induced alopecia
- Squamous epithelial proliferation induced by walleye dermal sarcoma retrovirus cyclin in transgenic mice
- Acute sensitivity of the oral mucosa to oncogenic <i>K‐ras</i>
- THE FREQUENCY OF VISCERAL AND PHENOTYPIC MARKERS IN PATIENTS WITH THE COMBINATION OF UNDIFFERENTIATED CONNECTIVE TISSUE DISEASE AND GASTROESOPHAGEAL REFLUX DISEASE
- Pathology in Practice
- Abstract 5202: Bone marrow-derived epithelial cells contribute to chronic skin inflammation and skin tumor formation in the mouse
- 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
- 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
- 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
- Histological and dermatoscopic description of sphynx cat skin