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Research 421–450 of 1000+
- Therapeutic Efficacy and Promise of Human Umbilical Cord Mesenchymal Stem Cell-Derived Extracellular Vesicles in Aging and Age-Related Disorders
- Biomedical applications of organoids in genetic diseases
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- The Genomic Variation in Textured Hair: Implications in Developing a Holistic Hair Care Routine
- Increasing GSH-Px Activity and Activating Wnt Pathway Promote Fine Wool Growth in FGF5-Edited Sheep
- Androgenetic Alopecia in Men: An Update On Genetics
- Bioengineered skin organoids: from development to applications
- Editor's evaluation: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Hair & Cutaneous Development
- Toxic and Metabolic Disorders of the Nervous System
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- Dysplastic nevi, cutaneous melanoma, and other skin neoplasms in patients with myotonic dystrophy type 1: A cross-sectional study
- Skin self-photography for dysplastic nevus monitoring is associated with a decrease in the number of biopsies at follow-up: A retrospective analytical study
- Follicular dysplasia and hair loss in white-tailed deer (<i>Odocoileus virginianus</i>)
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Ectodermal Dysplasia: Otolaryngologic Manifestations and Management
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Hypotrichosis and nail dysplasia: A novel hidrotic ectodermal dysplasia
- Follicular dysplasia in five Weimaraners
- The G60S Connexin43 Mutant Regulates Hair Growth and Hair Fiber Morphology in a Mouse Model of Human Oculodentodigital Dysplasia
- Epidermal dysplasia and <i>Malassezia</i> infection in two West Highland White Terrier siblings: an inherited skin disorder or reaction to severe <i>Malassezia</i> infection?
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- Follicular dysplasia in two cows
- Concurrent follicular dysplasia and interface dermatitis in Boxer dogs
- KID Syndrome: Report of a Case and Support for Its Reclassification as an Ectodermal Dysplasia
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay
- Topical cetirizine and oral vitamin D: a valid treatment for hypotrichosis caused by ectodermal dysplasia