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Research 241–270 of 1000+
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- Differentiation of Adipose Derived Stem Cells by Stimulating with Extracellular Vesicles Secreted from Dermal Papilla Cells Activated with Osteogenic and Adipogenic Inducers
- UNCONVENTIONAL PROTEIN SECRETION OF KERATIN 75 BY AMELOBLASTS IN VIVO
- Nociceptive and Nonnociceptive Roles of TRPV3 and Its “Druggability”
- British Society for Dermatopathology: Summaries of Papers
- Compartmentalized organization: a common and required feature of stem cell niches?
- Hyperandrogenism in Adolescent Girls
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- Autologous Platelet Concentrates in Periodontology : Science, Concept, Protocols and Clinical Applications
- Benign Cutaneous Eruptions After Transplantation
- A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease
- White piedra and pediculosis capitis in the same patient
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Long-Term Survival of Type XVII Collagen Revertant Cells in an Animal Model of Revertant Cell Therapy
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Effect of calcium supplementation on bone deformity and histopathological findings of skin papules in a pediatric patient with vitamin D–dependent rickets type 2A: a case report
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Unravelling the molecular basis for symbiotic signal transduction in legumes
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair
- Exploring the efficacy of testosterone undecanoate in male children with 5α‐reductase deficiency