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Research 841–870 of 1000+
- Cyproterone Acetate in the Treatment of Sexual Disorders: Pharmacological Base and Clinical Experience
- Programmable Artificial Skins Accomplish Antiscar Healing with Multiple Appendage Regeneration
- Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo “hairless” rat
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- Neurosteroid influence on affective tone
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- Evolution of Trichocyte Keratins
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Misdiagnosis as asphyxiating thoracic dystrophy and CMV-associated haemophagocytic lymphohistiocytosis in Shwachman-Diamond syndrome
- Identification of SNPs and expression patterns of FZD3 gene and its effect on wool traits in Chinese Merino sheep (Xinjiang Type)
- Androgen receptor activation integrates complex transcriptional effects in osteoblasts, involving the growth factors TGF-β and IGF-I, and transcription factor C/EBPδ
- Molecular cloning, characterization, and expression of sheep FGF5 gene
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- AN ATTEMPT TO ASSESS THE MAGNITUDE OF ENDOGENOUS ANDROGEN PRODUCTION IN A CASE OF THE ADRENOGENITAL SYNDROME*
- Physiological and transcriptomic analyses of brassinosteroid function in kiwifruit root
- Variation in the ovine trichohyalin gene and its association with wool curvature
- Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Genetic Susceptibility to Alopecia
- The use of minoxidil in the treatment of male and female androgenetic alopecia: a story of more than 30 years
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Umbilical cord‐derived mesenchymal stem cell secretome promotes skin regeneration and rejuvenation: From mechanism to therapeutics
- Pseudallescheria boydii infection associated with IgG4-related disease
- Estrogen regulates the expression of retinoic acid synthesis enzymes and binding proteins in mouse skin
- Generation of Induced Pluripotent Stem Cells from Hair Follicle Bulge Neural Crest Stem Cells
- Influence of glucocorticoids on a time-of-day-dependent variation in intradermal reactivity to histamine in dogs
- Qiu Baoguo's Experience in Treating Consumptive Syndromes after Radio-Chemotherapies
- Ocular manifestations in a case of Kallmann syndrome – An interesting case report on isolated gonadotropin-releasing hormone deficiency
- FAM19A5 negatively regulates cutaneous wound healing via PPARD-dependent inhibition of keratinocyte migration