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Research 781–810 of 1000+
- Evidence-Based and Potential Benefits of Metformin in the Polycystic Ovary Syndrome: A Comprehensive Review
- <i>Hoxc13</i> mutant mice lack external hair
- The PDGF/PDGFR pathway as a drug target
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Alopecia Areata: a Comprehensive Review of Pathogenesis and Management
- Cutaneous reactions to chemotherapeutic drugs and targeted therapy for cancer
- Wnt signaling in skin organogenesis
- Induced Pluripotent Stem Cells from Human Hair Follicle Mesenchymal Stem Cells
- Prolactin: an emerging force along the cutaneous–endocrine axis
- Oral Manifestations of Hematologic and Nutritional Diseases
- Nonclassic Congenital Adrenal Hyperplasia
- Alopecia areata update
- Expression and roles of steroidogenic acute regulatory (StAR) protein in ‘non-classical’, extra-adrenal and extra-gonadal cells and tissues
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Significance of the S100A4 Protein in Psoriasis
- Differences in Expression of Specific Biomarkers Distinguish Human Beard from Scalp Dermal Papilla Cells
- Identification of microRNAs in Wool Follicles during Anagen, Catagen, and Telogen Phases in Tibetan Sheep
- Aromatase deficiency in a male patient - Case report and review of the literature.
- Marie Antoinette Syndrome
- Sp6 downregulation of follistatin gene expression in ameloblasts
- Group IID, IIE, IIF and III secreted phospholipase A2s
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- INTERFERONS IN DERMATOLOGY
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Is there any relationship between decreased AgNOR protein synthesis and human hair loss?
- The probable destructive mechanisms behind COVID-19 on male reproduction system and fertility
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Upregulation of interfollicular epidermal and hair infundibulum β-catenin expression in Gsdma3 mutant mice
- Gonadal Dysgenesis: Associations between Clinical Features and Sex of Rearing.