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Research 181–210 of 290
- Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Vitamin D and the skin
- Aberrant Activation of the Hedgehog Signaling Pathway in Malignant Hematological Neoplasms
- Anabolic androgenic steroids and carcinogenicity focusing on Leydig cell: a literature review
- Bone Morphogenetic Protein Signaling Regulates Postnatal Hair Follicle Differentiation and Cycling
- Selective Androgen Receptor Modulators (SARMs) Negatively Regulate Triple-Negative Breast Cancer Growth and Epithelial:Mesenchymal Stem Cell Signaling
- Targeting Wnt Signaling for Gastrointestinal Cancer Therapy: Present and Evolving Views
- PPAR-<i>γ</i> Agonists and Their Role in Primary Cicatricial Alopecia
- Krtap11-1, a hair keratin-associated protein, as a possible crucial element for the physical properties of hair shafts
- Hypoxia in Cell Reprogramming and the Epigenetic Regulations
- Activation of liver X receptors inhibits experimental fibrosis by interfering with interleukin-6 release from macrophages
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Physiological Insights from the Vitamin D Receptor Knockout Mouse
- Runx3 is involved in hair shape determination
- A systematic summary of survival and death signalling during the life of hair follicle stem cells
- Thyroxine Differentially Modulates the Peripheral Clock: Lessons from the Human Hair Follicle
- Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene
- Dermal Adipose Tissue Secretes HGF to Promote Human Hair Growth and Pigmentation
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- The Vitamin D Receptor Is Required for Mouse Hair Cycle Progression but not for Maintenance of the Epidermal Stem Cell Compartment
- Wnt Signaling Is Deranged in Asthmatic Bronchial Epithelium and Fibroblasts
- Cooperation of TGF‐β and FGF signalling pathways in skin development
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Sebaceous immunobiology - skin homeostasis, pathophysiology, coordination of innate immunity and inflammatory response and disease associations
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- International Society for the Study of Women's Sexual Health Clinical Practice Guideline for the Use of Systemic Testosterone for Hypoactive Sexual Desire Disorder in Women
- Notch signaling is significantly suppressed in basal cell carcinomas and activation induces basal cell carcinoma cell apoptosis
- The 1,25-dihydroxyvitamin D3-independent actions of the vitamin D receptor in skin