Search
for
Sort by
Research 481–510 of 1000+
- Autoimmune polyglandular syndrome type 4 – case report
- 5 Diverse Skin Type Considerations and Applications for Nonsurgical Combinations
- Development of a novel, clinically-relevant model for investigating factors that stimulate human hair growth
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Chemically Induced Hair Loss/Alopecia
- Structural Stability of Wild Type and Mutated α-Keratin Fragments: Molecular Dynamics and Free Energy Calculations
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Office Diagnosis of Hair Shaft Defects
- Localization, Age- and Site-Dependent Expression, and Regulation of 11β-Hydroxysteroid Dehydrogenase Type 1 in Skin
- Vitamin D‐dependent rickets Type II with alopecia: two case reports and review of the literature
- Immunofluorescence analysis of the basement membrane zone components in human anagen hair follicles
- Novel and recurrent mutations in the <i>AIRE</i> gene of autoimmune polyendocrinopathy syndrome type 1 (APS1) patients
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Expression characteristics of BMP2, BMPR-IA and Noggin in different stages of hair follicle in yak skin
- Mrp3, a Mitogen-Regulated Protein/Proliferin Gene Expressed in Wound Healing and in Hair Follicles
- Avicequinone C Isolated from Avicennia marina Exhibits 5α-Reductase-Type 1 Inhibitory Activity Using an Androgenic Alopecia Relevant Cell-Based Assay System
- 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
- Patient satisfaction and complications following laser hair removal in ethnic skin
- Polyglandular autoimmune syndrome type III with a prevalence of cutaneous features
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Skin features in myotonic dystrophy type 1: An observational study
- The feasibility of quantitative analysis of androgen metabolism by use of single dermal papillae from human hair follicles
- Skin-Associated Cartilage Is a Distinct Type of Lipid-Filled Tissue
- 11β-Hydroxysteroid Dehydrogenase Type 1 Inhibition Attenuates the Adverse Effects of Glucocorticoids on Dermal Papilla Cells
- Alopecia in vitamin D-dependent rickets type II responding to 1<i>α</i>-hydroxycholecalciferol
- Identification of key genes in type 2 diabetes‐induced erectile dysfunction rats with stem cell therapy through high‐throughput sequencing and bioinformatic analysis
- Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1
- Shock: A possible presenting manifestation of autoimmune polyendocrine syndrome type II
- Polyglandular Autoimmune Syndrome Type 3D : A Case Report
- 258 11β-hydroxysteroid dehydrogenase type 1 inhibition attenuates the adverse effects of glucocorticoids on dermal papilla cells