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Research 241–270 of 737
- Hair transplantation surgery
- Management of hair loss diseases
- Polymeric micelle mediated follicular delivery of spironolactone: Targeting the mineralocorticoid receptor to prevent glucocorticoid-induced activation and delayed cutaneous wound healing
- Hair Transplantation Update
- Hair Transplantation in Females
- Skin Graft Harvesting and Donor Site Selection
- The Hair Transplant Megasession Technique: A Review
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Scarring Alopecia
- 3D bioprinting of hepatocyte-derived exosome-reinforced skin organoid for efficient skin regeneration
- Using Angulation of Implanters at 45 Degrees to the Scalp with the Bevel Facing toward the Skin to Enhance Follicular Entry at Minimal Pressure: A Randomized Clinical Trial in Hair Transplantation
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Understanding Polycystic Ovary Syndrome
- LAWSONIA INERMIS LINN’S POTENTIAL FOR PROMOTING WOUND HEALING: A REVIEW
- Myodegeneration in EDA-A2 Transgenic Mice Is Prevented by XEDAR Deficiency
- Specific receptor detection by a functional keratinocyte growth factor-immunoglobulin chimera.
- A novel nonsense CDH3 mutation in hypotrichosis with juvenile macular dystrophy
- Immunohistochemical, pharmacovigilance, and omics analyses reveal the involvement of ATP-sensitive K+ channel subunits in cancers: role in drug–disease interactions
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Myotonic Dystrophy—A Progeroid Disease?
- EGFR Controls Hair Shaft Differentiation in a p53-Independent Manner
- The roles of collagen XVIII and its endostatin domain in wound healing, hair follicle cycling and bone development
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance
- Molecular Genetics of Human Hair Diseases
- Molecular basis of androgen insensitivity
- Epigenetics of Colorectal Cancer
- The role of VEGF and thrombospondins in skin angiogenesis