Search
for
Sort by
Research 91–120 of 286
- Lineage Tracing of Hair Follicle Stem Cells in Epidermal Whole Mounts
- The Benefit of Donor‐Site Closure in Hair Transplantation
- Follicular Unit Hair Transplantation
- Scalp microbiome in male androgenetic alopecia: 16S rRNA sequencing-based clinical characterization, mouse model validation, and effects on hair follicle cells
- Clinical Snippets
- A RARE CASE OF VITAMIN D DEPENDENT RICKETS TYPE-2A PRESENTED AS ALOPECIA TOTALIS
- Alopecia Areata and Alopecia Areata Incognita
- Clinical interest of a nonchemical lotion in head lice management
- Surgical Management of Leukotrichia
- Pediatric Radiation-Induced Alopecia Post Intracranial Vascular Malformation Embolization: A Case Report with Dermoscopic Findings
- Keratin disorders: from gene to therapy
- Molecular Genetics of Alopecias
- Dissecting Microscope Versus Magnifying Loupes with Transilluntination in the Preparation of Follicular Unit Grafts
- Symmetrical alopecia in the dog
- Follicular Unit Transplantation: Comparison of Video Microscopic vs. Combination Methods
- MALE PATTERN ALOPECIA
- Ectodermal Organ Stem Cells: Morphogenesis, Population Regenerative Behavior, and Evo-Devo
- The human keratins: biology and pathology
- Follimmerlicular Transplantation
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Activin Controls Skin Morphogenesis and Wound Repair Predominantly via Stromal Cells and in a Concentration-Dependent Manner via Keratinocytes
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- The failure behavior of the anchorage of hairs during slow extraction
- Health hazard evaluation report: HETA-2000-0385-2813, Equifax Payment Services, St. Petersburg, Florida.
- Wavy changes in sinus hairs are correlated with feline leukaemia virus infection
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients