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Research 61–90 of 1000+
- Hair Loss in Children
- Edar Signaling in the Control of Hair Follicle Development
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Self-Activated Electrical Stimulation for Effective Hair Regeneration <i>via</i> a Wearable Omnidirectional Pulse Generator
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- WOOLY HAIR PALMOPLANTAR KERATODERMA : A CASE REPORT
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- Nε-(carboxymethyl) lysine represses hair follicle formation by inhibiting Sonic hedgehog expression in a NF-κB-independent manner
- Lanceolate Hair (lah): A Recessive Mouse Mutation with Alopecia and Abnormal Hair
- The dermatoscope in the hair clinic: Trichoscopy of scarring and nonscarring alopecia
- 14-3-3σ Is Required for Club Hair Retention
- A rare pediatric case of loose anagen hair syndrome
- Locations of synthesis of hair structural proteins in human anagen follicles
- Fibrosing alopecia in a pattern distribution in two brothers with pili multigemini
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Alopecia classifications
- [Trichothiodystrophy: a morphological and biochemical study].
- New Activators and Inhibitors in the Hair Cycle Clock: Targeting Stem Cells’ State of Competence
- Topical minoxidil and tretinoin combined with an oral vitamin D analog as a treatment for woolly hair
- Hair dysplasias
- Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Bamboo Hair Syndrome or Netherton Syndrome - A Case Report
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Overview of Facial Plastic Surgery and Current Developments
- [Netherton's syndrome in two sisters].
- Short anagen syndrome in an African American woman
- Human stratum corneum proteomics reveals cross‐linking of a broad spectrum of proteins in cornified envelopes
- Hair Shaft Dysplasias
- Hair shaft structures in EDAR induced ectodermal dysplasia