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Research 301–330 of 1000+
- Topically Applied Minoxidil in Baldness
- Nutritional Disorders of the Hair and Their Management
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- An Overview of Alopecias
- Congenital hypotrichosis due to short anagen
- Comprehensive Overview and Treatment Update on Hair Loss
- Hormone und Haarwachstum
- Short anagen syndrome
- The rising burden of alopecia: A review on aetiology, prevalence and role of homoeopathy
- Identification of the cell lineage at the origin of basal cell carcinoma
- Integrated single-cell chromatin and transcriptomic analyses of human scalp identify gene-regulatory programs and critical cell types for hair and skin diseases
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Therapeutic potential of bimatoprost for the treatment of eyebrow hypotrichosis
- Viral-associated trichodysplasia spinulosa: a case with electron microscopic and molecular detection of the trichodysplasia spinulosa-associated human polyomavirus
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- [The Netherton syndrome with alopecia and prolinuria].
- Congenital atrichia associated with nevus flammeus: A rare association
- Stabilization of epithelial β-catenin compromises mammary cell fate acquisition and branching morphogenesis
- Editor's evaluation: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Stimulation of ectodermal organ development by Ectodysplasin-A1
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- MmuPV1-Induced Cutaneous Squamous Cell Carcinoma Arises Preferentially from Lgr5+ Epithelial Progenitor Cells
- Identification of dkk4 as a target of Eda-A1/Edar pathway reveals an unexpected role of ectodysplasin as inhibitor of Wnt signalling in ectodermal placodes
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Sox21 Regulates Anapc10 Expression and Determines the Fate of Ectodermal Organ