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Research 721–750 of 1000+
- AIRE Deficiency Leads to the Development of Alopecia Areata‒Like Lesions in Mice
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Establishment of Tsc2-deficient rat embryonic stem cells
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Exosomes in stroke management: A promising paradigm shift in stroke therapy
- Platelet-rich Plasma Injection and Lipofilling-assisted Hair Transplantation on Residual Scalp Alopecia Post Aplasia Cutis Congenita Verticis (ACCV)
- Comprehensive Analysis of LncRNA AC010789.1 Delays Androgenic Alopecia Progression by Targeting MicroRNA-21 and the Wnt/β-Catenin Signaling Pathway in Hair Follicle Stem Cells
- Gene expression of FOXA1 and CCL2 in different phenotypes of infertile women with polycystic ovarian syndrome
- Involvement of Wnt, Eda and Shh at defined stages of sweat gland development
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- A Case Report of Cronkhite-Canada Syndrome Complicated by Membranous Nephropathy
- Novel recombinant R-spondin1 promotes hair regeneration by targeting the Wnt/β-catenin signaling pathway
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Platelet-rich plasma as a potential treatment for noncicatricial alopecias
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- A clinico-epidemiological study of scalp hair loss in children (0–18 years) in Kota Region, South-East Rajasthan
- Varying Presentation of Type 1 Polyglandular Failure in India
- Cronkhite–Canada Syndrome With Multiple Mesenteric Lymphadenopathy: A Case Report
- Hepatocyte growth factor-modified hair follicle stem cells ameliorate cerebral ischemia/reperfusion injury in rats
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
- Epithelial Stem Cells: Turning over New Leaves
- Human Wharton’s Jelly Mesenchymal Stem Cells Plasticity Augments Scar-Free Skin Wound Healing with Hair Growth
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Diphenylcyclopropenone-Induced Vitiligo in a Patient with Alopecia Universalis
- [The Netherton syndrome with alopecia and prolinuria].
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Diseases of Hair
- Congenital atrichia associated with nevus flammeus: A rare association
- Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1