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Research 601–630 of 1000+
- New approach to the understanding of keloid: psychoneuroimmune–endocrine aspects
- Transplanted hair follicle stem cells migrate to the penumbra and express neural markers in a rat model of cerebral ischaemia/reperfusion
- Horse hair follicles: A novel dermal stem cell source for equine regenerative medicine
- The HEDGEHOG-GLI1 pathway is important for fibroproliferative properties in keloids and as a candidate therapeutic target
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Co-delivery of bioactive peptides by nanoliposomes for promotion of hair growth
- Back to the Future: From Appendage Development Toward Future Human Hair Follicle Neogenesis
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- AIRE Deficiency Leads to the Development of Alopecia Areata‒Like Lesions in Mice
- 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
- Telogen Effluvium: A Review
- 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
- 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.
- 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