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Research 451–480 of 1000+
- Generation of folliculogenic human epithelial stem cells from induced pluripotent stem cells
- 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.
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- p63: a crucial player in epithelial stemness regulation
- Hair: Its structure and response to cosmetic preparations
- 1313 Fzd2 controls multiple aspects of epidermal development through distinct signaling mechanisms
- Introduction to JID Symposium Proceedings 52nd Annual Montagna Symposium on the Biology of Skin “Stem Cells in Skin” Held at Snowmass, Colorado, USA, June 13–17, 2003
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- 증례 : 모발의 황 농도 감소를 보인 모발유황이영양증
- An Extended Epidermal Response Heals Cutaneous Wounds in the Absence of a Hair Follicle Stem Cell Contribution
- Epidermal patterning and induction of different hair types during mouse embryonic development
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Interleukin 6 and STAT3 regulate p63 isoform expression in keratinocytes during regeneration
- Promotion effect of Schisandra nigra on the growth of hair
- Frontal fibrosing alopecia: a review of eleven patients
- A Case Report of Cronkhite-Canada Syndrome Complicated by Membranous Nephropathy
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Frequency of Types of Alopecia in a Single-centre Hair Referral Clinic Over a Ten Years Period
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Pax9 is required for filiform papilla development and suppresses skin-specific differentiation of the mammalian tongue epithelium
- Bioengineered skin organoids: from development to applications
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Keratins and disease at a glance
- A girl with loose anagen hair syndrome and concurrent uncombable hair syndrome
- Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- A decade of neglecting sublingual mass: A case report of epidermoid cyst
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans