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Research 421–450 of 1000+
- Targeted inactivation of integrin-linked kinase in hair follicle stem cells reveals an important modulatory role in skin repair after injury
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- A systematic simulation-based meta-analytical framework for prediction of physiological biomarkers in alopecia
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Impaired LEF1 Activation Accelerates iPSC-Derived Keratinocytes Differentiation in Hutchinson-Gilford Progeria Syndrome
- Viewpoint 4
- The involvement of Elf5 in regulating keratinocyte proliferation and differentiation processes in skin
- Notch Signaling in Hair Follicle Development
- Biology of the Hair Follicle: The Basics
- Tooth, hair and claw: Comparing epithelial stem cell niches of ectodermal appendages
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Human Scalp Hair Follicles Are Both a Target and a Source of Prolactin, which Serves as an Autocrine and/or Paracrine Promoter of Apoptosis-Driven Hair Follicle Regression
- Prolactin and the Skin: A Dermatological Perspective on an Ancient Pleiotropic Peptide Hormone
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- Unmet Medical Needs in Chronic, Non-communicable Inflammatory Skin Diseases
- Sebaceous adenitis in Swedish dogs, a retrospective study of 104 cases
- Hair in health and disease: an introduction
- New Activators and Inhibitors in the Hair Cycle Clock: Targeting Stem Cells’ State of Competence
- Genetic Susceptibility to Alopecia
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- 272 Structural changes in human skin after topical application of glucocorticoids assessed by in vivo imaging technologies
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- 270 A novel small compound HPH-15 antagonizes TGF-β/Smad signaling and ameliorates experimental skin fibrosis
- 267 Deep phenotyping of patients with xeroderma pigmentosum and trichothiodystrophy
- Oral cyclosporin does not arrest progression of androgenetic alopecia
- Hair growth promoting effects of adipose tissue-derived stem cells