Search
for
Sort by
Research 151–180 of 728
- Skin
- Hair and scalp disorders
- The Potential Application of Exosomes as Therapeutic Agents, Carriers, and Biomarkers in Skin Diseases
- From a stem-cell–centered to a niche-centered view: the core role of collagen networks in hair loss and hair follicle miniaturization
- Psychosocial Aspects of Skin Conditions and Diseases
- Cutaneous Lupus Erythematosus
- Abstracts from the 17th Congress of the European Society for Dermatology and Psychiatry
- The role of hair follicles and Edar signalling in cutaneous wound healing
- Extracellular vesicle-based drug overview: research landscape, quality control and nonclinical evaluation strategies
- Dermatologic Conditions of the Early Post-Transplant Period in Hematopoietic Stem Cell Transplant Recipients
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Pediatric Inpatients Requesting Dermatology Consultation in a Tertiary Care Hospital: Retrospective Analysis of 614 Patients
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Influence of Recombinant Codon-Optimized Plasmid DNA Encoding VEGF and FGF2 on Co-Induction of Angiogenesis
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- The epidermis: rising to the surface
- Keratins: the hair shaft's backbone revealed
- Faculty Opinions recommendation of Loss of desmocollin 3 in mice leads to epidermal blistering.
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- Isolation and Characterization of a Putative Keratin-Associated Protein Gene Expressed in Embryonic Skin of Mice
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia
- The molecular basis of human keratin disorders
- The Two Functional Keratin 6 Genes of Mouse Are Differentially Regulated and Evolved Independently from Their Human Orthologs
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review
- The Type I Keratin 19 Possesses Distinct and Context-dependent Assembly Properties
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- Non-FDA-Approved Uses of Apremilast in Dermatology: A Review of Current Available literature