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Research 31–60 of 1000+
- Keratin Expression Provides Novel Insight into the Morphogenesis and Function of the Companion Layer in Hair Follicles
- A novel immune competent murine hypertrophic scar contracture model: A tool to elucidate disease mechanism and develop new therapies
- CXXC5: A novel regulator and coordinator of TGF-β, BMP and Wnt signaling
- Pmg-1 and Pmg-2 constitute a novel family of KAP genes differentially expressed during skin and mammary gland development
- A Novel Approach for Skin Regeneration by a Potent Bioactive Placental-Loaded Microneedle Patch: Comparative Study of Deer, Goat, and Porcine Placentas
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- A novel cell-free regenerative therapy for hair loss: human fetal cartilage progenitor cell secretome
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- 1329 CENPV is a novel CYLD-interacting molecule regulating ciliary acetylated tubulin
- Evaluation of a novel hybrid polymer in hair treatment
- Evaluation of a Novel Hybrid Polymer in Hair Treatment
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- LB1777 A novel ex vivo model of human hair follicle immune privilege collapse reveals the potential of farudodstat, a DHODH inhibitor, as a therapeutic for alopecia areata treatment
- Characterization of novel TMEM173 mutation with additive IFIH1 risk allele
- Lactium: A Novel Drug for Psychocutaneous Skin Disorders
- 231 Novel protocol for the invitro maintenance and expansion of adult epidermal LGR5+ stem cells
- Molecular cloning of two novel types of peptidylarginine deiminase cDNAs from retinoic acid‐treated culture of a newborn rat keratinocyte cell line
- Identification of novel glucocorticoid receptor-regulated genes involved in epidermal homeostasis and hair follicle differentiation
- Targeting the Hippo/YAP/TAZ signalling pathway: Novel opportunities for therapeutic interventions into skin cancers
- DKK4 as a novel candidate marker for Zhexi Angora rabbit wool quality
- Topical metformin as a novel therapy for alopecia areata due to its immunologic effects
- LB788 Development of a novel three-dimensional human epidermal model from plucked hair follicle-derived keratinocytes
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- 51826 PRO-C22 - A Novel Serological Biomarker of Tissue Damage is Associated with Disease Severity, Disease Activity, and Systemic Inflammation in Patients with Hidradenitis Suppurativa
- Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies