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Research 721–750 of 1000+
- Hairless is a nuclear receptor corepressor essential for skin function
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- Prostaglandin E <sub>2</sub> Receptor 2 Modulates Macrophage Activity for Cardiac Repair
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Through the lens of hair follicle neogenesis, a new focus on mechanisms of skin regeneration after wounding
- Managing adverse events associated with vismodegib in the treatment of basal cell carcinoma
- Low iron stores: a risk factor for excessive hair loss in non-menopausal women.
- Skin manifestations among<i>GATA2</i>-deficient patients
- Peripheral Arterial Disease: Diagnosis and Management
- A case of monilethrix caused by novel compound heterozygous mutations in the desmoglein 4 (DSG4) gene
- New oral anticoagulants and their reversal agents
- Catalytic Antibodies in Norm and Systemic Lupus Erythematosus
- Leptin controls hair follicle cycling
- Cellular Activity in the Dermis Surrounding the Hair Bulb in Alopecia Areata
- Advancements in 3D skin bioprinting: processes, bioinks, applications and sensor integration
- Mettl3-catalyzed m <sup>6</sup> A regulates histone modifier and modification expression in self-renewing somatic tissue
- Molecular determinants for the chemical activation of the warmth-sensitive TRPV3 channel by the natural monoterpenoid carvacrol
- Atypical Protein Kinase C Isoform, aPKCλ, Is Essential for Maintaining Hair Follicle Stem Cell Quiescence
- Skin transcriptome reveals the dynamic changes in the Wnt pathway during integument morphogenesis of chick embryos
- Sex-specific Difference of Hippocampal Synaptic Plasticity in Response to Sex Neurosteroids
- Procyanidins attenuate neuropathic pain by suppressing matrix metalloproteinase-9/2
- PTEN Mediates Activation of Core Clock Protein BMAL1 and Accumulation of Epidermal Stem Cells
- DNA Damage-Inducible Transcript 4 Is an Innate Surveillant of Hair Follicular Stress in Vitamin D Receptor Knockout Mice and a Regulator of Wound Re-Epithelialization
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- US clinics marketing unproven and unlicensed adipose-derived autologous stem cell interventions
- An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome
- Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless gene
- Scalp Flaps
- Nilotinib-Induced Keratosis Pilaris