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Research 811–840 of 1000+
- Reduction of Intrafollicular Apoptosis in Chemotherapy-Induced Alopecia by Topical Calcitriol-Analogs
- A Systemic Review on Topical Marketed Formulations, Natural Products, and Oral Supplements to Prevent Androgenic Alopecia: A Review
- Intoxication massive au lithium associée à une alopécie télogène diffuse
- Nanogenerators in Biomedical Frontiers: Revolutionizing Self-Powered Healthcare Systems
- Erosive Pustular Dermatosis: Delving into Etiopathogenesis and Management
- Polymorphism of Keratin Gene KRT71 and Its Relationship with Wool Properties in Gansu Alpine Fine-Wool Sheep
- Linear alopecia areata
- Regulation of somatic cell reprogramming through inducible mir-302 expression
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- ATP-competitive mTOR kinase inhibitors delay plant growth by triggering early differentiation of meristematic cells but no developmental patterning change
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Human Peptidylarginine Deiminase Type III: Molecular Cloning and Nucleotide Sequence of the cDNA, Properties of the Recombinant Enzyme, and Immunohistochemical Localization in Human Skin
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- The role of PPAR<i>γ</i>-mediated signalling in skin biology and pathology: new targets and opportunities for clinical dermatology
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Dermatologic Manifestations of Polycystic Ovary Syndrome
- Bimatoprost in the treatment of eyelash hypotrichosis
- Microporous Dermal-Like Electrospun Scaffolds Promote Accelerated Skin Regeneration
- Psychosocial dimensions of SLE: implications for the health care team
- TREATMENT OF ALOPECIA AREATA
- A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath
- Barley disease susceptibility factor RACB acts in epidermal cell polarity and positioning of the nucleus
- Alopecias in lupus erythematosus
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Young coconut juice can accelerate the healing process of cutaneous wounds
- Postoperative permanent pressure alopecia
- Satisfaction with control of systemic lupus erythematosus and lupus nephritis: physician and patient perspectives
- Development of the Alopecia Areata Patient Priority Outcomes Instrument: A Qualitative Study