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Research 931–960 of 1000+
- Re-identification of anonymised MRI head images with publicly available software: investigation of the current risk to patient privacy
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Biotin and Acetazolamide for Treatment of an Unusual Child With Autism Plus Lack of Nail and Hair Growth
- Winding the clock back on female androgenetic alopecia
- Higher Levels of Serum Uric Acid Have a Significant Association with Lower Incidence of Lower Urinary Tract Symptoms in Healthy Korean Men
- Promotion of hair growth by newly synthesized ceramide mimetic compound
- Aromatic C-nitrosation of a bioactive molecule. Nitrosation of minoxidil
- William Harvey and the Discovery of the Circulation of the Blood
- Toward Optimal Health: The Experts Discuss Facial Skin and Related Concerns in Women
- Cutaneous Lymphadenoma Is a Distinct Trichoblastoma-like Lymphoepithelial Tumor With Diffuse Androgen Receptor Immunoreactivity, Notch1 Ligand in Reed-Sternberg–like Cells, and Common EGFR Somatic Mutations
- Wnt10a Is a Candidate as a Non-Cellular Agent for Induction of Dental Pulp Regeneration with Dentine-Inducing Capacity.
- Skin stem cells orchestrate <i>de novo</i> generation of extrathymic regulatory T cells to establish a temporary protective niche during wound healing
- Cell-based treatments for hair loss: research update on “hair cloning”
- The voices of adult offspring of sperm donation: forces for change within assisted reproductive technology in the United States
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- The Aqualon SLT: A novel device for measuring hair stiffness and lubricity
- Generative Artificial Intelligence Tools: Evaluating Ways to Automate Your SALT ( GATEWAYS ) Scoring of Alopecia Areata
- Novel <i>RNF113A</i> Variant Underlying X‐Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- CPC14 Blaschko-linear trichoepitheliomas: unveiling type 1 segmental mosaicism
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- 8242 A Case of Ayme Gripp Syndrome
- PA15 Becker naevus syndrome associated with a mosaic pathogenic variant in <i>ACTB</i>
- <i>In vivo</i>reprogramming of wound-resident cells generates skin with hair
- Feronia: A Malectin-Like Domain-Containing Receptor Kinase in Arabidopsis Thalina
- Author response: Coordinated hedgehog signaling induces new hair follicles in adult skin
- Topological Markers for Subcellular Chemical Mapping using TOF-SIMS
- Humane rapid tranquillization of an agitated patient with an implantable cardioverter defibrillator
- Enzymes
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