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Research 931–960 of 1000+
- Exosomes as Emerging Therapeutics in Aesthetic and Regenerative Medicine: A Scoping Review
- Association between SQSTM1 dysregulation and risk in alopecia areata: a Mendelian randomization study
- Artificial intelligence in trichology - usage and prospects
- Breaking the biofilm- A persistent case of deep pyoderma in a Bullykutta dog
- Exploring the Causal Relationship and Molecular Mechanisms Between Fasting Insulin and Androgenetic Alopecia: A Mendelian Randomization Study with Bioinformatics Analysis
- Diffuse loss of hair with papules
- Twist2 contributes to skin regeneration and hair follicle formation in mouse fetuses
- Lichen Planopilaris As Part of Multiple Autoimmune Syndrome: A Case Report of New Association
- IV Międzynarodowe Sympozjum Studenckich Kół Naukowych Środowisko – Roślina – Zwierzę – Produkt Streszczenia
- Efectos de la disminución de los depósitos tisulares de hierro sobre los factores de riesgo cardiovascular en pacientes con hiperandrogenismo ovárico funcional
- Molecular and Pathological Studies on Sarcoptes scabiei in Sheep in Ismailia Province, Egypt.
- Follikelhormone
- The Role of Propioni Bacterium acnes in Acne Vulgaris
- INVESTIGATING THE MECHANISMS UNDERLYING THE PATHOGENESIS OF ALOPECIA AREATA
- Penis Endocrinology
- B‐ RAF , naevi and melanoma: a complex relationship
- Syndromes of Severe Insulin Resistance (SSIRs)
- British Society for Dermatopathology: Summaries of Papers
- Testing the impact of trait prevalence priors in Bayesian-based genetic prediction modeling of human appearance traits
- Supplementary Methods, Tables 1-2 and Figures from Tumor Stroma–Derived Wnt5a Induces Differentiation of Basal Cell Carcinoma of <i>Ptch</i>-Mutant Mice via CaMKII
- 464 Phenotypic heterogeneity of epidermolysis bullosa associated with the recurrent pathogenic variant p.(Arg2000Trp) in plectin
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Genome-wide Target Enrichment-aided Chip Design: a 66 K SNP Chip for Cashmere Goat
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- Acne Syndromes and Mosaicism
- 302 Availability of mRNA Obtained from Peripheral Blood Mononuclear Cells for Mutational Analysis in Dystrophic Epidermolysis Bullosa
- Signposts to the Promised Land in Alopecia Areata
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1, TACR3 and SPPL2C associated with Alzheimer’s disease
- Clinicopathological insights into the phenotypic variation of autosomal recessive hypotrichosis/wooly hair by c.736T>A LIPH mutation
- Temporal expression and steroidal regulation of piRNA pathway genes (mael, piwi, vasa) during Silurana (Xenopus) tropicalis embryogenesis and early larval development