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Research 841–870 of 1000+
- Burden of Eosinophilic Esophagitis and Gastroesophageal Reflux Disease in Metabolic Dysfunction–Associated Steatotic Liver Disease: A Comprehensive US Healthcare Analysis
- GENOME-WIDE ANALYSIS REVEALS THE MOLECULAR BASIS OF GENETIC VARIATION OF IMPORTANT ECONOMIC TRAITS IN CASHMERE GOATS ON QINGHAI-TIBET PLATEAU
- Impaired LEF1 Activation Accelerates iPSC-Derived Keratinocytes Differentiation in Hutchinson-Gilford Progeria Syndrome
- Androgenetic alopecia: Prevalence and clinical characteristics in a South-West Nigerian spopulation
- 010 Development of a Desmocollin-3 Active Mouse Model Recapitulating Human Atypical Pemphigus
- Characterization of novel TMEM173 mutation with additive IFIH1 risk allele
- A Novel Androgen Receptor Gene Mutation in a 46,XY Patient: Complete Androgen Insensitivity Syndrome
- Unravelling the Genetics of Physical Appearance Variation in Modern Humans
- Reprogramming the wound microenvironment: identity remodeling strategies for fibroblasts, keratinocytes, and macrophages
- TREATMENT OF KERATOSIS PILARIS: A NARRATIVE LITERATURE REVIEW OF TOPICAL, PROCEDURAL, AND VARIANT-SPECIFIC THERAPIES
- Image 1_Resident T cell activation leads to human hair follicle immune privilege loss ex vivo, which is prevented by the DHODH inhibitor farudodstat: relevance for alopecia areata.pdf
- Disorganization of Transcriptional Regulation and Alteration of Keratin Family Gene Expression in Hairy Ear Mice
- Unveiling the Connection between Gut Microbiome and Polycystic Ovary Syndrome (PCOS)
- Neonatal ichthyosis-sclerosing cholangitis syndrome caused by a novel CLDN1 mutation: a case report and literature review
- BH28 Breaking the pattern: frontal fibrosing alopecia in men, a case series
- 9209 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- Finding Long-COVID: Temporal Topic Modeling of Electronic Health Records from the N3C and RECOVER Programs
- Chronic Overlapping Pain Conditions and Nociplastic Pain
- Novel insights into cardiocutaneous syndromes
- From hair colour to diagnosis
- The role of skin macrophages under conditions of stress and injury: ultraviolet irradiation and wound healing
- Compound Heterozygous Mutations in <i>Forkhead Box N1</i> (<i>FOXN1</i>) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients
- Il-10 family members as novel responders to genotoxic stress
- Dumhetens rum i bildningens mitt
- The Cutaneous Epidermal Growth Factor Network: Can it be Translated Clinically to Stimulate Hair Growth? - eScholarship
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Ivarmacitinib in atopic dermatitis presenting with prurigo nodularis-like lesions and alopecia areata: a case report
- Systemic testosterone induces structural, immunological, and sex steroid receptor changes in human XX skin
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Impaired turnover of autophagolysosomes in cathepsin L deficiency