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Research 721–750 of 1000+
- Finding Long-COVID: Temporal Topic Modeling of Electronic Health Records from the N3C and RECOVER Programs
- Novel insights into cardiocutaneous syndromes
- From hair colour to diagnosis
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- Síndrome de ovario poliquístico: la distancia anogenital como marcador del entorno androgénico prenatal y revisión y comparación de los criterios diagnósticos
- Dumhetens rum i bildningens mitt
- Mechanism of Vitamin D Receptor Action
- Comparison of two ASC-derived therapeutics in an in vitro OA model: secretome versus extracellular vesicles
- Novel TMEM173 Mutation and the Role of Disease Modifying Alleles
- Intermittent treatment with farnesyltransferase inhibitor and sulforaphane improves cellular homeostasis in Hutchinson-Gilford progeria fibroblasts
- Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome
- The G60S Connexin43 Mutant Regulates Hair Growth and Hair Fiber Morphology in a Mouse Model of Human Oculodentodigital Dysplasia
- Approach to androgen excess in women: Clinical and biochemical insights
- CYP21A2 Genotypes do not Predict the Severity of Hyperandrogenic Manifestations in the Nonclassical Form of Congenital Adrenal Hyperplasia
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- The impact of polycystic ovary syndrome on women’s quality of life: Nursing guidelines for its
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Androgenetic alopecia: Prevalence and clinical characteristics in a South-West Nigerian spopulation
- A Novel Androgen Receptor Gene Mutation in a 46,XY Patient: Complete Androgen Insensitivity Syndrome
- 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
- BH28 Breaking the pattern: frontal fibrosing alopecia in men, a case series
- Chronic Overlapping Pain Conditions and Nociplastic Pain
- 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
- The Cutaneous Epidermal Growth Factor Network: Can it be Translated Clinically to Stimulate Hair Growth? - eScholarship
- Laser-Induced Koebner-Related Skin Reactions: A Clinical Overview