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Research 691–720 of 1000+
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- The Female Pattern Hair Loss: Review of Etiopathogenesis and Diagnosis
- Epidemiological and investigative study of premature graying of hair in higher secondary and pre-university school children
- One of These Things Is Not Like the Others: The Idea of Precedence in Health Technology Assessment and Coverage Decisions
- SKIN AND HAIR COSMETIC ISSUES IN WOMEN OF COLOR
- 7 Regulation of androgen receptor and 5α-reductase in the skin of normal and hirsute women
- The character “hairless” in the mouse
- Assessment of the usefulness of dihydrotestosterone in the diagnostics of patients with androgenetic alopecia
- Origin, Clinical Presentation, and Diagnosis of Facial Hypermelanoses
- Divergent neuroactive steroid responses to stress and ethanol in rat and mouse strains: relevance for human studies
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair
- Gene Delivery to the Hair Follicle
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Madarosis
- A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients
- Multifactorial Classification of Male and Female Androgenetic Alopecia
- High-coverage genome of the Tyrolean Iceman reveals unusually high Anatolian farmer ancestry
- Identifying genes associated with the development of human polycystic ovary syndrome
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Hair physiology and its disorders
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Gsdma3 is required for hair follicle differentiation in mice
- Melanocyte and gonad activity as potential severity modifying factors in C3H/HeJ mouse alopecia areata
- Optimal processing for proteomic genotyping of single human hairs
- Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris
- Gata6 promotes hair follicle progenitor cell renewal by genome maintenance during proliferation
- Management of CAH during pregnancy
- Eyebrow Loss
- Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless