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Research 841–870 of 1000+
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Fine mapping of the human <i>AR/EDA2R</i> locus in androgenetic alopecia
- Localized Autosomal Recessive Hypotrichosis Due to a Frameshift Mutation in the Desmoglein 4 Gene Exhibits Extensive Phenotypic Variability within a Pakistani Family
- Predicting hair cortisol levels with hair pigmentation genes: a possible hair pigmentation bias
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- The Contribution of Endogenous and Exogenous Factors to Female Alopecia
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- Cutaneous immunopathology of androgenetic alopecia
- Gene-knockout mice with abnormal epidermal and hair follicular development
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Stable transfection and identification of a hair follicle-specific expression vector of IGFBP-5 in goat fetal fibroblasts
- Keratinocyte Cytokine Networks Associated with Human Melanocytic Nevus Development
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Missense mutation Y449H of the K10 gene in a patient with severe epidermolytic ichthyosis
- HLA‐B alleles associated with frontal fibrosing alopecia in Brazil may share similar peptide presentation and T‐cell interaction profiles
- <i>WNT10A</i> gene variants at the root of short anagen hair syndrome
- Multiple cell types guided by neurocytes orchestrate horn bud initiation in dairy goats
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Paxbp1 is Indispensable for the Maintenance of Hair Follicle Homeostasis
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- LB918 Analysis of National Inpatient Sample to characterize admissions for pediatric patients with dystrophic epidermolysis bullosa
- Effects of Biomaterials Derived from Germinated Hemp Seeds on Stressed Hair Stem Cells and Immune Cells
- Vpliv prehrane na pojavnost aken
- Hair follicle growth by stromal vascular fraction-enhanced adipose transplantation in baldness
- Cómo hacer que dos más dos sumen cinco
- Profile of 513 patients with alopecia areata: associations of disease subtypes with atopy, autoimmune disease and positive family history
- Συχνότητα και μελέτη του δασυτριχισμού στον ελληνικό πληθυσμό
- Keratin expression in the hair of different racial groups