Search
for
Sort by
Research 961–990 of 1000+
- Disorders of Sex Development
- Emerging Topics in Cardiometabolic and Psychologic Sequelae, Pathogenesis, and Treatment of Polycystic Ovarian Syndrome: A Review
- Evaluation of serum level of omentin‐1 in females with hirsutism
- Scalp basal cell carcinoma: A different entity?
- Hypotrichosis with juvenile macular dystrophy
- Intraethnic variation in steroid-5-alpha-reductase polymorphisms in prostate cancer patients: a potential factor implicated in 5-alpha-reductase inhibitor treatment
- Eruptive vellus hair cysts: an original case occurring in twins
- Marie-unna hereditary hypotrichosis
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- Comparison of the effectivity of different snare types for collecting and retaining hair from Eurasian Lynx (Lynx lynx)
- Mapping of a novel locus for keratosis follicularis squamosa on chromosome 7p14.3–7p12.1
- Animal fibre: connecting science and production
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Disorders of the Hair and Scalp in Childhood
- The exposome impact on hair health: etiology, pathogenesis and clinical features ‒ Part I
- Acne
- Spatiotemporal Labeling of Melanocytes in Mice
- Nutrients in Hair Supplements: Evaluation of their Function in Hair Loss Treatment
- Prior facility affects alopecia in adulthood for rhesus macaques
- Frontal Fibrosing Alopecia Part II: Etiopathogenesis and Management
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Oxidative stress and alopecia areata
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Understanding Pattern Hair Loss—Hair Biology Impacted by Genes, Androgens, Prostaglandins and Epigenetic Factors
- Alopecias in humans: biology, pathomechanisms and emerging therapies
- Hair Follicle Melanogenesis Reflected in Hair Pigmentation as a Developmental Factor in Alopecia Areata
- Identification of a recurrent nonsense mutation in <i>HR</i> gene responsible for atrichia with papular lesions in two Kashmiri families
- Mechanism of androgenic alopecia: Addressing speculations through empirical evidences
- Missense mutation Y449H of the K10 gene in a patient with severe epidermolytic ichthyosis
- SNP variation in male pattern hair loss in Russians with different dihydrotestosterone levels