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Research 571–600 of 1000+
- 268 Male-pattern baldness and its association with coronary heart disease
- 478 Mutation-specific siRNA Knockdown of GJB2 − Potential gene therapy for Keratitis-ichthyosis-deafness Syndrome
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- Decision letter: The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome
- BJD Editor's Choice
- 14. Wound Healing; Cutaneous Therapy; Hair
- Registrars’ Symposium: Summaries of Papers
- Histopathological Analysis on keratin2-6 g Expression in Hair Mutant Mouse Hague
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
- Alopecia Areata: A tissue specific autoimmune disease of the hair follicle
- Recent Advances in the Pathogenesis of Autoimmune Hair Loss Disease Alopecia Areata
- A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females
- Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne
- Mutation of the doublecortin gene in male patients with double cortex syndrome: Somatic mosaicism detected by hair root analysis
- Somatostatin Expression in Human Hair Follicles and Its Potential Role in Immune Privilege
- THERAPEUTIC HOTLINE: Genetic variations in the androgen receptor gene and finasteride response in women with androgenetic alopecia mediated by epigenetics
- MC4R variants rs12970134 and rs17782313 are associated with obese polycystic ovary syndrome patients in the Western region of Saudi Arabia
- Association of the KAP 8.1 Gene Polymorphisms with Fibre Traits in Inner Mongolian Cashmere Goats
- Lepromatous Leprosy in a Renal Transplant Recipient
- Joint study of the associations of HLA‐B and the transmembrane short tandem repeat polymorphism of MICA protein with alopecia areata shows independent associations of both with the disease
- Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair
- POS0080 TOFACITINIB TREATMENT IN CHILDREN WITH RHEUMATIC DISEASES: SINGLE-CENTER EXPERIENCE
- Updates from the British Association of Dermatologists 91st Annual Meeting, 5-7 July 2011, London, U.K.
- Cross-species amplification of human microsatellite markers in pig-tailed and stump-tailed macaques
- Beyond Appearances: The Hidden Coat Diversity of the Sicilian Mastiff Revealed by Integrated Phenotypic and Genetic Analyses
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Role of polymorphism of the androgen receptor gene and non-random X chromosome inactivation in the genesis of androgenic alopecia in women of childbearing potential
- Research Snippets
- 9. Immunology and Genetics