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Research 31–60 of 1000+
- The genetics of androgenetic alopecia
- Genetic and molecular aspects of androgenetic alopecia
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- Coexistence of psoriasis, and alopecia areata with trachyonychia in a pediatric patient with Turner Syndrome
- Cheveu, vieillissement et environnement : aspects cliniques épidémiologiques
- Androgenetic Alopecia in Men: An Update On Genetics
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- British Society for Dermatopathology
- Molecular genetics of androgen insensitivity
- 7 Pathogenesis and Classification of Male Pattern Hair Loss (Androgenic Alopecia)
- Social selection favours offspring prone to the development of androgenetic alopecia.
- Cosmeceutical Treatments for Androgenetic Alopecia
- Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
- Familial congenital generalized hypertrichosis
- ANDROGENIC ALOPECIA: PATHOGENETIC MECHANISMS AND THERAPEUTIC APPROACHES
- BRITISH ASSOCIATION OF DERMATOLOGY.
- Damage of hair follicle stem cells and alteration of keratin expression in external radiation-induced acute alopecia
- Keratosis Follicularis Spinulosa Decalvans. What Syndrome Is This?
- Molecular mechanisms of Y chromosome loss and <i>UTY</i> gene activity
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Acromegaloidism with normal growth hormone secretion associated with X-Tetrasomy
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Finding bald spots on chromosome 20p11
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- Immune mechanisms associated with sex-based differences in severe COVID-19 clinical outcomes
- Long non-coding RNA Xist contribution in systemic lupus erythematosus and rheumatoid arthritis