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Research 31–60 of 1000+
- Sex-limited chromosomes and non-reproductive traits
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- The X Factor in Immunity: Sex Differences Shaped by the X Chromosome
- Male-pattern baldness susceptibility locus at 20p11
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Atrichia with papular lesions
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Prediction of male-pattern baldness from genotypes
- 7 Pathogenesis and Classification of Male Pattern Hair Loss (Androgenic Alopecia)
- SEXUAL DIMORPHISM IN MAMMALS
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Pathophysiology of Alopecia Areata in the Pediatric Patient
- Imprinted Dlk1-Gtl2 cluster miRNAs are potential epigenetic regulators of lamb fur quality
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Lanceolate Hair (lah): A Recessive Mouse Mutation with Alopecia and Abnormal Hair
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Polycystic ovary syndrome (PCOS) trilogy: a translational and clinical review
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Treatment of alopecia areata: “What is new on the horizon?”
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Disease causing homozygous variants in the human hairless gene
- Identification of novel mutation in the<i>HR</i>gene responsible for atrichia with papular lesions in a Pakistani family
- <i>FOXN1</i> Duplication and Congenital Hypertrichosis
- The Roles of EDA2R in Ageing and Disease
- BRITISH ASSOCIATION OF DERMATOLOGY.