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Research 30 of 1000+
- Scraggly, a new hair loss mutation on mouse Chromosome 19
- Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes
- Sex-Chromosome-Related Dimorphism in Steroidogenic Enzymes and Androgen Receptor in Response to Testosterone Treatment: An In Vitro Study on Human Primary Skeletal Muscle Cells
- It’s X-Related: Biological Bases of Increased COVID-19 Morbidity and Mortality in Men
- Polycystic ovary syndrome (PCOS) trilogy: a translational and clinical review
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Balding: A New Mutation on Mouse Chromosome 18 Causing Hair Loss and Immunological Defects
- BRITISH ASSOCIATION OF DERMATOLOGY.
- Identification of the Ovine Keratin-Associated Protein 21-1 Gene and Its Association with Variation in Wool Traits
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Mapping of a novel locus for keratosis follicularis squamosa on chromosome 7p14.3–7p12.1
- Endocrine abnormalities in ring chromosome 11: a case report and review of the literature
- Genetic and hormonal influence on SARS-CoV-2-infection susceptibility
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- 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
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- Immune mechanisms associated with sex-based differences in severe COVID-19 clinical outcomes
- The X Factor in Immunity: Sex Differences Shaped by the X Chromosome
- Genetic correlation analysis does not associate male pattern baldness with COVID-19
- THE PATHOGENESIS OF ALOPECIA AREATA
- Toxicological Studies on Procyanidin B-2 for Extern?al Application as a Hair Growing Agent
- Molecular genetics of androgen insensitivity
- SEXUAL DIMORPHISM IN MAMMALS
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- A Group of Type I Keratin Genes on Human Chromosome 17: Characterization and Expression
- Characterisation of an Ovine Keratin Associated Protein (KAP) Gene, Which Would Produce a Protein Rich in Glycine and Tyrosine, but Lacking in Cysteine
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Comment on: The Gabrin sign
- An interview Drs. Felix Brockschmidt and Markus Nöthen about the genetics of androgenetic alopecia