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Research 30 of 1000+
- Genetic Variation at the MC1R Locus and the Time since Loss of Human Body Hair
- A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Mapping of a novel locus for keratosis follicularis squamosa on chromosome 7p14.3–7p12.1
- Male-pattern baldness susceptibility locus at 20p11
- Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men
- Fine mapping of the human <i>AR/EDA2R</i> locus in androgenetic alopecia
- Association between the D19S884 marker at the insulin receptor gene locus and polycystic ovary syndrome
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population
- Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
- Association study reveals a susceptibility locus with male pattern baldness in the Han Chinese population
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31
- W locus alleles of the KIT Gene in Turkish Van Cats and Their Association with Certain Phenotypes
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11
- 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
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Genetics of blond hair
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
- Genetic association of <i>HLA‐DQB1</i> and <i>HLA‐DRB1</i> polymorphisms with alopecia areata in the Italian population
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology