Search
for
Sort by
Research 30 of 1000+
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Genes for intermediate filament proteins and the draft sequence of the human genome
- Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- A mouse with bad hair and poor taste
- Sequence Data and Chromosomal Localization of Human Type I and Type II Hair Keratin Genes
- Identification of the Ovine Keratin-Associated Protein 21-1 Gene and Its Association with Variation in Wool Traits
- Role of polymorphism of the androgen receptor gene andnon-random x chromosome inactivation in the pathogenesisof androgenic alopecia
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
- Marie-unna hereditary hypotrichosis
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Finding bald spots on chromosome 20p11
- Chromosomal localization of acidic and basic keratin genes of the domestic dog
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- DYS459, DYS391, DYS388 and DYS19 genetic loci have high allelic frequency in patients with prostate cancer
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- An adolescent girl presenting with primary amenorrhea: A case report of complete androgen insensitivity syndrome
- Genetic association of wool quality characteristics in United States Rambouillet sheep
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
- Updates to Male Infertility: AUA/ASRM Guideline (2024)
- Hair follicle-specific keratins and their diseases
- Prevalence of MMP-1 rs1799750 Polymorphism in Androgenetic Alopecia: A Cross-Sectional Study in an Indonesia Population
- A 10 Mb duplication in chromosome band 5q31.3–5q33.1 associated with late-onset lipodystrophy, ichthyosis, epilepsy and glomerulonephritis
- Exploring the effects of wetting and free fatty acid deposition on an atomistic hair fiber surface model incorporating Keratin Associated Protein 5-1
- Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
- Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family