Search
for
Sort by
Research 30 of 1000+
- Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5
- Endocrine abnormalities in ring chromosome 11: a case report and review of the literature
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11*1
- A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes
- Expression of novel keratin associated protein 5 genes in the cuticle layer of human hair follicles
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
- Overexpression of Hoxc13 in differentiating keratinocytes results in downregulation of a novel hair keratin gene cluster and alopecia
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- Several variants on chromosome 10 are associated with coarse hair diameter in Dazu black goats (<i>Capra hircus</i>)
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- [Association of eight single nucleotide polymorphisms of chromosomes 20 and X with androgenetic alopecia among ethnic Han Chinese from Yunnan].
- Identification of the Ovine Keratin-Associated Protein 21-1 Gene and Its Association with Variation in Wool Traits
- Mapping of a novel locus for keratosis follicularis squamosa on chromosome 7p14.3–7p12.1
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- A group of type I keratin genes on human chromosome 17: characterization and expression.
- The first broad replication study of SNPs and a pilot genome‐wide association study for androgenetic alopecia in Asian populations
- Finding bald spots on chromosome 20p11
- A case of ophiasis type of alopecia areata in a patient with ring chromosome 18 syndrome
- The Majority of Multipotent Epidermal Stem Cells Do Not Protect Their Genome by Asymmetrical Chromosome Segregation
- A Group of Type I Keratin Genes on Human Chromosome 17: Characterization and Expression
- Basonuclin is associated with the ribosomal RNA genes on human keratinocyte mitotic chromosomes