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Research 31–60 of 1000+
- Alopecia Areata is associated with MICA and an extended HLA haplotype
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- A case of ophiasis type of alopecia areata in a patient with ring chromosome 18 syndrome
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- Genes for intermediate filament proteins and the draft sequence of the human genome
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- Chromosomal localization of acidic and basic keratin genes of the domestic dog
- Scraggly, a new hair loss mutation on mouse Chromosome 19
- A Group of Type I Keratin Genes on Human Chromosome 17: Characterization and Expression
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- The Tabby (Ta), Tabby-c (Tac), and Tabby-J (TaJ) Mutations, Chromosome X
- Molecular mechanisms of Y chromosome loss and <i>UTY</i> gene activity
- The diversity of sex development: What do conditions affecting sex development teach us about sexual diversity?
- The X Factor in Immunity: Sex Differences Shaped by the X Chromosome
- Sex-limited chromosomes and non-reproductive traits
- Genome Report: chromosome-scale genome assembly of the African spiny mouse (<i>Acomys cahirinus</i>)
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- Characterisation of Three Ovine KRTAP13 Family Genes and Their Association with Wool Traits in Chinese Tan Sheep
- A Small Deletion Hotspot in the Type II Keratin Gene<i>mK6irs1/Krt2-6g</i>on Mouse Chromosome 15, a Candidate for Causing the Wavy Hair of the Caracul (<i>Ca</i>) Mutation
- Characterisation of an Ovine Keratin Associated Protein (KAP) Gene, Which Would Produce a Protein Rich in Glycine and Tyrosine, but Lacking in Cysteine
- 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
- Fine Mapping and Identifying the Mutation Gene of snthr -1Bao ScantHair Mouse
- Comparative genomics of the keratin-associated protein (KAP) gene clusters in human, chimpanzee, and baboon
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- SEXUAL DIMORPHISM IN MAMMALS
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13