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Research 61–90 of 1000+
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- The X Factor in Immunity: Sex Differences Shaped by the X Chromosome
- Effects of anticonvulsant drugs on chromosomes.
- The human type I keratin gene family: Characterization of new hair follicle specific members and evaluation of the chromosome 17q21.2 gene domain
- 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
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11
- The role of the androgen receptor gene CAG repeat polymorphism and X-chromosome inactivation pattern in postmenopausal female pattern hair loss
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11*1
- Characterization of New Members of the Human Type II Keratin Gene Family and a General Evaluation of the Keratin Gene Domain on Chromosome 12q13.13
- 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
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Human Trichohyalin Gene Is Clustered with the Genes for Other Epidermal Structural Proteins and Calcium-Binding Proteins at Chromosomal Locus 1q21
- Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- SEXUAL DIMORPHISM IN MAMMALS
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Overexpression of Hoxc13 in differentiating keratinocytes results in downregulation of a novel hair keratin gene cluster and alopecia
- Male-pattern baldness susceptibility locus at 20p11
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- THE PATHOGENESIS OF ALOPECIA AREATA
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13