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Research 61–90 of 1000+
- 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
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- 7 Pathogenesis and Classification of Male Pattern Hair Loss (Androgenic Alopecia)
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- 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
- Genes for intermediate filament proteins and the draft sequence of the human genome
- 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
- 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
- Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes
- Sequence Data and Chromosomal Localization of Human Type I and Type II Hair Keratin Genes
- Lanceolate Hair (lah): A Recessive Mouse Mutation with Alopecia and Abnormal Hair
- Characterization and Chromosomal Localization of Human Hair-Specific Keratin Genes and Comparative Expression During the Hair Growth Cycle
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Size Polymorphisms in the Human Ultrahigh Sulfur Hair Keratin-Associated Protein 4, KAP4, Gene Family