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Research 91–120 of 1000+
- 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
- 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
- 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
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Lanceolate Hair (lah): A Recessive Mouse Mutation with Alopecia and Abnormal Hair
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- 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
- Polycystic ovary syndrome (PCOS) trilogy: a translational and clinical review
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Treatment of alopecia areata: “What is new on the horizon?”
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome