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Research 91–120 of 1000+
- 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
- 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
- Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition
- Bloom's syndrome–‐a first report from India
- Potential Role of the Epidermal Differentiation Complex in the Pathogenesis of Psoriasis
- Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes
- Human Adipose-Derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele