Search
for
Sort by
Research 61–90 of 1000+
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Woolly hair nevus
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Trichoscopy in Hair Shaft Disorders
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Dermatoscopy of hair shaft disorders
- Hair loss in infancy and childhood
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Biology of the wool follicle: an excursion into a unique tissue interaction system waiting to be re‐discovered
- Hair Shaft Dysplasias
- Congenital hair loss disorders: Rare, but not too rare
- Transcriptome Analysis of Improved Wool Production in Skin-Specific Transgenic Sheep Overexpressing Ovine β-Catenin
- Unruly hair
- WOOLY HAIR PALMOPLANTAR KERATODERMA : A CASE REPORT
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- A rare case of woolly hair with unusual associations
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Marie-unna hereditary hypotrichosis
- Keratin disorders: from gene to therapy
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Trichoscopy in genetic hair shaft abnormalities
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Genetic association of wool quality characteristics in United States Rambouillet sheep
- Polymorphism of Keratin Gene KRT71 and Its Relationship with Wool Properties in Gansu Alpine Fine-Wool Sheep
- Screened of long non-coding RNA related to wool development and fineness in Gansu alpine fine-wool sheep
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Screening of Protein Related to Wool Development and Fineness in Gansu Alpine Fine-Wool Sheep