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Research 181–210 of 1000+
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- Hair Follicle Disruption Facilitates Pathogenesis to UVB-Induced Cutaneous Inflammation and Basal Cell Carcinoma Development in Ptch+/− Mice
- Expression analysis of KAP9.2 and Hoxc13 genes during different cashmere growth stages by qRT-PCR method
- Growth of the Mouse Coat VII. Hair Cycles and Sebaceous Glands in Homozygous and Heterozygous Naked Mice
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Ancient Genomes Reveal the Evolutionary History and Origin of Cashmere-Producing Goats in China
- Differential gene expression profiles in foetal skin of Rex rabbits with different wool density
- Sequence of a Cashmere goat type I hair keratin gene and its expression in skin
- Detecting the Mechanism behind the Transition from Fixed Two-Dimensional Patterned Sika Deer (Cervus nippon) Dermal Papilla Cells to Three-Dimensional Pattern
- Investigating the Genetic Association of Selected Candidate Loci with Alopecia Areata Susceptibility in Jordanian Patients
- Aging Skin: A Window to the Body
- Biology of the Hair Follicle: The Basics
- Vitamin D metabolism and function in the skin
- Genetic Disorders and Defects in Vitamin D Action
- Learning from nudity: lessons from the nude phenotype
- Alopecia Areata. Current situation and perspectives
- Alopecia Areata
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Current Genetics in Hair Diseases
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Two females with hair loss
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Molecular Genetics of Human Hair Diseases
- Wound Healing and Skin Regeneration
- <i>Hoxc13</i> mutant mice lack external hair