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Research 181–210 of 1000+
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- CPK1 activates CNGCs through phosphorylation for Ca2+ signaling to promote root hair growth in Arabidopsis
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice
- Therapeutic inhibition of keratinocyte TRPV3 sensory channel by local anesthetic dyclonine
- Colourless side of the <i>nude</i> mutation: Foxn1 and hair pigmentation
- Skin abnormalities generated by temporally controlled RXRα mutations in mouse epidermis
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Phosphorus Uptake and Growth of Wild-Type Barley and Its Root-Hairless Mutant Cultured in Buffered-and Non-Buffered-P Solutions
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Arabidopsis ZINC FINGER PROTEIN1 Acts Downstream of GL2 to Repress Root Hair Initiation and Elongation by Directly Suppressing bHLH Genes
- Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene
- The Anti-atopic Lotions Containing Fucoidan Extracted from Ecklonia Cava Impact on Hairless Mice Atopic Dermatitis Skin
- 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
- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene
- Alopezien und Hypotrichosen im Kindesalter
- Central Centrifugal Cicatricial Alopecia (CCCA)
- <i>Hoxc13</i> mutant mice lack external hair
- Alopecia: possible causes and treatments, particularly in captive nonhuman primates.
- Quantification of the Vitamin D Receptor−Coregulator Interaction
- Increased rate of hair keratin gene loss in the cetacean lineage
- The nude gene and the skin
- Milestones in Photocarcinogenesis
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia