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Research 61–90 of 1000+
- TCF/Lef1-Mediated Control of Lipid Metabolism Regulates Skin Barrier Function
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Identification of the Ovine Keratin-Associated Protein 21-1 Gene and Its Association with Variation in Wool Traits
- Gender-Difference in Hair Length as Revealed by Crispr-Based Production of Long-Haired Mice with Dysfunctional FGF5 Mutations
- The Mean Staple Length of Wool Fibre Is Associated with Variation in the Ovine Keratin-Associated Protein 21-2 Gene
- New clinico‐genetic classification of trichothiodystrophy
- The extracellular matrix dictates regional competence for tumour initiation
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Boron deficiency responses in maize (<i>Zea mays</i> L.) roots
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- NUDT15 polymorphism explains serious toxicity to azathioprine in Indian patients with chronic immune thrombocytopenia and autoimmune hemolytic anemia: a case series
- Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- Polymorphisms of OCT1 and metformin effects in Iraqi women with polycystic ovary syndrome in Karbala city
- Molecular genetics of androgen insensitivity
- The <i>IRE</i> gene encodes a protein kinase homologue and modulates root hair growth in <i>Arabidopsis</i>
- A pair of transmembrane receptors essential for the retention and pigmentation of hair
- Molecular and physiological mechanisms underlying the antifungal and nutrient acquisition activities of beneficial microbes
- Auxin Input Pathway Disruptions Are Mitigated by Changes in Auxin Biosynthetic Gene Expression in Arabidopsis
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- Premature aging and cancer development in transgenic mice lacking functional CYLD
- Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Establishment of Tsc2-deficient rat embryonic stem cells
- A novel 22-bp InDel within <i>FGF7</i> gene is significantly associated with growth traits in goat
- Detection of a Second KAP22 Family Member in Sheep and Analysis of Its Genetic Variation and Associations with Selected Wool Fibre Traits
- Pathogenesis and management of TRPV3-related Olmsted syndrome