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Research 181–210 of 1000+
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
- A Ca <sup>2+</sup> /calmodulin-dependent protein kinase required for symbiotic nodule development: Gene identification by transcript-based cloning
- Genetic analysis of interleukin 18 gene polymorphisms in alopecia areata
- Correlation analysis of four KRTAP gene polymorphisms and cashmere fiber diameters in two cashmere goat breeds
- Elucidating the roles of three β-glucuronosyltransferases (GLCATs) acting on arabinogalactan-proteins using a CRISPR-Cas9 multiplexing approach in Arabidopsis
- MiRNA-24 downregulates KLF6 affecting STAT3 protein expression and phosphorylation regulating melanogenesis in cashmere goat coat
- The heme-responsive PrrH sRNA regulates <i>Pseudomonas aeruginosa</i> pyochelin gene expression
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- FGF5 is a crucial regulator of hair length in humans
- MicroRNA-149-Mediated MAPK1/ERK2 Suppression Attenuates Hair Follicle Stem Cell Differentiation
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Establishment of Tsc2-deficient rat embryonic stem cells
- Analogs of human genetic skin disease in domesticated animals
- miR-370-3p Inhibited the Proliferation of Sheep Dermal Papilla Cells by Inhibiting the Expression of SMAD4
- Interleukin-1 Induces Transcription of Keratin K6 in Human Epidermal Keratinocytes
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- UDP-GlcNAc-1-Phosphotransferase Is a Clinically Important Regulator of Human and Mouse Hair Pigmentation
- Skin morphology of the mutant hairless USP mouse
- Mechanism of JmjC-containing protein Hairless in the regulation of vitamin D receptor function
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization