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Research 871–900 of 1000+
- Characterisation of Ovine KRTAP19-3 and Its Impact on Wool Traits in Chinese Tan Sheep
- Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts
- Etude des multiples rôles des phosphatidylinositol-4-kinases betas dans la morphogenèse et les réponses de défense d'Arabidopsis thaliana
- How the leopard gets its spots: a transmembrane peptidase specifies feline pigmentation patterns
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- From signal to form: Nod factor as a morhogenetic signal molecule to induce symbiotic responses in legume root hairs
- Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- The RpoS Gatekeeper in Borrelia burgdorferi: An Invariant Regulatory Scheme That Promotes Spirochete Persistence in Reservoir Hosts and Niche Diversity
- White Lupin Cluster Root Acclimation to Phosphorus Deficiency and Root Hair Development Involve Unique Glycerophosphodiester Phosphodiesterases
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- An essential role for <i>Rxrα</i> in the development of Th2 responses
- Intelligent nanotherapeutic strategies for the delivery of CRISPR system
- Exploring Variation in Ovine KRTAP19-5 and Its Effect on Fine Wool Fibre Curvature in Chinese Tan Sheep
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Detection of a Second KAP22 Family Member in Sheep and Analysis of Its Genetic Variation and Associations with Selected Wool Fibre Traits
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Mettl3-catalyzed m <sup>6</sup> A regulates histone modifier and modification expression in self-renewing somatic tissue
- Targeted inactivation of integrin-linked kinase in hair follicle stem cells reveals an important modulatory role in skin repair after injury
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Somatic Mutations in Normal Tissues: New Perspectives on Early Carcinogenesis
- TGFβ signaling regulates lipogenesis in human sebaceous glands cells
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- B-Raf and C-Raf Are Required for Melanocyte Stem Cell Self-Maintenance
- Essential Role for Integrin-Linked Kinase in Melanoblast Colonization of the Skin