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Research 901–930 of 1000+
- Moderate water stress in rice induces rhizosheath formation associated with abscisic acid and auxin responses
- A novel immune competent murine hypertrophic scar contracture model: A tool to elucidate disease mechanism and develop new therapies
- An N-Ethyl-N-Nitrosourea Induced Corticotropin-Releasing Hormone Promoter Mutation Provides a Mouse Model for Endogenous Glucocorticoid Excess
- Bone vs. fat: Embryonic origin of progenitors determines response to androgen in adipocytes and osteoblasts
- <i>In Vitro</i> Analysis of Finasteride Activity against Candida albicans Urinary Biofilm Formation and Filamentation
- Insights learned from L457(3.43)R, an activating mutant of the human lutropin receptor
- Somatic Mutations in Normal Tissues: New Perspectives on Early Carcinogenesis
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Effect of Flightless I Expression on Epidermal Stem Cell Niche During Wound Repair
- Overexpression of hepatoma-derived growth factor in melanocytes does not lead to oncogenic transformation
- Functional analysis of vitamin D receptor (VDR) using adenovirus vector
- COVID-19: The question of genetic diversity and therapeutic intervention approaches
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- Drought-induced SlCLE10 coordinates ethylene biosynthesis and root hair development to confer osmotic stress tolerance in tomato
- Molecular mechanism for transcriptional regulation of the parathyroid hormone gene by Epiprofin
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Expression and Analysis of TBX3 Gene in the Skin from Three Locations on Dun Mongolian Bider Horse
- Phytochemical Analysis and Antioxidant Activities of Prunus africana Bark, Leea indica and Paullinia pinnata Leaf Extracts
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Semidominant Inheritance in Epidermolytic Ichthyosis
- MicroRNA-181a Targets GNAI2 and Affects the Proliferation and Induction Ability of Dermal Papilla Cells: The Potential Involvement of the Wnt/β-Catenin Signaling Pathway
- <i>OsPHR2</i> Is Involved in Phosphate-Starvation Signaling and Excessive Phosphate Accumulation in Shoots of Plants
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- GLI2 Is Expressed in Normal Human Epidermis and BCC and Induces GLI1 Expression by Binding to its Promoter
- Impact of estrogens in males and androgens in females