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Research 121–150 of 1000+
- Remodelling of cytoskeleton and plasma membrane proteins contributes to drought sensitivity of Arabidopsis<i>rhd2</i>mutant
- Quantifying effects of aging across structures of the mouse auditory system, with in-vitro brain slice preparations
- Metabolic Regulation of Stem Cells in Aging
- FOXN1 deficient nude severe combined immunodeficiency
- 507 Trial to investigate the role of ATP-sensitive potassium channels (KATPc) in dermal papilla cells (DPCs)
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- <i>egfl6</i> expression in the pharyngeal pouch is dispensable for craniofacial development
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome
- TON1 recruiting motif 21 positively regulates the flavonoid metabolic pathway at the translational level in Arabidopsis thaliana
- Concise Review: Wnt Signaling Pathways in Skin Development and Epidermal Stem Cells
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Lamins in development, tissue maintenance and stress
- The fundamentals of WNT10A
- Animal models of human skin disease
- Melanocytes: The new Black
- Desmogleins: Hair perspective
- How the leopard gets its spots: a transmembrane peptidase specifies feline pigmentation patterns
- Interaction of the vacuolar H+-pyrophosphatase AVP1 with the secondary transporters AtNHX1 and SOS1 in Arabidopsis thaliana: Implications in salt tolerance and mineral nutrition
- Commentary on: Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Bridging Personal and Population in Excitability Diseases: Will Studies of Rare Diseases Bring Generalizable Mechanisms From Monogenic Channelopathies?
- Reversing wrinkled skin and hair loss in mice by restoring mitochondrial function
- Mandibulofacial dysostosis with alopecia results from ETAR gain-of-function mutations via allosteric effects on ligand binding
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Loss of PIKFyve Kinase Function Driven by Platelet Factor 4 Promoter Results in Platelet Lysosomal Storage Defects and Infiltration of Multiple Organs with Vacuolated Macrophages
- Deciphering the functions of the hair follicle infundibulum in skin physiology and disease
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix