Search
for
Sort by
Research 781–810 of 1000+
- A protein kinase target of a PDK1 signalling pathway is involved in root hair growth in Arabidopsis
- Vitamin D: More Than a “Bone-a-Fide” Hormone
- O-Glycosylated Cell Wall Proteins Are Essential in Root Hair Growth
- The Catalog of Human Hair Keratins
- Reactive Oxygen Species (ROS): Beneficial Companions of Plants’ Developmental Processes
- Identification and Characterization of a Novel Lysophosphatidic Acid Receptor, p2y5/LPA6
- Melatonin in the skin: synthesis, metabolism and functions
- Biological Function of Long Non-coding RNA (LncRNA) Xist
- Intradermal adipocytes mediate fibroblast recruitment during skin wound healing
- The Catalog of Human Hair Keratins
- Induction of the hair growth phase in postnatal mice by localized transient expression of Sonic hedgehog
- Human Hair Keratin‐Associated Proteins (KAPs)
- A Novel Marker of Tissue Junctions, Collagen XXII
- The Biological Actions of Dehydroepiandrosterone Involves Multiple Receptors
- Lipoatrophy and severe metabolic disturbance in mice with fat-specific deletion of PPARγ
- The 5 Alpha-Reductase Isozyme Family: A Review of Basic Biology and Their Role in Human Diseases
- The cell-surface marker MTS24 identifies a novel population of follicular keratinocytes with characteristics of progenitor cells
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Keratin 15 Expression in Stratified Epithelia: Downregulation in Activated Keratinocytes
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Evolution and Function of Vitamin D
- Melatonin: A Cutaneous Perspective on its Production, Metabolism, and Functions
- ATP-dependent chromatin remodeling during mammalian development
- Evidence that Myc activation depletes the epidermal stem cell compartment by modulating adhesive interactions with the local microenvironment
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- GLI2 Is Expressed in Normal Human Epidermis and BCC and Induces GLI1 Expression by Binding to its Promoter
- Comparative Proteomics Indicates That Biosynthesis of Pectic Precursors Is Important for Cotton Fiber and Arabidopsis Root Hair Elongation