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Research 571–600 of 1000+
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Androgens Protect against Apolipoprotein E4-Induced Cognitive Deficits
- Lack of the Vitamin D Receptor is Associated with Reduced Epidermal Differentiation and Hair Follicle Growth
- Patched1 Functions as a Gatekeeper by Promoting Cell Cycle Progression
- Fundamental hair follicle biology and fine fibre production in animals
- Impaired wound healing in transgenic mice overexpressing the activin antagonist follistatin in the epidermis
- ATP-competitive mTOR kinase inhibitors delay plant growth by triggering early differentiation of meristematic cells but no developmental patterning change
- The Lysosomal Protease Cathepsin L Is an Important Regulator of Keratinocyte and Melanocyte Differentiation During Hair Follicle Morphogenesis and Cycling
- WNT Signaling in Disease
- Shh maintains dermal papilla identity and hair morphogenesis via a Noggin–Shh regulatory loop
- Intracrine androgen biosynthesis, metabolism and action revisited
- What’s Sex Got to Do With COVID-19? Gender-Based Differences in the Host Immune Response to Coronaviruses
- Stretching the limits: from homeostasis to stem cell plasticity in wound healing and cancer
- Frizzled Receptors in Development and Disease
- Integument pattern formation involves genetic and epigenetic controls: feather arrays simulated by digital hormone models.
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Identification of a link between Wnt/β-catenin signalling and the cell fusion pathway
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- NEDD4 and NEDD4L regulate Wnt signalling and intestinal stem cell priming by degrading LGR5 receptor
- TCF/Lef1 activity controls establishment of diverse stem and progenitor cell compartments in mouse epidermis
- Keratins and disease at a glance
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Temporal Layering of Signaling Effectors Drives Chromatin Remodeling during Hair Follicle Stem Cell Lineage Progression
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- <i>Arabidopsis</i> VILLIN4 is involved in root hair growth through regulating actin organization in a Ca<sup>2+</sup>‐dependent manner
- Pathology of Mouse Models of Accelerated Aging
- Inherited ichthyoses/generalized Mendelian disorders of cornification