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Research 181–210 of 1000+
- The structure and organization of lanceolate mechanosensory complexes at mouse hair follicles
- A slow-cycling LGR5 tumour population mediates basal cell carcinoma relapse after therapy
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Skin tissue engineering
- Stimuli-responsive nanoformulations for CRISPR-Cas9 genome editing
- Gender-Difference in Hair Length as Revealed by Crispr-Based Production of Long-Haired Mice with Dysfunctional FGF5 Mutations
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Mechanical forces across compartments coordinate cell shape and fate transitions to generate tissue architecture
- The Multifaceted Functions of TRPV4 and Calcium Oscillations in Tissue Repair
- Diseases of the Canine Prostate Gland
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Visualising Androgen Receptor Activity in Male and Female Mice
- High proliferation and delamination during skin epidermal stratification
- In vivo monitoring of hair cycle stages via bioluminescence imaging of hair follicle NG2 cells
- Resequencing Analyses Revealed Genetic Diversity and Selection Signatures during Rabbit Breeding and Improvement
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- 25th Annual meeting of the European Society for Pigment Cell Research, Marseille, France
- Human and animal cells under influence of different lighting and stimulus
- TSA restores hair follicle-inductive capacity of skin-derived precursors
- Keratin 17 modulates hair follicle cycling in a TN<i>Fα</i>-dependent fashion
- Cartilage to bone transformation during fracture healing is coordinated by the invading vasculature and induction of the core pluripotency genes