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Boreal caribou in northeastern British Columbia have significant health issues, including infections, tick infestations, and mineral deficiencies.

PBM therapy improves mitochondrial function and promotes tissue regeneration in dental pulp stem cells.

EVG staining helps tell apart follicular scars from follicular streamers, aiding in diagnosing different types of hair loss.

Reticulocyte hemoglobin content is the best indicator of iron deficiency in women with diffuse non-scarring hair loss.

Dermal papilla cells and bulge stem cells can help reconstruct hair follicles.

Permanent waving damages hair by disrupting its keratin structure.

A vitamin D receptor mutation causes rickets and affects immune responses.

Cell movements and forces shape feather growth in chicken skin.

PRP injections with tadalafil and stretching safely improved Peyronie's symptoms but didn't significantly change curvature long-term.

The study found that minor protein differences between curved and straight Japanese hair are unlikely to significantly affect hair structure.

Domain shape greatly affects pattern formation.

Basal cell epithelioma-like changes are most similar to normal basal cells.

The Oat mouse model shows mild retinal degeneration, useful for testing treatments.

Lack of Vitamin D receptor changes skin structure and increases certain immune cells in the skin.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

The dermal sheath's contraction is crucial for hair follicle regression and stem cell relocation.

The rib-sparing technique in breast reconstruction may lead to more complications without reducing the need for further surgery.

Rushton's hyaline bodies form from hair keratin and blood substances.

Fibroblast changes in systemic sclerosis may help understand disease severity and treatment.

Permanent wave treatment with thioglycolic acid changes hair structure by altering disulfide bonds.

Two cases showed skin abnormalities without bone or neural defects.

Collagen scaffolds in cell therapy can transform skin to be more resilient and pressure-responsive.

NM2 and RLC phosphorylation are essential for normal inner ear hair cell function.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

Scientists have made progress in understanding hair follicle stem cells, identifying specific genes and markers, and suggesting their use in treating hair and skin conditions.

Tissue-engineered skin substitutes can model junctional epidermolysis bullosa and may help develop gene therapy.

Simple centrifugation with calcium gluconate boosts PDGF-BB release in PRP.

Trichothiodystrophy causes abnormal protein deposits and distortion in hair follicles.

Injury changes how hair follicle stem cells behave, depending on the hair growth stage.

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.