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The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

Cyclic nucleotide-gated channels are crucial for proper root hair growth and calcium balance in plants.

TR3 is mainly found in hair follicle stem cells and may be involved in hair loss.

The vitamin D receptor has many roles in the body beyond managing calcium, affecting the immune system, hair growth, muscles, fat, bone marrow, and cancer cells.

Raltitrexed conjugates are less potent than the free drug but more effective at high concentrations.

BRG1 is essential for skin cells to move and heal wounds properly.

AVT is highly conserved and may have antimicrobial properties.

A girl had rickets due to a gene mutation affecting vitamin D response.

The Itpr3 gene causes a specific hair pattern in mice.

TTD hair is brittle due to fewer sulfur amino acids and unstable disulfide bonds.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

TIP39 and PTH2R help control calcium levels and skin cell development.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

A gene mutation causes curly hair and hair loss in rats.

Tiger tail banding and hair abnormalities are reliable indicators for diagnosing trichothiodystrophy.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Caribine from traditional Chinese medicine may help treat hair loss.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

Touch dome keratinocytes in adult skin have traits of different skin cell types.

Strontium ranelate helps cartilage growth by blocking a specific cell pathway.

Recognizing RSCC is crucial due to its aggressive nature and high risk of poor outcomes.

Trichohyalin is modified by enzymes to form strong structures in hair cells.

CARASIL can cause different symptoms even with the same genetic mutation.

Higher CRBP1 levels are linked to more severe alopecia areata.

TRPV4 slows hair growth by affecting hair follicle cells.

TRPV3 could be a target for treating pain, skin disorders, and hair problems, but more research is needed to create effective drugs.