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Trichohyalin is found in non-hair tissues and works with filaggrin in certain skin areas and conditions.

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

Scientists found a gene in mice that causes early hearing loss.

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Defective nuclear transport may cause gene expression changes in Progeria.

A new method helps grow skin stem cells better, which could improve skin grafts for burn victims.

PTHrP is important for bone formation and may be targeted for osteoporosis treatment and longevity therapies.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

Ginsenosides Rb₁ and Rd may help prevent hair loss by promoting hair cell growth.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

Toll-like receptor 3 helps repair the skin barrier after UV damage.

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

Aryl hydrocarbon receptor overexpression found in miniaturized hair follicles in female hair loss.

HDAC6 helps keep ovarian follicles dormant, extending female fertility.

A gene mutation causes monilethrix in a Chinese family.

AKR1D1 controls glucocorticoid levels and receptor activity in liver cells.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Modified HDL can better deliver drugs and genes, potentially improving treatments and reducing side effects.

Lgr5 is a marker for active, long-lasting stem cells in mouse hair follicles.

Hutchinson-Gilford Progeria Syndrome caused rapid aging due to a genetic mutation, with treatments to manage symptoms.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

A mutation in the KRTHB5 gene causes hair and nail issues.

The SbbHLH85 protein helps sweet sorghum grow more root hairs but makes the plant more sensitive to salt.

Prolactin contributes to hair loss by promoting hair follicle shrinkage and cell death.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

MPZL3 is important for controlling the hair growth cycle in mice and humans.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.