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A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

The human K5 promoter controls specific gene expression in skin cells, with key regulatory elements near the TATA box.

GAPO syndrome causes growth issues, hair loss, missing teeth, and vision problems.

Targeting ornithine decarboxylase can help prevent skin cancer.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Keratin mutations may cause scarring alopecia by damaging hair structure.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

Lactococcus lactis strain H61 may reduce some ageing symptoms.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

Inherited color dilution in rabbits is linked to DNA methylation changes.

CRISPR gene editing reduces harmful molecules in cells from Emery–Dreifuss Muscular Dystrophy patients.

Removing Gata6 causes hair follicle and sebaceous duct enlargement.

Lack of a certain enzyme causes hair to grey early by damaging stem cells, but an antioxidant can help prevent this.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

Patched1 helps prevent tumors by controlling cell growth.

Certain changes in the KAP6-1 gene affect the thickness and length of cashmere goat fibers.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

Minoxidil boosts hair growth in genetically modified mice.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

CRISPR/Cas9 gene editing in cashmere goats increases hair follicles and fiber length, boosting cashmere yield.

Mutations in the KLHL24 gene cause skin blistering in epidermolysis bullosa simplex.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.