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New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Editing the FGF5 gene in sheep increases wool length, confirming its role in hair growth.

A new enzyme, BSSP, is found in high amounts in the hair follicles of nude mice.

Certain gene variations may increase the risk of hair loss in Egyptians.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Cathepsin L deficiency causes large, abnormal cell structures and health issues in mice.

Finasteride may cause cataracts and floppy-iris syndrome.

Overexpressing SSAT enzyme reduces prostate tumor growth in mice.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Phospholipids help plant proteins move by regulating receptor interactions.

Researchers used CRISPR/Cas9 to create a goat with a gene that increased cashmere production by 74.5% without affecting quality.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

A specific gene mutation causes long hair in Angora rabbits.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

SLC3A2 is crucial for hair follicle stem cell function and hair growth.

A substance called Compound 2g can strongly block STS (a hormone-related enzyme) without affecting estrogen levels, making it potentially good for treating breast cancer.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

SEFFI is a safe and effective anti-aging treatment with few complications.

The research helps understand how finasteride works and aids drug development.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

Retinoids increase steroid sulfatase activity in leukemia cells through RARα/RXR and involves certain pathways like phosphoinositide 3-kinase and ERK-MAP kinase.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

The LEF-1 gene in cashmere goats was successfully cloned and analyzed, showing potential for improving cashmere production.