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Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

DNAJB9 cfRNA could help diagnose and treat female hair loss.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.

Gene variation affects prostate issues and hair loss.

Using special RNA to target a mutant gene fixed hair problems in mice.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

The LEF-1 binding site enhances gene expression in hair follicles, with other proteins aiding specific regulation.

Researchers found 15 new genetic links to skin traits in Japanese women.

Modified β-catenin causes different effects in hair and skin cells, leading to cysts or tumors.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

lncRNAs may help control cashmere goat hair growth by responding to light changes.

The KRTAP22-2 gene in sheep does not significantly affect wool traits.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

A mutation in the KRT25 gene causes woolly hair and hair loss.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

CK 19 expression is higher in more severe skin cancers.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Certain RNAs may help diagnose alopecia areata by affecting keratin genes.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.