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Overexpressing NSD3 in mice causes breast cancer-like tumors and gland abnormalities.

Scientists found genes linked to hair length in Brangus cattle that could help breed heat-tolerant cattle.

Genetic marker rs12558842 strongly linked to male hair loss.

Thymic stromal lymphopoietin (TSLP) promotes hair growth, especially after skin injury.

WNT10B is important for body functions and linked to diseases like osteoporosis, obesity, and cancer.

Wnt/ß-catenin signaling is crucial for regulating skin stem cells and hair growth, with the right levels and timing needed for proper function.

The Dfl mutation in mice causes poor sebaceous gland function and complete hair loss.

PCAT1 helps hair growth by controlling miR-329/Wnt10b.

The PML protein helps prevent skin cancer in mice.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Wavy sinus hairs in cats are linked to feline leukemia virus infection.

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Certain long non-coding RNAs are important for the growth of hair follicles in Inner Mongolian cashmere goats.

The enzyme PA-PLA1α is important for proper hair follicle development.

Activated LEF/TCF complexes are crucial for hair development and cycling.

The KRTAP21-2 gene affects wool length and quality in sheep.

Monoclonal antibodies LT-1, LT-2, and LT-7 help diagnose certain blood cancers.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

Runx1 controls fat-related genes important for normal and cancer cell growth, affecting skin and hair cell behavior.

The KRT84 gene is linked to better wool quality in Gansu Alpine Fine-wool sheep.

CD8A and FOXD2-AS1 may be key for diagnosing and treating alopecia areata.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

A gene-based model predicts lung adenocarcinoma outcomes and helps guide treatment decisions.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

p2y5, now called LPA6, is a receptor important for human hair growth.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

Variant G of the KRTAP20-1 gene improves wool curliness in Chinese Tan sheep.

Certain genetic changes in the STX17 and KRT82 genes contribute to hair loss in alopecia areata.