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The research identified genes and non-coding RNAs in cells that could be affected by testosterone, which may help understand hair loss and prostate cancer.

Thymic transplantation normalized some T-cells but not others, maintaining immune function.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Several genes, including Hox-7A, Stra6, and Lim-1, are involved in normal palate formation.

LONRF1 is important for oxidative damage response and tissue remodeling during wound healing.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

Researchers created a new mouse model for studying scleroderma.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

PLIN2 affects hair growth in cashmere goats, potentially improving cashmere quality.

Inhibiting connective tissue sheath contraction may improve hair growth in male pattern baldness.

The MTR gene affects wool quality and production in Chinese Merino sheep.

Genetic profiling can improve androgenetic alopecia treatment by predicting drug response and minimizing side effects.

Desmoglein 4 is controlled by specific proteins that affect hair growth.

AtZP1 protein stops root hair growth in plants by blocking certain genes.

Lactate production is important for activating hair growth stem cells.

The HCR gene contributes to psoriasis risk.

miR-5110 affects alpaca pigmentation by altering specific gene expressions.

Specific keratin gene mutations can cause monilethrix.

Glioblastoma cells can make androgens, which might help the tumor grow.

The treatment showed significant hair regrowth in alopecia areata patients without side effects.

A mouse gene mutation increases the risk of skin cancer.

Activated ras can protect kidney cells from a certain substance that causes cell death.

ATP6AP1‐CDG can cause hearing loss, hair loss, and protein issues, even in female carriers.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

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

GLI and EGF signalling affect Basal Cell Carcinoma development and could be therapeutic targets.

Phospholipase C-δ1 is crucial for normal hair development.