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Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

ESR2 gene linked to female-pattern hair loss.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

SQSTM1 is linked to increased risk of alopecia areata.

Reducing SOX2 in colorectal cancer cells decreases tumor growth and self-renewal.

Sox6 is important in heart and kidney health, affecting diseases like diabetes, heart disease, and high blood pressure.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

Runx1 affects hair growth, cancer development, and autoimmune diseases in epithelial tissues.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Trps1 is essential for proper hair follicle development.

The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

A new gene mutation causes insulin resistance in a girl and her mother.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

SOX18 helps sheep hair cells grow by activating a specific cell growth pathway.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

Lhx2 helps retinal cells respond to signals for eye development.

Lhx2 is essential for effective Sonic Hedgehog signaling in early retinal development.

Sebaceous gland atrophy and abnormal function may contribute to hair loss in psoriasis.

Trps1 plays a key role in hair follicle development and cycling.

RAR-gamma 1 is important for normal skin maintenance and differentiation.

Understanding snoRNA regulation may help slow skin aging.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

A young patient with unusual insulin resistance and high testosterone levels had a rare INSR gene mutation.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.