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Overactive Stat3 in mouse skin causes hair loss and cell structure damage.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

Fadrozole and finasteride change gene expression related to sex hormones and thyroid hormones in frog larvae development.

In STSD patients, the body compensates for low androgen levels by increasing another enzyme's activity.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

PTCH gene mutations contribute to basal cell carcinoma development.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Overexpressing a specific enzyme in mice causes hair loss and female infertility.

Poliosis causes white hair patches due to lack of melanin.

A specific gene mutation causes different hair defects in Indian monilethrix families.

Two gene variants cause white spots in cattle.

Different types of polycystic ovary syndrome show varying levels of insulin resistance, with the 'PHO' type being the most insulin resistant.

Steroid sulfatase is important for activating hormones that affect memory, brain function, and certain diseases, and could be a target for treating hormone-related disorders.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

Both enzyme forms can sulfate minoxidil.

Some women with PCOS have CYP21 mutations and IRS1 variants, but these genetic factors are not major contributors to PCOS.

SIPHL1 from tomato enhances plants' response to low phosphate levels.

Polycomb Repressive Complex 2 is not needed for hair regeneration.

Defective nuclear transport may cause gene expression changes in Progeria.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

Thyroid hormones and androgens affect gene expression in frog reproductive organs differently between males and females.

SQSTM1 gene issues may increase the risk of alopecia areata.

Men with more CAG repeats in the androgen receptor gene and lower testosterone levels may experience more severe COVID-19.