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The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

Certain gene variations may increase the risk of PCOS in South Indian women.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

A new gene, JMJD1C, may affect testosterone levels in men.

Genetic defects in the Wnt/PCP pathway may cause congenital yellow nail syndrome.

Enzymes called PADIs play a key role in hair growth and loss.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Phytoconstituents from Cyperus Rotundus may help treat hirsutism by interacting with the 5 α reductase enzyme.

Genetic differences within ethnic groups may affect prostate cancer treatment effectiveness.

Mutations in the p63 gene affect skin adhesion, barrier integrity, and hair growth.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Cyclic nucleotide-gated channels are crucial for proper root hair growth and calcium balance in plants.

Certain gene variants may raise the risk of prostate enlargement, but taking NSAIDs could reduce this risk.

Hair loss in androgenic alopecia patients is linked to changes in certain genes that control cell growth and death.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

Finasteride doesn't affect antipyrine metabolism, so interactions with cytochrome P-450 enzyme drugs are unlikely.

NCBP3, SDHA, and PTPRA are the best genes for normalizing goat skin experiments.

Certain herbal compounds, especially from bitter melon, can inhibit cancer growth and promote hair growth by blocking PAK1.

A new DSG4 gene mutation causes hair defects in a young girl.

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

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

Hair follicles can be used to study gene mutations in Stargardt disease.

LY191704 is a compound that effectively blocks a specific enzyme involved in hormone conversion and could help treat enlarged prostate and hair loss.