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Fasting in hens affects thyroid hormones, which regulate feather and hair growth.

Sex and sex hormones can affect brain inflammation in Parkinson's disease, with male mice being more affected and female mice showing a protective effect.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

Newly divided skin cells quickly move to join skin structures due to tissue tension and specific signals.

The document concludes that blocking the internal pathways that create androgens might help treat cancers that depend on sex hormones.

Tadalafil and Finasteride may help treat aggressive melanoma.

Fingerprints form uniquely before birth due to specific genetic pathways and local signals.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

A new mutation in the HR gene causes hair loss in a specific family.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

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

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.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Disrupting Stat3 in hair follicle stem cells greatly reduces skin tumor formation.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

Mutations in the enzyme don't significantly change how it binds to its specific substances.