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ΔNp63α helps control a protein that stops cancer cells from spreading.

Lamins are vital for cell survival, organ development, and preventing premature aging.

RANK is a key target in breast cancer treatment due to its role in tumor growth and bone metastasis.

Melatonin affects many body functions beyond sleep by interacting with specific receptors in various tissues.

Human skin can make serotonin and melatonin.

The document concludes that understanding the anatomical changes of the ageing face is important for effective rejuvenation treatments.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

Hair color is determined by melanin produced and transferred in hair follicles.

Low oxygen areas help maintain and protect blood stem cells by using a simple sugar breakdown process for energy and managing their activity levels.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

Eph receptors and ephrins may be promising targets for treating diseases, but more understanding is needed for effective and safe therapies.

Found different proteins in balding and non-balding cells, giving insight into hair loss causes.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

Hairless protein is key for hair growth, cell differences cause gene expression variation, and the N-end rule pathway senses nitric oxide for protein breakdown.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

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

The document concludes that pig iPSCs show promise for transplant therapies and the field is advancing in controlling cell behavior for biology and medicine.

The document concludes that treating androgen excess needs patience, managing expectations is important, and many drugs used are not officially approved, suggesting cosmetic options for mild cases.