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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Certain gene variations are linked to better memory in healthy Chinese women.

Finasteride effectively treats male hair loss, increasing length and thickness.

PRP treatment may promote hair growth and improve hair density in women with AGA, but more research is needed.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

Hairless HRS/J mice resist Bacillus anthracis skin infections due to high numbers of immune cells, not because they lack hair follicles.

Women with myotonic dystrophy might get diseases related to male hormones because their body tissues are extra sensitive to these hormones.

Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.

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.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

Topical botanical lotion increases hair density and improves quality of life in women with hair loss.

Women with hair loss have more androgen receptors in certain hair follicles.

The Itpr3 gene causes a specific hair pattern in mice.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

KLF4 is important for maintaining stem cells and has potential in cancer treatment and wound healing.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

Dihydrotestosterone (DHT) is crucial for conditions like male-pattern baldness and acne, and measuring a byproduct, androstanediol glucuronide, is a better way to assess DHT's effects than DHT blood levels.

5α-reductase inhibitors can interfere with doping tests by masking banned substances.

Feather patterns are influenced by enhancers and chromatin looping, and the structure of protein complexes important for hair growth has been detailed.

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.

Hair loss in men is mainly caused by hormones and genes, and while current treatments can slow it down, they can't fully stop it.

New drug shows promise for better hair growth in baldness treatment.

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