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The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

CPK1 helps root hair growth in Arabidopsis by activating channels for calcium signaling.

The patient's hair had unique damage and a lower sulfur-to-nitrogen ratio compared to relatives, but not compared to healthy controls.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

B6.Cg-Tyr c−2J Hr hr /J mice have a stronger delayed sunburn reaction and are good for UV research.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

hHb1, hHb3, and hHb6 mRNAs start expressing at the same time in hair follicles.

Botryococcus braunii's three chemical races should be reclassified as separate species.

The microenvironment affects the behavior and survival of melanocytes with the GNAQ oncogene in melanoma.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

SGK3 is essential for proper hair growth and health.

BTNL2 helps protect hair follicles from immune attacks, which could aid in treating alopecia areata.

The FGF5 gene variant causes long hair in Akitas, and genetic testing is advised to manage coat length and welfare.

CD98hc's role in skin health decreases with age.

SQSTM1 is linked to increased risk of alopecia areata.

Box A of HMGB1 can improve stem cell function, aiding anti-aging therapy.

A group has developed therapies that show promise for treating cancer and various other conditions.

Multiple mouse desmoglein 1 isoforms have distinct roles in skin and hair development.

In alopecia areata, certain immune cells increase and express a protein linked to immune activation.

The G allele of IFITM3 rs12252 is linked to more severe COVID-19.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Strontium and cerium are most effective for tissue repair.

Seven new genetic risk areas for prostate cancer were found.

Researchers found a non-functional sheep keratin gene due to mutations.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

CG2001 is safe, well-tolerated, and a promising treatment for hair loss with fewer side effects.

Certain SHBG gene variants, like rs727428, are linked to higher testosterone levels in women with PCOS.

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