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Disodium folinate can safely and effectively replace calcium folinate in colorectal cancer treatment.

Protein profiling of forehead skin can help distinguish between frontal fibrosing alopecia and androgenetic alopecia.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Neurosteroids like allopregnanolone help control cell death and growth in the developing fetal brain.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps from birth.

Frontal fibrosing alopecia may be caused by an autoimmune reaction and hormonal imbalance.

Long non-coding RNA Xist plays a key role in sex bias in lupus and rheumatoid arthritis, especially in females.

A 308 nm excimer laser successfully treated a boy with a rare skin condition after about a year of weekly sessions.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

Hair follicle stem cells are crucial for touch sensation and proper nerve structure in mice.

New treatments for Frontal Fibrosing Alopecia show promise, especially finasteride and dutasteride, with most patients seeing improvement or stabilization.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

An elderly Chinese man lost all his hair after taking a new heart medication.

Erk signaling helps zebrafish fins regrow to the right size by using memory of the original size.

Researchers found a new early sign of Frontal Fibrosing Alopecia that could help avoid misdiagnosis.

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.

PADI4 enzyme slows down cell growth in developing hair follicles.

PF-05314882 selectively activates androgen receptors without much effect on prostate and may help in prostate cancer treatment and hair loss prevention.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

SFRP-4 might be an early indicator of diabetes and hypertension in men with androgenic alopecia.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps due to a gene mutation.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

Channels stay open for 24 hours, making laser treatment potentially effective for hair loss.

Palmaris longus muscle absence is uncommon and not linked to gender, hand side, or finger ratio.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

A new method using nanolipogels with fucosterol can help regrow hair by targeting follicles, reducing inflammation, and improving blood flow.

"20-nail dystrophy" can have multiple causes.

Mice without the p21 gene can fully regenerate injured ears due to reduced Sdf1 increase and leukocyte recruitment, suggesting new ways to induce tissue regeneration in mammals.