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Phaeodactylum tricornutum extract helps hair follicle cells grow by activating the ERK1/2 pathway.

Probiotics may help improve health markers in women with PCOS.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

Platycladus orientalis leaf extract helps hair grow by activating certain proteins.

Frontal fibrosing alopecia has occurred in two related male families.

Nano-PROTACs could improve drug targeting and delivery by using nanotechnology.

Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

FOXC1 boosts SFRP1 in hair loss, suggesting new treatments.

Finasteride may help treat frontal fibrosing alopecia, but more research is needed.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

The document concludes that stopping shaving or removing affected hair can alleviate Pseudofolliculitis barbae (PFB).

The combination of propylene glycol and Tween® 80 improves finasteride gel effectiveness.

Finasteride 1 mg/day reduces semen quality without affecting hormones or sexual function.

Using topical prostaglandin F2α for glaucoma may cause loss of eyelash or eyebrow pigment.

A 46-year-old man was diagnosed with frontal fibrosing alopecia, a condition usually seen in postmenopausal women.

Riboflavin 5′-phosphate (FMN) shows potential for treating androgen-related conditions but may be limited in treating prostate cancer.

Eflornithine improved symptoms in Bachmann–Bupp Syndrome patients.

Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

Topical latanoprost acid at 0.05% concentration improved hair growth in women with androgenetic alopecia.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

FucoPol hydrogel membranes are promising for delivering drugs on the skin.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

CAP7.1 is generally safe at 200 mg/m²/day, but can cause fatigue, nausea, hair loss, fever, and blood-related issues.