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The drug BAY 1158061 is safe, well-tolerated, and shows potential for treating diseases related to prolactin.

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.

A Turkish woman has a hair condition caused by a LIPH gene mutation.

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Hair transplant assistants in the UK must follow certain behavior and quality rules.

Combining laser and corticosteroid is not better than corticosteroid alone for treating frontal fibrosing alopecia.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

BKN-1 antibody targets specific keratin in basal cell epithelioma and normal skin basal cells.

A genetic marker linked to a type of hair loss was found in most patients studied.

The treatment effectively reduces hair loss and improves hair growth with minimal side effects.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

BFNB could be a promising treatment for hair growth.

Hair transplant surgeons in the British Association of Hair Restoration Surgery must follow specific behavior and performance rules.

Hedgehog pathway inhibitors for advanced basal cell carcinoma can cause side effects, but managing them helps maintain treatment.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

People were generally happy with the home light therapy devices for hair loss.

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ULBP3 could be a marker for diagnosing alopecia areata incognita and may be linked to its cause and development.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

Truncated LTBP-1 disrupts TGF-beta signaling, affecting hair growth.

Certain genetic variants in PRLR and PCCA genes may lead to shorter hair in cattle, which could help with heat tolerance.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

The new method improves bone repair by enhancing cell loading and stability in bioprinted scaffolds.

Follistatin helps hair growth and cycling, while activin prevents it.