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The treatment effectively promotes hair regrowth in androgenetic alopecia without causing skin irritation.

Dihydrotestosterone increases growth and spread of human brain cancer cells, and blocking its formation might help treat this cancer.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

CCT128930 is a promising new drug that effectively targets and inhibits a cancer-related protein, showing potential for cancer treatment.

TTD patients don't have a higher skin cancer risk because their main issue is with transcription, not DNA repair.

Vitamin D receptor gene variations are not linked to alopecia areata.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

Dystonia may be part of PAS-4 and linked to immune issues.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.

DMBT1 and galectin-3 may help suppress epithelial skin cancer.

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

Gsdma3 affects hair growth by controlling Wnt5a, which influences hair cell development.

Removing REDD1 in mice increases skin fat by making fat cells larger and more numerous.

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

Blocking a certain signal in the gp130 receptor can improve tissue healing and lessen osteoarthritis symptoms.

Using both TGA and DTDG in hair straightening reduces hair damage compared to using TGA alone.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Activated β-catenin affects hair growth and skin thickness, and changes are reversible.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

The RNA AL136131.3 slows down hair growth and speeds up hair loss by affecting sugar breakdown in hair follicles.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Androgens and estrogens are crucial for insulin secretion in males.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

A certain gene variation can affect protein production and is linked to male pattern baldness.

The research found that androgens help control blood flow in the rat prostate through a specific binding site.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.