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Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

GLI2 increases follistatin production in human skin cells.

Certain proteins are essential for the growth of root hairs in barley.

EGM2 and SOX2 help form beige adipocytes by maintaining ASC immaturity and activating brown adipocytes.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

Alopecia areata involves specific T-cells, unlike androgenetic alopecia.

Gene variation affects prostate issues and hair loss.

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

TAF4 is important for skin cell growth and helps prevent skin cancer in mice.

A specific gene change is linked to severe hair loss.

Increasing COX-2 in mouse skin causes bigger sebaceous glands and thinner hair, but stopping COX-2 can reverse hair thinning.

PGD2 stops hair growth and is higher in bald men with AGA.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

The research found a way to develop hair growth materials by targeting a specific signaling pathway.

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

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

A defective protein in progeria causes cell death and atherosclerosis, but a treatment targeting cell stress may reduce these effects.

Cyclooxygenase-2 overexpression in mice skin causes hair loss like human androgenetic alopecia.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

Human hair follicles have a scent receptor that can influence hair growth.

Botulinum toxin type A helps treat hair loss by stopping cell death in hair follicles through a process involving certain non-coding RNAs and a protein called Bax.

New genes linked to male pattern baldness were found on chromosome 20p11.

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

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Certain gene combinations may affect prostate cancer risk, and GSTP1 methylation is linked to tumor aggressiveness.

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