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The extract from Bacillus/Trapa japonica fruit helps increase hair growth and could be a potential treatment for hair loss.

Foxp1 helps control hair stem cell growth and response to stress during hair growth cycles.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

A specific RNA can help hair growth in baldness by boosting stem cell activity.

Tebentafusp-tebn improves survival rates in uveal melanoma patients but has common side effects like rash and fatigue.

Hair becomes less stiff as we age because of a decrease in zinc, which is linked to lower levels of the protein TG3.

FilaggrinHigh melanomas have active FGFR signaling and weak GNA14 and Th1 signatures.

Human hair follicles have their own thyroid hormone system.

Ayme-Gripp Syndrome was confirmed in a woman through genetic testing, highlighting the need to consider rare genetic conditions in diagnoses.

Reducing SFRP1 can promote hair growth and may help treat hair loss.

Claudin-1 is important for the barrier function and growth of hair.

Sirtuin 1 could be a potential drug target for treating hypertrophic scars.

A specific gene mutation causes sparse, brittle hair in a family.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Removing Lrig1-positive cells in mice leads to temporary loss of sebaceous glands.

FoxN1 overexpression in young mice harms immune cell and skin development.

Fibroblast growth factors could be a better, safer treatment for hair loss than current options.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

TMPRSS6 is crucial for controlling hepcidin and normal iron absorption.

A new gene, JMJD1C, may affect testosterone levels in men.

People with polycystic ovary syndrome have higher levels of Gremlin-1.

The new gel formula could improve the delivery of a hair loss treatment through the skin and might be an alternative to taking it by mouth.

Certain changes in the KAP6-1 gene affect the thickness and length of cashmere goat fibers.

Trichothiodystrophy causes abnormal protein deposits and distortion in hair follicles.

Tmem50b and 2610305D13Rik genes play key roles in early mouse embryo development.

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

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Fz3 and Fz6 can partially replace each other in tissue polarity and axon guidance.