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Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Human skin cells contain Protease Nexin-1, and male hormones can decrease its levels, potentially affecting hair growth.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The PIP5K1A gene helps cashmere growth in goats by promoting cell proliferation, and melatonin boosts its expression.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

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

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

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Cytokeratin 19 and cytokeratin 15 are key markers for monitoring the quality and self-renewing potential of engineered skin.

CTCF protein is essential for skin and hair follicle development in mice.

The reconstructed skin model from hair follicles functions like human skin in processing chemicals and can be used to test ingredient safety.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

The ACE1 gene variant doesn't affect long-COVID symptoms.

Cytokeratins 15 and 19 may help track vitiligo treatment progress.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

Non-classical 21-hydroxylase deficiency can be missed in newborn screenings and should be considered in cases of early puberty or virilization.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

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

KAP9.2 and Hoxc13 genes are important for cashmere growth and vary in activity during different stages.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

CXXC5 is a protein that prevents hair growth and could be a target for hair loss treatment.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

Testosterone changes how certain channels work in male rat reproductive tracts, affecting fertility-related fluid balance.