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Fewer GGC sequences in the androgen receptor gene improve finasteride treatment for hair loss.

Lnc056 helps hair follicle stem cells grow by increasing TRIP6 expression.

Hoxc13 gene is essential for hair, nail, and papilla development.

MOF controls skin development by regulating genes for mitochondria and cilia.

Monilethrix is a genetic hair disorder affecting hair shape, seen in two brothers.

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

The research found specific genes and proteins that affect how fast chickens' feathers grow, which is not solely determined by traditional inheritance patterns.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Different gene mutations cause different types of ichthyosis, with some new mutations found.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

CD61 is important for mouse tooth cell growth and works through Lgr5.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

X-linked mental retardation includes various syndromes with both mental and physical abnormalities.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

Personalized sonidegib dosing can effectively treat Gorlin-Goltz syndrome with fewer side effects.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

Fadrozole and Finasteride change frog sex ratios and cause intersex animals with altered gene expressions.

A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

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

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

Gene differences affect finasteride side effects in men with hair loss.

The 1298CC genotype in RA patients leads to higher methotrexate toxicity, while the 1298AA genotype results in better treatment response.

Certain gene variations might increase the risk of a hair loss condition in Koreans.

Using Armillaria strain A541 boosts Polyporus umbellatus yield and polysaccharide content.