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Biotin helps regulate proteins in the blood, which may explain its role in hair growth.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

The PLP2 gene affects cashmere fiber quality in goats and is linked to hair growth and loss.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Gut flora changes could potentially indicate depression, but more research is needed.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Sex steroids affect the MafB gene differently in male and female hamsters.

The gene Ascl4 is not necessary for the development of hair, teeth, or mammary glands.

A new gene mutation causes insulin resistance in a girl and her mother.

A new gene variant causes glucocorticoid resistance in a mother and son.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

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

Certain gene variants may raise the risk of prostate enlargement, but taking NSAIDs could reduce this risk.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

New treatments targeting specific genes show promise for treating keratin disorders.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

Obese women with PCOS show a male-like pattern in certain fat tissue gene expressions.

Hair loss is common in lupus patients and can be permanent or reversible, depending on the type, with various treatments available.

Mutations in the KRT85 gene cause hair and nail problems.

Finger length ratios are not linked to the number of specific gene repeats affecting testosterone sensitivity.

Men's hair loss is caused by hormones and genes, and can be treated with medication and surgery, while graying is due to aging and has no prevention except dyeing.

Sp6 promotes tooth development by reducing follistatin levels.

Certain SHBG gene variants, like rs727428, are linked to higher testosterone levels in women with PCOS.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.