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Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

RXRα is crucial for proper immune response and links diet to immune function.

A mutation in the KRT25 gene causes a rare hair disorder with thin, woolly hair.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

Removing both KLK5 and KLK7 proteins can prevent death and skin issues in Netherton syndrome.

Female mice with disrupted 5α-reductase 1 had significant metabolic issues, including stress response problems, insulin resistance, liver fat buildup, and obesity.

LIPH mutations cause woolly hair in some Chinese people.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

5α-Reductase helps regulate hormone action in toad testes, especially during breeding season.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

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

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

5-alpha reductase inhibitors don't increase breast cancer or benign breast disorder risk in women.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Loss of Pten in certain hair follicle stem cells increases skin cancer risk.

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

5α-reductase affects dopamine receptors linked to sensorimotor gating, which may help understand disorders like schizophrenia.

RXRα is crucial for hair growth and skin cell function.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

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

Friedreich's ataxia causes thin, weak hair with surface damage and cavities.

A new mutation in the ST14 gene was found in a patient with ARIH syndrome, showing milder symptoms and no tooth issues.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

Four genes are potential markers for hair loss condition alopecia areata, linked to a specific type of cell death.

Homozygous K5Cre transgenic mice have wavy hair and faster cancer progression.