Search

everythinglearnresearchcommunity

for

Search:↓

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

The enzyme steroid sulfatase is linked to breast cancer and other conditions, and inhibitors are being developed for treatment.

New steroids were effective in blocking male hormone receptors in hamster prostates.

Altered DHEA metabolism in hair follicles may be linked to hair loss in balding men.

A new compound, 3a, effectively fights prostate cancer better than finasteride.

The chemicals 17βC and its methyl ester can block the effects of testosterone on hamster skin but not the effects of DHT.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

A boy with severe Vitamin D-resistant rickets did not respond to treatment and lacked a common symptom, suggesting a need for alternative treatments.

Minoxidil affects collagen-related genes, potentially helping treat fibrosis.

The study concluded that androstendione and DHEA are important for diagnosing high male hormone levels in women with excessive hair growth.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

Alopecia in these mice is caused by defective hair cycle communication due to missing vitamin D receptor function, not vitamin D levels.

Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

Human skin releases different steroids, with some coming from sebaceous glands and others from sweat glands.

Hairless protein can block vitamin D activation in skin cells.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

1 alpha,25-dihydroxy-vitamin D3 and calcipotriol speed up cell differentiation in hair follicles.

A new method accurately measures nine steroid hormones in human serum with high sensitivity.

Non-classical 21 hydroxylase deficiency is an underdiagnosed cause of female hair loss and polycystic ovarian syndrome.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Enzyme purified and characterized for minoxidil sulphation in rat liver.

17-beta estradiol and prednisolone may help regrow hair damaged by chemotherapy.

A reliable model for screening type II 5α-reductase inhibitors was created and validated.

GI197111X is best dissolved in Capmul MCM for trials.

The vitamin D receptor helps maintain hair and bone health even without binding vitamin D.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.