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11α-Hydroxyprogesterone is changed into different substances by certain enzymes and may play a role in prostate cancer.

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

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

A trial showed that a new treatment is safe and effective for male pattern baldness, with most participants growing new hair.

Hedgehog pathway inhibitors used for skin cancer can cause significant hair loss, which may improve after stopping the medication.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Measuring 24-OHase induction helps identify defects in vitamin D processing and predict treatment response.

Trodelvy™ helped some patients with advanced breast cancer, but had side effects.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Finasteride improves hidradenitis suppurativa in children with no adverse effects.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Optimizing the structure of a specific compound greatly improved its effectiveness and precision for treating diabetic complications.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

Capivasertib improves survival in certain breast cancer cases but requires careful management of side effects.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Blocking CYP17A1 enzyme may help improve certain brain function issues related to dopamine.

The UK's EDS National Diagnostic Service found that early diagnosis, lifestyle advice, and regular check-ups are crucial for managing vascular Ehlers-Danlos syndrome. A combination of losartan and bisoprolol can reduce vascular events, improving survival and quality of life.

Farudodstat may effectively treat alopecia areata without harmful side effects.

Drospirenone can hide symptoms of certain hormonal disorders, complicating diagnosis.

LY191704 is a compound that effectively blocks a specific enzyme involved in hormone conversion and could help treat enlarged prostate and hair loss.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

Isotretinoin may effectively treat hereditary hypotrichosis simplex, a rare hair loss condition.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.

Researchers successfully made new compounds for hormone level tests, but one attempt led to an unexpected product, correcting a past error.

Antiviral drugs, especially daclatasvir, may be a new treatment for a rare skin disease, improving survival and reducing symptoms in mice.

A single amino acid change in the vitamin D receptor can disrupt its function and lead to hair loss.