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A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

The study found that certain mutations in the vitamin D receptor can cause rickets and potentially affect hair growth.

A specific gene mutation causes long hair in Angora rabbits.

RXR agonists may promote hair growth in humans.

The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Nirogacestat can cause severe skin issues like hidradenitis suppurativa.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

The research found that compound 6, a newly created steroid, is more effective at inhibiting 5α-reductase (an enzyme) than current treatments, suggesting it could be a better option for treating urinary tract symptoms in men.

New chemical compounds were made that effectively block an enzyme linked to prostate growth.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Dihydrotestosterone increases the activity of an enzyme in pubic skin cells that converts testosterone to dihydrotestosterone.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

Ch55 may help reduce skin scarring and fibrosis.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

Rat hair-follicle stem cells can become heart cells with specific supplements.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

A genetic variant in the KRT25 gene causes tightly curled hair.

High LGR5 levels in glioblastoma indicate poor prognosis and are essential for cancer stem cell survival.

Different keratins have unique expression patterns in mouse skin cells.

Men taking 5α-reductase inhibitors for enlarged prostate have a higher chance of experiencing reduced sexual desire and erectile dysfunction.

Targeting CD200 could be a new treatment for rheumatoid arthritis.

Vitamin D receptor helps control hair growth genes in skin cells.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.