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Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

Parental support and gender-affirming care are crucial for the mental health of transgender adolescents.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

High levels of 3 alpha-diol glucuronide in the blood are a marker of increased androgen action in women with excessive hair growth of unknown cause.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

Low-dose finasteride reduces excessive hair growth in teenage girls safely and affordably.

Finasteride improves hidradenitis suppurativa in children with no adverse effects.

Whale genes show changes that help them live in water, like less hair and better flippers.

Glutamic acid helps increase hair growth in mice.

Lipid–polymer hybrid nanoparticles can improve genome editing delivery and outcomes.

Researchers created a model to understand heart aging, highlighting the role of microRNAs and identifying key genes and pathways involved.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Blocking the enzyme 11β-HSD1 might help treat obesity and metabolic issues.

A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

Finasteride is effective and safe for treating hidradenitis suppurativa in both adults and some younger patients.

CDH3-related disease causes worsening eye and hair issues.

The fragrance cyclohexyl salicylate helps promote hair growth and increase hair stem cell numbers.

Cyclohexyl salicylate promotes human hair growth and increases certain hair follicle stem cell progeny.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

A 22-year-old woman with a rare genetic condition was successfully treated to develop normal female characteristics and regular menstruation.

Non-classical 21-hydroxylase deficiency can be missed in newborn screenings and should be considered in cases of early puberty or virilization.

NSC167409 can effectively inhibit the virus causing hand, foot, and mouth disease.

Early detection of specific VDR mutations is crucial for effective treatment and better dental outcomes in children with hereditary vitamin D–resistant rickets.

The patient had complex urinary tract issues and ambiguous genitalia, with physical features suggesting a hormonal imbalance.

New method, hair distribution width (HDW), improves accuracy in diagnosing androgenetic alopecia (AGA).

The method can measure multiple steroids in human hair to study long-term steroid metabolism, especially in newborns and children.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

The gene HDC is important for the development of hair follicles in newborn mice.