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Children with classic congenital adrenal hyperplasia have thicker heart fat and more heart and blood vessel risk factors, especially if their condition is not well-controlled.

The ACE1 gene variant doesn't affect long-COVID symptoms.

SHH protein helps nerve regeneration in hypertensive rats.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

PF-05314882 selectively activates androgen receptors without much effect on prostate and may help in prostate cancer treatment and hair loss prevention.

HGF combined with ADA is highly accurate for diagnosing tuberculous pleural effusion, especially in younger females.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

Mutations in certain receptors can cause diseases and offer new treatment options.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

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

Airway issues can occur in Conradi–Hünermann–Happle syndrome and can be managed with minimally invasive procedures.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

RXR-alpha is strongly expressed in both normal and psoriatic skin and may help in skin cell differentiation and hair growth.

SARMs work differently in tissues due to unique interactions and structures.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

DPR can show different hair characteristics, as seen in two brothers with normal hair.

AMPK activation may reduce melanoma risk in red-haired individuals.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

Androgen treatment with dihydrotestosterone may help maintain height in patients with 5-α-reductase type 2 deficiency, especially before puberty.

Natural 5α-reduced glucocorticoids might be anti-inflammatory with fewer side effects than current options.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

Vitamin D receptor interacts with certain dietary components to help prevent diseases and regulate hair growth.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Mutations in the hHb6 gene cause the hair disorder monilethrix.