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MicroRNA-214 is important for skin and hair growth because it affects the Wnt pathway.

Prostaglandin D2 blocks new hair growth after skin injury through the Gpr44 receptor.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

Certain genes in Iranian sheep are linked to wool production and heat adaptation.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

α3β1-integrin is crucial for maintaining normal hair follicle shape and function but not needed for the development of the surrounding skin.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

The review found no clear link between vitamin D receptor gene variations and polycystic ovary syndrome.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.

The study found that a specific area of the hair follicle helps start hair growth by reducing the blocking effects on certain cells and controlling growth signals.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Protein hydrolysates applied to roots or leaves differently improved lettuce yield and quality, with the best results seen in specific combined treatments for each type.

Runx1 controls fat-related genes important for normal and cancer cell growth, affecting skin and hair cell behavior.

Genetic variation in the KRTAP15-1 gene affects wool yield in sheep.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Some patients treated with peginterferon and ribavirin for chronic hepatitis C had mild to moderate skin reactions, but treatment did not need to be stopped.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Metformin works better for adolescent girls with PCOS who have certain genetic variations.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

Progesterone and its byproducts control a specific receptor in the brain independently of progesterone receptors, affecting conditions related to the menstrual cycle.

sPLA2-IIA increases growth in hair follicle stem cells and cancer cells, suggesting it could be targeted for hair growth and cancer treatment.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.