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A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

This enzyme helps metabolize fatty acids and isoleucine, and could be key in treating neurological diseases and certain cancers.

Polygenic risk scores can predict the risk and outcomes of benign prostatic hyperplasia.

Hair loss is linked to eating less soy, having lower blood vanadium, and a specific genetic variation in Taiwanese communities.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

A specific genetic mutation causes POMC deficiency, leading to symptoms like weight gain and red hair.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

Mice without the enzyme HSD17B3 still produce normal testosterone, suggesting they have different ways to make it compared to humans.

Lack of functional CYLD in mice leads to early aging and cancer.

Certain gene variants may raise the risk of prostate enlargement, but taking NSAIDs could reduce this risk.

A new DSG4 gene mutation causes hair defects in a young girl.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

The study found genetic variations in sheep that affect traits like milk production, growth, and health.

All Indian dromedary camel breeds have the same KRTAP7 gene affecting hair quality.

Certain gene variations in the Vitamin D Receptor are linked to higher risk of female hair loss.

CCDC22 and CCDC93 are essential for root and root hair growth in Arabidopsis.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

The rs6152 allele is not a good marker for baldness in the Indonesian population, but family history, age, gender, high blood pressure, and body weight are linked to the risk.

21-hydroxylase deficiency causes hormone imbalances leading to various symptoms, and diagnosis involves clinical and genetic tests.

TACE/ADAM17 is essential for maintaining healthy hair and hair follicle stem cells.

Higher IL-37 levels are linked to more severe alopecia areata, but the gene variation doesn't affect disease risk.

Noncoding RNAs help determine cashmere quality in goats.

ETC-159 was safe up to 30 mg, but no tumor shrinkage was seen.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

The article's correction clarifies scientific and methodological concerns about miR-200c-3p's role in alopecia areata.

CDP is crucial for lung and hair follicle cell development.

Increased energy use in Pik3r1-related insulin resistance isn't due to Ucp1 thermogenesis.

Higher levels of miR-1199-5p may reduce the effectiveness of certain prostate treatments.

CIPK13 and CIPK18 genes are crucial for root hair growth in plants.

Mutations at Val-889 and Arg-752 disrupt key interactions in androgen receptor dimerization.