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Testosterone replacement therapy improved blood sugar and fat levels without raising prostate cancer risk in Japanese men with low testosterone.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.

A unique gene mutation was found in a family with monilethrix.

New, eco-friendly methods accurately measure TDF and FNS in a new urologic medication.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

Thulium laser therapy is a safe and effective short-term treatment for hair regrowth.

RY-023, a specific drug, can improve early stage memory learning without affecting general activity in rats, but it's less effective for later learning stages and doesn't impact memory recall.

A woman's sudden hair loss was linked to azathioprine use despite normal enzyme levels, and improved after stopping the drug and starting treatment.

Rapamycin and anti-EGFR antibody reduce LAM/TSC cell migration and blood vessel growth in the uterus.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Specific brain and bone imaging findings can help diagnose Trichothiodystrophy.

Combining medication and minimally invasive techniques can effectively manage Marine-Lenhart syndrome.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

The 308-nm excimer laser is a promising treatment for vitiligo with varying success and mild side effects.

The levonorgestrel implant increases free testosterone and lowers SHBG more than DMPA-IM and the copper IUD.

XP-endo Finisher R removes more root filling material than PUI in curved canals.

Overexpressing Tβ4 in cashmere goats improves hair fiber traits and increases cashmere yield.

Oxytocin receptor changes in hair cells may help identify autism, especially in males.

Newly designed proteins can effectively degrade specific proteins in cells, offering a potential new therapy method.

The guidelines ensure accurate genetic testing and reporting for 21-hydroxylase deficiency.

New treatment effectively reverses hair thinning in most patients with mild side effects.

Tridax procumbens extracts can harm cell division and increase cell death in onion roots.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

The model predicts minoxidil's effectiveness and side effects better than traditional methods.

TGF-β1 and 2 may play a role in hair loss in AGA.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.