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A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

The new ELISA method is reliable and eco-friendly for checking the quality of Pueraria candollei.

A method was developed to test the breakdown of Finasteride capsules, showing it can tell the difference between different brands and highlighting the need for standard tests and ingredient consistency.

The article guides practitioners on how to effectively assess skin problems.

A KRT32 gene variant causes loose anagen hair syndrome.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

The document's conclusion cannot be provided because the document is not accessible or understandable.

Probe detects finasteride with high selectivity and low detection limit.

The method accurately and quickly measures silodosin and dutasteride in mixtures.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

The 3D printed scaffold with SB216763 and copper helps heal wounds and regrow skin and hair.

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

Scientists made a carbon-14 labeled version of a drug with a 48% yield and over 99% purity.

Selective Androgen Receptor Modulators (SARMs) are drugs that can control the effects of androgens in different tissues, potentially having fewer side effects and promising for treating various conditions.

We need better ways to test and understand SARMs to make safer and more effective treatments.

The document's conclusion cannot be provided because the document is not accessible or understandable.

The new silk suture with silver and curcumin helps heal wounds faster and fights bacteria.

Finasteride's polymorphic form affects capsule quality and drug effect, requiring strict control.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

Sesn2 protects inner ear hair cells from damage by regulating certain cell survival pathways.

A reliable method was developed to measure Finasteride and Tadalafil together, showing they degrade under certain conditions.

SARMs show promise but need more evidence to prove they're better than traditional androgens.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

A rare ovarian tumor was successfully treated with surgery and chemotherapy.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.