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A specific DNA pattern in Malassezia restricta may be linked to hair loss in men.

SIPHL1 from tomato enhances plants' response to low phosphate levels.

ASLNC168501 may help restore hair growth in androgenetic alopecia by improving hair follicle stem cell function.

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

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

lncRNA MRPS28 regulates hair follicle development in cashmere goats, affecting cashmere quality.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

A gene variation is linked to hair thickness in Asians.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

ESR2 gene linked to female-pattern hair loss.

The document confirms the structures of major metabolites of the CRTh2 antagonist Setipiprant and identifies minor metabolites.

The UK Intellectual Property Office allows granting of supplementary protection certificates with negative terms.