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Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

A new mouse mutation causes skin and hair defects due to a gene change.

Certain genetic differences may affect how likely someone is to get COVID-19 and how severe it might be.

LIPH mutations cause woolly hair in some Chinese people.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

Croton membranaceus root extract can change how drugs are processed in the body.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

PDCD4 protein levels, affected by genetics and breastfeeding, may predict breast cancer treatment response.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Heart-specific steroid metabolism is crucial in cardiac hypertrophy.

The LEF-1 gene in cashmere goats was successfully cloned and analyzed, showing potential for improving cashmere production.

Narrowband UVB treatment increases certain gene expressions in psoriasis skin and improves symptoms.

Cinnamomi cortex may help treat prostate enlargement by reducing related proteins.

Noncoding RNAs help determine cashmere quality in goats.

Certain gene variations may increase the risk of PCOS in South Indian women.

Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

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

A new mouse mutation causes skin and hair issues, influenced by another gene.

Pygo2 is important for early growth and progression of intestinal tumors, and could be a target for treating cancers with certain mutations.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

Phospholipase C-δ1 is crucial for normal hair development.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.