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Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Higher Lnk protein levels in ovaries may lead to insulin resistance in women with PCOS.

Polycomb Repressive Complex 1 is crucial for keeping stem cells stable and maintaining healthy adult tissues.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

Human hair keratin genes have unique simple sequence repeats that may help track genetic variations.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

A20 protein is crucial for normal skin and hair development.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Keratins are crucial for cell structure, growth, and disease risk.

Gene variation affects prostate issues and hair loss.

Inflammation may cause nail issues in Cronkhite–Canada Syndrome.

TB and BCC tumors show similar follicular differentiation patterns.

Kv1.3 blockers may help treat alopecia areata and promote hair regrowth.

The MTR gene affects wool quality and production in Chinese Merino sheep.

Blocking Wnt signaling in young mice causes thymus shrinkage and cell loss, but recovery is possible when the block is removed.

A single recessive gene causes sparse hair in certain Japanese White rabbits.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

Researchers found genes that may explain why some pigs grow winter hair, which could help breed cold-resistant pigs.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Cronkhite-Canada syndrome is a rare, non-inherited condition causing various symptoms like polyps, hair loss, and weight loss.

Variants on chromosome 10 affect hair thickness in Dazu black goats.

CK 15, follistatin, and Bmi-1 can help differentiate basal cell carcinoma from squamous cell carcinoma.

Mouse hair keratins mHa1 and mHb4 can't form a strong network on their own in cells.

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

Folliculin slows hair growth, and blocking it might help treat hair loss.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

A new genetic tool improves the study of hair growth and potential hair disorder treatments.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.