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Measuring minimal residual disease on day 15 helps identify high-risk leukemia patients.

Rabies virus was found in specific skin cells of rabid dogs' muzzles, suggesting these cells could help diagnose rabies.

Genetic differences affect how people respond to COVID-19.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

A gene mutation in mice causes permanent hair loss and skin issues.

Researchers made a detailed map of gene activity for different parts of human hair follicles to help create targeted hair disorder treatments.

Certain changes in the VEGF gene can increase or decrease the risk of polycystic ovary syndrome.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

pCLCA2 protein may help maintain skin structure and function.

The KRTAP36-1 gene affects wool quality in Chinese Tan lambs.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

FGFR2 signaling controls Merkel cell formation in different skin regions.

The VDR gene polymorphism does not affect BDNF levels in autoimmune thyroiditis and hypothyroidism patients.

TRF1 is crucial for creating and maintaining stem cells and marks both pluripotent and adult stem cells.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

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

The LMNA mutation affects skin structure even in asymptomatic carriers.

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

Scientists found new genetic areas that affect how rice root hairs grow and develop.

Connexin 30 is usually absent in normal skin but can appear in certain skin conditions.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

A newly found RNA in Cashmere goats may play a role in hair growth and development.

These gene variations are not linked to alopecia areata in Egyptians.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

Steroid treatment improved both gut and nerve symptoms in a man with Cronkhite–Canada syndrome.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

The FA2H gene improves cashmere fineness by enhancing hair growth in goats.

Different Hairless isoforms affect Vitamin D receptor activity in hair regulation, with one repressing and the other stimulating it.