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The technique effectively shows how human skin and hair cells form into ball-like structures.

The transporter protein SH1446 in Staphylococcus hominis is key to underarm odor production.

Pig skin cells can turn into mesodermal cells but lose their ability to become neural cells.

Early diagnosis, genetic testing, and personalized care are essential for managing tuberous sclerosis.

NCBP3, SDHA, and PTPRA are the best genes for accurate goat skin research.

Lidocaine-loaded microparticles effectively relieve pain and fight bacteria in wounds.

Wnt/β-catenin signaling is crucial for cell fusion in placental development.

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

BBS7 is crucial for maintaining healthy periodontal ligaments by supporting Shh signaling.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Lack of Cisd2 disrupts calcium balance in cells, leading to poorly functioning neutrophils.

Ca²⁺-mediated protein citrullination controls cell growth in the CNS and may help treat brain tumors.

The DiLiCre mouse model is an effective tool for precise genome editing using light.

Lower GPX4 mRNA levels are linked to higher disease activity and symptoms in lupus patients.

Low-penetration genes might help personalize colorectal cancer prevention.

A comprehensive human skin cell atlas was created to better understand skin biology and disease.

A(1-7) treatment reduces symptoms of lupus in mice.

A new method helps grow skin stem cells better, which could improve skin grafts for burn victims.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.

ICP5249 helps hair grow by activating a specific cell pathway.

Vitamin D receptor helps control hair growth genes in skin cells.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

The SOSTDC1 gene is crucial for determining sheep wool type.

New genetic mutations linked to rare skin disorders were found in three newborns.

Newly designed proteins can effectively degrade specific proteins in cells, offering a potential new therapy method.

scMC effectively separates biological signals from technical noise in single-cell genomics data.

PCL nanoscaffold-based liver spheroids are effective for drug screening and studying liver toxicity.