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Cannabinoid receptor-1 signaling is essential for the survival and growth of human hair follicle stem cells.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

Genomic approach finds new possible treatments for hair loss.

Scientists found genes linked to the growth of high-quality brush hair in Chinese Haimen goats.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Mitochondrial therapy and platelet-rich plasma therapy both stimulated hair regrowth in aging mice, with mitochondrial therapy showing similar effectiveness to plasma therapy.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

Selective breeding caused the unique curly hair in Mangalitza pigs.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Injecting CHIR-99021 into goose embryos improves feather growth by changing gene activity and energy processes.

The circadian clock in skin cells controls their growth and rest cycles.

Mice genetically modified to produce more Del1 protein had faster hair regrowth.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Hair follicle samples effectively show how well the drug MK-0752 targets and engages with the Notch pathway.

Researchers found four genes that could help diagnose severe alopecia areata early.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Mechanical forces are crucial for shaping cells and forming tissues during development.

Certain long non-coding RNAs are important for the growth of hair follicles in Inner Mongolian cashmere goats.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

The research found a way to identify and study skin cells with stem cell traits, revealing they behave differently in culture and questioning current stemness assessment methods.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

PCOS has a strong genetic basis, but more research is needed to fully understand it.

ARWH is a rare hair disorder with no cure, but potential treatments include minoxidil and other therapies.

Rhamnose may help hair growth and pigmentation, making it a potential treatment for hair loss.

Woodhouse-Sakati syndrome shows varied symptoms and genetic differences within families.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

The research found genes that may protect certain scalp cells from hair loss.