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

Genomic approach finds new possible treatments for hair loss.

Hair and skin can regenerate without bulge stem cells due to other compensating cells.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Lack of cystatin M/E causes thin hair and dry skin.

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.

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

Different cell types work together to repair skin, and targeting them may improve healing and reduce scarring.

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

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.

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

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.

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

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

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.

DNA methylation likely doesn't cause different lambskin patterns in Hu sheep.

The SOSTDC1 gene is crucial for determining sheep wool type.

Deleting the EDAR gene in Cashmere goats affects genes and proteins related to hair growth.

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.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

STK11 gene polymorphism does not predict metformin response in PCOS.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

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

The FRZB gene slows hair growth in rabbits.

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

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.