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Stem cell behavior varies with stimuli, and lineage changes can happen without affecting stem cell division.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

CEC levels may be a useful marker for predicting prostate cancer progression.

Genetic changes in specific proteins contribute to hair loss in some women of African descent.

GPC1 is important for blood vessel growth in hair follicles and could help treat hair loss.

Recombinant thrombomodulin can effectively treat severe complications in Cronkhite-Canada syndrome.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

Mice without the Sept4/ARTS gene heal wounds better due to more stem cells that don't die easily.

CRH promotes fat production in skin cells, affecting conditions like acne.

Vav2 and Vav3 proteins help control skin stem cell numbers and activity in both healthy and cancerous cells.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

The CTLA-4 gene change studied does not affect Polycystic Ovarian Syndrome in the women tested.

Septin4 helps kill colon cancer cells by working with the protein BAX.

Cupric chloride treatment corrected abnormal Purkinje cell development in brindled mice.

Activated protein C helps protect mice from radiation damage.

The CTLA-4 gene polymorphism does not affect polycystic ovarian syndrome.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

SCF helps heal diabetic wounds by promoting stem cell migration.

TCHHL1 is a protein important for hair growth, found in hair follicles.

Mice with more Flightless I protein grew back their claws better after amputation.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

Patients with mycosis fungoides have a higher risk of heart disease.

DNA methylation of miR-365-1 causes hair follicle stem cell death by affecting DAP3.

Cystatin M/E strongly inhibits cathepsin V and cathepsin L, important for skin formation.

CD80CD86 deficiency causes hair loss by disrupting regulatory T cells.

Rac1 is crucial for normal hair structure and pigmentation.

Certain CD8+ T cells attack hair follicles in alopecia areata, suggesting they could be targeted for treatment.

CD200- cells in hair follicles have a higher ability to regenerate hair.