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Measuring 24-OHase induction helps identify defects in vitamin D processing and predict treatment response.

Normal cells outcompete and remove mutant cells in the pancreas with the help of the EphA2 receptor.

RpoS helps Borrelia burgdorferi survive in hosts and adapt to different environments.

Ribonucleotide excision repair is crucial to prevent skin cancer.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

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

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

LTBP1 is a key regulator in diseases and a potential target for new treatments.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

BTNL2 helps protect hair follicles from immune attacks, which could aid in treating alopecia areata.

Keratin 2e shows a unique pattern in developing fetal skin, different from other keratins.

Eribulin-based chemotherapy is more effective and has fewer side effects for advanced triple-negative breast cancer.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

Plakophilin 1 helps control skin cell immune responses to prevent excessive inflammation.

Certain genes may help Bulgarians live longer.

Specialized ribosomes affect aging in human skin cells.

Netherton syndrome has two subtypes with shared immune traits but different allergic and immune responses, suggesting targeted treatments.

Modulating BMP activity changes the number, size, shape, and type of ectodermal organs.

Endoglin is important for proper hair growth cycles and stem cell activation in hair follicles.

The protein ARA70/ELE1 is involved in male pattern baldness, and lower levels of its short form may lead to hair thinning.

R-spondin2 may help treat hair loss, gene differences could explain baldness, a peptide's regulation is linked to psoriasis, B-defensin gene copies may affect a skin condition's risk and severity, and potential markers and targets for alopecia areata were identified.

Mechanoreceptors convert physical touch into electrical signals through specialized nerve structures.

Different body areas have unique skin cell communication patterns, explaining why certain skin diseases occur in specific regions.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Androgens help motor neurons grow by increasing neuritin.

5alpha-reductase 2 is crucial for proper male brain development and sexual differentiation.

Communication between blood vessel and hair follicle cells decreases with age, affecting hair growth and blood vessel formation.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.