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A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.

The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

Vitamin D affects Msx1 protein expression and may influence mineralized tissue health.

The study created a mouse model that survives longer and shows fewer symptoms of pemphigus vulgaris.

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

SCD1 is important for hair growth by keeping the connection in skin cells where hair stem cells live stable.

PCPA induces hypersexual behavior in male rats regardless of age or castration status.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

NAC1 controls certain enzymes that reduce root hair growth in Arabidopsis.

Mice without the p21 gene can fully regenerate injured ears due to reduced Sdf1 increase and leukocyte recruitment, suggesting new ways to induce tissue regeneration in mammals.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Calprotectin starves Pseudomonas aeruginosa of essential metals, affecting its growth and resistance.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Pvalb8 is essential for zebrafish hearing and hair cell development, and its mutation causes hearing loss.

Mycophenolic acid may help treat hair loss by promoting hair growth and cell proliferation.

S-1 treatment led to a complete response in pancreatic cancer with manageable side effects.

PHGDH promotes cancer growth by aiding cell proliferation and tumor progression.

The study created a mouse model to mimic degenerative diseases for testing tissue repair and new therapies.

The flaky skin mouse mutation is a natural model for studying human psoriasis.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

The ZIP13 variant is linked to abnormal hair quality.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

NSG mice had the most mites, and genetic factors affect immune response and susceptibility.

A girl initially thought to have a psychiatric disorder was later found to have a lupus-related condition, which improved with proper treatment.

Higher levels of certain proteins may increase or decrease rosacea risk.