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A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

The LMNA mutation affects skin structure even in asymptomatic carriers.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.

The skin's ability to produce hormones is linked to various skin conditions, and better understanding this process could lead to new treatments.

Certain fats in the blood are linked to an increased risk of male pattern baldness.

Removing Lrig1-positive cells in mice leads to temporary loss of sebaceous glands.

A rare scalp condition caused scarring hair loss in a woman, improved slightly with treatment.

5-aminolevulinic acid therapy reduces acne by decreasing fat production in skin cells.

SLHA can be hard to diagnose and needs teamwork between specialists.

The SLICK1 allele in Holstein heifers affects hair and immune traits without altering prolactin signaling.

Lhx2 helps retinal cells respond to signals for eye development.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

The study suggests that changes in immune system receptors and their interaction with a cell component may be important in the development of a type of hair loss condition.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

Blocking TSLP reduces skin inflammation and cell overgrowth in psoriasis.

Cholesterol balance is important for hair health, and problems with it can lead to hair loss conditions.

Dermoscopy helps diagnose rare GLPLS in males.

The mTOR pathway may be involved in the development of hair follicle tumors, with higher activity in malignant tumors.

Age-related changes in scalp glands may affect hair health, but sulforaphane might help.

Scalp seborrheic dermatitis is a common skin condition linked to oil production and bacteria, with specific diagnostic features and treatments like antifungals and corticosteroids.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

Mitochondrial Complex I reduces inflammation and increases bone breakdown by affecting certain immune cells.

PCL nanoscaffold-based liver spheroids are effective for drug screening and studying liver toxicity.

Inducing ferroptosis in hepatic stellate cells is crucial for treating liver fibrosis.

Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Women with early onset androgenetic alopecia have worse lipid profiles.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.