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A new neural network helps identify key regulators in cell changes, aiding in understanding diseases and finding new treatments.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

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.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Cathepsin L deficiency causes large, abnormal cell structures and health issues in mice.

Prolactin affects when mice shed and grow hair.

The piRNA pathway genes are crucial in early development and may influence sex differentiation through hormone regulation.

The Foxn1 gene is essential for normal nail and hair development.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

RANKL causes lymph nodes to grow by making certain cells multiply.

Foxn1 is crucial for skin development and healing, and altering its expression may aid regenerative medicine.

Scientists successfully created and analyzed the structure of a part of the human androgen receptor with specific modulators and a peptide to understand how it binds differently in various tissues.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

LY191704 is a compound that effectively blocks a specific enzyme involved in hormone conversion and could help treat enlarged prostate and hair loss.

Prolactin affects when mice shed and grow hair.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

Androgen receptors in the brain affect metabolism and reproduction differently in males and females, and may help manage PCOS symptoms in females.

CD98hc's role in skin health decreases with age.

Thymic transplantation normalized some T-cells but not others, maintaining immune function.

Lgr5+ stem cells do not cause skin tumors.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

High-throughput LC-MS screening is effective for finding new autotaxin inhibitors for asthma treatment.

Krt15+ cells in the mouse intestine resist radiation and can start tumors.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Hox proteins help maintain keratinocyte identity by regulating miRNA expression.

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

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.