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

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Enhanced stem cells from the placenta can reduce fat cell formation in eye disease.

Progesterone affects GABA_A receptor function by altering δ subunit levels.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.

People with PCOS have higher levels of PAI-1, which may increase their risk of heart disease and fertility issues.

Caspase-1 helps hair stem cells move to heal wounded or inflamed skin.

GFC injections significantly improved hair growth and quality with minimal side effects.

The assay quickly identifies substances that increase or decrease blood vessel growth.

Targeting glucocorticoid action might help treat type-2 diabetes, but human trials are needed.

Simple centrifugation with calcium gluconate boosts PDGF-BB release in PRP.

Chinese medicine may help treat hair loss by affecting genes and enzyme activity.

Hair follicle samples effectively show how well the drug MK-0752 targets and engages with the Notch pathway.

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

Alkaline Ceramidase 1 prevents early hair loss in mice by keeping hair follicle stem cells balanced.

Plasma protein binding significantly affects glucocorticosteroid concentration in blood, saliva, and hair.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

A new method accurately measures a drug in skin for cancer therapy research.

PDGF-D boosts stem cell growth and movement, enhancing hair regeneration.

A specific genetic mutation causes POMC deficiency, leading to symptoms like weight gain and red hair.

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.

Certain gene variations are linked to better memory in healthy Chinese women.

NonClassic Congenital Adrenal Hyperplasia is a less severe form of a genetic disorder affecting adrenal gland function.

The research found how GPCR Class A Rhodopsin receptors are related and suggested possible substances they interact with.

Genomics can improve patient care by using DNA to create personalized treatment plans.

Blocking Oncostatin M's role in the JAK-STAT pathway can stimulate hair growth in mice.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.