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The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A specific mutation in PA-PLA1α causes abnormal hair growth.

Diphenyl cresyl phosphate has low toxicity but can harm the liver, kidneys, adrenal glands, and testicles at high doses.

Clascoterone is safe for the heart, even at high doses.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

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

The -866G/A polymorphism in the UCP2 gene is not linked to polycystic ovary syndrome.

Standard treatment for congenital erythropoietic porphyria was ineffective over five years.

PDF2 senses specific lipids and regulates root growth and gene expression in Arabidopsis.

BioPlex-11 improves DNA profiling from telogen hair roots in forensic work.

CCC1 is essential for pH balance and normal cell function in plants.

CNGC14 is crucial for calcium entry needed for root hair growth in plants.

CLE14 peptide promotes root hair growth in Arabidopsis.

MPA increases cancer spread by boosting Eph A2 activity.

A mouse gene mutation increases the risk of skin cancer.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

VPS13C variants are linked to more severe REM sleep disorder and faster progression to Parkinson's disease.

The document confirms the structures of major metabolites of the CRTh2 antagonist Setipiprant and identifies minor metabolites.

Adding TERT and BMI1 to certain skin cells can improve their ability to create hair follicles in mice.

A new type of pachyonychia congenita may exist, caused by a different keratin mutation.

Immortalized human dermal papilla cells were created that grow better and can still help form hair.

Type XVII collagen may help prevent skin aging.

Ceramide may help delay hair aging by restoring stressed hair cells.

Certain derivatives are more effective 5α-reductase type 2 inhibitors than finasteride.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

New probes were created to effectively measure specific enzymes involved in fat metabolism, which could help develop new drugs.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

PPARγ signaling modulation can protect hair follicle stem cells from chemotherapy-induced damage.

Low androgen levels can still cause female pattern hair loss.