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Phosphorylation of certain parts of the PIN3 protein is crucial for its role in plant root growth and response to gravity.

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

Par3 protein is essential for skin cell balance and stability.

Impaired ABCA5 activity disrupts cholesterol balance in hair follicle cells, affecting hair growth.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Kv1.3 blockers may help treat alopecia areata and promote hair regrowth.

The new assay can help develop products for hair re-growth.

Blocking CRF1 receptors improved male hormone levels and reduced testicular tumor size in men with a specific adrenal condition.

Actin filaments help stabilize and reshape cell membranes.

Cortexolone 17a-propionate may be an effective new treatment for hair loss.

AGD1's PH domain is essential for its role in root hair growth and polarity.

A protein called COMP is part of the connective tissue in normal human hair follicles and may be important for hair health.

CaM7 and CNGC14 interaction controls root hair growth in Arabidopsis.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

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

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

ULBP3 could be a marker for diagnosing alopecia areata incognita and may be linked to its cause and development.

The chitosan-peptide system helps cartilage regeneration using fat-derived cells.

Type 3 5α-reductase is more common and finasteride and dutasteride strongly inhibit it.

CD73 may regulate hair growth and could be targeted for hair growth treatments.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

A more sensitive assay was developed to detect enzyme activity converting arginine to citrulline in hair follicles.

3,4,5-tri-O-caffeoylquinic acid promotes hair growth by activating the β-catenin pathway.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

CCCA may be caused by both hair traction and an immune response.

Different PADI isoforms help cells develop diverse functions.