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Hox proteins help maintain keratinocyte identity by regulating miRNA expression.

Hair loss and aging are caused by the breakdown of a key protein in hair stem cells.

Using steroids can increase the risk of heart problems.

The conclusion is that a combination of noninvasive treatments and lifestyle changes can improve skin health during menopause.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

Folliculotropic mycosis fungoides can affect the central nervous system in advanced stages.

A Turkish woman has a hair condition caused by a LIPH gene mutation.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

EZH1 and EZH2 are crucial for healthy hair growth and skin repair.

Targeting adipocyte-to-mesenchymal transition could help treat fibrosis.

Tet1/2/3 enzymes affect hair follicle cell development by influencing BMP signaling.

The hr gene is linked to hair loss in Valle del Belice sheep.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

miR-21 increases skin aging by reducing SATB1, affecting skin cell function.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Temporal triangular alopecia is a harmless, non-progressive hair loss condition.

Lipid-antigen stimulation may play a role in folliculotropic mycosis fungoides.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

Telogen effluvium is a common, reversible hair loss condition treatable with patient education and sometimes Minoxidil.

Translation levels actively determine keratinocyte cell fate.

Monilethrix is a genetic hair disorder affecting hair shape, seen in two brothers.

Mitochondrial problems in tooth cells lead to bad enamel and dentin development in mice.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

DNMT1 may help treat hypospadias by improving cell function and preventing unwanted cell changes.

New mutations in the hairless gene may cause hair loss and affect bone development.