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MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.

Dicer is crucial for hair growth in mice.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Vitamin D receptor helps prevent skin tumors.

Overactive Stat3 in mouse skin causes hair loss and cell structure damage.

Gene regulatory regions evolve faster than protein coding regions, allowing new gene relationships without changing transcription factors.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

Thymosin beta 4 protects cells from damage by blocking a harmful microRNA and boosting a protective gene.

CDKN2AIP gene is less active in nevus sebaceous, affecting related RNA networks.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

The LAMTOR3 gene is involved in cashmere goat hair growth and is affected by certain treatments and other genes.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

ETC-159 was safe up to 30 mg, but no tumor shrinkage was seen.

The HCR gene contributes to psoriasis risk.

Robertsonian translocation can cause recurrent miscarriages.

TRH stimulates human hair growth and extends the hair growth phase.

Arabidopsis Formin 2 stabilizes actin filaments to aid cell-to-cell trafficking.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

The keratin tail is crucial for skin structure and function.

Human adrenals and gonads have a unique enzyme for steroid hormone production.

Deleting the p63 gene in certain cells causes problems in thymus development and severe hair loss in mice.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

A new therapy for a skin blistering condition has not been developed yet.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

The Ovol2-Zeb1 circuit is crucial for skin healing and hair growth by guiding cell movement and growth.