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FGF9 from certain cells can trigger new hair growth during wound healing, but humans have fewer of these cells, which may limit hair regrowth.

Non-viral delivery systems and stimuli-responsive nanoformulations can improve CRISPR-Cas9 gene therapy.

NAC1 controls certain enzymes that reduce root hair growth in Arabidopsis.

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Rac1 is crucial for normal hair structure and pigmentation.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

Nevus comedonicus is a rare skin condition causing dark bumps, treatable with retinoic acid or surgery.

Moles may stop growing because of cell cooperation, not just because of aging cells.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

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

LHX2 and SOX9 identify unique hair follicle cell groups, crucial for hair maintenance.

An 11-month-old boy with Menkes disease had severe brain shrinkage and abnormal blood vessels, and didn't respond well to treatment.

The GG genotype of the KRT71 gene leads to longer wool in Gansu alpine fine-wool sheep.

Certain genetic markers on the Y-chromosome may influence prostate cancer risk in Iraqi males.

Early diagnosis and multidisciplinary care are crucial for managing CNOT3 syndrome.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

Modified pep7, named EPM peptide, effectively promotes hair growth at low concentrations and works well with minoxidil.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

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

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

Miz1 is essential for proper hair structure and growth.

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.

Zebrafish helped find new ways to prevent drug-induced hair cell death and potential treatments for hearing loss.