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The research found changes in gene expression related to cell death in mouse skin that help understand hair follicle development and skin health.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

New treatments targeting specific genes show promise for treating keratin disorders.

Blocking CXCR4 may help treat hidradenitis suppurativa.

Removing both Atr and Trp53 genes in adult mice causes severe tissue damage and death due to DNA damage.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Kremen is crucial for proper development and preventing tumors by regulating Wnt signaling.

Deleting the CDSN gene causes severe skin and hair problems, leading to death.

Smart nano-PROTACs improve cancer treatment by targeting proteins more precisely and reducing side effects.

Mice without the Sept4/ARTS gene heal wounds better due to more stem cells that don't die easily.

PROTACs show promise in cancer treatment by effectively degrading specific harmful proteins.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Different body areas have unique skin cell communication patterns, explaining why certain skin diseases occur in specific regions.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

A new gene mutation causes a rare type of hair loss.

A gene mutation in mice causes skin defects and early death.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

Crisaborole may help regrow hair in children with alopecia areata.

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

The improved genome of the African spiny mouse helps study its tissue regeneration.

Non-coding RNAs are crucial for skin development and health.

Researchers found a new mutation causing total hair loss from birth.

Deleting part of a gene in mice causes wavy hair and high pup loss.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.