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A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

Men with more CAG repeats in the androgen receptor gene and lower testosterone levels may experience more severe COVID-19.

Sea cucumbers have unique genes that help them regenerate their intestines.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

Polycomb Repressive Complex 2 is not needed for hair regeneration.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

Very-long-chain acyl-CoA synthetases and fatty acid transport proteins play key roles in fatty acid metabolism and lipid processing in different tissues.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

Connexin 30 is usually absent in normal skin but can appear in certain skin conditions.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

KAP6 genes are conserved across species and active in hair follicles.

PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.

Certain genetic variants in PRLR and PCCA genes may lead to shorter hair in cattle, which could help with heat tolerance.

New probes were created to effectively measure specific enzymes involved in fat metabolism, which could help develop new drugs.

CaBP1 and CaBP2 are important for continuous hearing by preventing inactivation of calcium currents in ear cells, with CaBP2 also able to restore hearing when reintroduced.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

The PCL/PHB blend allows for slower, more controlled curcumin release than individual polymers.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

miR-26b-5p in macrophage exosomes helps keloids grow.

Tcf3 helps cells move and heal wounds by controlling lipocalin 2.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

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