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Low-frequency skin massage helps nanoparticles penetrate hair follicles better.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Birds can lose neck feathers due to a genetic change that increases a gene's activity, helping them adapt to heat.

Nano-quercetin improves quercetin's effectiveness in treating diseases but faces challenges in safety and production.

RNA delivery is best for in-body use, while RNP delivery is good for outside-body use. Both methods are expected to greatly impact future treatments.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

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

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

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

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

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Mutations in the SNRPE gene cause hereditary hair loss.

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

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

The HCR gene contributes to psoriasis risk.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Portable point-of-care testing can improve quick and accurate genetic disorder detection.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

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