Search

everythinglearnresearchcommunity

for

Search:↓

Shampoo with heat-killed Lacticaseibacillus paracasei GMNL-653 improves scalp health and hair growth by changing scalp bacteria.

The 2012 criteria are better for diagnosing atypical lupus cases.

Proteomics combined with other technologies can lead to a better understanding of skin diseases.

Thermal spring waters and their microbes could be good for skin health and treating some skin conditions in skincare products.

K6 gene expression can be controlled and manipulated in mice for studying skin disorders.

KRT72 gene helps form hair.

Mutations in the KRT16 gene can cause skin and nail disorders.

Only one K16 gene on chromosome 17 makes a functional keratin protein.

Two new gene clusters important for hair formation were found on human chromosome 11.

Two new gene clusters important for hair formation were found on human chromosome 11.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

Only one of the two K16 genes on chromosome 17 makes a functional protein for keratin filaments.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

A specific gene mutation causes woolly hair and hair loss.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

A KRT32 gene variant causes loose anagen hair syndrome.

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

Krtap11-1 is important for hair strength and structure.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A cluster of 21 keratin-associated protein genes important for hair growth was found on human chromosome 21.

A specific DNA region controls skin cell gene expression by working with certain proteins.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.