Search

everythinglearnresearchcommunity

for

Search:↓

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

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

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

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

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

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Keratin 15 helps maintain skin cell growth and repair.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

EBF1 controls hair type and length.

aPKCλ is essential for hair follicle stem cell maintenance and wound healing.

Keratins K6 and K16 are expressed more freely in regenerating mouse skin than K1 and K10.

The protein aPKCλ is crucial for keeping hair follicle stem cells inactive and for hair growth and regeneration.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

The vector successfully directed specific gene expression in hair follicles.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

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

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

K16 can partially replace K14 but causes hair loss and skin issues.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

A genetic variant in the KRT25 gene causes tightly curled hair.

K6hf is found in specific parts of hair follicles, nails, and tongue, and is linked to hair growth and structure.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

BMP receptor IA is essential for proper hair cell differentiation in mice.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

CIP/KIP proteins help stop cell division and support hair growth.