Search

everythinglearnresearchcommunity

for

Search:↓

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

The p53 protein helps control hair follicle shrinking by promoting cell death in mice.

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

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

PRMT5 inhibitors effectively fight adenoid cystic carcinoma in salivary glands.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

The IRE gene is important for normal root hair growth in Arabidopsis plants.

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Newly designed proteins can effectively degrade specific proteins in cells, offering a promising alternative for targeted protein degradation.

α-parvin is necessary for skin and hair growth and for the correct orientation of skin cells.

Grasp protein helps maintain skin health after UVB exposure.

A new mutation in mice causes crooked whiskers and messy hair.

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

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Dermal EZH2 controls skin cell development and hair growth in mice.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

PINCH-1 is crucial for skin cell adhesion and movement, working with EPLIN and ILK.

A new gene mutation linked to a skin condition was found in a Spanish family.

Hoxc13 gene is essential for hair, nail, and papilla development.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Mice without the p21 gene can fully regenerate injured ears due to reduced Sdf1 increase and leukocyte recruitment, suggesting new ways to induce tissue regeneration in mammals.

PTCH gene mutations contribute to basal cell carcinoma development.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.