Search

everythinglearnresearchcommunity

for

Search:↓

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

A new genetic mutation was found causing hair and eye issues in a boy.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

Researchers created a cell line to study hair growth and found specific genes affected by dihydrotestosterone.

The enzyme PA-PLA1α is important for proper hair follicle development.

Different keratins have unique expression patterns in mouse skin cells.

CaBP1 and 2 are important for maintaining the activity of calcium channels necessary for hearing in inner ear cells.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Collagen XVIII is crucial for maintaining tissue structure and function in the brain, kidneys, and hair.

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

The Hr protein binds to DNA, interacts with p53, and affects cell cycle genes.

Inhibiting ACE2 improves skin regeneration during tissue expansion.

LPR1 regulates root growth under low phosphate stress independently of SIZ1 in Arabidopsis thaliana.

The TIP1 gene is crucial for normal plant cell growth in Arabidopsis.

Activin A and Follistatin affect how mouse hair follicles grow.

Keratin 19 expression in certain skin cells is temporary and not a reliable stem cell marker.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

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

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

Foxn1 helps skin cells mature by controlling a specific protein's activity.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

H19 may help prevent hair loss by keeping hair cells young.

A mutation in the KRT25 gene causes woolly hair and hair loss.

Collagen XVII is important for cell functions and its absence can worsen cancer outcomes.