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YAP and TAZ proteins are necessary for the development of two types of skin cancer.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

Astrotactin-2 is cleaved in a specific way that helps understand its maturation.

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

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

BAP1 mutations are rare in pediatric melanocytic tumors and may develop later in life.

Sox21 is crucial for tooth development and enamel formation by preventing cells from changing into a different type.

Grasp protein helps maintain skin health after UVB exposure.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

N1-acetylspermidine promotes hair follicle stem cell self-renewal.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

Loss of Rap1 protein speeds up heart aging in mice.

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

Pmg-1 and Pmg-2 are new genes important for skin and mammary gland development.

A specific gene change in APCDD1 increases the risk of hair loss.

Mutations in hKAP1 genes may cause hereditary hair disorders.

PP2Acα is essential for proper hair and skin development.

A peptide from hair follicle stem cells can boost hair growth.

ANXA1 influences hair growth in mice through the EGF signaling pathway.

Overexpressing a specific enzyme in mice causes hair loss and female infertility.

Deleting NIPP1 in mouse skin cells causes early aging and chronic skin issues.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Smad1 and Smad5 are essential for hair follicle development and stem cell sleepiness.