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A specific mutation in Kras causes abnormal tissue changes by making a cell signal continuously active, which disrupts normal cell coordination.

Progeria, a disease that causes early aging, is linked to a gene mutation and helps us understand normal aging.

Zebrafish helped find new ways to prevent drug-induced hair cell death and potential treatments for hearing loss.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

Hairless protein and putrescine regulate each other, affecting hair growth and skin balance.

Hair follicle stem cells are crucial for touch sensation and proper nerve structure in mice.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

Hair follicles supply a crucial brain development protein to the brain via platelets.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

GALT5 and GALT2 are important for plant growth and development because they help with protein glycosylation.

Gab1 protein is crucial for hair growth and stem cell renewal, and Mapk signaling helps maintain these processes.

Melanocyte stem cells are crucial for skin pigmentation and have potential in disease modeling and regenerative medicine.

Different species use the same genes for tooth regeneration.

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

Lipases, especially gehB, are crucial for Staphylococcus aureus to enter and colonize hair follicles.

Antiviral drugs, especially daclatasvir, may be a new treatment for a rare skin disease, improving survival and reducing symptoms in mice.

Pulsed red light boosts collagen and energy in cells faster than continuous red light.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

The best animal model for studying male-pattern baldness is the stumptailed macaque, not rats or mice.

The research found that different types of fibroblasts are involved in wound healing and that some blood cells can turn into fat cells during this process.

Modulating BMP activity changes the number, size, shape, and type of ectodermal organs.

Normal skin cell renewal doesn't need RAR signaling, but vitamin A-related skin thickening does.

Formyl-peptide receptor agonists could be new anti-inflammatory drugs.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Maintaining DNA health in stem cells is key to preventing aging and tissue breakdown.

Notch-related genes play a key role in the development and cycling of hair follicles.

Wnt, Eda, and Shh pathways are crucial for different stages of sweat gland development in mice.