Search

everythinglearnresearchcommunity

for

Search:↓

Some viruses can cause cancer by changing cell processes and avoiding the immune system; vaccines and targeted treatments help reduce these cancers.

The document concludes that certain mutations may contribute to the inflammation in hidradenitis suppurativa and suggests that targeting TNFα could be a treatment strategy.

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

Involucrin gene expression is controlled by specific proteins and signaling pathways.

Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

Both classical and L-type atypical BSE from cattle can infect goats with different incubation times, and tests can distinguish between the two strains.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

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

Recombinant keratin K31 makes damaged hair thicker, stronger, and straighter.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

MIM is crucial for hair follicle formation and regeneration by controlling cilia formation and hedgehog signaling through its interaction with Cortactin and Src.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

Alk1 in specific cells is crucial for proper nerve branching and hair function.

Blocking the Wnt pathway could lead to new treatments for cancer and tissue repair but requires careful development to avoid side effects.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

Pitx2 helps outer root sheath cells differentiate but can't start hair growth on its own.

LEF1 interacts with Vitamin D Receptor, affecting hair follicle regeneration and this could be linked to hair loss conditions.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

ΔNp63α stops TAp73β from working in skin cancer by blocking its access to specific genes, not by directly interacting with it.

New treatments for advanced skin cancer are improving patient outcomes, but drug resistance and finding the right treatment combinations are still big challenges.

Apoptosis contributes to hair loss in androgenetic alopecia.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.

RNA aptamers can specifically block FGF5-related cell growth, potentially treating related diseases or hair disorders.

Recombinant keratins can form useful structures for medical applications, overcoming natural keratin limitations.

Lack of cystatin M/E causes thin hair and dry skin.

Researchers found 44 proteins that change during different hair growth stages and may be important for hair follicle function.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

Genetic defects and UV radiation cause skin damage and aging.