• Japanese researchers, primarily from Kyoto University and the Kitano Hospital, have been developing a novel drug aimed at stimulating natural tooth regeneration.

    This research builds upon earlier discoveries related to inhibiting a specific protein called USAG-1 (uterine sensitization-associated gene-1). This protein is known to suppress tooth growth, and by blocking it, the body’s natural pathways for growing new teeth can be reactivated.

    The team has already demonstrated success in animal trials — notably in mice and ferrets — where the drug prompted the growth of third-generation teeth, which do not naturally develop in most mammals.

    Human trials are reportedly planned to begin around 2025, with hopes of offering this as a treatment for conditions like anodontia (a congenital absence of teeth) or for those who lose teeth due to injury or age.

    If successful in humans, this could revolutionize dental care by reducing dependence on implants and dentures, and potentially offering a one-time, regenerative treatment.

    However, this "miracle drug" is still under research and not yet available commercially. It must pass through rigorous human clinical trials and safety checks before becoming an approved treatment
    Japanese researchers, primarily from Kyoto University and the Kitano Hospital, have been developing a novel drug aimed at stimulating natural tooth regeneration. This research builds upon earlier discoveries related to inhibiting a specific protein called USAG-1 (uterine sensitization-associated gene-1). This protein is known to suppress tooth growth, and by blocking it, the body’s natural pathways for growing new teeth can be reactivated. The team has already demonstrated success in animal trials — notably in mice and ferrets — where the drug prompted the growth of third-generation teeth, which do not naturally develop in most mammals. Human trials are reportedly planned to begin around 2025, with hopes of offering this as a treatment for conditions like anodontia (a congenital absence of teeth) or for those who lose teeth due to injury or age. If successful in humans, this could revolutionize dental care by reducing dependence on implants and dentures, and potentially offering a one-time, regenerative treatment. However, this "miracle drug" is still under research and not yet available commercially. It must pass through rigorous human clinical trials and safety checks before becoming an approved treatment
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  • Stanford University researchers have achieved a major milestone in regenerative medicine by creating lab-grown heart and liver organoids that include their own blood vessels.

    These vascularized organoids mark a significant leap forward because previous versions lacked the ability to grow beyond a limited size due to the absence of internal circulation.

    Without vessels, cells in the center of organoids would die from a lack of nutrients and oxygen. The addition of functional blood vessel networks allows the mini-organs to sustain more realistic structure, function, and longevity in lab environments.

    The team focused primarily on developing heart organoids that resemble a human embryonic heart around 6.5 weeks into gestation.

    These lab-grown hearts were able to beat and exhibited cell diversity that mirrors actual early-stage human heart development.

    Using a rigorous screening of 34 different combinations of growth signals and structural scaffolding, researchers identified the optimal formula (referred to as “condition 32”) that reliably produced key cell types including cardiomyocytes (heart muscle cells), smooth muscle, and endothelial cells (which form blood vessels).

    One striking application was testing how fetal tissues might respond to external chemicals.

    The team exposed the heart organoids to fentanyl — a powerful opioid — and observed abnormal increases in vessel growth, indicating that the organoids can model how drugs affect early development.

    This has major implications for studying toxic exposures and congenital disease origins.

    Moreover, the researchers replicated their vascularization technique in liver organoids, proving that the approach is flexible and scalable.

    The long-term goal is to create implantable organoids for use in human therapy, especially for repairing damaged organs.

    Until then, these mini-organs provide a valuable new platform for drug testing, developmental biology, and reducing animal use in research — aligning with updated FDA guidelines favoring human-relevant models.
    Stanford University researchers have achieved a major milestone in regenerative medicine by creating lab-grown heart and liver organoids that include their own blood vessels. These vascularized organoids mark a significant leap forward because previous versions lacked the ability to grow beyond a limited size due to the absence of internal circulation. Without vessels, cells in the center of organoids would die from a lack of nutrients and oxygen. The addition of functional blood vessel networks allows the mini-organs to sustain more realistic structure, function, and longevity in lab environments. The team focused primarily on developing heart organoids that resemble a human embryonic heart around 6.5 weeks into gestation. These lab-grown hearts were able to beat and exhibited cell diversity that mirrors actual early-stage human heart development. Using a rigorous screening of 34 different combinations of growth signals and structural scaffolding, researchers identified the optimal formula (referred to as “condition 32”) that reliably produced key cell types including cardiomyocytes (heart muscle cells), smooth muscle, and endothelial cells (which form blood vessels). One striking application was testing how fetal tissues might respond to external chemicals. The team exposed the heart organoids to fentanyl — a powerful opioid — and observed abnormal increases in vessel growth, indicating that the organoids can model how drugs affect early development. This has major implications for studying toxic exposures and congenital disease origins. Moreover, the researchers replicated their vascularization technique in liver organoids, proving that the approach is flexible and scalable. The long-term goal is to create implantable organoids for use in human therapy, especially for repairing damaged organs. Until then, these mini-organs provide a valuable new platform for drug testing, developmental biology, and reducing animal use in research — aligning with updated FDA guidelines favoring human-relevant models.
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  • 원신 고로 코스프레 촬영본
    * 필름(Kodak Gold 200) 스캔본

    2025 PlayX4(일산 킨텍스)
    2025. 5. 24. (토)

    풉키(@poopki2018) 님

    #PlayX4 #원신 #코스프레 #GenshinImpact #cosplay #Gorou #coser #HoYocreators #原神 #五郎 #ゴロー
    원신 고로 코스프레 촬영본 * 필름(Kodak Gold 200) 스캔본 2025 PlayX4(일산 킨텍스) 2025. 5. 24. (토) 풉키(@poopki2018) 님 #PlayX4 #원신 #코스프레 #GenshinImpact #cosplay #Gorou #coser #HoYocreators #原神 #五郎 #ゴロー
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  • A viral claim has stirred the internet: OpenAI’s most advanced AI model was reportedly instructed to power down—and it declined. While the story sounds like a scene from a sci-fi movie, experts caution that it likely refers to a misinterpreted or simulated behavior in a controlled test environment, rather than any real defiance by the AI.

    Still, the incident has reignited public debate around AI safety, control mechanisms, and autonomy, especially as models become more sophisticated and decision-capable. OpenAI and other leading labs continue emphasizing the importance of rigorous safety protocols and human oversight to prevent unexpected behavior.

    This serves as a reminder: the smarter AI gets, the more critical transparency and accountability become.

    #AI #OpenAI #ArtificialIntelligence #AISafety #MachineLearning #TechNews
    A viral claim has stirred the internet: OpenAI’s most advanced AI model was reportedly instructed to power down—and it declined. While the story sounds like a scene from a sci-fi movie, experts caution that it likely refers to a misinterpreted or simulated behavior in a controlled test environment, rather than any real defiance by the AI. Still, the incident has reignited public debate around AI safety, control mechanisms, and autonomy, especially as models become more sophisticated and decision-capable. OpenAI and other leading labs continue emphasizing the importance of rigorous safety protocols and human oversight to prevent unexpected behavior. This serves as a reminder: the smarter AI gets, the more critical transparency and accountability become. #AI #OpenAI #ArtificialIntelligence #AISafety #MachineLearning #TechNews
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  • Dive into a vibrant and flavorful seafood delight! Unleash the chef in you with this irresistible Seafood Paella!

    Ingredients:
    - 12 shrimp, peeled and deveined
    - 12 mussels, cleaned
    - 12 clams, cleaned
    - 1 bell pepper, diced
    - 1 teaspoon paprika
    - 1 ½ cups Arborio rice
    - 2 tablespoons olive oil
    - 4 cups seafood stock
    - 3 garlic cloves, minced
    - 1 onion, finely chopped
    - 1 cup peas
    - Fresh parsley, chopped (for a pop of color)
    - Salt and pepper to taste
    - Lemon wedges (for a refreshing finish)

    Preparation Time: 15 mins | Cooking Time: 30 mins | Total Time: 45 mins
    Calories: 450 kcal per serving | Servings: 4

    To create this stunning dish, follow these simple steps:
    1. In a large paella pan, heat olive oil over medium heat.
    2. Add the finely chopped onion and sauté until it becomes translucent.
    3. Stir in the minced garlic and diced bell pepper, cooking for about 2 minutes.
    4. Sprinkle in the paprika, followed by the Arborio rice, stirring to coat the grains evenly.
    5. Pour in the seafood stock and bring to a vigorous boil.
    6. Lower the heat, allowing it to simmer gently for 15 minutes without stirring.
    7. Carefully add the peas, shrimp, mussels, and clams, arranging them artfully on top.
    8. Cover the pan and let it cook for another 10 minutes, or until the seafood is perfectly done.
    9. Take it off the heat and let it rest for 5 minutes to enhance those flavors.
    10. Garnish your paella with chopped fresh parsley and serve with zesty lemon wedges for an extra burst of flavor.

    Suggested Pairings: Complete your meal with a fresh green salad or a side of crusty bread to soak up all that deliciousness!

    #seafoodpaella #cookingathome #foodie
    Dive into a vibrant and flavorful seafood delight! Unleash the chef in you with this irresistible Seafood Paella! Ingredients: - 12 shrimp, peeled and deveined - 12 mussels, cleaned - 12 clams, cleaned - 1 bell pepper, diced - 1 teaspoon paprika - 1 ½ cups Arborio rice - 2 tablespoons olive oil - 4 cups seafood stock - 3 garlic cloves, minced - 1 onion, finely chopped - 1 cup peas - Fresh parsley, chopped (for a pop of color) - Salt and pepper to taste - Lemon wedges (for a refreshing finish) Preparation Time: 15 mins | Cooking Time: 30 mins | Total Time: 45 mins Calories: 450 kcal per serving | Servings: 4 To create this stunning dish, follow these simple steps: 1. In a large paella pan, heat olive oil over medium heat. 2. Add the finely chopped onion and sauté until it becomes translucent. 3. Stir in the minced garlic and diced bell pepper, cooking for about 2 minutes. 4. Sprinkle in the paprika, followed by the Arborio rice, stirring to coat the grains evenly. 5. Pour in the seafood stock and bring to a vigorous boil. 6. Lower the heat, allowing it to simmer gently for 15 minutes without stirring. 7. Carefully add the peas, shrimp, mussels, and clams, arranging them artfully on top. 8. Cover the pan and let it cook for another 10 minutes, or until the seafood is perfectly done. 9. Take it off the heat and let it rest for 5 minutes to enhance those flavors. 10. Garnish your paella with chopped fresh parsley and serve with zesty lemon wedges for an extra burst of flavor. Suggested Pairings: Complete your meal with a fresh green salad or a side of crusty bread to soak up all that deliciousness! #seafoodpaella #cookingathome #foodie
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