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  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Doi.org Make Money
  6. Keywords
  7. Topics
  8. Schema
  9. External Links
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We began analyzing https://link.springer.com/article/10.1007/s007740170042, but it redirected us to https://link.springer.com/article/10.1007/s007740170042. The analysis below is for the second page.

Title[redir]:
Central control of bone formation | Journal of Bone and Mineral Metabolism
Description:
Vertebrates constantly remodel bone to maintain a constant bone mass. Bone remodeling comprises two phases: bone resorption by the osteoclasts followed by bone formation by the osteoblasts. Although the prevailing view about the control of bone remodeling is that it is an autocrine/paracrine phenomenon, the bone resorption arm of bone remodeling is under a tight endocrine control. To date little is known about the regulation of bone formation. We took the observations that gonadal failure favors bone loss and obesity protects from it as an indication that bone mass, body weight, and reproduction could be regulated by the same hormone(s). Leptin is one of these hormones. Leptin inhibits bone formation by the osteoblasts. This function is dominant, and leptin deficiency results in a high bone mass phenotype despite the hypogonadism characterizing these animals. Genetic biochemical and physiological studies demonstrate that leptin inhibits bone formation following its binding to its receptor in the hypothalamus. These results are the first evience that bone remodeling is a hypothalamic process; they imply necessarily that osteoporosis, the most frequent bone remodeling disease, is partly at least a hypothalamic disease. This finding also has therapeutic implications.

Matching Content Categories {πŸ“š}

  • Health & Fitness
  • Science
  • News & Politics

Content Management System {πŸ“}

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Custom-built

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Traffic Estimate {πŸ“ˆ}

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πŸ™οΈ Massive Traffic: 50M - 100M visitors per month


Based on our best estimate, this website will receive around 80,479,999 visitors per month in the current month.

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Keywords {πŸ”}

bone, article, formation, control, remodeling, privacy, cookies, content, journal, central, leptin, information, publish, search, mass, access, chapter, data, log, research, metabolism, takeda, karsenty, regulation, discover, remodelling, springer, function, optional, personal, parties, policy, find, track, mineral, cite, shu, gerard, explore, resorption, osteoblasts, hormones, inhibits, results, genetic, hypothalamic, disease, institution, molecular, related,

Topics {βœ’οΈ}

month download article/chapter central control bone formation published bone remodeling comprises tight endocrine control privacy choices/manage cookies constant bone mass bone resorption arm central regulation mineral metabolism aims article takeda full article pdf leptin deficiency results european economic area autocrine/paracrine phenomenon physiological studies demonstrate bone formation bone remodeling conditions privacy policy bone metabolism accepting optional cookies related subjects bone mass journal finder publish main content log bone resorption check access instant access karsenty article journal privacy policy control personal data books a optional cookies bone manage preferences hypothalamic disease molecular article log journal publish data protection essential cookies cookies skip subscription content similar content article cite institution subscribe leptin usage analysis

Schema {πŸ—ΊοΈ}

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         headline:Central control of bone formation
         description: Vertebrates constantly remodel bone to maintain a constant bone mass. Bone remodeling comprises two phases: bone resorption by the osteoclasts followed by bone formation by the osteoblasts. Although the prevailing view about the control of bone remodeling is that it is an autocrine/paracrine phenomenon, the bone resorption arm of bone remodeling is under a tight endocrine control. To date little is known about the regulation of bone formation. We took the observations that gonadal failure favors bone loss and obesity protects from it as an indication that bone mass, body weight, and reproduction could be regulated by the same hormone(s). Leptin is one of these hormones. Leptin inhibits bone formation by the osteoblasts. This function is dominant, and leptin deficiency results in a high bone mass phenotype despite the hypogonadism characterizing these animals. Genetic biochemical and physiological studies demonstrate that leptin inhibits bone formation following its binding to its receptor in the hypothalamus. These results are the first evience that bone remodeling is a hypothalamic process; they imply necessarily that osteoporosis, the most frequent bone remodeling disease, is partly at least a hypothalamic disease. This finding also has therapeutic implications.
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      headline:Central control of bone formation
      description: Vertebrates constantly remodel bone to maintain a constant bone mass. Bone remodeling comprises two phases: bone resorption by the osteoclasts followed by bone formation by the osteoblasts. Although the prevailing view about the control of bone remodeling is that it is an autocrine/paracrine phenomenon, the bone resorption arm of bone remodeling is under a tight endocrine control. To date little is known about the regulation of bone formation. We took the observations that gonadal failure favors bone loss and obesity protects from it as an indication that bone mass, body weight, and reproduction could be regulated by the same hormone(s). Leptin is one of these hormones. Leptin inhibits bone formation by the osteoblasts. This function is dominant, and leptin deficiency results in a high bone mass phenotype despite the hypogonadism characterizing these animals. Genetic biochemical and physiological studies demonstrate that leptin inhibits bone formation following its binding to its receptor in the hypothalamus. These results are the first evience that bone remodeling is a hypothalamic process; they imply necessarily that osteoporosis, the most frequent bone remodeling disease, is partly at least a hypothalamic disease. This finding also has therapeutic implications.
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