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  2. Genetics of obesity - Wikipedia

    en.wikipedia.org/wiki/Genetics_of_obesity

    Like many other medical conditions, obesity is the result of an interplay between environmental and genetic factors. [2] [3] Studies have identified variants in several genes that may contribute to weight gain and body fat distribution; although, only in a few cases are genes the primary cause of obesity.

  3. Human genome - Wikipedia

    en.wikipedia.org/wiki/Human_genome

    The complete human genome (without Y chromosome) was published in 2021, while with Y chromosome in January 2022. [3] [4] [73] In 2023, a draft human pangenome reference was published. [8] It is based on 47 genomes from persons of varied ethnicity. [8] Plans are underway for an improved reference capturing still more biodiversity from a still ...

  4. Pathophysiology of obesity - Wikipedia

    en.wikipedia.org/wiki/Pathophysiology_of_obesity

    Pathophysiology of obesity is the study of disordered physiological processes that cause, result from, or are otherwise associated with obesity. A number of possible pathophysiological mechanisms have been identified which may contribute in the development and maintenance of obesity.

  5. Overweight vs. Obesity: Do You Really Know the Difference? - AOL

    www.aol.com/overweight-vs-obesity-really-know...

    Obesity is a disease characterized by having excessive body fat, increasing a person’s risk for many serious health problems, such as heart disease, diabetes, and even some cancers.

  6. Eukaryotic chromosome structure - Wikipedia

    en.wikipedia.org/wiki/Eukaryotic_chromosome...

    In eukaryotes, such as humans, roughly 3.2 billion nucleotides are spread out over 23 different chromosomes (males have both an X chromosome and a Y chromosome instead of a pair of X chromosomes as seen in females). Each chromosome consists enormously long linear DNA molecule associated with proteins that fold and pack the fine thread of DNA ...

  7. 16p11.2 deletion syndrome - Wikipedia

    en.wikipedia.org/wiki/16p11.2_deletion_syndrome

    16p11.2 deletion syndrome is a rare genetic condition caused by microdeletion on the short arm of chromosome 16. Most affected individuals experience global developmental delay and intellectual disability, as well as childhood-onset obesity. [1] 16p11.2 deletion is estimated to account for approximately 1% of autism spectrum disorder cases. [3] [4]

  8. Gene mapping - Wikipedia

    en.wikipedia.org/wiki/Gene_mapping

    There are two distinctive mapping approaches used in the field of genome mapping: genetic maps (also known as linkage maps) [7] and physical maps. [3] While both maps are a collection of genetic markers and gene loci, [8] genetic maps' distances are based on the genetic linkage information, while physical maps use actual physical distances usually measured in number of base pairs.

  9. New study finds first US obesity decline in 10 years. Is ...

    www.aol.com/study-finds-first-us-obesity...

    Published in JAMA Health Forum on Friday, the study, "Changes in Adult Obesity Trends in the US," found that between 2022 and 2023, obesity in American adults between ages 26-75 dropped about 0.15%.