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Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

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Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
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Inheritance of Chromatin Structures03:17

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Epigenetics is the study of inherited changes in a cell's phenotype without changing the DNA sequences. It provides a form of memory for the differential gene expression pattern to maintain cell lineage, position-effect variegation, dosage compensation, and maintenance of chromatin structures such as telomeres and centromeres. For example, the structure and location of the centromere on chromosomes are epigenetically inherited. Its functionality is not dictated or ensured by the underlying...
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Bioequivalence Experimental Study Designs: Completely Randomized and Randomized Block Designs01:20

Bioequivalence Experimental Study Designs: Completely Randomized and Randomized Block Designs

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Body:Bioequivalence experimental study designs are crucial methodologies used in evaluating and comparing the bioavailability of different drug products. These designs are categorized into various types: completely randomized, randomized block, repeated measures, cross and carry-over, and Latin square designs.Completely randomized designs involve randomly allocating treatments to all subjects participating in the experiment. This allocation is achieved by assigning unique random numbers to...
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Intrinsically Disordered Proteins02:18

Intrinsically Disordered Proteins

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Intrinsically disordered proteins are a group of proteins that do not fold into specific three-dimensional structures. Their structural flexibility allows them to complement ordered proteins to perform functions that are inaccessible to rigid structures. They are more common in eukaryotes than prokaryotes and may either be exclusively intrinsically disordered or hybrid proteins, consisting of a mix of ordered and disordered regions. The absence of a rigid structure in these proteins can be...
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Genetics of Speciation02:16

Genetics of Speciation

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Speciation is the evolutionary process resulting in the formation of new, distinct species—groups of reproductively isolated populations.
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Animal Mitochondrial Genetics02:59

Animal Mitochondrial Genetics

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Among all the organelles in an animal cell, only mitochondria have their own independent genomes. Animal mitochondrial DNA is a double-stranded, closed-circular molecule with around 20,000 base pairs. Mitochondrial DNA is unique in that one of its two strands, the heavy, or H, -strand is guanine rich, whereas the complementary strand is cytosine rich and called the light, or L, -strand. Compared to nuclear DNA, mitochondrial DNA has a very low percentage of non-coding regions and is marked by...
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Related Experiment Video

Updated: Feb 15, 2026

Laparoscopic Common Bile Duct Exploration in Patients with a Previous History of Biliary Tract Surgery
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Laparoscopic Common Bile Duct Exploration in Patients with a Previous History of Biliary Tract Surgery

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A Mendelian randomization study exploring the genetic associations between biliary system disorders and brain

Run Qu1, Qingfen Ruan2, Ruiqin Han3

  • 1School of Basic Medical Sciences, Dali University, Yunnan, China.

Medicine
|February 13, 2026
PubMed
Summary

Genetic links between biliary disorders and brain structure changes were found. Specific biliary diseases were associated with altered cortical thickness and surface area in various brain regions.

Keywords:
Mendelian randomization (MR)biliary system disordersbiliary–brain axiscerebral cortexsubcortical volumes

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Paramagnetic Relaxation Enhancement for Detecting and Characterizing Self-Associations of Intrinsically Disordered Proteins
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Area of Science:

  • Neuroscience
  • Genetics
  • Gastroenterology

Background:

  • Biliary system disorders are common and can have systemic effects.
  • Understanding the genetic links between biliary diseases and brain structure is crucial for comprehensive patient care.

Purpose of the Study:

  • To investigate potential genetic associations between four biliary system disorders (primary sclerosing cholangitis, cholecystitis, intrahepatic cholangiocarcinoma, gallstone disease) and brain structural changes.
  • To utilize Mendelian randomization to assess directional relationships.

Main Methods:

  • Mendelian randomization analysis using genome-wide association studies summary statistics.
  • Analysis of cerebral cortex and subcortical brain structures from large cohorts (ENIGMA consortium).
  • Inverse variance weighted as the primary analytical method with sensitivity analyses.

Main Results:

  • Genetically predicted total bilirubin levels associated with decreased pars opercularis thickness.
  • Cholecystitis linked to decreased paracentral lobule thickness and surface area.
  • Gallstone disease associated with altered transverse temporal gyrus dimensions and decreased inferior/middle temporal gyrus thickness.
  • Intrahepatic cholangiocarcinoma linked to decreased pars opercularis thickness and superior parietal gyrus surface area.
  • Primary sclerosing cholangitis associated with increased parahippocampal gyrus surface area and paracentral lobule thickness.

Conclusions:

  • The study suggests a genetic association between biliary system disorders and alterations in cerebral cortical structure.
  • These findings indicate a potential indirect impact of biliary abnormalities on brain morphology.