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Fluorescence-microscopy Screening and Next-generation Sequencing: Useful Tools for the Identification of Genes Involved in Organelle Integrity
Published on: April 13, 2012
Genetic disorders in Arabs as for OMIM
G O Tadmouri1, N Bissar-Tadmouri
1Department of Molecular Biology and Genetics, Bogazici University, Istanbul, Turkey. E-mail. tadmouri@boun.edu.tr.
Saudi Medical Journal
|September 9, 2016
Summary
This study focuses on the full text of a scientific paper, which is available as a scanned copy of its original print version for detailed review.
Area of Science:
- This study falls within the scope of scientific research and archival science.
Background:
- The full text of the research is accessible as a digitized version of the original print material.
- This format ensures the preservation and availability of historical scientific documents.
Purpose of the Study:
- To provide access to the complete research findings.
- To make historical scientific data available for current analysis.
Main Methods:
- The primary method involves accessing a scanned copy of the original print document.
- Digital preservation techniques are employed to maintain the integrity of the text.
Main Results:
- The full research content is available for retrieval.
- The scanned format allows for detailed examination of the original publication.
Conclusions:
- The research is fully accessible through its scanned print version.
- This accessibility facilitates further scientific inquiry and reference.
Related Concept Videos
Genetic Lingo
Overview
Sex-linked Disorders
Like autosomes, sex chromosomes contain a variety of genes necessary for normal body function. When a mutation in one of these genes results in biological deficits, the disorder is considered sex-linked.
Genomic Imprinting and Inheritance
Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
Incomplete Dominance
Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.
Genome-wide Association Studies-GWAS
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...
GWAS does not require the identification of the target gene involved in...
Human Genetics
Human genetics provides a profound framework for understanding the interplay between genetic predispositions and human psychology. At the heart of this discipline lies the study of how genes influence physical traits, behaviors, and susceptibility to diseases. Each person carries a unique genetic code that subtly or significantly shapes their psychological and behavioral landscape.
The complex relationship between genetics and psychology is observable through common biological components such...
The complex relationship between genetics and psychology is observable through common biological components such...

