International Journal of Science and Research (IJSR)

International Journal of Science and Research (IJSR)
Call for Papers | Fully Refereed | Open Access | Double Blind Peer Reviewed

ISSN: 2319-7064


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Review Papers | Genetics Science | India | Volume 7 Issue 1, January 2018 | Popularity: 7 / 10


     

A Review in Mitochondria and Some of its Diseases

B. Aruthra


Abstract: A cell is said to be a unit of life since its function, make the organisms to stay alive. Cellular functions are regulated and performed by various cell organelles. One such important cell organelle is mitochondria, which is said to be power house of the cell, because mitochondria generate energy for cellular metabolism. Mitochondria, generates energy by various biochemical reactions which result in the synthesis of energy in the form of ATP (adenosine tri-phosphate). Many different enzymes, co-factors, substrate involves in the ATP synthesis are encoded by mitochondrial DNA (mtDNA). When these mtDNA gets mutated, it leads to mitochondrial diseases. Mitochondrial diseases cause biochemical malfunction of a cell. Since mitochondria are inherited from mother to offspring, mitochondrial diseases also get inherited from a carrier mother. This condition is known as maternal inheritance during fertilization. These mitochondrial diseases has no cure but can be diagnosed by prenatal screening as well as by comparing mtDNA sequence of a patient with Cambridge reference sample of mtDNA, which is the first mtDNA sequence analysed in Europe. This comparison pays way for phyogenetic analysis. Mitochondrial diseases result in mortality.


Keywords: mtDNA, ATP synthesis, maternal inheritance


Edition: Volume 7 Issue 1, January 2018


Pages: 793 - 795



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B. Aruthra, "A Review in Mitochondria and Some of its Diseases", International Journal of Science and Research (IJSR), Volume 7 Issue 1, January 2018, pp. 793-795, URL: https://www.ijsr.net/getabstract.php?paperid=ART20179415, DOI: https://www.doi.org/10.21275/ART20179415



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Genetics Science, Morocco, Volume 8 Issue 1, January 2019

Pages: 429 - 432

Toward Primary Congenital Glaucoma GLC3B Gene Identification: The Case of Kazrin Gene

Soumaya El Akil, Ahmed Belmouden


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Genetics Science, Guatemala, Volume 7 Issue 10, October 2018

Pages: 176 - 177

Scientific Discovery on the Way of its Validation

Juan Carlos Perez Velazquez


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Genetics Science, India, Volume 8 Issue 9, September 2019

Pages: 1601 - 1618

Genetic Engineering in Pediatric Dentistry

Arya M V, Rani Somani, Deepti Jawa


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Genetics Science, India, Volume 7 Issue 4, April 2018

Pages: 114 - 116

Ambiguous Genitalia: A Case Report

Dr. Anjali Sabnis, Dr. Vijay N Kamale


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