نتایج جستجو برای: polg gene

تعداد نتایج: 1141492  

Journal: :Pediatric Neurology Briefs 2012

Journal: :Movement Disorders Clinical Practice 2015

2016
Joonil Kim Eungu Kang Yoonmyung Kim Jae-Min Kim Beom Hee Lee Kei Murayama Gu-Hwan Kim In Hee Choi Kyung Mo Kim Han-Wook Yoo

MPV17-related hepatocerebral mitochondrial DNA depletion syndrome (MDS) is a very rare condition, and only a few cases have been reported in East Asian countries. Here, we describe four Korean children affected by hepatocerebral MDS. The DGUOK, POLG1, and MPV17 genes were analyzed, and all patients had MPV17 mutations.

Journal: :Genetics 2007
Emma J Bowles Joon-Hee Lee Ramiro Alberio Rhiannon E I Lloyd Dov Stekel Keith H S Campbell Justin C St John

Mitochondrial DNA (mtDNA) is normally only inherited through the oocyte. However, nuclear transfer (NT), the fusion of a donor cell with an enucleated oocyte, can transmit both donor cell and recipient oocyte mtDNA. mtDNA replication is under the control of nuclear-encoded replication factors, such as polymerase gamma (POLG) and mitochondrial transcription factor A (TFAM). These are first expre...

2009
Ivana Bratic Jürgen Hench Johan Henriksson Adam Antebi Thomas R Bürglin Aleksandra Trifunovic

A number of studies showed that the development and the lifespan of Caenorhabditis elegans is dependent on mitochondrial function. In this study, we addressed the role of mitochondrial DNA levels and mtDNA maintenance in development of C. elegans by analyzing deletion mutants for mitochondrial polymerase gamma (polg-1(ok1548)). Surprisingly, even though previous studies in other model organisms...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2005
Lawrence A Loeb Douglas C Wallace George M Martin

M itochondria are cellular energy factories that generate ATP via the reaction of hydrocarbons with oxygen. Every human cell contains hundreds of mitochondria, and each mitochondrion contains multiple copies of mitochondrial DNA (mtDNA). The ancestry of the mitochondrial genome can be traced to early eubacteria, and it is therefore unexpected that this organelle may have a major role in governi...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2013
Amy Reeve Martin Meagher Nichola Lax Eve Simcox Philippa Hepplewhite Evelyn Jaros Doug Turnbull

Mitochondrial defects within substantia nigra (SN) neurons are implicated in the pathogenesis of Parkinson's disease. SN neurons show increased mitochondrial defects, mitochondrial DNA deletion levels, and susceptibility to such dysfunction, although the role of mitochondria in neuronal degeneration remains uncertain. In this study, we addressed this important question by exploring changes with...

Journal: :Archives of Neurology 2010

Journal: :Frontiers in bioscience 2017
Rachel Krasich William C Copeland

Since 1970, the DNA polymerase gamma (PolG) has been known to be the DNA polymerase responsible for replication and repair of mitochondrial DNA, and until recently it was generally accepted that this was the only polymerase present in mitochondria. However, recent data has challenged that opinion, as several polymerases are now proposed to have activity in mitochondria. To date, their exact rol...

2010
Sarah A. Martin Nuala McCabe Michelle Mullarkey Robert Cummins Darren J. Burgess Yusaku Nakabeppu Sugako Oka Elaine Kay Christopher J. Lord Alan Ashworth

Synthetic sickness/lethality (SSL) can be exploited to develop therapeutic strategies for cancer. Deficiencies in the tumor suppressor proteins MLH1 and MSH2 have been implicated in cancer. Here we demonstrate that deficiency in MSH2 is SSL with inhibition of the DNA polymerase POLB, whereas deficiency in MLH1 is SSL with DNA polymerase POLG inhibition. Both SSLs led to the accumulation of 8-ox...

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