نتایج جستجو برای: trna mitochondrial mutation repeated pregnancy loss

تعداد نتایج: 1060873  

Journal: :Mitochondrion 2015
Rachael M Duff Anne-Marie J Shearwood Judith Ermer Giulia Rossetti Rebecca Gooding Tara R Richman Shanti Balasubramaniam David R Thorburn Oliver Rackham Phillipa J Lamont Aleksandra Filipovska

Leigh syndrome (LS) is a progressive mitochondrial neurodegenerative disorder, whose symptoms most commonly include psychomotor delay with regression, lactic acidosis and a failure to thrive. Here we describe three siblings with LS, but with additional manifestations including hypertrophic cardiomyopathy, hepatosplenomegaly, cholestatic hepatitis, and seizures. All three affected siblings were ...

Objective(s): As mitochondrial oxidative stress is probably entailed in ATP production, a candidate modifier factor for the long QT syndrome (LQTS) could be mitochondrial DNA (mtDNA). It has been notified that ion channels' activities in cardiomyocytes are sensitive to the ATP level. Materials and Methods: The sample of the research was an Iranian family with LQTS for mutations by PCR-SSCP and...

Journal: :iranian red crescent medical journal 0
elham yousefian department of midwifery, islamic azad university falavarjan branch, isfahan, ir iran; department of midwifery, islamic azad university falavarjan branch, isfahan, ir iran. tel: +98-3123120136 mohammad taghi kardi department of biology, university of isfahan, isfahan, ir iran azra allahveisi department of anatomy, faculty of medicine, kurdistan university of medical sciences, sannandaj, ir iran

background recurrent pregnancy loss (rpl) is a serious problem for pregnancy. there is evidence that vascular complications play a principal role in rpl. methylenetetrahydrofolate reductase (mthfr) is a key enzyme in folate metabolism. polymorphisms (c677t, a1298c) of mthfr gene are associated with decreased mthfr activity. objectives the aim of this study was to determine the association betwe...

2008
Joanna Rorbach Abdul Aziz Yusoff Helen Tuppen Dyg P. Abg-Kamaludin Zofia M.A. Chrzanowska-Lightowlers Robert W. Taylor Douglass M. Turnbull Robert McFarland Robert N. Lightowlers

Phenotypic diversity associated with pathogenic mutations of the human mitochondrial genome (mtDNA) has often been explained by unequal segregation of the mutated and wild-type genomes (heteroplasmy). However, this simple hypothesis cannot explain the tissue specificity of disorders caused by homoplasmic mtDNA mutations. We have previously associated a homoplasmic point mutation (1624C>T) in MT...

Journal: :Journal of medical genetics 2010
M Nakamura I Yabe A Sudo K Hosoki H Yaguchi S Saitoh H Sasaki

BACKGROUND Myoclonic epilepsy with ragged-red fibres (MERRF) and mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) are established phenotypes of mitochondrial encephalomyopathy. The m.8356T>C transition in the mitochondrial tRNA(Lys) gene is a pathogenic mutations of MERRF. The m.3243A>G transition in the mitochondrial tRNA(Leu) gene is detected in most MELAS patien...

2015
Mariella Simon Elodie M. Richard Xinjian Wang Mohsin Shahzad Vincent H. Huang Tanveer A. Qaiser Prasanth Potluri Sarah E. Mahl Antonio Davila Sabiha Nazli Saege Hancock Margret Yu Jay Gargus Richard Chang Nada Al-sheqaih William G. Newman Jose Abdenur Arnold Starr Rashmi Hegde Thomas Dorn Anke Busch Eddie Park Jie Wu Hagen Schwenzer Adrian Flierl Catherine Florentz Marie Sissler Shaheen N. Khan Ronghua Li Min-Xin Guan Thomas B. Friedman Doris K. Wu Vincent Procaccio Sheikh Riazuddin Douglas C. Wallace Zubair M. Ahmed Taosheng Huang Saima Riazuddin

Here we demonstrate association of variants in the mitochondrial asparaginyl-tRNA synthetase NARS2 with human hearing loss and Leigh syndrome. A homozygous missense mutation ([c.637G>T; p.Val213Phe]) is the underlying cause of nonsyndromic hearing loss (DFNB94) and compound heterozygous mutations ([c.969T>A; p.Tyr323*] + [c.1142A>G; p.Asn381Ser]) result in mitochondrial respiratory chain defici...

Journal: :international journal of reproductive biomedicine 0
majid teremmahi ardestani hossein hadi nodushan abbas aflatoonian nasrin ghasemi mohammad hasan sheikhha

background: recurrent pregnancy loss (rpl) caused by various genetic and non-genetic factors. after chromosome abnormality, thrombophilia is one of the most important genetic factors that could cause rpl. factor v leiden and factor ii g20210a mutation were the most common mutations cause thrombophilia in the world. objective: the purpose of this study was to determine the frequency of factor v ...

2014
Daria Diodato Laura Melchionda Tobias B Haack Cristina Dallabona Enrico Baruffini Claudia Donnini Tiziana Granata Francesca Ragona Paolo Balestri Maria Margollicci Eleonora Lamantea Alessia Nasca Christopher A Powell Michal Minczuk Tim M Strom Thomas Meitinger Holger Prokisch Costanza Lamperti Massimo Zeviani Daniele Ghezzi

By way of whole-exome sequencing, we identified a homozygous missense mutation in VARS2 in one subject with microcephaly and epilepsy associated with isolated deficiency of the mitochondrial respiratory chain (MRC) complex I and compound heterozygous mutations in TARS2 in two siblings presenting with axial hypotonia and severe psychomotor delay associated with multiple MRC defects. The nucleoti...

2013
Rojeen Shahni Yehani Wedatilake Maureen A Cleary Keith J Lindley Keith R Sibson Shamima Rahman

Nuclear-encoded disorders of mitochondrial translation are clinically and genetically heterogeneous. Genetic causes include defects of mitochondrial aminoacyl-tRNA synthetases, and factors required for initiation, elongation and termination of protein synthesis as well as ribosome recycling. We report on a new case of myopathy, lactic acidosis and sideroblastic anemia (MLASA) syndrome caused by...

2011
Haris Kokotas Maria Grigoriadou George S. Korres Elisabeth Ferekidou Dimitrios Kandiloros Stavros Korres Michael B. Petersen

Mitochondrion harbors its own DNA, known as mtDNA, encoding certain essential components of the mitochondrial respiratory chain and protein synthesis apparatus. mtDNA mutations have an impact on cellular ATP production and many of them are undoubtedly a factor that contributes to sensorineural deafness, including both syndromic and non-syndromic forms. Hot spot regions for deafness mutations ar...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید