Literature DB >> 17662684

A multiplex real-time PCR method to detect and quantify mitochondrial DNA deletions in individual cells.

Kim J Krishnan1, Andreas Bender, Robert W Taylor, Douglass M Turnbull.   

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Year:  2007        PMID: 17662684     DOI: 10.1016/j.ab.2007.06.024

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


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  49 in total

1.  SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder.

Authors:  Valentina Del Dotto; Farid Ullah; Ivano Di Meo; Pamela Magini; Mirjana Gusic; Alessandra Maresca; Leonardo Caporali; Flavia Palombo; Francesca Tagliavini; Evan Harris Baugh; Bertil Macao; Zsolt Szilagyi; Camille Peron; Margaret A Gustafson; Kamal Khan; Chiara La Morgia; Piero Barboni; Michele Carbonelli; Maria Lucia Valentino; Rocco Liguori; Vandana Shashi; Jennifer Sullivan; Shashi Nagaraj; Mays El-Dairi; Alessandro Iannaccone; Ioana Cutcutache; Enrico Bertini; Rosalba Carrozzo; Francesco Emma; Francesca Diomedi-Camassei; Claudia Zanna; Martin Armstrong; Matthew Page; Nicholas Stong; Sylvia Boesch; Robert Kopajtich; Saskia Wortmann; Wolfgang Sperl; Erica E Davis; William C Copeland; Marco Seri; Maria Falkenberg; Holger Prokisch; Nicholas Katsanis; Valeria Tiranti; Tommaso Pippucci; Valerio Carelli
Journal:  J Clin Invest       Date:  2020-01-02       Impact factor: 14.808

2.  Depression, telomeres and mitochondrial DNA: between- and within-person associations from a 10-year longitudinal study.

Authors:  J E Verhoeven; D Révész; M Picard; E E Epel; O M Wolkowitz; K A Matthews; B W J H Penninx; E Puterman
Journal:  Mol Psychiatry       Date:  2017-03-28       Impact factor: 15.992

3.  Genome-wide mitochondrial DNA sequence variations and lower expression of OXPHOS genes predict mitochondrial dysfunction in oral cancer tissue.

Authors:  Esita Chattopadhyay; Navonil De Sarkar; Richa Singh; Anindita Ray; Roshni Roy; Ranjan Rashmi Paul; Mousumi Pal; Sandip Ghose; Subhrendu Ghosh; Debajyoti Kabiraj; Raja Banerjee; Bidyut Roy
Journal:  Tumour Biol       Date:  2016-04-07

4.  Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease.

Authors:  Lyndsey Craven; Helen A Tuppen; Gareth D Greggains; Stephen J Harbottle; Julie L Murphy; Lynsey M Cree; Alison P Murdoch; Patrick F Chinnery; Robert W Taylor; Robert N Lightowlers; Mary Herbert; Douglass M Turnbull
Journal:  Nature       Date:  2010-04-14       Impact factor: 49.962

5.  Gastrointestinal dysmotility in mitochondrial neurogastrointestinal encephalomyopathy is caused by mitochondrial DNA depletion.

Authors:  Carla Giordano; Mariangela Sebastiani; Roberto De Giorgio; Claudia Travaglini; Andrea Tancredi; Maria Lucia Valentino; Marzio Bellan; Andrea Cossarizza; Michio Hirano; Giulia d'Amati; Valerio Carelli
Journal:  Am J Pathol       Date:  2008-09-11       Impact factor: 4.307

6.  Dopaminergic midbrain neurons are the prime target for mitochondrial DNA deletions.

Authors:  Andreas Bender; Rachel-Maria Schwarzkopf; Anja McMillan; Kim J Krishnan; Gabriele Rieder; Manuela Neumann; Matthias Elstner; Douglas M Turnbull; Thomas Klopstock
Journal:  J Neurol       Date:  2008-07-11       Impact factor: 4.849

7.  Associations Between Cellular Aging Markers and Metabolic Syndrome: Findings From the CARDIA Study.

Authors:  Dóra Révész; Josine E Verhoeven; Martin Picard; Jue Lin; Stephen Sidney; Elissa S Epel; Brenda W J H Penninx; Eli Puterman
Journal:  J Clin Endocrinol Metab       Date:  2018-01-01       Impact factor: 5.958

8.  Loss of myelin-associated glycoprotein in kearns-sayre syndrome.

Authors:  Nichola Z Lax; Graham R Campbell; Amy K Reeve; Nobuhiko Ohno; Jessica Zambonin; Emma L Blakely; Robert W Taylor; Eduardo Bonilla; Kurenai Tanji; Salvatore DiMauro; Evelyn Jaros; Hans Lassmann; Doug M Turnbull; Don J Mahad
Journal:  Arch Neurol       Date:  2012-04

9.  Mitochondrial DNA defects and selective extraocular muscle involvement in CPEO.

Authors:  Laura C Greaves; Patrick Yu-Wai-Man; Emma L Blakely; Kim J Krishnan; Nina E Beadle; Jamie Kerin; Martin J Barron; Philip G Griffiths; Alison J Dickinson; Douglass M Turnbull; Robert W Taylor
Journal:  Invest Ophthalmol Vis Sci       Date:  2010-02-17       Impact factor: 4.799

10.  A p.R369G POLG2 mutation associated with adPEO and multiple mtDNA deletions causes decreased affinity between polymerase γ subunits.

Authors:  Kate Craig; Matthew J Young; Emma L Blakely; Matthew J Longley; Douglass M Turnbull; William C Copeland; Robert W Taylor
Journal:  Mitochondrion       Date:  2011-12-04       Impact factor: 4.160

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