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There are 31631 results for: content related to: Mitochondrial DNA and disease

  1. Mitochondrial disorders: genetics, counseling, prenatal diagnosis and reproductive options

    American Journal of Medical Genetics

    Volume 106, Issue 1, Spring 2001, Pages: 102–114, David R. Thorburn and Hans-Henrik M. Dahl

    Version of Record online : 17 MAY 2001, DOI: 10.1002/ajmg.1380

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    Detection of mitochondrial deoxyribonucleic acid alterations in urine from urothelial cell carcinoma patients

    International Journal of Cancer

    Volume 131, Issue 1, 1 July 2012, Pages: 158–164, Santanu Dasgupta, Chunbo Shao, Thomas E. Keane, David P. Duberow, Richard A. Mathies, Paul B. Fisher, Lambertus A. Kiemeney and David Sidransky

    Version of Record online : 30 AUG 2011, DOI: 10.1002/ijc.26357

  3. mtDNA mutations variously impact mtDNA maintenance throughout the human embryofetal development

    Clinical Genetics

    Volume 88, Issue 5, November 2015, Pages: 416–424, J. Steffann, S. Monnot and J.-P. Bonnefont

    Version of Record online : 3 FEB 2015, DOI: 10.1111/cge.12557

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    A transgenic model to study the pathogenesis of somatic mtDNA mutation accumulation in β-cells

    Diabetes, Obesity and Metabolism

    Volume 9, Issue s2, November 2007, Pages: 74–80, K. G. Bensch, W. DeGraaf, P. A. Hansen, H. P. Zassenhaus and J. A. Corbett

    Version of Record online : 4 OCT 2007, DOI: 10.1111/j.1463-1326.2007.00776.x

  5. You have full text access to this OnlineOpen article
    Mitochondrial DNA deletions and depletion within paraspinal muscles

    Neuropathology and Applied Neurobiology

    Volume 39, Issue 4, June 2013, Pages: 377–389, G. R. Campbell, A. Reeve, I. Ziabreva, T. M. Polvikoski, R. W. Taylor, R. Reynolds, D. M. Turnbull and D. J. Mahad

    Version of Record online : 25 APR 2013, DOI: 10.1111/j.1365-2990.2012.01290.x

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    Mitochondrial DNA deletions and neurodegeneration in multiple sclerosis

    Annals of Neurology

    Volume 69, Issue 3, March 2011, Pages: 481–492, Graham R. Campbell, Iryna Ziabreva, Amy K. Reeve, Kim J. Krishnan, Richard Reynolds, Owen Howell, Hans Lassmann, Doug M. Turnbull and Don J. Mahad

    Version of Record online : 8 NOV 2010, DOI: 10.1002/ana.22109

  7. Mouse models for mitochondrial disease

    American Journal of Medical Genetics

    Volume 106, Issue 1, Spring 2001, Pages: 71–93, Douglas C. Wallace

    Version of Record online : 22 JUN 2001, DOI: 10.1002/ajmg.1393

  8. You have full text access to this OnlineOpen article
    Human stem cell aging: do mitochondrial DNA mutations have a causal role?

    Aging Cell

    Volume 13, Issue 2, April 2014, Pages: 201–205, Holly L. Baines, Douglass M. Turnbull and Laura C. Greaves

    Version of Record online : 28 JAN 2014, DOI: 10.1111/acel.12199

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    Genetic basis of Alzheimer's dementia: role of mtDNA mutations

    Genes, Brain and Behavior

    Volume 5, Issue s2, June 2006, Pages: 92–107, M. Grazina, J. Pratas, F. Silva, S. Oliveira, I. Santana and C. Oliveira

    Version of Record online : 26 APR 2006, DOI: 10.1111/j.1601-183X.2006.00225.x

  10. Mitochondrial Mutations and Disease

    Mitochondria, Second Edition

    Immo E. Scheffler, Pages: 345–416, 2007

    Published Online : 30 APR 2007, DOI: 10.1002/9780470191774.ch7

  11. Mitochondrial DNA mutations in human disease

    American Journal of Medical Genetics

    Volume 106, Issue 1, Spring 2001, Pages: 18–26, Salvatore DiMauro and Eric A. Schon

    Version of Record online : 25 MAY 2001, DOI: 10.1002/ajmg.1392

  12. Mitochondrial myopathies

    Acta Physiologica Scandinavica

    Volume 171, Issue 3, March 2001, Pages: 385–393, N.-G. Larsson and A. Oldfors

    Version of Record online : 9 OCT 2008, DOI: 10.1046/j.1365-201x.2001.00842.x

  13. Molecular Analysis of Oxidative Phosphorylation Diseases for Detection of Mitochondrial DNA Mutations

    Unit

    Current Protocols in Human Genetics

    9:9.9.1–9.9.26

    John M. Shoffner

    Published Online : 1 MAY 2001, DOI: 10.1002/0471142905.hg0909s13

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    Mouse models of mitochondrial DNA defects and their relevance for human disease

    EMBO reports

    Volume 10, Issue 2, February 2009, Pages: 137–143, Henna Tyynismaa and Anu Suomalainen

    Version of Record online : 16 JAN 2009, DOI: 10.1038/embor.2008.242

  15. Frequent Intracellular Clonal Expansions of Somatic mtDNA Mutations

    Annals of the New York Academy of Sciences

    Volume 959, Issue 1, April 2002, Pages: 434–447, HILARY A. COLLER, NATALYA D. BODYAK and KONSTANTIN KHRAPKO

    Version of Record online : 24 JAN 2006, DOI: 10.1111/j.1749-6632.2002.tb02113.x

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    Mitochondrial DNA mutations in human disease

    IUBMB Life

    Volume 58, Issue 3, March 2006, Pages: 143–151, Laura C. Greaves and Robert W. Taylor

    Version of Record online : 3 JAN 2008, DOI: 10.1080/15216540600686888

  17. Transition to Next Generation Analysis of the Whole Mitochondrial Genome: A Summary of Molecular Defects

    Human Mutation

    Volume 34, Issue 6, June 2013, Pages: 882–893, Sha Tang, Jing Wang, Victor Wei Zhang, Fang-Yuan Li, Megan Landsverk, Hong Cui, Cavatina K. Truong, Guoli Wang, Li Chieh Chen, Brett Graham, Fernando Scaglia, Eric S. Schmitt, William J. Craigen and Lee-Jun C. Wong

    Version of Record online : 2 APR 2013, DOI: 10.1002/humu.22307

  18. Diagnostic screening of mitochondrial DNA mutations in Australian adults 1990–2001

    Internal Medicine Journal

    Volume 34, Issue 1-2, January 2004, Pages: 10–19, R. Marotta, J. Chin, A. Quigley, S. Katsabanis, R. Kapsa, E. Byrne and S. Collins

    Version of Record online : 23 SEP 2008, DOI: 10.1111/j.1444-0903.2004.t01-3-.x

  19. Preventing the transmission of mitochondrial DNA disorders using prenatal or preimplantation genetic diagnosis

    Annals of the New York Academy of Sciences

    Volume 1350, Issue 1, September 2015, Pages: 29–36, Hubert J.M. Smeets, Suzanne C.E.H. Sallevelt, Jos C.F.M. Dreesen, Christine E.M. de Die-Smulders and Irenaeus F.M. de Coo

    Version of Record online : 27 AUG 2015, DOI: 10.1111/nyas.12866

  20. Mitochondrial DNA mutations in respiratory complex-I in never-smoker lung cancer patients contribute to lung cancer progression and associated with EGFR gene mutation

    Journal of Cellular Physiology

    Volume 227, Issue 6, June 2012, Pages: 2451–2460, Santanu Dasgupta, Ethan Soudry, Nitai Mukhopadhyay, Chunbo Shao, John Yee, Stephan Lam, Wan Lam, Wei Zhang, Adi F Gazdar, Paul B Fisher and David Sidransky

    Version of Record online : 24 FEB 2012, DOI: 10.1002/jcp.22980