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There are 81986 results for: content related to: Where and When Do Somatic mtDNA Mutations Occur?

  1. You have free access to this content
    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

  2. 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

  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

  4. 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

  5. You have free access to this content
    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

  6. 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

  7. You have free access to this content
    High-frequency minisatellite instability of the mitochondrial genome in colorectal cancer tissue associated with clinicopathological values

    International Journal of Cancer

    Volume 131, Issue 6, 15 September 2012, Pages: 1332–1341, Sang Woo Lim, Hye Ran Kim, Hwan Young Kim, Jung Wook Huh, Young Jin Kim, Jong Hee Shin, Soon Pal Suh, Dong Wook Ryang, Hyeong Rok Kim and Myung Geun Shin

    Version of Record online : 11 JAN 2012, DOI: 10.1002/ijc.27375

  8. 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

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    Concise Review: Heteroplasmic Mitochondrial DNA Mutations and Mitochondrial Diseases: Toward iPSC-Based Disease Modeling, Drug Discovery, and Regenerative Therapeutics

    STEM CELLS

    Volume 34, Issue 4, April 2016, Pages: 801–808, Hideyuki Hatakeyama and Yu-ichi Goto

    Version of Record online : 13 FEB 2016, DOI: 10.1002/stem.2292

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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

  11. Complex-I Alteration and Enhanced Mitochondrial Fusion Are Associated With Prostate Cancer Progression

    Journal of Cellular Physiology

    Volume 231, Issue 6, June 2016, Pages: 1364–1374, Julie V. Philley, Anbarasu Kannan, Wenyi Qin, Edward R. Sauter, Mitsuo Ikebe, Kate L. Hertweck, Dean A. Troyer, Oliver J. Semmes and Santanu Dasgupta

    Version of Record online : 24 NOV 2015, DOI: 10.1002/jcp.25240

  12. You have full text access to this OnlineOpen article
    Concise Reviews: Assisted Reproductive Technologies to Prevent Transmission of Mitochondrial DNA Disease

    STEM CELLS

    Volume 33, Issue 3, March 2015, Pages: 639–645, Jessica Richardson, Laura Irving, Louise A. Hyslop, Meenakshi Choudhary, Alison Murdoch, Douglass M. Turnbull and Mary Herbert

    Version of Record online : 17 FEB 2015, DOI: 10.1002/stem.1887

  13. You have free access to this content
    Toward a mtDNA locus-specific mutation database using the LOVD platform

    Human Mutation

    Volume 33, Issue 9, September 2012, Pages: 1352–1358, Joanna L. Elson, Mary G. Sweeney, Vincent Procaccio, John W. Yarham, Antonio Salas, Qing-Peng Kong, Francois H. van der Westhuizen, Robert D.S. Pitceathly, David R. Thorburn, Marie T. Lott, Douglas C. Wallace, Robert W. Taylor and Robert McFarland

    Version of Record online : 2 JUL 2012, DOI: 10.1002/humu.22118

  14. Testing for contributions of mitochondrial DNA mutations to complex diseases

    Genetic Epidemiology

    Volume 15, Issue 5, 1998, Pages: 451–469, Fengzhu Sun, Allison E. Ashley-Koch, L. Kathryn Durham, Eleanor Feingold, M. Elizabeth Halloran, Amita K. Manatunga and Stephanie L. Sherman

    Version of Record online : 7 DEC 1998, DOI: 10.1002/(SICI)1098-2272(1998)15:5<451::AID-GEPI2>3.0.CO;2-3

  15. 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

  16. Somatic mutations of the mitochondrial genome in human breast cancers

    Genes, Chromosomes and Cancer

    Volume 50, Issue 10, October 2011, Pages: 800–811, Ling-Ming Tseng, Pen-Hui Yin, Chu-Wen Yang, Yi-Fang Tsai, Chih-Yi Hsu, Chin-Wen Chi and Hsin-Chen Lee

    Version of Record online : 11 JUL 2011, DOI: 10.1002/gcc.20901

  17. 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

  18. You have full text access to this Open Access content
    Does premature aging of the mtDNA mutator mouse prove that mtDNA mutations are involved in natural aging?

    Aging Cell

    Volume 5, Issue 3, June 2006, Pages: 279–282, Konstantin Khrapko, Yevgenya Kraytsberg, Aubrey DNJ De Grey, Jan Vijg and Eric A. Schon

    Version of Record online : 26 APR 2006, DOI: 10.1111/j.1474-9726.2006.00209.x

  19. NOVEL MITOCHONDRIAL DNA MUTATIONS ASSOCIATED WITH CHINESE FAMILIAL HYPERTROPHIC CARDIOMYOPATHY

    Clinical and Experimental Pharmacology and Physiology

    Volume 36, Issue 9, September 2009, Pages: 933–939, Yan-Ling Wei, Chang-An Yu, Peng Yang, Ai-Li Li, Jian-Yan Wen, Shu-Min Zhao, Hong-Xing Liu, Yuan-Nan Ke, William Campbell, Yi-Guan Zhang, Xiao-Hui Li and Wen-Qiang Liao

    Version of Record online : 27 MAR 2009, DOI: 10.1111/j.1440-1681.2009.05183.x

  20. You have free access to this content
    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