Works by Robert W. Taylor

Results: 295

Delineating the mechanisms of cerebellar degeneration in paediatric and adult primary mitochondrial disease.

Published in:

Acta Neuropathologica, 2025, v. 149, n. 1, p. 1, doi. 10.1007/s00401-025-02891-6

By:

Smith, Laura A.;
Olkhova, Elizaveta A.;
Lax, Nichola Z.;
Ng, Yi Shiau;
Taylor, Robert W.;
Gorman, Grainne S.;
Erskine, Daniel;
McFarland, Robert

Publication type:

Article

PET Imaging of Bacterial Infections with Fluorine-18-Labeled Maltohexaose.

Published in:

Angewandte Chemie, 2014, v. 126, n. 51, p. 14320, doi. 10.1002/ange.201408533

By:

Ning, Xinghai;
Seo, Wonewoo;
Lee, Seungjun;
Takemiya, Kiyoko;
Rafi, Mohammad;
Feng, Xuli;
Weiss, Daiana;
Wang, Xiaojian;
Williams, Larry;
Camp, Vernon M.;
Eugene, Malveaux;
Taylor, W. Robert;
Goodman, Mark;
Murthy, Niren

Publication type:

Article

Loss‐of‐function mutations in <italic>ISCA2</italic> disrupt 4Fe–4S cluster machinery and cause a fatal leukodystrophy with hyperglycinemia and mtDNA depletion.

Published in:

Human Mutation, 2018, v. 39, n. 4, p. 537, doi. 10.1002/humu.23396

By:

Alaimo, Joseph T.;
Besse, Arnaud;
Alston, Charlotte L.;
Pang, Ki;
Appadurai, Vivek;
Samanta, Monisha;
Smpokou, Patroula;
McFarland, Robert;
Taylor, Robert W.;
Bonnen, Penelope E.

Publication type:

Article

A novel inborn error of the coenzyme Q10 biosynthesis pathway: cerebellar ataxia and static encephalomyopathy due to COQ5 C-methyltransferase deficiency.

Published in:

Human Mutation, 2018, v. 39, n. 1, p. 69, doi. 10.1002/humu.23345

By:

Malicdan, May Christine V.;
Vilboux, Thierry;
Ben‐Zeev, Bruria;
Guo, Jennifer;
Eliyahu, Aviva;
Pode‐Shakked, Ben;
Dori, Amir;
Kakani, Sravan;
Chandrasekharappa, Settara C.;
Ferreira, Carlos R.;
Shelestovich, Natalia;
Marek‐Yagel, Dina;
Pri‐Chen, Hadass;
Blatt, Ilan;
Niederhuber, John E.;
He, Langping;
Toro, Camilo;
Taylor, Robert W.;
Deeken, John;
Yardeni, Tal

Publication type:

Article

MTO1 Mutations are Associated with Hypertrophic Cardiomyopathy and Lactic Acidosis and Cause Respiratory Chain Deficiency in Humans and Yeast.

Published in:

Human Mutation, 2013, v. 34, n. 11, p. 1501, doi. 10.1002/humu.22393

By:

Baruffini, Enrico;
Dallabona, Cristina;
Invernizzi, Federica;
Yarham, John W.;
Melchionda, Laura;
Blakely, Emma L.;
Lamantea, Eleonora;
Donnini, Claudia;
Santra, Saikat;
Vijayaraghavan, Suresh;
Roper, Helen P.;
Burlina, Alberto;
Kopajtich, Robert;
Walther, Anett;
Strom, Tim M.;
Haack, Tobias B.;
Prokisch, Holger;
Taylor, Robert W.;
Ferrero, Ileana;
Zeviani, Massimo

Publication type:

Article

Pathogenic Mitochondrial t RNA Point Mutations: Nine Novel Mutations Affirm Their Importance as a Cause of Mitochondrial Disease.

Published in:

Human Mutation, 2013, v. 34, n. 9, p. 1260, doi. 10.1002/humu.22358

By:

Blakely, Emma L.;
Yarham, John W.;
Alston, Charlotte L.;
Craig, Kate;
Poulton, Joanna;
Brierley, Charlotte;
Park, Soo‐Mi;
Dean, Andrew;
Xuereb, John H.;
Anderson, Kirstie N.;
Compston, Alistair;
Allen, Chris;
Sharif, Saba;
Enevoldson, Peter;
Wilson, Martin;
Hammans, Simon R.;
Turnbull, Douglass M.;
McFarland, Robert;
Taylor, Robert W.

Publication type:

Article

Toward a mtDNA locus-specific mutation database using the LOVD platform.

Published in:

Human Mutation, 2012, v. 33, n. 9, p. 1352, doi. 10.1002/humu.22118

By:

Elson, Joanna L.;
Sweeney, Mary G.;
Procaccio, Vincent;
Yarham, John W.;
Salas, Antonio;
Kong, Qing-Peng;
van der Westhuizen, Francois H.;
Pitceathly, Robert D.S.;
Thorburn, David R.;
Lott, Marie T.;
Wallace, Douglas C.;
Taylor, Robert W.;
McFarland, Robert

Publication type:

Article

A comparative analysis approach to determining the pathogenicity of mitochondrial tRNA mutations.

Published in:

Human Mutation, 2011, v. 32, n. 11, p. 1319, doi. 10.1002/humu.21575

By:

Yarham, John W.;
Al-Dosary, Mazhor;
Blakely, Emma L.;
Alston, Charlotte L.;
Taylor, Robert W.;
Elson, Joanna L.;
McFarland, Robert

Publication type:

Article

Pathogenic mitochondrial tRNA mutations - Which mutations are inherited and why?

Published in:

Human Mutation, 2009, v. 30, n. 11, p. E984, doi. 10.1002/humu.21113

By:

Elson, Joanna L.;
Swalwell, Helen;
Blakely, Emma L.;
McFarland, Robert;
Taylor, Robert W.;
Turnbull, Doug M.

Publication type:

Article

Exaggerated status of 'novel' and 'pathogenic' mtDNA sequence variants due to inadequate database searches.

Published in:

2009

By:

Bandelt, Hans-Jürgen;
Salas, Antonio;
Taylor, Robert W.;
Yao, Yong-Gang

Publication type:

Other

A Novel Pathogenic Variant in MT-CO2 Causes an Isolated Mitochondrial Complex IV Deficiency and Late-Onset Cerebellar Ataxia.

Published in:

Journal of Clinical Medicine, 2019, v. 8, n. 6, p. 789, doi. 10.3390/jcm8060789

By:

Zierz, Charlotte M.;
Baty, Karen;
Blakely, Emma L.;
Hopton, Sila;
Falkous, Gavin;
Schaefer, Andrew M.;
Hadjivassiliou, Marios;
Sarrigiannis, Ptolemaios G.;
Ng, Yi Shiau;
Taylor, Robert W.

Publication type:

Article

Cognitive deficits in adult m.3243A>G‐ and m.8344A>G‐related mitochondrial disease: importance of correcting for baseline intellectual ability.

Published in:

Annals of Clinical & Translational Neurology, 2019, v. 6, n. 5, p. 826, doi. 10.1002/acn3.736

By:

Moore, Heather L.;
Kelly, Thomas;
Bright, Alexandra;
Field, Robert H.;
Schaefer, Andrew M.;
Blain, Alasdair P.;
Taylor, Robert W.;
McFarland, Robert;
Turnbull, Doug M.;
Gorman, Gráinne S.

Publication type:

Article

Phenotypic heterogeneity in m.3243A>G mitochondrial disease: The role of nuclear factors.

Published in:

Annals of Clinical & Translational Neurology, 2018, v. 5, n. 3, p. 333, doi. 10.1002/acn3.532

By:

Pickett, Sarah J.;
Grady, John P.;
Ng, Yi Shiau;
Gorman, Gráinne S.;
Schaefer, Andrew M.;
Wilson, Ian J.;
Cordell, Heather J.;
Turnbull, Doug M.;
Taylor, Robert W.;
McFarland, Robert

Publication type:

Article

POLG2 deficiency causes adult-onset syndromic sensory neuropathy, ataxia and parkinsonism.

Published in:

Annals of Clinical & Translational Neurology, 2017, v. 4, n. 1, p. 4, doi. 10.1002/acn3.361

By:

Van Maldergem, Lionel;
Besse, Arnaud;
De Paepe, Boel;
Blakely, Emma L.;
Appadurai, Vivek;
Humble, Margaret M.;
Piard, Juliette;
Craig, Kate;
He, Langping;
Hella, Pierre;
Debray, François‐Guillaume;
Martin, Jean‐Jacques;
Gaussen, Marion;
Laloux, Patrice;
Stevanin, Giovanni;
Van Coster, Rudy;
Taylor, Robert W.;
Copeland, William C.;
Mormont, Eric;
Bonnen, Penelope E.

Publication type:

Article

ORGANIZED CRIME.

Published in:

1987

By:

TAYLOR, ROBERT W.

Publication type:

Book Review

INTEGRATED MANAGEMENT DECISION-MAKING: A FUTURISTIC MODEL FOR POLICE ORGANIZATIONS.

Published in:

American Journal of Criminal Justice, 1984, v. 9, n. 1, p. 31, doi. 10.1007/BF03373754

By:

Taylor, Robert W.

Publication type:

Article

Abandoned Underground Storage Tank Location Using Fluxgate Magnetic Surveying: A Case Study.

Published in:

Ground Water Monitoring & Remediation, 2002, v. 22, n. 1, p. 116, doi. 10.1111/j.1745-6592.2002.tb00660.x

By:

Biersel, Thomas P.;
Bristoll, Bill C.;
Taylor, Robert W.;
Rose, James

Publication type:

Article

The Application of Combined Seismic and Electrical Measurements to the Determination of the Hydraulic Conductivity of a Lake Bed.

Published in:

Ground Water Monitoring & Remediation, 1984, v. 4, n. 4, p. 78, doi. 10.1111/j.1745-6592.1984.tb00897.x

By:

Taylor, Robert W.;
Cherkauer, Douglas S.

Publication type:

Article

Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease.

Published in:

JAMA Neurology, 2016, v. 73, n. 6, p. 668, doi. 10.1001/jamaneurol.2016.0355

By:

Martikainen, Mika H.;
Yi Shiau Ng;
Gorman, Gráinne S.;
Alston, Charlotte L.;
Blakely, Emma L.;
Schaefer, Andrew M.;
Chinnery, Patrick F.;
Burn, David J.;
Taylor, Robert W.;
McFarland, Robert;
Turnbull, Doug M.

Publication type:

Article

Clinical and Pathological Features of Mitochondrial DNA Deletion Disease Following Antiretroviral Treatment.

Published in:

JAMA Neurology, 2015, v. 72, n. 5, p. 603, doi. 10.1001/jamaneurol.2015.0150

By:

Payne, Brendan A. I.;
Gardner, Kristian;
Blakely, Emma L.;
Maddison, Paul;
Horvath, Rita;
Taylor, Robert W.;
Chinnery, Patrick F.

Publication type:

Article

Clonal Expansion of Secondary Mitochondrial DNA Deletions Associated With Spinocerebellar Ataxia Type 28.

Published in:

JAMA Neurology, 2015, v. 72, n. 1, p. 106, doi. 10.1001/jamaneurol.2014.1753

By:

Gorman, Gráinne S.;
Pfeffer, Gerald;
Griffin, Helen;
Blakely, Emma L.;
Kurzawa-Akanbi, Marzena;
Gabriel, Jessica;
Sitarz, Kamil;
Roberts, Mark;
Schoser, Benedikt;
Pyle, Angela;
Schaefer, Andrew M.;
McFarland, Robert;
Turnbull, Douglass M.;
Horvath, Rita;
Chinnery, Patrick F.;
Taylor, Robert W.

Publication type:

Article

Near-Identical Segregation of mtDNA Heteroplasmy in Blood, Muscle, Urinary Epithelium, and Hair Follicles in Twins With Optic Atrophy, Ptosis, and Intractable Epilepsy.

Published in:

JAMA Neurology, 2013, v. 70, n. 12, p. 1552, doi. 10.1001/jamaneurol.2013.4111

By:

Spyropoulos, Achilles;
Manford, Mark;
Horvath, Rita;
Alston, Charlotte L.;
Yu-Wai-Man, Patrick;
Langping He;
Taylor, Robert W.;
Chinnery, Patrick F.

Publication type:

Article

POLICE REFERRALS OF CRIME VICTIMS TO COMPENSATION SOURCES: AN EMPIRICAL ANALYSIS OF ATTITUDINAL AND STRUCTURAL IMPEDIMENTS.

Published in:

Police Quarterly, 2004, v. 7, n. 3, p. 372, doi. 10.1177/1098611103257691

By:

Fritsch, Eric J.;
Caeti, Tory J.;
Tobolowsky, Peggy M.;
Taylor, Robert W.

Publication type:

Article

Investigating complex I deficiency in Purkinje cells and synapses in patients with mitochondrial disease.

Published in:

Neuropathology & Applied Neurobiology, 2016, v. 42, n. 5, p. 477, doi. 10.1111/nan.12282

By:

Chrysostomou, Alexia;
Grady, John P.;
Laude, Alex;
Taylor, Robert W.;
Turnbull, Doug M.;
Lax, Nichola Z.

Publication type:

Article

Mitochondrial and inflammatory changes in sporadic inclusion body myositis.

Published in:

Neuropathology & Applied Neurobiology, 2015, v. 41, n. 3, p. 288, doi. 10.1111/nan.12149

By:

Rygiel, Karolina A.;
Miller, James;
Grady, John P.;
Rocha, Mariana C.;
Taylor, Robert W.;
Turnbull, Doug M.

Publication type:

Article

Interrogating Mitochondrial Biology and Disease Using CRISPR/Cas9 Gene Editing.

Published in:

Genes, 2021, v. 12, n. 10, p. 1604, doi. 10.3390/genes12101604

By:

Tang, Jia-Xin;
Pyle, Angela;
Taylor, Robert W.;
Oláhová, Monika

Publication type:

Article

Ultrasensitive deletion detection links mitochondrial DNA replication, disease, and aging.

Published in:

Genome Biology, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s13059-020-02138-5

By:

Lujan, Scott A.;
Longley, Matthew J.;
Humble, Margaret H.;
Lavender, Christopher A.;
Burkholder, Adam;
Blakely, Emma L.;
Alston, Charlotte L.;
Gorman, Grainne S.;
Turnbull, Doug M.;
McFarland, Robert;
Taylor, Robert W.;
Kunkel, Thomas A.;
Copeland, William C.

Publication type:

Article

Alginate microencapsulation of human mesenchymal stem cells as a strategy to enhance paracrine-mediated vascular recovery after hindlimb ischaemia.

Published in:

Journal of Tissue Engineering & Regenerative Medicine, 2016, v. 10, n. 3, p. 222, doi. 10.1002/term.1680

By:

Landázuri, Natalia;
Levit, Rebecca D.;
Joseph, Giji;
Ortega‐Legaspi, Juan Manuel;
Flores, Cristina A.;
Weiss, Daiana;
Sambanis, Athanassios;
Weber, Collin J.;
Safley, Susan A.;
Taylor, W. Robert

Publication type:

Article

A homoplasmic mtDNA variant can influence the phenotype of the pathogenic m.7472Cins MTTS1 mutation: are two mutations better than one?

Published in:

European Journal of Human Genetics, 2008, v. 16, n. 10, p. 1265, doi. 10.1038/ejhg.2008.65

By:

Swalwell, Helen;
Blakely, Emma L.;
Sutton, Ruth;
Tonska, Kasia;
Elstner, Matthias;
Langping He;
Taivassalo, Tanja;
Burns, Dennis K.;
Turnbull, Douglass M.;
Haller, Ronald G.;
Davidson, Mercy M.;
Taylor, Robert W.

Publication type:

Article

LHON/MELAS overlap syndrome associated with a mitochondrial MTND1 gene mutation.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 5, p. 623, doi. 10.1038/sj.ejhg.5201363

By:

Blakely, Emma L.;
de Silva, Rajith;
King, Andrew;
Schwarzer, Verena;
Harrower, Tim;
Dawidek, Gervase;
Turnbull, Douglass M.;
Taylor, Robert W.

Publication type:

Article

Noninvasive diagnosis of the 3243A>G mitochondrial DNA mutation using urinary epithelial cells.

Published in:

European Journal of Human Genetics, 2004, v. 12, n. 9, p. 778, doi. 10.1038/sj.ejhg.5201216

By:

Mcdonnell, Martina T.;
Schaefer, Andrew M.;
Blakely, Emma L.;
McFarland, Robert;
Chinnery, Patrick F.;
Turnbull, Douglass M.;
Taylor, Robert W.

Publication type:

Article

A novel point mutation in the mitochondrial tRNA<sup>Trp</sup> gene produces a neurogastrointestinal syndrome.

Published in:

European Journal of Human Genetics, 2004, v. 12, n. 6, p. 509, doi. 10.1038/sj.ejhg.5201185

By:

Maniura-Weber, Katharina;
Taylor, Robert W.;
Johnson, Margaret A.;
Chrzanowska-Lightowlers, Zofia;
Morris, Andrew A. M.;
Charlton, Charles P. J.;
Turnbull, Douglas M.;
Bindoff, Laurence A.

Publication type:

Article

Leigh disease associated with a novel mitochondrial DNA ND5 mutation.

Published in:

European Journal of Human Genetics, 2002, v. 10, n. 2, p. 141, doi. 10.1038/sj.ejhg.5200773

By:

Taylor, Robert W.;
Morris, Andrew A.M.;
Hutchinson, Michael;
Turnbull, Douglass M.

Publication type:

Article

Association between inhaled nitric oxide treatment and long-term pulmonary function in survivors of acute respiratory distress syndrome.

Published in:

2012

By:

Dellinger, R Phillip;
Trzeciak, Stephen W;
Criner, Gerard J;
Zimmerman, Janice L;
Taylor, Robert W;
Usansky, Helen;
Young, Joseph;
Goldstein, Brahm

Publication type:

journal article

Activated protein C in septic shock: a propensity-matched analysis.

Published in:

2011

By:

Sadaka, Farid;
O'Brien, Jacklyn;
Migneron, Matthew;
Stortz, Julie;
Vanston, Alexander;
Taylor, Robert W

Publication type:

journal article

iNaturalist is useful at enhancing biodiversity studies as evident from southern African freshwater crabs (Decapoda: Brachyura: Potamonautidae).

Published in:

Journal of Crustacean Biology, 2022, v. 42, n. 3, p. 1, doi. 10.1093/jcbiol/ruac042

By:

Daniels, Savel R;
Barnes, Aaron;
Peer, Nasreen;
Egan, Vincent T;
Taylor, Ricky;
Taylor, Robert W;
van der Colff, Dewidine

Publication type:

Article

Hydrocyanines: A Class of Fluorescent Sensors That Can Image Reactive Oxygen Species in Cell Culture, Tissue, and In Vivo.

Published in:

Angewandte Chemie International Edition, 2009, v. 48, n. 2, p. 299, doi. 10.1002/anie.200804851

By:

Kundu, Kousik;
Knight, Sarah F.;
Willett, Nick;
Lee, Sungmun;
Taylor, W. Robert;
Murthy, Niren

Publication type:

Article

Dissecting the neuronal vulnerability underpinning Alpers' syndrome: a clinical and neuropathological study.

Published in:

Brain Pathology, 2019, v. 29, n. 1, p. 97, doi. 10.1111/bpa.12640

By:

Hayhurst, Hannah;
Anagnostou, Maria‐Eleni;
Bogle, Helen J.;
Grady, John P.;
Taylor, Robert W.;
Bindoff, Laurence A.;
McFarland, Robert;
Turnbull, Doug M.;
Lax, Nichola Z.

Publication type:

Article

What causes mitochondrial DNA deletions in human cells?

Published in:

Nature Genetics, 2008, v. 40, n. 3, p. 275, doi. 10.1038/ng.f.94

By:

Krishnan, Kim J.;
Reeve, Amy K.;
Samuels, David C.;
Chinnery, Patrick F.;
Blackwood, John K.;
Taylor, Robert W.;
Wanrooij, Sjoerd;
Spelbrink, Johannes N.;
Lightowlers, Robert N.;
Turnbull, Doug M.

Publication type:

Article

High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 515, doi. 10.1038/ng1769

By:

Bender, Andreas;
Krishnan, Kim J.;
Morris, Christopher M.;
Taylor, Geoffrey A.;
Reeve, Amy K.;
Perry, Robert H.;
Jaros, Evelyn;
Hersheson, Joshua S.;
Betts, Joanne;
Klopstock, Thomas;
Taylor, Robert W.;
Turnbull, Douglass M.

Publication type:

Article

Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutation.

Published in:

Nature Genetics, 2002, v. 30, n. 2, p. 145, doi. 10.1038/ng819

By:

McFarland, Robert;
Clark, Kim M.;
Morris, Andrew A.M.;
Taylor, Robert W.;
Macphail, Sheila;
Lightowlers, Robert N.;
Turnbull, Douglass M.

Publication type:

Article

Determination of Cation Exchange Capacity of Calcareous Soils: Comparison of Summation Method and Direct Replacement Method.

Published in:

Communications in Soil Science & Plant Analysis, 2023, v. 54, n. 6, p. 743, doi. 10.1080/00103624.2022.2118765

By:

Jain, Amita;
Taylor, Robert W.

Publication type:

Article

Incidence of carpal tunnel syndrome in adult patients with mitochondrial disease.

Published in:

Journal of the Peripheral Nervous System, 2013, v. 18, n. 1, p. 59, doi. 10.1111/jns5.12009

By:

Whittaker, Roger G.;
Hall, Elizabeth;
Mansoor, Muhammad K.;
Taylor, Robert W.;
Turnbull, Douglass M.

Publication type:

Article

Scientific and Ethical Issues in Mitochondrial Donation.

Published in:

New Bioethics, 2018, v. 24, n. 1, p. 57, doi. 10.1080/20502877.2018.1440725

By:

Craven, Lyndsey;
Murphy, Julie;
Turnbull, Doug M.;
Taylor, Robert W.;
Gorman, Grainne S.;
McFarland, Robert

Publication type:

Article

Remuscularization with triiodothyronine and β<sub>1</sub>-blocker therapy reverses post-ischemic left ventricular dysfunction and adverse remodeling.

Published in:

Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-12723-2

By:

Bogush, Nikolay;
Tan, Lin;
Naqvi, Emmen;
Calvert, John W.;
Graham, Robert M.;
Taylor, W. Robert;
Naqvi, Nawazish;
Husain, Ahsan

Publication type:

Article

A novel missense mutation in ISCA2 causes aberrant splicing and leads to multiple mitochondrial dysfunctions syndrome 4.

Published in:

Frontiers in Psychiatry, 2024, p. 1, doi. 10.3389/fpsyt.2024.1428175

By:

Al-Hassnan, Zuhair;
AlDosary, Mazhor;
AlHargan, Aljouhra;
AlQudairy, Hanan;
Almass, Rawan;
Alahmadi, Khaled Omar;
AlShahrani, Saif;
AlBakheet, Albandary;
Almuhaizea, Mohammad A.;
Taylor, Robert W.;
Colak, Dilek;
Kaya, Namik

Publication type:

Article

Delineating selective vulnerability of inhibitory interneurons in Alpers' syndrome.

Published in:

Neuropathology & Applied Neurobiology, 2022, v. 48, n. 6, p. 1, doi. 10.1111/nan.12833

By:

Smith, Laura A.;
Erskine, Daniel;
Blain, Alasdair;
Taylor, Robert W.;
McFarland, Robert;
Lax, Nichola Z.

Publication type:

Article

Mitochondrial DNA mutations induce mitochondrial biogenesis and increase the tumorigenic potential of Hodgkin and Reed–Sternberg cells.

Published in:

Carcinogenesis, 2020, v. 41, n. 12, p. 1735, doi. 10.1093/carcin/bgaa032

By:

Haumann, Sophie;
Boix, Julia;
Knuever, Jana;
Bieling, Angela;
Sanjurjo, Anton Vila;
Elson, Joanna L;
Blakely, Emma L;
Taylor, Robert W;
Riet, Nicole;
Abken, Hinrich;
Kashkar, Hamid;
Hornig-Do, Hue-Tran;
Wiesner, Rudolf J

Publication type:

Article

2-Deoxy-D-glucose couples mitochondrial DNA replication with mitochondrial fitness and promotes the selection of wild-type over mutant mitochondrial DNA.

Published in:

Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-26829-0

By:

Pantic, Boris;
Ives, Daniel;
Mennuni, Mara;
Perez-Rodriguez, Diego;
Fernandez-Pelayo, Uxoa;
Lopez de Arbina, Amaia;
Muñoz-Oreja, Mikel;
Villar-Fernandez, Marina;
Dang, Thanh-mai Julie;
Vergani, Lodovica;
Johnston, Iain G.;
Pitceathly, Robert D. S.;
McFarland, Robert;
Hanna, Michael G.;
Taylor, Robert W.;
Holt, Ian J.;
Spinazzola, Antonella

Publication type:

Article

Mitochondrial DNA mutations in human disease.

Published in:

IUBMB Life, 2006, v. 58, n. 3, p. 143, doi. 10.1080/15216540600686888

By:

Greaves, Laura C.;
Taylor, Robert W.

Publication type:

Article