Works by Shoubridge, Eric A.

Results: 80

Mutations in the Mitochondrial Methionyl-tRNA Synthetase Cause a Neurodegenerative Phenotype in Flies and a Recessive Ataxia (ARSAL) in Humans.

Published in:

PLoS Biology, 2012, v. 10, n. 3, p. 1, doi. 10.1371/journal.pbio.1001288

By:

Bayat, Vafa;
Thiffault, Isabelle;
Jaiswal, Manish;
Tétreault, Martine;
Donti, Taraka;
Sasarman, Florin;
Bernard, Geneviève;
Demers-Lamarche, Julie;
Dicaire, Marie-Josée;
Mathieu, Jean;
Vanasse, Michel;
Bouchard, Jean-Pierre;
Rioux, Marie-France;
Lourenco, Charles M.;
Zhihong Li;
Haueter, Claire;
Shoubridge, Eric A.;
Graham, Brett H.;
Brais, Bernard;
Bellen, Hugo J.

Publication type:

Article

RNA modification landscape of the human mitochondrial tRNALys regulates protein synthesis.

Published in:

Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-06471-z

By:

Richter, Uwe;
Evans, Molly E.;
Clark, Wesley C.;
Marttinen, Paula;
Shoubridge, Eric A.;
Suomalainen, Anu;
Wredenberg, Anna;
Wedell, Anna;
Pan, Tao;
Battersby, Brendan J.

Publication type:

Article

SLC25A46 is required for mitochondrial lipid homeostasis and cristae maintenance and is responsible for Leigh syndrome.

Published in:

EMBO Molecular Medicine, 2016, v. 8, n. 9, p. 1019, doi. 10.15252/emmm.201506159

By:

Janer, Alexandre;
Prudent, Julien;
Paupe, Vincent;
Fahiminiya, Somayyeh;
Majewski, Jacek;
Sgarioto, Nicolas;
Des Rosiers, Christine;
Forest, Anik;
Lin, Zhen‐Yuan;
Gingras, Anne‐Claude;
Mitchell, Grant;
McBride, Heidi M;
Shoubridge, Eric A

Publication type:

Article

Aerobic conditioning in patients with mitochondrial myopathies: physiological, biochemical, and genetic effects.

Published in:

2001

By:

Taivassalo, Tanja;
Shoubridge, Eric A.;
Chen, Jacqueline;
Kennaway, Nancy G.;
DiMauro, Salvatore;
Arnold, Douglas L.;
Haller, Ronald G.;
Taivassalo, T;
Shoubridge, E A;
Chen, J;
Kennaway, N G;
DiMauro, S;
Arnold, D L;
Haller, R G

Publication type:

journal article

Oxidative phosphorylation defect in the brains of carriers of the tRNAleu(UUR) A3243G mutation in a MELAS pedigree.

Published in:

Annals of Neurology, 2000, v. 47, n. 2, p. 179, doi. 10.1002/1531-8249(200002)47:2<179::AID-ANA7>3.0.CO;2-Z

By:

Dubeau, François;
De Stefano, Nicola;
Zifkin, Benjamin G.;
Arnold, Douglas L.;
Shoubridge, Eric A.

Publication type:

Article

Autosomal dominant chronic progressive external ophthalmoplegia: A tale of two genomes.

Published in:

Annals of Neurology, 1996, v. 40, n. 5, p. 693, doi. 10.1002/ana.410400503

By:

Shoubridge, Eric A.

Publication type:

Article

Reply.

Published in:

Annals of Neurology, 1995, v. 38, n. 2, p. 274, doi. 10.1002/ana.410380226

By:

Karpati, George;
Shoubridge, Eric

Publication type:

Article

Late-onset mitochondrial myopathy.

Published in:

Annals of Neurology, 1995, v. 37, n. 1, p. 16, doi. 10.1002/ana.410370106

By:

Johnston, Wendy;
Karpati, George;
Carpenter, Stirling;
Arnold, Douglas;
Shoubridge, Eric A.

Publication type:

Article

Myoblast transfer in duchenne muscular dystrophy.

Published in:

Annals of Neurology, 1993, v. 34, n. 1, p. 8, doi. 10.1002/ana.410340105

By:

Karpati, George;
Ajdukovic, Djordje;
Arnold, Douglas;
Gledhill, Robert B.;
Guttmann, Ronald;
Holland, Paul;
Koch, Penelope A.;
Shoubridge, Eric;
Spence, Desmond;
Vanasse, Michel;
Watters, Gordon V.;
Abrahamowicz, Michael;
Duff, Catherine;
Worton, Ronald G.

Publication type:

Article

Mitochondrial dysfunction in multiple symmetrical lipomatosis.

Published in:

Annals of Neurology, 1991, v. 29, n. 5, p. 566, doi. 10.1002/ana.410290519

By:

Berkovic, Samuel F.;
Andermann, Frederick;
Shoubridge, Eric A.;
Carpenter, Stirling;
Robitaille, Yvon;
Andermann, Eva;
Melmed, Calvin;
Karpati, George

Publication type:

Article

Alkalosis monitored by 31P NMR in a human glioma cell line exposed to the anti-tumor drug 1, 3-bis (2-chloroethyl)-1-nitrosourea.

Published in:

Magnetic Resonance in Medicine, 1991, v. 22, n. 2, p. 394, doi. 10.1002/mrm.1910220247

By:

Commodari, Fernando;
Sanctuary, Bryan C.;
Feindel, William;
Shoubridge, Eric A.

Publication type:

Article

Developmental biology: Asexual healing.

Published in:

Nature, 2009, v. 461, n. 7262, p. 354, doi. 10.1038/461354a

By:

Shoubridge, Eric A.

Publication type:

Article

A pseudouridine synthase module is essential for mitochondrial protein synthesis and cell viability.

Published in:

EMBO Reports, 2017, v. 18, n. 1, p. 28, doi. 10.15252/embr.201643391

By:

Antonicka, Hana;
Choquet, Karine;
Lin, Zhen‐Yuan;
Gingras, Anne‐Claude;
Kleinman, Claudia L;
Shoubridge, Eric A

Publication type:

Article

Missense mutations in SURF1 associated with deficient cytochrome c oxidase assembly in Leigh syndrome patients.

Published in:

Human Genetics, 2000, v. 106, n. 2, p. 194, doi. 10.1007/s004390051028

By:

Poyau, Alain;
Buchet, Karine;
Fouad Bouzidi, Mohamed;
Zabot, Marie-Thérèse;
Echenne, Bernard;
Jianbo Yao;
Shoubridge, Eric A.;
Godinot, Catherine

Publication type:

Article

Mitochondrial molecular genetics and human disease.

Published in:

Human Molecular Genetics, 2024, v. 33, p. R1, doi. 10.1093/hmg/ddae049

By:

Shoubridge, Eric A;
Barrientos, Antoni

Publication type:

Article

Multi-OMICS study of a CHCHD10 variant causing ALS demonstrates metabolic rewiring and activation of endoplasmic reticulum and mitochondrial unfolded protein responses.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 8, p. 687, doi. 10.1093/hmg/ddab078

By:

Straub, Isabella R;
Weraarpachai, Woranontee;
Shoubridge, Eric A

Publication type:

Article

The mitochondrial DNA genetic bottleneck results from replication of a subpopulation of genomes.

Published in:

Nature Genetics, 2008, v. 40, n. 12, p. 1484, doi. 10.1038/ng.258

By:

Wai, Timothy;
Teoli, Daniella;
Shoubridge, Eric A.

Publication type:

Article

Reactive oxygen species and the segregation of mtDNA sequence variants.

Published in:

2007

By:

Battersby, Brendan J;
Shoubridge, Eric A.

Publication type:

Letter

Erratum: Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type.

Published in:

2006

By:

Lerner-Ellis, Jordan P.;
Tirone, Jamie C.;
Pawelek, Peter D.;
Doré, Carole;
Atkinson, Janet L.;
Watkins, David;
Morel, Chantal F.;
Fujiwara, T. Mary;
Moras, Emily;
Hosack, Angela R.;
Dunbar, Gail V.;
Antonicka, Hana;
Forgetta, Vince;
Dobson, C. Melissa;
Leclerc, Daniel;
Gravel, Roy A.;
Shoubridge, Eric A.;
Coulton, James W.;
Lepage, Pierre;
Rommens, Johanna M.

Publication type:

Correction Notice

Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 93, doi. 10.1038/ng1683

By:

Lerner-Ellis, Jordan P;
Tirone, Jamie C;
Pawelek, Peter D;
Doré, Carole;
Atkinson, Janet L;
Watkins, David;
Morel, Chantal F;
Fujiwara, T Mary;
Moras, Emily;
Hosack, Angela R;
Dunbar, Gail V;
Antonicka, Hana;
Forgetta, Vince;
Dobson, C Melissa;
Leclerc, Daniel;
Gravel, Roy A;
Shoubridge, Eric A;
Coulton, James W;
Lepage, Pierre;
Rommens, Johanna M

Publication type:

Article

Nuclear genetic control of mitochondrial DNA segregation.

Published in:

Nature Genetics, 2003, v. 33, n. 2, p. 183, doi. 10.1038/ng1073

By:

Battersby, Brendan J.;
Loredo-Osti, J.C.;
Shoubridge, Eric A.

Publication type:

Article

The ABcs of mitochondrial transcription.

Published in:

Nature Genetics, 2002, v. 31, n. 3, p. 227, doi. 10.1038/ng0702-227

By:

Shoubridge, Eric A.

Publication type:

Article

A debut for mito-mouse.

Published in:

Nature Genetics, 2000, v. 26, n. 2, p. 132, doi. 10.1038/79832

By:

Shoubridge, Eric A

Publication type:

Article

SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome.

Published in:

Nature Genetics, 1998, v. 20, n. 4, p. 337, doi. 10.1038/3804

By:

Zhu, Zhiqing;
Yao, Jianbo;
Johns, Timothy;
Fu, Katherine;
Bie, Isabelle De;
Macmillan, Carol;
Cuthbert, Andrew P.;
Newbold, Robert F.;
Wang, Jia-chi;
Chevrette, Mario;
Brown, Garry K.;
Brown, Ruth M.;
Shoubridge, Eric A.

Publication type:

Article

Whole-exome sequencing identifies novel ECHS1 mutations in Leigh syndrome.

Published in:

Human Genetics, 2015, v. 134, n. 9, p. 981, doi. 10.1007/s00439-015-1577-y

By:

Tetreault, Martine;
Fahiminiya, Somayyeh;
Antonicka, Hana;
Mitchell, Grant;
Geraghty, Michael;
Lines, Matthew;
Boycott, Kym;
Shoubridge, Eric;
Mitchell, John;
Michaud, Jacques;
Majewski, Jacek

Publication type:

Article

Mitochondrial biogenesis: which part of 'NO' do we understand?

Published in:

BioEssays, 2003, v. 25, n. 6, p. 538, doi. 10.1002/bies.10298

By:

Leary, Scot C.;
Shoubridge, Eric A.

Publication type:

Article

Mitochondrial genetics and human disease.

Published in:

BioEssays, 1996, v. 18, n. 12, p. 983, doi. 10.1002/bies.950181208

By:

Grossman, Lawrence I.,;
Shoubridge, Eric A.,

Publication type:

Article

Loss of mitochondrial Chchd10 or Chchd2 in zebrafish leads to an ALS‐like phenotype and Complex I deficiency independent of the mitochondrial integrated stress response.

Published in:

Developmental Neurobiology (19328451), 2023, v. 83, n. 1, p. 54, doi. 10.1002/dneu.22909

By:

Petel Légaré, Virginie;
Rampal, Christian J.;
Gurberg, Tyler J. N.;
Aaltonen, Mari J.;
Janer, Alexandre;
Zinman, Lorne;
Shoubridge, Eric A.;
Armstrong, Gary A. B.

Publication type:

Article

Autosomal recessive cerebellar ataxia caused by a homozygous mutation in PMPCA.

Published in:

2016

By:

Choquet, Karine;
Zurita-Rendón, Olga;
La Piana, Roberta;
Sharon Yang;
Dicaire, Marie-Joseè;
Boycott, Kym M.;
Majewski, Jacek;
Shoubridge, Eric A.;
Brais, Bernard;
Tètreault, Martine;
Yoon, Grace;
Delague, Valèrie;
Mègarbane, Andrè;
Isaya, Grazia;
Yang, Sharon;
Dicaire, Marie-Josée;
Care4Rare Consortium;
Tétreault, Martine

Publication type:

Case Study

LONP1 Is Required for Maturation of a Subset of Mitochondrial Proteins, and Its Loss Elicits an Integrated Stress Response.

Published in:

Molecular & Cellular Biology, 2018, v. 38, n. 20, p. 1, doi. 10.1128/MCB.00412-17

By:

Rendón, Olga Zurita;
Shoubridge, Eric A.

Publication type:

Article

A Mutation in the Flavin Adenine Dinucleotide-Dependent Oxidoreductase FOXRED1 Results in Cell-Type-Specific Assembly Defects in Oxidative Phosphorylation Complexes I and II.

Published in:

Molecular & Cellular Biology, 2016, v. 36, n. 16, p. 2132, doi. 10.1128/MCB.00066-16

By:

Rendón, Olga Zurita;
Antonicka, Hana;
Horvath, Rita;
Shoubridge, Eric A.

Publication type:

Article

1H NMR characterization of normal human cerebrospinal fluid and the detection of methylmalonic acid in a vitamin B12 deficient patient.

Published in:

NMR in Biomedicine, 1991, v. 4, n. 4, p. 192, doi. 10.1002/nbm.1940040407

By:

Commodari, Fernando;
Arnold, Douglas L.;
Sanctuary, Bryan C.;
Shoubridge, Eric A.

Publication type:

Article

Matchmaking facilitates the diagnosis of an autosomal-recessive mitochondrial disease caused by biallelic mutation of the tRNA isopentenyltransferase ( TRIT1) gene.

Published in:

Human Mutation, 2017, v. 38, n. 5, p. 511, doi. 10.1002/humu.23196

By:

Kernohan, Kristin D.;
Dyment, David A.;
Pupavac, Mihaela;
Cramer, Zvi;
McBride, Arran;
Bernard, Genevieve;
Straub, Isabella;
Tetreault, Martine;
Hartley, Taila;
Huang, Lijia;
Sell, Erick;
Majewski, Jacek;
Rosenblatt, David S.;
Shoubridge, Eric;
Mhanni, Aziz;
Myers, Tara;
Proud, Virginia;
Vergano, Samanta;
Spangler, Brooke;
Farrow, Emily

Publication type:

Article

Inborn Error of Cobalamin Metabolism Associated with the Intracellular Accumulation of Transcobalamin-Bound Cobalamin and Mutations in ZNF143, Which Codes for a Transcriptional Activator.

Published in:

Human Mutation, 2016, v. 37, n. 9, p. 976, doi. 10.1002/humu.23037

By:

Pupavac, Mihaela;
Watkins, David;
Petrella, Francis;
Fahiminiya, Somayyeh;
Janer, Alexandre;
Cheung, Warren;
Gingras, Anne‐Claude;
Pastinen, Tomi;
Muenzer, Joseph;
Majewski, Jacek;
Shoubridge, Eric A.;
Rosenblatt, David S.

Publication type:

Article

Mutation in The Nuclear-Encoded Mitochondrial Isoleucyl-tRNA Synthetase IARS2 in Patients with Cataracts, Growth Hormone Deficiency with Short Stature, Partial Sensorineural Deafness, and Peripheral Neuropathy or with Leigh Syndrome.

Published in:

Human Mutation, 2015, v. 36, n. 2, p. 281, doi. 10.1002/humu.22756

By:

Schwartzentruber, Jeremy;
Buhas, Daniela;
Majewski, Jacek;
Sasarman, Florin;
Papillon‐Cavanagh, Simon;
Thiffault, Isabelle;
Sheldon, Katherine M.;
Massicotte, Christine;
Patry, Lysanne;
Simon, Mariella;
Zare, Amir S.;
McKernan, Kevin J.;
Consortium, FORGE Canada;
Michaud, Jacques;
Boles, Richard G.;
Deal, Cheri L.;
Desilets, Valerie;
Shoubridge, Eric A.;
Samuels, Mark E.

Publication type:

Article

Mutation in The Nuclear-Encoded Mitochondrial Isoleucyl-t RNA Synthetase IARS2 in Patients with Cataracts, Growth Hormone Deficiency with Short Stature, Partial Sensorineural Deafness, and Peripheral Neuropathy or with Leigh Syndrome.

Published in:

Human Mutation, 2014, v. 35, n. 11, p. 1285, doi. 10.1002/humu.22629

By:

Schwartzentruber, Jeremy;
Buhas, Daniela;
Majewski, Jacek;
Sasarman, Florin;
Papillon‐Cavanagh, Simon;
Thiffaut, Isabelle;
Sheldon, Katherine M.;
Massicotte, Christine;
Patry, Lysanne;
Simon, Mariella;
Zare, Amir S.;
McKernan, Kevin J.;
Michaud, Jacques;
Boles, Richard G.;
Deal, Cheri L.;
Desilets, Valerie;
Shoubridge, Eric A.;
Samuels, Mark E.

Publication type:

Article

Novel Mutations in SCO1 as a Cause of Fatal Infantile Encephalopathy and Lactic Acidosis.

Published in:

Human Mutation, 2013, v. 34, n. 10, p. 1366, doi. 10.1002/humu.22385

By:

Leary, Scot C.;
Antonicka, Hana;
Sasarman, Florin;
Weraarpachai, Woranontee;
Cobine, Paul A.;
Pan, Min;
Brown, Garry K.;
Brown, Ruth;
Majewski, Jacek;
Ha, Kevin C. H.;
Rahman, Shamima;
Shoubridge, Eric A.

Publication type:

Article

A novel mutation in YARS2 causes myopathy with lactic acidosis and sideroblastic anemia.

Published in:

Human Mutation, 2012, v. 33, n. 8, p. 1201, doi. 10.1002/humu.22098

By:

Sasarman, Florin;
Nishimura, Tamiko;
Thiffault, Isabelle;
Shoubridge, Eric A.

Publication type:

Article

Repopulation of ρ0 cells with mitochondria from a patient with a mitochondrial DNA point mutation in tRNAGly results in respiratory chain dysfunction.

Published in:

Human Mutation, 1999, v. 13, n. 3, p. 245, doi. 10.1002/(SICI)1098-1004(1999)13:3<245::AID-HUMU9>3.0.CO;2-B

By:

Raha, Sandeep;
Merante, Frank;
Shoubridge, Eric;
Myint, A. Tomoko;
Tein, Ingrid;
Benson, Lee;
Johns, Tim;
Robinson, Brian H.

Publication type:

Article

ESYT1 tethers the ER to mitochondria and is required for mitochondrial lipid and calcium homeostasis.

Published in:

Life Science Alliance, 2024, v. 7, n. 1, p. 1, doi. 10.26508/lsa.202302335

By:

Janer, Alexandre;
Morris, Jordan L.;
Krols, Michiel;
Antonicka, Hana;
Aaltonen, Mari J.;
Zhen-Yuan Lin;
Anand, Hanish;
Gingras, Anne-Claude;
Prudent, Julien;
Shoubridge, Eric A.

Publication type:

Article

The role of the mitochondrial outer membrane protein SLC25A46 in mitochondrial fission and fusion.

Published in:

Life Science Alliance, 2023, v. 6, n. 6, p. 1, doi. 10.26508/lsa.202301914

By:

Schuettpelz, Jana;
Janer, Alexandre;
Antonicka, Hana;
Shoubridge, Eric A.

Publication type:

Article

Serine palmitoyltransferase assembles at ER--mitochondria contact sites.

Published in:

Life Science Alliance, 2022, v. 5, n. 2, p. 1, doi. 10.26508/lsa.202101278

By:

Aaltonen, Mari J.;
Alecu, Irina;
König, Tim;
Bennett, Steffany A. L.;
Shoubridge, Eric A.

Publication type:

Article

Human GTPBP5 (MTG2) fuels mitoribosome large subunit maturation by facilitating 16S rRNA methylation.

Published in:

Nucleic Acids Research, 2020, v. 48, n. 14, p. 7924, doi. 10.1093/nar/gkaa592

By:

Maiti, Priyanka;
Antonicka, Hana;
Gingras, Anne-Claude;
Shoubridge, Eric A;
Barrientos, Antoni

Publication type:

Article

RMND1 deficiency associated with neonatal lactic acidosis, infantile onset renal failure, deafness, and multiorgan involvement.

Published in:

European Journal of Human Genetics, 2015, v. 23, n. 10, p. 1301, doi. 10.1038/ejhg.2014.293

By:

Janer, Alexandre;
van Karnebeek, Clara DM;
Sasarman, Florin;
Antonicka, Hana;
Al Ghamdi, Malak;
Shyr, Casper;
Dunbar, Mary;
Stockler-Ispiroglu, Sylvia;
Ross, Colin J;
Vallance, Hilary;
Dionne, Janis;
Wasserman, Wyeth W;
Shoubridge, Eric A

Publication type:

Article

Loss of CHCHD10-CHCHD2 complexes required for respiration underlies the pathogenicity of a CHCHD10 mutation in ALS.

Published in:

Human Molecular Genetics, 2018, v. 27, n. 1, p. 178, doi. 10.1093/hmg/ddx393

By:

Straub, Isabella R.;
Janer, Alexandre;
Weraarpachai, Woranontee;
Zinman, Lorne;
Robertson, Janice;
Rogaeva, Ekaterina;
Shoubridge, Eric A.

Publication type:

Article

Loss of hepatic LRPPRC alters mitochondrial bioenergetics, regulation of permeability transition and trans-membrane ROS diffusion.

Published in:

Human Molecular Genetics, 2017, v. 26, n. 16, p. 3186, doi. 10.1093/hmg/ddx202

By:

Cuillerier, Alexanne;
Honarmand, Shamisa;
Cadete, Virgilio J. J.;
Ruiz, Matthieu;
Forest, Anik;
Deschênes, Sonia;
Beauchamp, Claudine;
Charron, Guy;
Rioux, John D.;
Rosiers, Christine Des;
Shoubridge, Eric A.;
Burelle, Yan

Publication type:

Article

An N-terminal formyl methionine on COX 1 is required for the assembly of cytochrome c oxidase.

Published in:

Human Molecular Genetics, 2015, v. 24, n. 14, p. 4103, doi. 10.1093/hmg/ddv149

By:

Hinttala, Reetta;
Sasarman, Florin;
Nishimura, Tamiko;
Antonicka, Hana;
Brunel-Guitton, Catherine;
Schwartzentruber, Jeremy;
Fahiminiya, Somayyeh;
Majewski, Jacek;
Faubert, Denis;
Ostergaard, Elsebet;
Smeitink, Jan A.;
Shoubridge, Eric A.

Publication type:

Article

The 3' addition of CCA to mitochondrial tRNASer(AGY) is specifically impaired in patients with mutations in the tRNA nucleotidyl transferase TRNT1.

Published in:

Human Molecular Genetics, 2015, v. 24, n. 10, p. 2841, doi. 10.1093/hmg/ddv044

By:

Sasarman, Florin;
Thiffault, Isabelle;
Weraarpachai, Woranontee;
Salomon, Steven;
Maftei, Catalina;
Gauthier, Julie;
Ellazam, Benjamin;
Webb, Neil;
Antonicka, Hana;
Janer, Alexandre;
Brunel-Guitton, Catherine;
Elpeleg, Orly;
Mitchell, Grant;
Shoubridge, Eric A.

Publication type:

Article

Sacs knockout mice present pathophysiological defects underlying autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Published in:

Human Molecular Genetics, 2015, v. 24, n. 3, p. 727, doi. 10.1093/hmg/ddu491

By:

Larivière, Roxanne;
Gaudet, Rébecca;
Gentil, Benoit J.;
Girard, Martine;
Conte, Talita Cristiane;
Minotti, Sandra;
Leclerc-Desaulniers, Kim;
Gehring, Kalle;
McKinney, R. Anne;
Shoubridge, Eric A.;
McPherson, Peter S.;
Durham, Heather D.;
Brais, Bernard

Publication type:

Article

Tissue-specific responses to the LRPPRC founder mutation in French Canadian Leigh Syndrome.

Published in:

Human Molecular Genetics, 2015, v. 24, n. 2, p. 480, doi. 10.1093/hmg/ddu46

By:

Sasarman, Florin;
Nishimura, Tamiko;
Antonicka, Hana;
Weraarpachai, Woranontee;
Shoubridge, Eric A.

Publication type:

Article