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Joanna Poulton

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Robert D S Pitceathly; Ute Pohl; Joanna Poulton; Mark E Roberts; Andrew M Schaefer; Zarfishan Shabbir; Conrad Smith; John Taylor; Robert W Taylor; Douglass M Turnbull; Peter D Turnpenny; Charlotte L Alston; Emma L Blakely; Patrick F Chinnery; Kate Craig; Marcus Deschauer; Julie C Evans; Carl Fratter; Christopher A Halfpenny; Michael G Hanna; Langping He; Rita Horvath; Matthew C Jackson; Peter W Lunt; Robert McFarland; Gráinne S Gorman
Adults with RRM2B-related mitochondrial disease have distinct clinical and molecular characteristics.
Joanna Poulton; Pippa Oakeshott
Nuclear transfer to prevent maternal transmission of mitochondrial DNA disease.
J Uusimaa; Massimo Zeviani; C A Sewry; E P Treacy; J Birks; Garry K Brown; G Crisponi; L Feng; Carl Fratter; I Hughes; Heinz Jungbluth; M McDermott; Francesco Muntoni; Joanna Poulton
Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease.

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All Publications

2012: Robert D S Pitceathly; Ute Pohl; Joanna Poulton; Mark E Roberts; Andrew M Schaefer; Zarfishan Shabbir; Conrad Smith; John Taylor; Robert W Taylor; Douglass M Turnbull; Peter D Turnpenny; Charlotte L Alston; Emma L Blakely; Patrick F Chinnery; Kate Craig; Marcus Deschauer; Julie C Evans; Carl Fratter; Christopher A Halfpenny; Michael G Hanna; Langping He; Rita Horvath; Matthew C Jackson; Peter W Lunt; Robert McFarland; Gráinne S Gorman
Adults with RRM2B-related mitochondrial disease have distinct clinical and molecular characteristics.
Brain : a journal of neurology 2012;135(Pt 11):3392-403.
2012: Joanna Poulton; Pippa Oakeshott
Nuclear transfer to prevent maternal transmission of mitochondrial DNA disease.
BMJ (Clinical research ed.) 2012;345():e6651.
2011: J Uusimaa; Massimo Zeviani; C A Sewry; E P Treacy; J Birks; Garry K Brown; G Crisponi; L Feng; Carl Fratter; I Hughes; Heinz Jungbluth; M McDermott; Francesco Muntoni; Joanna Poulton
Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease.
Journal of medical genetics 2011;48(10):660-8.
2011: Marcos Roberto Chiaratti; Flávio Meirelles; Dagan Wells; Joanna Poulton
Therapeutic treatments of mtDNA diseases at the earliest stages of human development.
Mitochondrion 2011;11(5):820-8.
2010: Joanna Poulton; Marcos R Chiaratti; Flávio Meirelles; Stephen Kennedy; Dagan Wells; Ian J Holt
Transmission of mitochondrial DNA diseases and ways to prevent them.
PLoS genetics 2010;6(8):.
2010: Joanna Poulton; A L Bredenoord
174th ENMC international workshop: Applying pre-implantation genetic diagnosis to mtDNA diseases: implications of scientific advances 19-21 March 2010, Naarden, The Netherlands.
Neuromuscular disorders : NMD 2010;20(8):559-63.
2010: Carl Fratter; G S Gorman; J D Stewart; M Buddles; C Smith; J Evans; A Seller; Joanna Poulton; M Roberts; M G Hanna; S Rahman; S E Omer; T Klopstock; B Schoser; C Kornblum; B Czermin; B Lecky; E L Blakely; K Craig; P F Chinnery; D M Turnbull; R Horvath; R W Taylor
The clinical, histochemical, and molecular spectrum of PEO1 (Twinkle)-linked adPEO.
Neurology 2010;74(20):1619-26.
2009: Neil Ashley; Joanna Poulton
Anticancer DNA intercalators cause p53-dependent mitochondrial DNA nucleoid re-modelling.
Oncogene 2009;28(44):3880-91.
2009: Joanna Poulton; Ian J Holt
163rd ENMC International Workshop: nucleoid and nucleotide biology in syndromes of mitochondrial DNA depletion myopathy 12-14 December 2008, Naarden, The Netherlands.
Neuromuscular disorders : NMD 2009;19(6):439-43.
2009: Neil Ashley; Joanna Poulton
Mitochondrial DNA is a direct target of anti-cancer anthracycline drugs.
Biochemical and biophysical research communications 2009;378(3):450-5.
2007: Karl J Morten; Neil Ashley; Frits A Wijburg; Nedim Hadzic; Jeremy Parr; Sandeep Jayawant; Susan Adams; Laurence A Bindoff; Henk D Bakker; Giorgina Mieli-Vergani; Massimo Zeviani; Joanna Poulton
Liver mtDNA content increases during development: a comparison of methods and the importance of age- and tissue-specific controls for the diagnosis of mtDNA depletion.
Mitochondrion 2007;7(6):386-95.
2007: Lodovica Vergani; Adriana Malena; Patrizia Sabatelli; Emanuele Loro; Lucia Cavallini; Paolo Magalhaes; Lucia Valente; Federica Bragantini; Franco Carrara; Bertrand Leger; Joanna Poulton; Aaron P Russell; Ian J Holt
Cultured muscle cells display defects of mitochondrial myopathy ameliorated by anti-oxidants.
Brain : a journal of neurology 2007;130(Pt 10):2715-24.
2007: Sreena Das; Amanda J Bennett; Ulla Sovio; Aimo Ruokonen; Hannu Martikainen; Anneli Pouta; Anna-Liisa Hartikainen; Stephen Franks; Paul Elliott; Joanna Poulton; Marjo-Riitta Järvelin; Mark I McCarthy
Detailed analysis of variation at and around mitochondrial position 16189 in a large Finnish cohort reveals no significant associations with early growth or metabolic phenotypes at age 31 years.
The Journal of clinical endocrinology and metabolism 2007;92(8):3219-23.
2007: Neil Ashley; Susan Adams; Abdelhamid Slama; Massimo Zeviani; Anu Suomalainen; Antonio L Andreu; Robert K Naviaux; Joanna Poulton
Defects in maintenance of mitochondrial DNA are associated with intramitochondrial nucleotide imbalances.
Human molecular genetics 2007;16(12):1400-11.
2007: Joanna Poulton; P Oakeshott; Stephen Kennedy
Difficulties and possible solutions in the genetic management of mtDNA disease in the preimplantation embryo.
Current topics in developmental biology 2007;77():213-25.
2006: David R Marchington; Martin Scott Brown; David H Barlow; Joanna Poulton
Mosaicism for mitochondrial DNA polymorphic variants in placenta has implications for the feasibility of prenatal diagnosis in mtDNA diseases.
European journal of human genetics : EJHG 2006;14(7):816-23.
2006: Emma L Blakely; Katherine J Rennie; Linda Jones; Matthias Elstner; Zofia M A Chrzanowska-Lightowlers; Christopher B White; Julian P H Shield; Daniela T Pilz; Douglass M Turnbull; Joanna Poulton; Robert W Taylor
Sporadic intragenic inversion of the mitochondrial DNA MTND1 gene causing fatal infantile lactic acidosis.
Pediatric research 2006;59(3):440-4.
2005: Wendy M Hutchison; Dominic Thyagarajan; Joanna Poulton; David R Marchington; Denise M Kirby; Shehnaaz S M Manji; Hans-Henrik M Dahl
Clinical and molecular features of encephalomyopathy due to the A3302G mutation in the mitochondrial tRNA(Leu(UUR)) gene.
Archives of neurology 2005;62(12):1920-3.
2005: Karl J Morten; P Field; Neil Ashley; K A Williams; D Harris; M Hartley; A Clark; Joanna Poulton
Fetal and neonatal exposure to AZT and low-protein diet affects glucose homeostasis: a model with implications for AIDS prevention.
American journal of physiology. Endocrinology and metabolism 2005;289(6):E1115-8.
2005: Ellen Parker; David I W Phillips; Richard A Cockington; Carole Cull; Joanna Poulton
A common mitchondrial DNA variant is associated with thinness in mothers and their 20-yr-old offspring.
American journal of physiology. Endocrinology and metabolism 2005;289(6):E1110-4.
2005: Teeratorn Pulkes; Danae Liolitsa; Louise H Eunson; M Rose; Isabelle P Nelson; Shamina Rahman; Joanna Poulton; David R Marchington; David N Landon; A G Debono; JA Morgan-Hughes; Michael G Hanna
New phenotypic diversity associated with the mitochondrial tRNA(SerUCN) gene mutation.
Neuromuscular disorders : NMD 2005;15(5):364-71.
2005: Neil Ashley; Dot Harris; Joanna Poulton
Detection of mitochondrial DNA depletion in living human cells using PicoGreen staining.
Experimental cell research 2005;303(2):432-46.
2004: Henna Tyynismaa; Hiroshi Sembongi; Monika Bokori-Brown; Caroline Granycome; Neil Ashley; Joanna Poulton; Anu Jalanko; Johannes N Spelbrink; Ian J Holt; Anu Suomalainen
Twinkle helicase is essential for mtDNA maintenance and regulates mtDNA copy number.
Human molecular genetics 2004;13(24):3219-27.
2004: Emma L Blakely; Joanna Poulton; Michael Pike; Fenella Wojnarowska; Douglass M Turnbull; Robert McFarland; Robert W Taylor
Childhood neurological presentation of a novel mitochondrial tRNA(Val) gene mutation.
Journal of the neurological sciences 2004;225(1-2):99-103.
2004: Patrick F Chinnery; Salvatore DiMauro; Sara Shanske; Eric A Schon; Massimo Zeviani; Caterina Mariotti; Franco Carrara; Anne Lombes; Pascal Laforet; Helène Ogier; Michaela Jaksch; Hanns Lochmüller; Rita Horvath; Marcus Deschauer; David R Thorburn; Laurence A Bindoff; Joanna Poulton; Robert W Taylor; J N S Matthews; Douglass M Turnbull
Risk of developing a mitochondrial DNA deletion disorder.
Lancet 2004;364(9434):592-6.
2004: Anja T Rovio; Josef Abel; Arja L Ahola; Aida M Andres; Jaume Bertranpetit; Antoine Blancher; Ronald E Bontrop; Leona G Chemnick; Howard J Cooke; Jim Cummins; Heidi A Davis; David J Elliott; Ellen Fritsche; Timothy B Hargreave; Susan M G Hoffman; Anne M Jequier; Shu-Huei Kao; Heui-Soo Kim; David R Marchington; Denise Mehmet; Nel Otting; Joanna Poulton; Oliver A Ryder; Hans-Christian Schuppe; Osamu Takenaka; Yau-Huei Wei; Lars Wichmann; Howard T Jacobs
A prevalent POLG CAG microsatellite length allele in humans and African great apes.
Mammalian genome : official journal of the International Mammalian Genome Society 2004;15(6):492-502.
2002: Joanna Poulton; AL Bednarz; Martin Scott Brown; C Thompson; V A Macaulay; D Simmons
The presence of a common mitochondrial DNA variant is associated with fasting insulin levels in Europeans in Auckland.
Diabetic medicine : a journal of the British Diabetic Association 2002;19(11):969-71.
2002: David R Marchington; Martin Scott Brown; V K Lamb; Ron J T Van Golde; Jan A M Kremer; Joep H A M Tuerlings; Edwin C M Mariman; Adam H Balen; Joanna Poulton
No evidence for paternal mtDNA transmission to offspring or extra-embryonic tissues after ICSI.
Molecular human reproduction 2002;8(11):1046-9.
2002: Joanna Poulton; Jian'an Luan; Vincent Macaulay; Susie Hennings; Jo Mitchell; Nicholas J Wareham
Type 2 diabetes is associated with a common mitochondrial variant: evidence from a population-based case-control study.
Human molecular genetics 2002;11(13):1581-3.
2002: Joanna Poulton; David R Marchington
Segregation of mitochondrial DNA (mtDNA) in human oocytes and in animal models of mtDNA disease: clinical implications.
Reproduction (Cambridge, England) 2002;123(6):751-5.
2001: Anja T Rovio; David R Marchington; S Donat; Hans-Christian Schuppe; J Abel; Ellen Fritsche; David J Elliott; P Laippala; A L Ahola; D McNay; R F Harrison; B Hughes; T Barrett; D M Bailey; Denise Mehmet; Anne M Jequier; Timothy B Hargreave; S H Kao; Jim Cummins; David Barton; H J Cooke; Y H Wei; L Wichmann; Joanna Poulton; Howard T Jacobs
Mutations at the mitochondrial DNA polymerase (POLG) locus associated with male infertility.
Nature genetics 2001;29(3):261-2.
2001: Johannes N Spelbrink; FY Li; Valeria Tiranti; Kaisu Nikali; Qiu-Ping Yuan; M Tariq; Sjoerd Wanrooij; Nuria Garrido; G Comi; L Morandi; L Santoro; A Toscano; G M Fabrizi; Hannu Somer; Rebecca Croxen; David Beeson; Joanna Poulton; Anu Suomalainen; Howard T Jacobs; Massimo Zeviani; Catharina Larsson
Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria.
Nature genetics 2001;28(3):223-31.
2001: C F Emmerson; G K Brown; Joanna Poulton
Synthesis of mitochondrial DNA in permeabilised human cultured cells.
Nucleic acids research 2001;29(2):E1.
2001: Shamina Rahman; Joanna Poulton; David R Marchington; Anu Suomalainen
Decrease of 3243 A-->G mtDNA mutation from blood in MELAS syndrome: a longitudinal study.
American journal of human genetics 2001;68(1):238-40.
2000: Olli A Kajander; Anja T Rovio; K Majamaa; Joanna Poulton; Johannes N Spelbrink; Ian J Holt; Pekka J Karhunen; Howard T Jacobs
Human mtDNA sublimons resemble rearranged mitochondrial genoms found in pathological states.
Human molecular genetics 2000;9(19):2821-35.
2000: Joanna Poulton; David R Marchington
Progress in genetic counselling and prenatal diagnosis of maternally inherited mtDNA diseases.
Neuromuscular disorders : NMD 2000;10(7):484-7.
2000: T G Barrett; Martin Scott Brown; A Seller; AL Bednarz; K Poulton; Joanna Poulton
The mitochondrial genome in Wolfram syndrome.
Journal of medical genetics 2000;37(6):463-6.
1999: C Hardy; Farhat L Khanim; R Torres; Martin Scott Brown; A Seller; Joanna Poulton; D Collier; J Kirk; Mihael H Polymeropoulos; Farida Latif; Timothy Barrett
Clinical and molecular genetic analysis of 19 Wolfram syndrome kindreds demonstrating a wide spectrum of mutations in WFS1.
American journal of human genetics 1999;65(5):1279-90.
1999: Olli A Kajander; Joanna Poulton; Johannes N Spelbrink; Anja T Rovio; P J Karhunen; H T Jacobs
The dangers of extended PCR in the clinic.
Nature medicine 1999;5(9):965-6.
1999: David R Marchington; D Barlow; Joanna Poulton
Transmitochondrial mice carrying resistance to chloramphenicol on mitochondrial DNA: developing the first mouse model of mitochondrial DNA disease.
Nature medicine 1999;5(8):957-60.
1999: Anja T Rovio; Valeria Tiranti; AL Bednarz; Anu Suomalainen; Johannes N Spelbrink; N Lecrenier; Atle Melberg; Massimo Zeviani; Joanna Poulton; Françoise Foury; Howard T Jacobs
Analysis of the trinucleotide CAG repeat from the human mitochondrial DNA polymerase gene in healthy and diseased individuals.
European journal of human genetics : EJHG 1999;7(2):140-6.
1998: David R Marchington; Vincent Macaulay; G M Hartshorne; D Barlow; Joanna Poulton
Evidence from human oocytes for a genetic bottleneck in an mtDNA disease.
American journal of human genetics 1998;63(3):769-75.
1998: Joanna Poulton; Vincent Macaulay; David R Marchington
Mitochondrial genetics '98 is the bottleneck cracked?
American journal of human genetics 1998;62(4):752-7.
1998: Joanna Poulton
Mitochondrial gene mutations.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 1998;2(2):99-103.
1998: Joanna Poulton; M S Brown; A Cooper; David R Marchington; David Phillips
A common mitochondrial DNA variant is associated with insulin resistance in adult life.
Diabetologia 1998;41(1):54-8.
1997: David R Marchington; G M Hartshorne; D Barlow; Joanna Poulton
Homopolymeric tract heteroplasmy in mtDNA from tissues and single oocytes: support for a genetic bottleneck.
American journal of human genetics 1997;60(2):408-16.
1996: Joanna Poulton; David R Marchington
Prospects for DNA-based prenatal diagnosis of mitochondrial disorders.
Prenatal diagnosis 1996;16(13):1247-56.
1996: Graeme C M Black; K Morten; A Laborde; Joanna Poulton
Leber's hereditary optic neuropathy: heteroplasmy is likely to be significant in the expression of LHON in families with the 3460 ND1 mutation.
The British journal of ophthalmology 1996;80(10):915-7.
1996: D A Mackey; R J Oostra; T Rosenberg; E Nikoskelainen; J Bronte-Stewart; Joanna Poulton; A E Harding; G Govan; P A Bolhuis; S Norby
Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy.
American journal of human genetics 1996;59(2):481-5.
1996: David R Marchington; Joanna Poulton; A Sellar; I J Holt
Do sequence variants in the major non-coding region of the mitochondrial genome influence mitochondrial mutations associated with disease?
Human molecular genetics 1996;5(4):473-9.
1996: K J Morten; C Freeman Emmerson; Joanna Poulton
Functional mtDNA replication defect in a fibroblast line from a patient with mtDNA depletion.
Journal of inherited metabolic disease 1996;19(2):123-6.
1995: Joanna Poulton; H G Harley; J Dasmahapatra; Garry K Brown; C G Potter; B Sykes
Mitochondrial DNA does not appear to influence the congenital onset type of myotonic dystrophy.
Journal of medical genetics 1995;32(9):732-5.
1995: K J Morten; Joanna Poulton; B Sykes
Multiple independent occurrence of the 3243 mutation in mitochondrial tRNA(leuUUR) in patients with the MELAS phenotype.
Human molecular genetics 1995;4(9):1689-91.
1995: Paul Matthews; Ruth M Brown; K Morten; David R Marchington; Joanna Poulton; G Brown
Intracellular heteroplasmy for disease-associated point mutations in mtDNA: implications for disease expression and evidence for mitotic segregation of heteroplasmic units of mtDNA.
Human genetics 1995;96(3):261-8.
1995: Joanna Poulton; Garry K Brown
Investigation of mitochondrial disease.
Archives of disease in childhood 1995;73(2):94-7.
1995: Joanna Poulton
28th ENMC international workshop: mitochondrial diseases.
Neuromuscular disorders : NMD 1995;5(4):345-6.
1995: Joanna Poulton; S O'Rahilly; K J Morten; A Clark
Mitochondrial DNA, diabetes and pancreatic pathology in Kearns-Sayre syndrome.
Diabetologia 1995;38(7):868-71.
1995: Joanna Poulton; A Rötig; K Weber; Garry K Brown; David R Marchington; Karl J Morten; Laurence A Bindoff
Duplications of mitochondrial DNA in Kearns-Sayre syndrome.
Muscle & nerve. Supplement 1995;(3):S154-8.
1995: Joanna Poulton; C Sewry; C G Potter; T Bougeron; D Chretien; F A Wijburg; K J Morten; G Brown
Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome.
Journal of inherited metabolic disease 1995;18(1):4-20.
1995: Joanna Poulton; K J Morten; David R Marchington; K Weber; Garry K Brown; A Rötig; Laurence A Bindoff
Duplications of mitochondrial DNA in Kearns-Sayre syndrome.
Muscle & nerve. Supplement 1995;3():S154-8.
1995: Graeme C M Black; IW Craig; R J Oostra; S Norby; T Rosenberg; K Morten; A Laborde; Joanna Poulton
Leber's hereditary optic neuropathy: implications of the sex ratio for linkage studies in families with the 3460 ND1 mutation.
Eye (London, England) 1995;9 ( Pt 4)():513-6.
1994: Joanna Poulton; K Morten; C Freeman-Emmerson; C Potter; C Sewry; V Dubowitz; H Kidd; J Stephenson; W Whitehouse; F J Hansen
Deficiency of the human mitochondrial transcription factor h-mtTFA in infantile mitochondrial myopathy is associated with mtDNA depletion.
Human molecular genetics 1994;3(10):1763-9.
1994: Joanna Poulton; K J Morten; K Weber; Garry K Brown; Laurence A Bindoff
Are duplications of mitochondrial DNA characteristic of Kearns-Sayre syndrome?
Human molecular genetics 1994;3(6):947-51.
1993: K J Morten; J M Cooper; Garry K Brown; B D Lake; D Pike; Joanna Poulton
A new point mutation associated with mitochondrial encephalomyopathy.
Human molecular genetics 1993;2(12):2081-7.
1993: Laurence A Bindoff; Neil Howell; Joanna Poulton; D A McCullough; K J Morten; Robert N Lightowlers; Douglass M Turnbull; K Weber
Abnormal RNA processing associated with a novel tRNA mutation in mitochondrial DNA. A potential disease mechanism.
The Journal of biological chemistry 1993;268(26):19559-64.
1993: Joanna Poulton
Mitochondrial DNA and genetic disease.
Developmental medicine and child neurology 1993;35(9):833-40.
1993: Joanna Poulton; K Morten
Noninvasive diagnosis of the MELAS syndrome from blood DNA.
Annals of neurology 1993;34(1):116.
1993: Joanna Poulton; M E Deadman; Laurence A Bindoff; K Morten; J Land; G Brown
Families of mtDNA re-arrangements can be detected in patients with mtDNA deletions: duplications may be a transient intermediate form.
Human molecular genetics 1993;2(1):23-30.
1992: Joanna Poulton
Mitochondrial DNA and genetic disease.
BioEssays : news and reviews in molecular, cellular and developmental biology 1992;14(11):763-8.
1992: Joanna Poulton
Duplications of mitochondrial DNA: implications for pathogenesis.
Journal of inherited metabolic disease 1992;15(4):487-98.
1991: Neil Howell; Laurence A Bindoff; D A McCullough; I Kubacka; Joanna Poulton; D Mackey; L Taylor; Douglass M Turnbull
Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees.
American journal of human genetics 1991;49(5):939-50.
1991: Joanna Poulton; M E Deadman; J Bronte-Stewart; W S Foulds; R M Gardiner
Analysis of mitochondrial DNA in Leber's hereditary optic neuropathy.
Journal of medical genetics 1991;28(11):765-70.
1991: Joanna Poulton; M E Deadman; S Ramacharan; R M Gardiner
Germ-line deletions of mtDNA in mitochondrial myopathy.
American journal of human genetics 1991;48(4):649-53.
1991: Joanna Poulton; M E Deadman; D M Turnbull; B Lake; R M Gardiner
Detection of mitochondrial DNA deletions in blood using the polymerase chain reaction: non-invasive diagnosis of mitochondrial myopathy.
Clinical genetics 1991;39(1):33-8.
1990: M Gardiner; A Sandford; M Deadman; Joanna Poulton; William O C M Cookson; S Reeders; I Jokiaho; L Peltonen; H Eiberg; C Julier
Batten disease (Spielmeyer-Vogt disease, juvenile onset neuronal ceroid-lipofuscinosis) gene (CLN3) maps to human chromosome 16.
Genomics 1990;8(2):387-90.
1990: N J Watmough; Laurence A Bindoff; Mark A Birch-Machin; S Jackson; K Bartlett; C I Ragan; Joanna Poulton; R M Gardiner; H S Sherratt; Douglass M Turnbull
Impaired mitochondrial beta-oxidation in a patient with an abnormality of the respiratory chain. Studies in skeletal muscle mitochondria.
The Journal of clinical investigation 1990;85(1):177-84.
1989: Joanna Poulton; M E Deadman; R M Gardiner
Tandem direct duplications of mitochondrial DNA in mitochondrial myopathy: analysis of nucleotide sequence and tissue distribution.
Nucleic acids research 1989;17(24):10223-9.
1989: Joanna Poulton; M E Deadman; R M Gardiner
Duplications of mitochondrial DNA in mitochondrial myopathy.
Lancet 1989;1(8632):236-40.
1988: Joanna Poulton; D M Turnbull; A B Mehta; J Wilson; R M Gardiner
Restriction enzyme analysis of the mitochondrial genome in mitochondrial myopathy.
Journal of medical genetics 1988;25(9):600-5.
1988: Joanna Poulton
Mitochondrial DNA and genetic disease.
Archives of disease in childhood 1988;63(8):883-5.