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Items: 42

1.

Genetic Basis of Severe Childhood-Onset Cardiomyopathies.

Vasilescu C, Ojala TH, Brilhante V, Ojanen S, Hinterding HM, Palin E, Alastalo TP, Koskenvuo J, Hiippala A, Jokinen E, Jahnukainen T, Lohi J, Pihkala J, Tyni TA, Carroll CJ, Suomalainen A.

J Am Coll Cardiol. 2018 Nov 6;72(19):2324-2338. doi: 10.1016/j.jacc.2018.08.2171.

PMID:
30384889
2.

Metabolomes of mitochondrial diseases and inclusion body myositis patients: treatment targets and biomarkers.

Buzkova J, Nikkanen J, Ahola S, Hakonen AH, Sevastianova K, Hovinen T, Yki-Järvinen H, Pietiläinen KH, Lönnqvist T, Velagapudi V, Carroll CJ, Suomalainen A.

EMBO Mol Med. 2018 Dec;10(12). pii: e9091. doi: 10.15252/emmm.201809091.

3.

A reality check for climate change experiments: Do they reflect the real world?

Knapp AK, Carroll CJW, Griffin-Nolan RJ, Slette IJ, Chaves FA, Baur LE, Felton AJ, Gray JE, Hoffman AM, Lemoine NP, Mao W, Post AK, Smith MD.

Ecology. 2018 Oct;99(10):2145-2151. doi: 10.1002/ecy.2474. Epub 2018 Sep 4.

PMID:
30054917
4.

Reply to 'Letter to Editor by Finsterer J and Zarrouk-Mahjoub S: Phenotypic manifestations of the m.8969G>A variant'.

Isohanni P, Carroll CJ, Jackson CB, Pohjanpelto M, Lönnqvist T, Suomalainen A.

Neurogenetics. 2018 May;19(2):133-134. doi: 10.1007/s10048-018-0542-z. Epub 2018 Feb 26. No abstract available.

PMID:
29480378
5.

A urinary biosignature for mitochondrial myopathy, encephalopathy, lactic acidosis and stroke like episodes (MELAS).

Esterhuizen K, Lindeque JZ, Mason S, van der Westhuizen FH, Suomalainen A, Hakonen AH, Carroll CJ, Rodenburg RJ, de Laat PB, Janssen MCH, Smeitink JAM, Louw R.

Mitochondrion. 2018 Feb 19. pii: S1567-7249(17)30237-4. doi: 10.1016/j.mito.2018.02.003. [Epub ahead of print]

PMID:
29471047
6.

Defective mitochondrial ATPase due to rare mtDNA m.8969G>A mutation-causing lactic acidosis, intellectual disability, and poor growth.

Isohanni P, Carroll CJ, Jackson CB, Pohjanpelto M, Lönnqvist T, Suomalainen A.

Neurogenetics. 2018 Jan;19(1):49-53. doi: 10.1007/s10048-018-0537-9. Epub 2018 Jan 19.

PMID:
29350304
7.

Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia.

Nguyen TTM, Murakami Y, Sheridan E, Ehresmann S, Rousseau J, St-Denis A, Chai G, Ajeawung NF, Fairbrother L, Reimschisel T, Bateman A, Berry-Kravis E, Xia F, Tardif J, Parry DA, Logan CV, Diggle C, Bennett CP, Hattingh L, Rosenfeld JA, Perry MS, Parker MJ, Le Deist F, Zaki MS, Ignatius E, Isohanni P, Lönnqvist T, Carroll CJ, Johnson CA, Gleeson JG, Kinoshita T, Campeau PM.

Am J Hum Genet. 2017 Nov 2;101(5):856-865. doi: 10.1016/j.ajhg.2017.09.020.

8.

Defective mitochondrial RNA processing due to PNPT1 variants causes Leigh syndrome.

Matilainen S, Carroll CJ, Richter U, Euro L, Pohjanpelto M, Paetau A, Isohanni P, Suomalainen A.

Hum Mol Genet. 2017 Sep 1;26(17):3352-3361. doi: 10.1093/hmg/ddx221.

PMID:
28645153
9.

Absence of Hikeshi, a nuclear transporter for heat-shock protein HSP70, causes infantile hypomyelinating leukoencephalopathy.

Vasilescu C, Isohanni P, Palomäki M, Pihko H, Suomalainen A, Carroll CJ.

Eur J Hum Genet. 2017 Feb;25(3):366-370. doi: 10.1038/ejhg.2016.189. Epub 2016 Dec 21.

10.

Pushing precipitation to the extremes in distributed experiments: recommendations for simulating wet and dry years.

Knapp AK, Avolio ML, Beier C, Carroll CJ, Collins SL, Dukes JS, Fraser LH, Griffin-Nolan RJ, Hoover DL, Jentsch A, Loik ME, Phillips RP, Post AK, Sala OE, Slette IJ, Yahdjian L, Smith MD.

Glob Chang Biol. 2017 May;23(5):1774-1782. doi: 10.1111/gcb.13504. Epub 2016 Nov 1.

11.

Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy.

Haack TB, Ignatius E, Calvo-Garrido J, Iuso A, Isohanni P, Maffezzini C, Lönnqvist T, Suomalainen A, Gorza M, Kremer LS, Graf E, Hartig M, Berutti R, Paucar M, Svenningsson P, Stranneheim H, Brandberg G, Wedell A, Kurian MA, Hayflick SA, Venco P, Tiranti V, Strom TM, Dichgans M, Horvath R, Holinski-Feder E, Freyer C, Meitinger T, Prokisch H, Senderek J, Wredenberg A, Carroll CJ, Klopstock T.

Am J Hum Genet. 2016 Sep 1;99(3):735-743. doi: 10.1016/j.ajhg.2016.06.026. Epub 2016 Aug 18.

12.

Mitochondrial DNA Replication Defects Disturb Cellular dNTP Pools and Remodel One-Carbon Metabolism.

Nikkanen J, Forsström S, Euro L, Paetau I, Kohnz RA, Wang L, Chilov D, Viinamäki J, Roivainen A, Marjamäki P, Liljenbäck H, Ahola S, Buzkova J, Terzioglu M, Khan NA, Pirnes-Karhu S, Paetau A, Lönnqvist T, Sajantila A, Isohanni P, Tyynismaa H, Nomura DK, Battersby BJ, Velagapudi V, Carroll CJ, Suomalainen A.

Cell Metab. 2016 Apr 12;23(4):635-48. doi: 10.1016/j.cmet.2016.01.019. Epub 2016 Feb 25.

13.

Endothelial disruptive proinflammatory effects of nicotine and e-cigarette vapor exposures.

Schweitzer KS, Chen SX, Law S, Van Demark M, Poirier C, Justice MJ, Hubbard WC, Kim ES, Lai X, Wang M, Kranz WD, Carroll CJ, Ray BD, Bittman R, Goodpaster J, Petrache I.

Am J Physiol Lung Cell Mol Physiol. 2015 Jul 15;309(2):L175-87. doi: 10.1152/ajplung.00411.2014. Epub 2015 May 15.

14.

Differential sensitivity to regional-scale drought in six central US grasslands.

Knapp AK, Carroll CJ, Denton EM, La Pierre KJ, Collins SL, Smith MD.

Oecologia. 2015 Apr;177(4):949-57. doi: 10.1007/s00442-015-3233-6. Epub 2015 Feb 5.

PMID:
25651805
15.

Effective treatment of mitochondrial myopathy by nicotinamide riboside, a vitamin B3.

Khan NA, Auranen M, Paetau I, Pirinen E, Euro L, Forsström S, Pasila L, Velagapudi V, Carroll CJ, Auwerx J, Suomalainen A.

EMBO Mol Med. 2014 Jun;6(6):721-31. doi: 10.1002/emmm.201403943.

16.

Next-generation sequencing for mitochondrial disorders.

Carroll CJ, Brilhante V, Suomalainen A.

Br J Pharmacol. 2014 Apr;171(8):1837-53. doi: 10.1111/bph.12469. Review.

17.

Regulation of myocardial interleukin-6 expression by p53 and STAT1.

Carroll CJ, Sayan BS, Bailey SG, McCormick J, Stephanou A, Latchman DS, Townsend PA.

J Interferon Cytokine Res. 2013 Sep;33(9):542-8. doi: 10.1089/jir.2012.0165. Epub 2013 May 15.

PMID:
23675777
18.

Whole-exome sequencing identifies a mutation in the mitochondrial ribosome protein MRPL44 to underlie mitochondrial infantile cardiomyopathy.

Carroll CJ, Isohanni P, Pöyhönen R, Euro L, Richter U, Brilhante V, Götz A, Lahtinen T, Paetau A, Pihko H, Battersby BJ, Tyynismaa H, Suomalainen A.

J Med Genet. 2013 Mar;50(3):151-9. doi: 10.1136/jmedgenet-2012-101375. Epub 2013 Jan 12.

PMID:
23315540
19.

Mitochondrial phenylalanyl-tRNA synthetase mutations underlie fatal infantile Alpers encephalopathy.

Elo JM, Yadavalli SS, Euro L, Isohanni P, Götz A, Carroll CJ, Valanne L, Alkuraya FS, Uusimaa J, Paetau A, Caruso EM, Pihko H, Ibba M, Tyynismaa H, Suomalainen A.

Hum Mol Genet. 2012 Oct 15;21(20):4521-9. Epub 2012 Jul 23.

PMID:
22833457
20.

Transgenic overexpression of HSP56 does not result in cardiac hypertrophy nor protect from ischaemia/reperfusion injury.

Carroll CJ, Suleman N, Davidson SM, Faulkes DJ, Diss JK, Knight R, Stephanou A, Latchman DS, Townsend PA.

Int J Biochem Cell Biol. 2011 Jan;43(1):74-9. doi: 10.1016/j.biocel.2010.09.020. Epub 2010 Oct 29.

PMID:
20932935
21.

Mitochondrial myopathy induces a starvation-like response.

Tyynismaa H, Carroll CJ, Raimundo N, Ahola-Erkkilä S, Wenz T, Ruhanen H, Guse K, Hemminki A, Peltola-Mjøsund KE, Tulkki V, Oresic M, Moraes CT, Pietiläinen K, Hovatta I, Suomalainen A.

Hum Mol Genet. 2010 Oct 15;19(20):3948-58. doi: 10.1093/hmg/ddq310. Epub 2010 Jul 23.

PMID:
20656789
22.

Effects of polyclonal IgG derived from patients with different clinical types of the antiphospholipid syndrome on monocyte signaling pathways.

Lambrianides A, Carroll CJ, Pierangeli SS, Pericleous C, Branch W, Rice J, Latchman DS, Townsend P, Isenberg DA, Rahman A, Giles IP.

J Immunol. 2010 Jun 15;184(12):6622-8. doi: 10.4049/jimmunol.0902765. Epub 2010 May 17.

23.

Ketogenic diet slows down mitochondrial myopathy progression in mice.

Ahola-Erkkilä S, Carroll CJ, Peltola-Mjösund K, Tulkki V, Mattila I, Seppänen-Laakso T, Oresic M, Tyynismaa H, Suomalainen A.

Hum Mol Genet. 2010 May 15;19(10):1974-84. doi: 10.1093/hmg/ddq076. Epub 2010 Feb 17.

PMID:
20167576
24.

Urocortin prevents mitochondrial permeability transition in response to reperfusion injury indirectly by reducing oxidative stress.

Townsend PA, Davidson SM, Clarke SJ, Khaliulin I, Carroll CJ, Scarabelli TM, Knight RA, Stephanou A, Latchman DS, Halestrap AP.

Am J Physiol Heart Circ Physiol. 2007 Aug;293(2):H928-38. Epub 2007 May 4.

25.

Urocortin inhibits Beclin1-mediated autophagic cell death in cardiac myocytes exposed to ischaemia/reperfusion injury.

Valentim L, Laurence KM, Townsend PA, Carroll CJ, Soond S, Scarabelli TM, Knight RA, Latchman DS, Stephanou A.

J Mol Cell Cardiol. 2006 Jun;40(6):846-52. Epub 2006 May 12.

PMID:
16697404
26.

The cotton rat provides a novel model to study genital herpes infection and to evaluate preventive strategies.

Yim KC, Carroll CJ, Tuyama A, Cheshenko N, Carlucci MJ, Porter DD, Prince GA, Herold BC.

J Virol. 2005 Dec;79(23):14632-9.

27.

Cardioprotection mediated by urocortin is dependent on PKCepsilon activation.

Lawrence KM, Kabir AM, Bellahcene M, Davidson S, Cao XB, McCormick J, Mesquita RA, Carroll CJ, Chanalaris A, Townsend PA, Hubank M, Stephanou A, Knight RA, Marber MS, Latchman DS.

FASEB J. 2005 May;19(7):831-3. Epub 2005 Mar 10.

PMID:
15764590
28.

The cardioprotective effect of urocortin during ischaemia/reperfusion involves the prevention of mitochondrial damage.

Lawrence KM, Townsend PA, Davidson SM, Carroll CJ, Eaton S, Hubank M, Knight RA, Stephanou A, Latchman DS.

Biochem Biophys Res Commun. 2004 Aug 20;321(2):479-86.

PMID:
15358201
29.

Signal-transduction pathways involved in the hypertrophic effect of hsp56 in neonatal cardiomyocytes.

Jamshidi Y, Zourlidou A, Carroll CJ, Sinclair J, Latchman DS.

J Mol Cell Cardiol. 2004 Mar;36(3):381-92.

PMID:
15010277
30.

BAG-1 proteins protect cardiac myocytes from simulated ischemia/reperfusion-induced apoptosis via an alternate mechanism of cell survival independent of the proteasome.

Townsend PA, Cutress RI, Carroll CJ, Lawrence KM, Scarabelli TM, Packham G, Stephanou A, Latchman DS.

J Biol Chem. 2004 May 14;279(20):20723-8. Epub 2004 Feb 20.

31.

Urocortin protects cardiac myocytes from ischemia/reperfusion injury by attenuating calcium-insensitive phospholipase A2 gene expression.

Lawrence KM, Scarabelli TM, Turtle L, Chanalaris A, Townsend PA, Carroll CJ, Hubank M, Stephanou A, Knight RA, Latchman DS.

FASEB J. 2003 Dec;17(15):2313-5. Epub 2003 Oct 16.

PMID:
14563694
32.

YAC transgenic mice carrying pathological alleles of the MJD1 locus exhibit a mild and slowly progressive cerebellar deficit.

Cemal CK, Carroll CJ, Lawrence L, Lowrie MB, Ruddle P, Al-Mahdawi S, King RH, Pook MA, Huxley C, Chamberlain S.

Hum Mol Genet. 2002 May 1;11(9):1075-94.

PMID:
11978767
33.

Rescue of the Friedreich's ataxia knockout mouse by human YAC transgenesis.

Pook MA, Al-Mahdawi S, Carroll CJ, Cossée M, Puccio H, Lawrence L, Clark P, Lowrie MB, Bradley JL, Cooper JM, Koenig M, Chamberlain S.

Neurogenetics. 2001 Oct;3(4):185-93.

PMID:
11714098
34.

The medical building: here's a way to turn it into pure investment.

Isselhard TJ, Carroll CJ Jr, Picone CL.

Group Pract J. 1982 Sep-Oct;31(5):10-2. No abstract available.

PMID:
10257375
35.

Selective induction of labour.

O'Driscol K, Carroll CJ, Coughlan M.

Br Med J. 1975 Dec 27;4(5999):727-9.

36.

Carbohydrate intolerance: its influence on maternal and fetal levels of cortisol and cortisone.

Chattoraj SC, Carroll CJ, Turner AK, Gillespie L, Pinkus JL, Charles D.

Obstet Gynecol. 1974 Nov;44(5):646-56. No abstract available.

PMID:
4422809
37.

Simultaneous competitive protein binding assay for cortissol, cortisone, and prednisolone in plasma, and its clinical application.

Turner AK, Carroll CJ, Pinkus JL, Charles D, Chattoraj SC.

Clin Chem. 1973 Jul;19(7):731-6. No abstract available.

38.

Criteria for diagnosis of candida vulvovaginitis in pregnant women.

Carroll CJ, Hurley R, Stanley VC.

J Obstet Gynaecol Br Commonw. 1973 Mar;80(3):258-63. No abstract available.

PMID:
4574090
39.

Distribution and significance of candida precipitins in sera from pregnant women.

Stanley VC, Hurley R, Carroll CJ.

J Med Microbiol. 1972 Aug;5(3):313-20. No abstract available.

PMID:
4627060
40.

Infantile cortical hyperostosis presenting with exophthalmos. Case report.

BYWATERS TW Jr, BAILEY RW, CARROLL CJ, O'CONNOR GA.

J Mich State Med Soc. 1963 Mar;62:285-8. No abstract available.

PMID:
14017524
41.

Antibody response of pregnant women to poliomyelitis vaccine and passive transfer to infants.

BROWN GC, CARROLL CJ.

J Immunol. 1958 Nov;81(5):389-95. No abstract available.

PMID:
13598920
42.

Reaction of Pyo compounds with sodium hypoiodite.

WELLS IC, HAYS EE, THAYER SA, DOISY EA, GABY WL, CARROLL CJ, JONES LR.

J Biol Chem. 1952 May;196(1):341-5. No abstract available.

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