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Items: 1 to 50 of 489

1.

The ADP/ATP translocase drives mitophagy independent of nucleotide exchange.

Hoshino A, Wang WJ, Wada S, McDermott-Roe C, Evans CS, Gosis B, Morley MP, Rathi KS, Li J, Li K, Yang S, McMannus MJ, Bowman C, Potluri P, Levin M, Damrauer S, Wallace DC, Holzbaur ELF, Arany Z.

Nature. 2019 Oct 16. doi: 10.1038/s41586-019-1667-4. [Epub ahead of print]

PMID:
31618756
2.

Sleep, Nutrition, Disordered Eating, Problematic Tobacco and Alcohol Use, and Exercise in College Students With and Without Diabetes.

Cockroft MC, Bartlett TR, Wallace DC.

J Psychosoc Nurs Ment Health Serv. 2019 Sep 27:1-10. doi: 10.3928/02793695-20190919-04. [Epub ahead of print]

PMID:
31566702
3.

BKCa (Slo) Channel Regulates Mitochondrial Function and Lifespan in Drosophila melanogaster.

Gururaja Rao S, Bednarczyk P, Towheed A, Shah K, Karekar P, Ponnalagu D, Jensen HN, Addya S, Reyes BAS, Van Bockstaele EJ, Szewczyk A, Wallace DC, Singh H.

Cells. 2019 Aug 21;8(9). pii: E945. doi: 10.3390/cells8090945.

4.

Persistent Mitochondrial Dysfunction Linked to Prolonged Organ Dysfunction in Pediatric Sepsis.

Weiss SL, Zhang D, Bush J, Graham K, Starr J, Tuluc F, Henrickson S, Kilbaugh T, Deutschman CS, Murdock D, McGowan FX Jr, Becker L, Wallace DC.

Crit Care Med. 2019 Oct;47(10):1433-1441. doi: 10.1097/CCM.0000000000003931.

PMID:
31385882
5.

Are Emergency Departments in the United States Following Recommendations by the Emergency Severity Index to Promote Quality Triage and Reliability?

Worth M, Davis LL, Wallace DC, Bartlett R, Travers D.

J Emerg Nurs. 2019 Nov;45(6):677-684. doi: 10.1016/j.jen.2019.05.006. Epub 2019 Aug 2.

PMID:
31383365
6.

H+ transport is an integral function of the mitochondrial ADP/ATP carrier.

Bertholet AM, Chouchani ET, Kazak L, Angelin A, Fedorenko A, Long JZ, Vidoni S, Garrity R, Cho J, Terada N, Wallace DC, Spiegelman BM, Kirichok Y.

Nature. 2019 Jul;571(7766):515-520. doi: 10.1038/s41586-019-1400-3. Epub 2019 Jul 24.

PMID:
31341297
7.

Host mitochondria influence gut microbiome diversity: A role for ROS.

Yardeni T, Tanes CE, Bittinger K, Mattei LM, Schaefer PM, Singh LN, Wu GD, Murdock DG, Wallace DC.

Sci Signal. 2019 Jul 2;12(588). pii: eaaw3159. doi: 10.1126/scisignal.aaw3159.

PMID:
31266851
8.

Regulation of nuclear epigenome by mitochondrial DNA heteroplasmy.

Kopinski PK, Janssen KA, Schaefer PM, Trefely S, Perry CE, Potluri P, Tintos-Hernandez JA, Singh LN, Karch KR, Campbell SL, Doan MT, Jiang H, Nissim I, Nakamaru-Ogiso E, Wellen KE, Snyder NW, Garcia BA, Wallace DC.

Proc Natl Acad Sci U S A. 2019 Aug 6;116(32):16028-16035. doi: 10.1073/pnas.1906896116. Epub 2019 Jun 28.

9.

Scanning Microwave Microscopy of Vital Mitochondria in Respiration Buffer.

Li J, Nemati Z, Haddadi K, Wallace DC, Burke PJ.

IEEE MTTS Int Microw Symp. 2018 Jun;2018:115-118. doi: 10.1109/MWSYM.2018.8439645. Epub 2018 Aug 20.

10.

Premature Lambs Exhibit Normal Mitochondrial Respiration after Long-Term Extrauterine Support.

Rossidis AC, Angelin A, Lawrence KM, Baumgarten HD, Kim AG, Mejaddam AY, Coons BE, Hartman HA, Hwang G, Monos S, Peranteau WH, Davey MG, Murdock D, Wallace DC, Flake AW.

Fetal Diagn Ther. 2019 Mar 12:1-7. doi: 10.1159/000496232. [Epub ahead of print]

PMID:
30861524
11.

Nutrition and its role in human evolution.

James WPT, Johnson RJ, Speakman JR, Wallace DC, Frühbeck G, Iversen PO, Stover PJ.

J Intern Med. 2019 May;285(5):533-549. doi: 10.1111/joim.12878. Epub 2019 Feb 17. Review.

PMID:
30772945
12.

The phenotype modifier: is the mitochondrial DNA background responsible for individual differences in disease severity.

Morava E, Kozicz T, Wallace DC.

J Inherit Metab Dis. 2019 Jan;42(1):3-4. doi: 10.1002/jimd.12050. No abstract available.

PMID:
30740738
13.

Highly efficient 5' capping of mitochondrial RNA with NAD+ and NADH by yeast and human mitochondrial RNA polymerase.

Bird JG, Basu U, Kuster D, Ramachandran A, Grudzien-Nogalska E, Towheed A, Wallace DC, Kiledjian M, Temiakov D, Patel SS, Ebright RH, Nickels BE.

Elife. 2018 Dec 12;7. pii: e42179. doi: 10.7554/eLife.42179.

14.

Hispanic Families' Action Plans for a Healthier Lifestyle for Diabetes Management.

Amirehsani KA, Hu J, Wallace DC, Silva ZA, Dick S.

Diabetes Educ. 2019 Feb;45(1):87-95. doi: 10.1177/0145721718812478. Epub 2018 Nov 23. No abstract available.

PMID:
30466357
15.

Mitochondrial genetic medicine.

Wallace DC.

Nat Genet. 2018 Dec;50(12):1642-1649. doi: 10.1038/s41588-018-0264-z. Epub 2018 Oct 29. Review.

PMID:
30374071
16.

Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma.

Singh LN, Crowston JG, Lopez Sanchez MIG, Van Bergen NJ, Kearns LS, Hewitt AW, Yazar S, Mackey DA, Wallace DC, Trounce IA.

Invest Ophthalmol Vis Sci. 2018 Sep 4;59(11):4598-4602. doi: 10.1167/iovs.18-25085.

17.

Mitochondrial DNA Variation Dictates Expressivity and Progression of Nuclear DNA Mutations Causing Cardiomyopathy.

McManus MJ, Picard M, Chen HW, De Haas HJ, Potluri P, Leipzig J, Towheed A, Angelin A, Sengupta P, Morrow RM, Kauffman BA, Vermulst M, Narula J, Wallace DC.

Cell Metab. 2019 Jan 8;29(1):78-90.e5. doi: 10.1016/j.cmet.2018.08.002. Epub 2018 Aug 30.

18.

Mitochondrial DNA associations with East Asian metabolic syndrome.

Chalkia D, Chang YC, Derbeneva O, Lvova M, Wang P, Mishmar D, Liu X, Singh LN, Chuang LM, Wallace DC.

Biochim Biophys Acta Bioenerg. 2018 Sep;1859(9):878-892. doi: 10.1016/j.bbabio.2018.07.002. Epub 2018 Jul 8.

19.

Women's Mental Health After Retirement.

Sheppard FH, Wallace DC.

J Psychosoc Nurs Ment Health Serv. 2018 Jul 1;56(7):37-45. doi: 10.3928/02793695-20180619-07.

PMID:
29975397
20.

USMG5 Ashkenazi Jewish founder mutation impairs mitochondrial complex V dimerization and ATP synthesis.

Barca E, Ganetzky RD, Potluri P, Juanola-Falgarona M, Gai X, Li D, Jalas C, Hirsch Y, Emmanuele V, Tadesse S, Ziosi M, Akman HO, Chung WK, Tanji K, McCormick EM, Place E, Consugar M, Pierce EA, Hakonarson H, Wallace DC, Hirano M, Falk MJ.

Hum Mol Genet. 2018 Oct 1;27(19):3305-3312. doi: 10.1093/hmg/ddy231.

21.

Mitochondrial Etiology of Psychiatric Disorders-Reply.

Wallace DC, Chalkia D, Singh LN.

JAMA Psychiatry. 2018 May 1;75(5):527-528. doi: 10.1001/jamapsychiatry.2017.4468. No abstract available.

PMID:
29541750
22.

MSeqDR mvTool: A mitochondrial DNA Web and API resource for comprehensive variant annotation, universal nomenclature collation, and reference genome conversion.

Shen L, Attimonelli M, Bai R, Lott MT, Wallace DC, Falk MJ, Gai X.

Hum Mutat. 2018 Jun;39(6):806-810. doi: 10.1002/humu.23422. Epub 2018 Apr 6.

23.

Mitochondrial Etiology of Neuropsychiatric Disorders.

Pei L, Wallace DC.

Biol Psychiatry. 2018 May 1;83(9):722-730. doi: 10.1016/j.biopsych.2017.11.018. Epub 2017 Nov 20. Review.

24.

Homozygous boricua TBCK mutation causes neurodegeneration and aberrant autophagy.

Ortiz-González XR, Tintos-Hernández JA, Keller K, Li X, Foley AR, Bharucha-Goebel DX, Kessler SK, Yum SW, Crino PB, He M, Wallace DC, Bönnemann CG.

Ann Neurol. 2018 Jan;83(1):153-165. doi: 10.1002/ana.25130.

25.

Predicting the pathogenicity of novel variants in mitochondrial tRNA with MitoTIP.

Sonney S, Leipzig J, Lott MT, Zhang S, Procaccio V, Wallace DC, Sondheimer N.

PLoS Comput Biol. 2017 Dec 11;13(12):e1005867. doi: 10.1371/journal.pcbi.1005867. eCollection 2017 Dec.

26.

Loss of Drosophila FMRP leads to alterations in energy metabolism and mitochondrial function.

Weisz ED, Towheed A, Monyak RE, Toth MS, Wallace DC, Jongens TA.

Hum Mol Genet. 2018 Jan 1;27(1):95-106. doi: 10.1093/hmg/ddx387.

27.

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

Malicdan MCV, Vilboux T, Ben-Zeev B, Guo J, Eliyahu A, Pode-Shakked B, Dori A, Kakani S, Chandrasekharappa SC, Ferreira CR, Shelestovich N, Marek-Yagel D, Pri-Chen H, Blatt I, Niederhuber JE, He L, Toro C, Taylor RW, Deeken J, Yardeni T, Wallace DC, Gahl WA, Anikster Y.

Hum Mutat. 2018 Jan;39(1):69-79. doi: 10.1002/humu.23345. Epub 2017 Nov 8.

28.

Association Between Mitochondrial DNA Haplogroup Variation and Autism Spectrum Disorders.

Chalkia D, Singh LN, Leipzig J, Lvova M, Derbeneva O, Lakatos A, Hadley D, Hakonarson H, Wallace DC.

JAMA Psychiatry. 2017 Nov 1;74(11):1161-1168. doi: 10.1001/jamapsychiatry.2017.2604. Erratum in: JAMA Psychiatry. 2017 Dec 1;74(12):1279.

29.

US Healthcare Experiences of Hispanic Patients with Diabetes and Family Members: A Qualitative Analysis.

Amirehsani KA, Hu J, Wallace DC, Silva ZA, Dick S, West-Livingston LN, Hussami CR.

J Community Health Nurs. 2017 Jul-Sep;34(3):126-135. doi: 10.1080/07370016.2017.1340556.

30.

Resistive flow sensing of vital mitochondria with nanoelectrodes.

Zand K, Pham TDA, Li J, Zhou W, Wallace DC, Burke PJ.

Mitochondrion. 2017 Nov;37:8-16. doi: 10.1016/j.mito.2017.06.003. Epub 2017 Jun 24.

31.

A Mitochondrial Etiology of Neuropsychiatric Disorders.

Wallace DC.

JAMA Psychiatry. 2017 Sep 1;74(9):863-864. doi: 10.1001/jamapsychiatry.2017.0397. No abstract available.

PMID:
28614546
32.

Mitochondrial DNA 3243A>G heteroplasmy is associated with changes in cytoskeletal protein expression and cell mechanics.

Kandel J, Picard M, Wallace DC, Eckmann DM.

J R Soc Interface. 2017 Jun;14(131). pii: 20170071. doi: 10.1098/rsif.2017.0071.

33.

An X-chromosome linked mouse model (Ndufa1S55A) for systemic partial Complex I deficiency for studying predisposition to neurodegeneration and other diseases.

Kim C, Potluri P, Khalil A, Gaut D, McManus M, Compton S, Wallace DC, Yadava N.

Neurochem Int. 2017 Oct;109:78-93. doi: 10.1016/j.neuint.2017.05.003. Epub 2017 May 12.

34.

Foxp3 Reprograms T Cell Metabolism to Function in Low-Glucose, High-Lactate Environments.

Angelin A, Gil-de-Gómez L, Dahiya S, Jiao J, Guo L, Levine MH, Wang Z, Quinn WJ 3rd, Kopinski PK, Wang L, Akimova T, Liu Y, Bhatti TR, Han R, Laskin BL, Baur JA, Blair IA, Wallace DC, Hancock WW, Beier UH.

Cell Metab. 2017 Jun 6;25(6):1282-1293.e7. doi: 10.1016/j.cmet.2016.12.018. Epub 2017 Apr 13.

35.

Precancer Atlas to Drive Precision Prevention Trials.

Spira A, Yurgelun MB, Alexandrov L, Rao A, Bejar R, Polyak K, Giannakis M, Shilatifard A, Finn OJ, Dhodapkar M, Kay NE, Braggio E, Vilar E, Mazzilli SA, Rebbeck TR, Garber JE, Velculescu VE, Disis ML, Wallace DC, Lippman SM.

Cancer Res. 2017 Apr 1;77(7):1510-1541. doi: 10.1158/0008-5472.CAN-16-2346.

36.

Deleterious variants in TRAK1 disrupt mitochondrial movement and cause fatal encephalopathy.

Barel O, Malicdan MCV, Ben-Zeev B, Kandel J, Pri-Chen H, Stephen J, Castro IG, Metz J, Atawa O, Moshkovitz S, Ganelin E, Barshack I, Polak-Charcon S, Nass D, Marek-Yagel D, Amariglio N, Shalva N, Vilboux T, Ferreira C, Pode-Shakked B, Heimer G, Hoffmann C, Yardeni T, Nissenkorn A, Avivi C, Eyal E, Kol N, Glick Saar E, Wallace DC, Gahl WA, Rechavi G, Schrader M, Eckmann DM, Anikster Y.

Brain. 2017 Mar 1;140(3):568-581. doi: 10.1093/brain/awx002. Erratum in: Brain. 2018 Apr 1;141(4):e34.

37.

Leber Hereditary Optic Neuropathy: Exemplar of an mtDNA Disease.

Wallace DC, Lott MT.

Handb Exp Pharmacol. 2017;240:339-376. doi: 10.1007/164_2017_2. Review.

PMID:
28233183
38.

Mitochondrial energy deficiency leads to hyperproliferation of skeletal muscle mitochondria and enhanced insulin sensitivity.

Morrow RM, Picard M, Derbeneva O, Leipzig J, McManus MJ, Gouspillou G, Barbat-Artigas S, Dos Santos C, Hepple RT, Murdock DG, Wallace DC.

Proc Natl Acad Sci U S A. 2017 Mar 7;114(10):2705-2710. doi: 10.1073/pnas.1700997114. Epub 2017 Feb 21.

39.

V-T theory for the self-intermediate scattering function in a monatomic liquid.

Wallace DC, Chisolm ED, De Lorenzi-Venneri G.

J Phys Condens Matter. 2017 Feb 8;29(5):055101. doi: 10.1088/1361-648X/29/5/055101. Epub 2016 Dec 12.

PMID:
27941219
40.

Frailty Assessment in Hospitalized Older Adults Using the Electronic Health Record.

Lekan DA, Wallace DC, McCoy TP, Hu J, Silva SG, Whitson HE.

Biol Res Nurs. 2017 Mar;19(2):213-228. doi: 10.1177/1099800416679730. Epub 2017 Jan 25.

41.

Metabolic and Growth Rate Alterations in Lymphoblastic Cell Lines Discriminate Between Down Syndrome and Alzheimer's Disease.

Coskun P, Helguera P, Nemati Z, Bohannan RC, Thomas J, Samuel SE, Argueta J, Doran E, Wallace DC, Lott IT, Busciglio J.

J Alzheimers Dis. 2017;55(2):737-748.

PMID:
27802222
42.

Cristae remodeling causes acidification detected by integrated graphene sensor during mitochondrial outer membrane permeabilization.

Pham TD, Pham PQ, Li J, Letai AG, Wallace DC, Burke PJ.

Sci Rep. 2016 Oct 27;6:35907. doi: 10.1038/srep35907.

43.

Mitochondrial respiration is sensitive to cytoarchitectural breakdown.

Kandel J, Angelin AA, Wallace DC, Eckmann DM.

Integr Biol (Camb). 2016 Nov 7;8(11):1170-1182.

44.

The rise of mitochondria in medicine.

Picard M, Wallace DC, Burelle Y.

Mitochondrion. 2016 Sep;30:105-16. doi: 10.1016/j.mito.2016.07.003. Epub 2016 Jul 14. Review.

45.

Microchambers with Solid-State Phosphorescent Sensor for Measuring Single Mitochondrial Respiration.

Pham TD, Wallace DC, Burke PJ.

Sensors (Basel). 2016 Jul 9;16(7). pii: E1065. doi: 10.3390/s16071065.

46.

Genetics: Mitochondrial DNA in evolution and disease.

Wallace DC.

Nature. 2016 Jul 28;535(7613):498-500. Epub 2016 Jul 6. No abstract available.

PMID:
27383787
47.

Targeting ACLY sensitizes castration-resistant prostate cancer cells to AR antagonism by impinging on an ACLY-AMPK-AR feedback mechanism.

Shah S, Carriveau WJ, Li J, Campbell SL, Kopinski PK, Lim HW, Daurio N, Trefely S, Won KJ, Wallace DC, Koumenis C, Mancuso A, Wellen KE.

Oncotarget. 2016 Jul 12;7(28):43713-43730. doi: 10.18632/oncotarget.9666.

48.

Atomic motion from the mean square displacement in a monatomic liquid.

Wallace DC, De Lorenzi-Venneri G, Chisolm ED.

J Phys Condens Matter. 2016 May 11;28(18):185101. doi: 10.1088/0953-8984/28/18/185101. Epub 2016 Apr 8.

PMID:
27058024
49.

Differential Mitochondrial Requirements for Radially and Non-radially Migrating Cortical Neurons: Implications for Mitochondrial Disorders.

Lin-Hendel EG, McManus MJ, Wallace DC, Anderson SA, Golden JA.

Cell Rep. 2016 Apr 12;15(2):229-37. doi: 10.1016/j.celrep.2016.03.024. Epub 2016 Mar 31.

50.

Deficiency in the mouse mitochondrial adenine nucleotide translocator isoform 2 gene is associated with cardiac noncompaction.

Kokoszka JE, Waymire KG, Flierl A, Sweeney KM, Angelin A, MacGregor GR, Wallace DC.

Biochim Biophys Acta. 2016 Aug;1857(8):1203-1212. doi: 10.1016/j.bbabio.2016.03.026. Epub 2016 Apr 24.

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