Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 474

1.

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.

2.

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. 2018 Aug 23. pii: S1550-4131(18)30503-5. doi: 10.1016/j.cmet.2018.08.002. [Epub ahead of print]

PMID:
30174309
3.

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.

PMID:
29997041
4.

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
5.

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.

PMID:
29917077
6.

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
7.

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.

PMID:
29539190
8.

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.

PMID:
29290371
9.

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.

PMID:
29283439
10.

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.

11.

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.

12.

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.

PMID:
29044765
13.

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.

14.

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.

15.

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.

PMID:
28655663
16.

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
17.

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.

18.

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.

19.

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.

20.

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.

Supplemental Content

Loading ...
Support Center