Name | Wallace Douglas C, Prof., Dr. |
---|---|
Institution |
Center for Mitochondrial and Epigenomic Medicine (CMEM) The Children's Hospital of Philadelphia - Research Institute Colket Translational Research Building |
Address | 3501 Civic Center Blvd, 6th Floor, Office 6060, 19104 |
City | Philadelphia |
State/Province | Pennsylvania (PA) |
Country | USA |
WallaceD1@email.chop.edu | |
Weblink | Center for Mitochondrial and Epigenomic Medicine (CMEM) |
O2k-Network Lab | US PA Philadelphia Wallace DC |
Labels:
Publications
Published | Reference | |
---|---|---|
Song 2024 Commun Biol | 2024 | Song A, Zhao N, Hilpert DC, Perry C, Baur JA, Wallace DC, Schaefer PM (2024) Visualizing subcellular changes in the NAD(H) pool size versus redox state using fluorescence lifetime imaging microscopy of NADH. Commun Biol 7:428. https://doi.org/10.1038/s42003-024-06123-7 |
Lee 2024 ACS Nano | 2024 | Lee CH, Wallace DC, Burke PJ (2024) Super-resolution imaging of voltages in the interior of individual, vital mitochondria. ACS Nano 18:1345β56. https://doi.org/10.1021/acsnano.3c02768 |
Weiss 2022 Shock | 2022 | Weiss SL, Henrickson SE, Lindell RB, Sartori LF, Zhang D, Bush J, Farooqi S, Starr J, Deutschman CS, McGowan FX Jr, Becker L, Tuluc F, Wherry EJ, Picard M, Wallace DC (2022) Influence of immune cell subtypes on mitochondrial measurements in peripheral blood mononuclear cells from children with sepsis. Shock 57:630-8. https://doi.org/10.1097/SHK.0000000000001903 |
Weiss 2022 J Cell Mol Med | 2022 | Weiss SL, Zhang D, Farooqi S, Wallace DC (2022) Sodium butyrate reverses lipopolysaccharide-induced mitochondrial dysfunction in lymphoblasts. https://doi.org/10.1111/jcmm.17342 |
Weiss 2021 Crit Care Explor | 2021 | Weiss SL, Bittinger K, Lee JJ, Friedman ES, Mattei LM, Graham K, Zhang D, Bush J, Balamuth F, McGowan FX Jr, Bushman FD, Baldassano RN, Wu GD, Wallace DC, Collman RG (2021) Decreased intestinal microbiome diversity in pediatric sepsis: a conceptual framework for intestinal dysbiosis to influence immunometabolic function. Crit Care Explor 3:0360. |
Yardeni 2021 Proc Natl Acad Sci U S A | 2021 | Yardeni T, Cristancho AG, McCoy AJ, Schaefer PM, McManus MJ, Marsh ED, Wallace DC (2021) An mtDNA mutant mouse demonstrates that mitochondrial deficiency can result in autism endophenotypes. Proc Natl Acad Sci U S A 118:e2021429118. |
Gururaja Rao 2019 Cells | 2019 | 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 (2019) BKCa (Slo) channel regulates mitochondrial function and lifespan in Drosophila melanogaster. Cells 8:E945. |
Kopinski 2019 Proc Natl Acad Sci U S A | 2019 | 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 (2019) Regulation of nuclear epigenome by mitochondrial DNA heteroplasmy. Proc Natl Acad Sci U S A 116:16028-35. |
McManus 2019 Cell Metab | 2019 | 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 (2019) Mitochondrial DNA variation dictates expressivity and progression of nuclear DNA mutations causing cardiomyopathy. Cell Metab 29:78-90. |
Barca 2018 Hum Mol Genet | 2018 | 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 E, Place E, Consugar M, Pierce EA, Hakonarson H, Wallace DC, Hirano M, Falk MJ (2018) USMG5 Ashkenazi Jewish founder mutation impairs mitochondrial complex V dimerization and ATP synthesis. Hum Mol Genet 27:3305-12. |
Weisz 2018 Hum Mol Genet | 2018 | Weisz ED, Towheed A, Monyak RE, Toth MS, Wallace DC, Jongens TA (2018) Loss of Drosophila FMRP leads to alterations in energy metabolism and mitochondrial function. Hum Mol Genet 27:95-106. |
Zand 2017 Mitochondrion | 2017 | Zand K, Pham TDA, Li J, Zhou W, Wallace DC, Burke PJ (2017) Resistive flow sensing of vital mitochondria with nanoelectrodes. Mitochondrion 37:8-16. |
Morrow 2017 Proc Natl Acad Sci U S A | 2017 | Morrow RM, Picard M, Derbeneva O, Leipzig J, McManus MJ, Gouspillou G, Barbat-Artigas S, Dos Santos C, Hepple RT, Murdock DG, Wallace DC (2017) Mitochondrial energy deficiency leads to hyperproliferation of skeletal muscle mitochondria and enhanced insulin sensitivity. Proc Natl Acad Sci U S A 114:2705-10. |
Pham 2016 Sensors (Basel) | 2016 | Pham TD, Wallace DC, Burke PJ (2016) Microchambers with solid-state phosphorescent sensor for measuring single mitochondrial respiration. Sensors (Basel) 16 pii: E1065. |
Beier 2015 FASEB J | 2015 | Beier UH, Angelin A, Akimova T, Wang L, Liu Y, Xiao H, Koike MA, Hancock SA, Bhatti TR, Han R, Jiao J, Veasey SC, Sims CA, Baur JA, Wallace DC, Hancock WW (2015) Essential role of mitochondrial energy metabolism in Foxp3βΊ T-regulatory cell function and allograft survival. FASEB J 29:2315-26. https://doi.org/10.1096/fj.14-268409 |
Kilbaugh 2015 PLoS One | 2015 | Kilbaugh TJ, Lvova M, Karlsson M, Zhang Z, Leipzig J, Wallace DC, Margulies SS (2015) Peripheral blood mitochondrial DNA as a biomarker of cerebral mitochondrial dysfunction following traumatic brain injury in a porcine model. PLoS One 10:e0130927. |
Wallace 2010 Annu Rev Pathol | 2010 | Wallace DC, Fan W, Procaccio V (2010) Mitochondrial energetics and therapeutics. Annu Rev Pathol 5:297-348. |
Ruiz-Pesini 2004 Science | 2004 | Ruiz-Pesini E, Mishmar D, Brandon M, Procaccio V, Wallace DC (2004) Effects of purifying and adaptive selection on regional variation in human mtDNA. Science 303:223-6. |
Mishmar 2003 Proc Natl Acad Sci U S A | 2003 | Mishmar D, Ruiz-Pesini E, Golik P, Macaulay V, Clark AG, Hosseini S, Brandon M, Easley K, Chen E, Brown MD, Sukernik RI, Olckers A, Wallace DC (2003) Natural selection shaped regional mtDNA variation in humans. Proc Natl Acad Sci U S A 100:171-6. |
Wallace 1988 Science | 1988 | Wallace DC, Singh G, Lott MT, Hodge JA, Schurr TG, Lezza AM, Elsas LJ 2nd, Nikoskelainen EK (1988) Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. https://doi.org/10.1126/science.3201231 |
Abstracts
Published | Reference | |
---|---|---|
McManus 2015 Abstract MiP2015 | 2015 | The etiology of age-dependent disease: a story of two genomes. |
Picard 2014 Abstract MiP2014 | 2014 | Quantitative regulation of nuclear gene expression by mitochondrial DNA heteroplasmy. |