Wallace DC

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Name Wallace Douglas C, Prof., Dr.
Institution
Doug Wallace 1600.JPG

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
Email WallaceD1@email.chop.edu
Weblink Center for Mitochondrial and Epigenomic Medicine (CMEM)
O2k-Network Lab US PA Philadelphia Wallace DC


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Publications

 PublishedReference
McManus 2019 Cell Metab2019McManus 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.
Kopinski 2019 Proc Natl Acad Sci U S A2019Kopinski 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 [Epub ahead of print].
Gururaja Rao 2019 Cells2019Gururaja 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.
Weisz 2018 Hum Mol Genet2018Weisz 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.
Barca 2018 Hum Mol Genet2018Barca 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.
Morrow 2017 Proc Natl Acad Sci U S A2017Morrow 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.
Zand 2017 Mitochondrion2017Zand K, Pham TDA, Li J, Zhou W, Wallace DC, Burke PJ (2017) Resistive flow sensing of vital mitochondria with nanoelectrodes. Mitochondrion 37:8-16.
Pham 2016 Sensors (Basel)2016Pham TD, Wallace DC, Burke PJ (2016) Microchambers with solid-state phosphorescent sensor for measuring single mitochondrial respiration. Sensors (Basel) 16 pii: E1065.
Kilbaugh 2015 PLoS One2015Kilbaugh 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.
Ruiz-Pesini 2004 Science2004Ruiz-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 A2003Mishmar 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.

Abstracts

 PublishedReference
McManus 2015 Abstract MiP20152015The etiology of age-dependent disease: a story of two genomes.
Picard 2014 Abstract MiP20142014Quantitative regulation of nuclear gene expression by mitochondrial DNA heteroplasmy.

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