McManus MJ: Difference between revisions
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{{Person | {{Person | ||
|lastname=McManus | |lastname=McManus | ||
|firstname=Meagan | |firstname=Meagan J | ||
|title=PhD | |||
|institution=[[File:Meagan McManus.png|right|80px|Meagan McManus]] | |institution=[[File:Meagan McManus.png|right|80px|Meagan McManus]] | ||
Center for Mitochondrial and Epigenomic Medicine (CMEM) | Center for Mitochondrial and Epigenomic Medicine (CMEM) | ||
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}} | }} | ||
{{Labelingperson | {{Labelingperson | ||
|field of research=Basic | |field of research=Basic, Pharmacological | ||
}} | }} | ||
== Participated at == | == Participated at == | ||
* [[MiPNet20.10 IOC106 Schroecken|IOC106 Schroecken]] | * [[MiPNet20.10 IOC106 Schroecken|IOC106 Schroecken]] | ||
* [[MiP2015]] | * [[MiP2015]] |
Revision as of 16:02, 14 September 2015
Name | McManus Meagan J, PhD |
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Institution |
Center for Mitochondrial and Epigenomic Medicine (CMEM) Children's Hospital of Philadelphia Colket Translational Research Building |
Address | 3501 Civic Center Blvd, Room 6100, 19104 |
City | Philadelphia |
State/Province | Pennsylvania (PA) |
Country | USA |
[email protected] | |
Weblink | |
O2k-Network Lab | US PA Philadelphia Wallace DC |
Labels:
Field of research: Basic, Pharmacological
Publications
Published | Reference | |
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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. |
Marquez 2020 J Am Heart Assoc | 2020 | Marquez AM, Morgan RW, Ko T, Landis WP, Hefti MM, Mavroudis CD, McManus MJ, Karlsson M, Starr J, Roberts AL, Lin Y, Nadkarni V, Licht DJ, Berg RA, Sutton RM, Kilbaugh TJ (2020) Oxygen exposure during cardiopulmonary resuscitation is associated with cerebral oxidative injury in a randomized, blinded, controlled, preclinical trial. J Am Heart Assoc 9:015032. |
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. |
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. |
Abstracts
Published | Reference | |
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McManus 2016 Abstract MitoFit Science Camp 2016 | 2016 | A multi-tiered mitochondrial approach to predictive biomarkers of neurodegenerative disease. |
McManus 2015 Abstract MiP2015 | 2015 | The etiology of age-dependent disease: a story of two genomes. |