The DOI matches its Crossref record; 59 of the 59 references it cites were found in a registry or an index.
Transcriptional coactivators PGC-1α and PGC-lβ control overlapping programs required for perinatal maturation of the heart
Open accessAbstract
Oxidative tissues such as heart undergo a dramatic perinatal mitochondrial biogenesis to meet the high-energy demands after birth. PPARγ coactivator-1 (PGC-1) α and β have been implicated in the transcriptional control of cellular energy metabolism. Mice with combined deficiency of PGC-1α and PGC-1β (PGC-1αβ −/− mice) were generated to investigate the convergence of their functions in vivo. The phenotype of PGC-1β −/− mice was minimal under nonstressed conditions, including normal heart function, similar to that of PGC-1α −/− mice generated previously. In striking contrast to the singly deficient PGC-1 lines, PGC-1αβ −/− mice died shortly after birth with small hearts, bradycardia, intermittent heart block, and a markedly reduced cardiac output. Cardiac-specific ablation of the PGC-1β gene on a PGC-1α-deficient background phenocopied the generalized PGC-1αβ −/− mice. The hearts of the PGC-1αβ −/− mice exhibited signatures of a maturational defect including reduced growth, a late fetal arrest in mitochondrial biogenesis, and persistence of a fetal pattern of gene expression. Brown adipose tissue (BAT) of PGC-1αβ −/− mice also exhibited a severe abnormality in function and mitochondrial density. We conclude that PGC-1α and PGC-1β share roles that collectively are necessary for the postnatal metabolic and functional maturation of heart and BAT.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Previous work has established that repression of either or both co-activators (PGC-1α or PGC-1β) decreases mitochondrial biogenesis and function, elicits cardiomyopathy and impairs de novo glucose production23-25.”
From Telomere dysfunction induces metabolic and mitochondrial compromise (2011) · cites this paper as [25]
In the citing paper
“The existence of compensation for PGC-1 deficiency by PGC-1␣ and vice versa is evidenced by the phenotype of double PGC-1␣ and PGC-1 muscle-specific knockout mice (62).”
From The role of mitochondria in the pathogenesis of type 2 diabetes (2010) · cites this paper as [62]
In the citing paper
“PGC-1-null mice (59, 62, 65, 66) display phenotypes similar to, but not identical to, those of PGC-1␣ knockouts, including reduced expression of OXPHOS genes, reduced ATP synthesis, reduced exercise capacity, and impaired thermogenesis (59,62).”
From The role of mitochondria in the pathogenesis of type 2 diabetes (2010) · cites this paper as [62]
In the citing paper
“These animals display normal mitochondrial biogenesis during development but die early after birth due to failure of perinatal mitochondrial proliferation and consequent cardiac failure (62).”
From The role of mitochondria in the pathogenesis of type 2 diabetes (2010) · cites this paper as [62]
In the citing paper
“Insulin sensitivity in these animals is reported to be normal.”
From The role of mitochondria in the pathogenesis of type 2 diabetes (2010) · cites this paper as [62]
In the citing paper
“Lai, 2008 (62) PGC-1␣ and PGC-1 2 60%, heart | muscle-specific KO”
From The role of mitochondria in the pathogenesis of type 2 diabetes (2010) · cites this paper as [62]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION
Bligh, E. G., & Dyer, W. J. (1959) · Canadian Journal of Biochemistry and Physiology · doi:10.1139/o59-099 · Cited by 54,751
Wu, Z., Puigserver, P., Andersson, U., Zhang, C., Adelmant, G., Mootha, V., Troy, A., Cinti, S., Lowell, B., Scarpulla, R. C., et al. (1999) · Cell · doi:10.1016/s0092-8674(00)80611-x · Cited by 4,139
A Cold-Inducible Coactivator of Nuclear Receptors Linked to Adaptive Thermogenesis
Puigserver, P., Wu, Z., Park, C. W., Graves, R., Wright, M., & Spiegelman, B. M. (1998) · Cell · doi:10.1016/s0092-8674(00)81410-5 · Cited by 3,864
Transcriptional co-activator PGC-1α drives the formation of slow-twitch muscle fibres
Lin, J., Wu, H., Tarr, P. T., Zhang, C.-Y., Wu, Z., Boss, O., Michael, L. F., Puigserver, P., Isotani, E., Olson, E. N., et al. (2002) · Nature · doi:10.1038/nature00904 · Cited by 2,546
Puigserver, P., & Spiegelman, B. M. (2003) · Endocrine Reviews · doi:10.1210/er.2002-0012 · Cited by 2,076
Control of hepatic gluconeogenesis through the transcriptional coactivator PGC-1
Yoon, J. C., Puigserver, P., Chen, G., Donovan, J., Wu, Z., Rhee, J., Adelmant, G., Stafford, J., Kahn, C. R., Granner, D. K., et al. (2001) · Nature · doi:10.1038/35093050 · Cited by 1,821
Tei, C., Ling, L. H., Hodge, D. O., Bailey, K. R., Oh, J. K., Rodeheffer, R. J., Tajik, A. J., & Seward, J. B. (1995) · PubMed · Cited by 1,547
Insulin-regulated hepatic gluconeogenesis through FOXO1–PGC-1α interaction
Puigserver, P., Rhee, J., Donovan, J., Walkey, C. J., Yoon, J. C., Oriente, F., Kitamura, Y., Altomonte, J., Dong, H., Accili, D., et al. (2003) · Nature · doi:10.1038/nature01667 · Cited by 1,487
PGC-1 coactivators: inducible regulators of energy metabolism in health and disease
Finck, B. N. (2006) · Journal of Clinical Investigation · doi:10.1172/jci27794 · Cited by 1,461
CREB regulates hepatic gluconeogenesis through the coactivator PGC-1
Herzig, S., Long, F., Jhala, U. S., Hedrick, S., Quinn, R., Bauer, A., Rudolph, D., Schutz, G., Yoon, C., Puigserver, P., et al. (2001) · Nature · doi:10.1038/35093131 · Cited by 1,440
Flagged first, then by citations
Cited by
Sorted by citations
Items 201–300 of 327
Metabolic regulation by the PGC-1α and PGC-1β coactivators in larval zebrafish (Danio rerio)
Northam, C., & LeMoine, C. M. R. (2019) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2019.04.011 · Cited by 20
Zou, J., Wang, W., Lü, Y., Ayala, J. D., Dong, K., Zhou, H., Wang, J., Chen, W., Weintraub, N. L., Zhou, J., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112018 · Cited by 20
Miranda, D., Jara, C., Ibañez-Vega, J., Ahumada, V., Acuña‐Castillo, C., Martín, A., Córdova, A., & Montoya, M. (2016) · Mediators of Inflammation · doi:10.1155/2016/9605253 · Cited by 20
Development, activation, and therapeutic potential of thermogenic adipocytes
Emont, M. P., Kim, D., & Wu, J. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2018.05.004 · Cited by 20
Accelerated Cardiac Aging in Patients With Congenital Heart Disease
Iacobazzi, D., Alvino, V. V., Caputo, M., & Madeddu, P. R. (2022) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2022.892861 · Cited by 19
Hypertrophic Cardiomyopathy in Infants from the Perspective of Cardiomyocyte Maturation
Seok, H., & Oh, J.-H. (2021) · Korean Circulation Journal · doi:10.4070/kcj.2021.0153 · Cited by 18
Cardiac-Specific Overexpression of ERRγ in Mice Induces Severe Heart Dysfunction and Early Lethality
Lasheras, J., Pardo, R., Velilla, M., Poncelas, M., Salvatella, N., Simó, R., Ruiz‐Meana, M., Zamora, M., & Villena, J. A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22158047 · Cited by 17
He, L., & Maheshwari, A. (2022) · Current Pediatric Reviews · doi:10.2174/1573396319666221221110728 · Cited by 17
Reclaiming Warburg: using developmental biology to gain insight into human metabolic diseases
Drummond‐Barbosa, D., & Tennessen, J. M. (2020) · Development · doi:10.1242/dev.189340 · Cited by 17
Phosphoproteomics of the developing heart identifies PERM1 - An outer mitochondrial membrane protein
Aravamudhan, S., Türk, C., Bock, T., Keufgens, L., Nolte, H., Lang, F., Krishnan, R. K., König, T., Hammerschmidt, P., Schindler, N., et al. (2021) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2021.01.010 · Cited by 18
Preobrazenski, N., Islam, H., & Gurd, B. J. (2021) · European Journal of Applied Physiology · doi:10.1007/s00421-021-04669-6 · Cited by 18
Mitochondria Cripple without Krüppel
Jang, C., & Arany, Z. P. (2015) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2015.08.004 · Cited by 17
Wu, C.-W. J., Hung, C.-Y., Hirase, H., Tain, Y., Lee, W., Chan, J. Y. H., Fu, M., Chen, L.-W., Liu, W., Liang, C., et al. (2019) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00408.2018 · Cited by 17
Managing risky assets – mitophagy in vivo
Narendra, D. P. (2021) · Journal of Cell Science · doi:10.1242/jcs.240465 · Cited by 16
Development and Functions of Mitochondria in Early Life
Maheshwari, A., Peng, J., Ramatchandirin, B., Pearah, A., & He, L. (2022) · Newborn · doi:10.5005/jp-journals-11002-0013 · Cited by 17
Lee, S., Leone, T. C., Rogosa, L., Rumsey, J. W., Ayala, J. E., Coen, P. M., Fitts, R. H., Vega, R. B., & Kelly, D. P. (2017) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00380.2016 · Cited by 16
Self-citationHellen, N., Ricardo, C. P., Vauchez, K., Whiting, G. C., Wheeler, J. X., & Harding, S. E. (2019) · Stem Cells and Development · doi:10.1089/scd.2018.0210 · Cited by 14
Prolonged cardiac NR4A2 activation causes dilated cardiomyopathy in mice
Ashraf, S., Taegtmeyer, H., & Harmancey, R. (2022) · Basic Research in Cardiology · doi:10.1007/s00395-022-00942-7 · Cited by 16
Metzler, M. A., Venkatesh, S. G., Lakshmanan, J., Carenbauer, A. L., Perez, S. M., Andres, S. A., Appana, S. N., Brock, G. N., Wittliff, J. L., & Darling, D. S. (2015) · PLoS ONE · doi:10.1371/journal.pone.0125153 · Cited by 15
Liu, Y., Shim, E., Crespo-Mejias, Y., Nguyen, P., Gibbons, A. T., Liu, D. D., Shide, E. D., & Poirier, M. C. (2014) · Cardiovascular Toxicology · doi:10.1007/s12012-014-9288-5 · Cited by 15
Age‐dependent electrocardiographic changes in Pgc‐1β deficient murine hearts
Ahmad, S., Valli, H., Salvage, S., Grace, A., Jeevaratnam, K., & Huang, C. (2017) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/1440-1681.12863 · Cited by 14
Dumont, S., Pennec, S. L., Donnart, A., Teusan, R., Steenman, M., Chevalier, C., Houlgatte, R., & Savagner, F. (2018) · Oncotarget · doi:10.18632/oncotarget.24633 · Cited by 15
Fatty acid-based monolayer culture to promote in vitro neonatal rat cardiomyocyte maturation
Isu, G., Diaz, D. R., Grussenmeyer, T., Gaudiello, E., Eckstein, F. S., Brink, M., & Marsano, A. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2019.118561 · Cited by 15
Gestational Hypoxia and Programing of Lung Metabolism
Rood, K., Lopez, V., Frano, M. R. L., Fiehn, O., Zhang, L., Blood, A. B., & Wilson, S. M. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.01453 · Cited by 15
Kiebish, M. A., Young, D. M., Lehman, J. J., & Han, X. (2011) · Journal of Lipid Research · doi:10.1194/jlr.m020628 · Cited by 15
Ahmad, S., Valli, H., Chadda, K. R., Cranley, J. J., Jeevaratnam, K., & Huang, C. L.-H. (2018) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2018.05.004 · Cited by 15
Links between telomere dysfunction and hallmarks of aging
Li, S., Liu, Z., Zhang, J., & Li, L. (2023) · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · doi:10.1016/j.mrgentox.2023.503617 · Cited by 15
Mitonuclear Communication in Stem Cell Function
Peng, B., Wang, Y., & Zhang, H. (2024) · Cell Proliferation · doi:10.1111/cpr.13796 · Cited by 14
Metabolic remodeling in chronic heart failure
Wang, J., & Guo, T. (2013) · Journal of Zhejiang University SCIENCE B · doi:10.1631/jzus.b1300137 · Cited by 14
Keeping the beat against time: Mitochondrial fitness in the aging heart
Mendoza, A., & Karch, J. M. (2022) · Frontiers in Aging · doi:10.3389/fragi.2022.951417 · Cited by 13
Rubio‐Tomás, T., Soler‐Botija, C., Martínez-Estrada, O. M., & Villena, J. A. (2024) · Biochemical Pharmacology · doi:10.1016/j.bcp.2024.116185 · Cited by 13
A transcriptional regulatory mechanism of genes in the tricarboxylic acid cycle in the heart
Veera, S., Tang, F., Mourad, Y., Kim, S., Liu, T., Hong Li, A., Wang, Y., Warren, J. S., Park, J., Van, C., et al. (2024) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2024.107677 · Cited by 12
Brain nuclear receptors and cardiovascular function
Wang, M., Yang, Y., & Xu, Y. (2023) · Cell & Bioscience · doi:10.1186/s13578-023-00962-3 · Cited by 12
Chai, N., Zheng, H., Zhang, H., Li, L., Yu, X. M., Wang, L., Bi, X., Yang, L., Niu, T., Liu, X., et al. (2023) · Iranian journal of pharmaceutical research · doi:10.5812/ijpr-133776 · Cited by 11
Recent Advances in Modeling Mitochondrial Cardiomyopathy Using Human Induced Pluripotent Stem Cells
Pávez, M., & Cyganek, L. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.800529 · Cited by 12
Dittrich, A., Hansen, K., Simonsen, M. I. T., Busk, M., Alstrup, A. K. O., & Lauridsen, H. (2020) · BioEssays · doi:10.1002/bies.202000054 · Cited by 10
The role of metabolism in cardiac development
Nakano, H., & Nakano, A. (2024) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2024.01.005 · Cited by 10
Palzkill, V. R., Tan, J., Moparthy, D., Tice, A. L., Ferreira, L. F., & RYAN, T. E. (2024) · JACC Basic to Translational Science · doi:10.1016/j.jacbts.2024.08.011 · Cited by 9
Mitochondrial Dynamics during Development
Maheshwari, A., He, L., & Tronstad, K. J. (2023) · Newborn · doi:10.5005/jp-journals-11002-0053 · Cited by 10
Ruiz, M., Khairallah, M., Dingar, D. D., Vaniotis, G., Khairallah, R. J., Lauzier, B., Thibault, S., Trépanier, J., Shi, Y., Douillette, A., et al. (2021) · Journal of the American Heart Association · doi:10.1161/jaha.120.017791 · Cited by 10
Ji, H. L., Lu, R., Chang, Z., Su, S., & Yang, G. (2011) · Reproduction in Domestic Animals · doi:10.1111/j.1439-0531.2011.01894.x · Cited by 11
Modulation of PPAR ‐α and PPAR ‐γ Influences Cardiomyocyte Growth and Cardiac Remodeling
Xuan, Q., Li, J., Feng, Z., Zhu, L., Jiang, T., Li, H., Liu, M., Qian, X., & Ma, X. (2025) · IUBMB Life · doi:10.1002/iub.70035 · Cited by 9
Li, S., Yan, B., Wu, B., Su, J., Lu, J., Lam, T.-W., Boheler, K. R., Poon, E. N.-Y., & Luo, R. (2023) · Stem Cell Research & Therapy · doi:10.1186/s13287-023-03442-0 · Cited by 9
Günthel, M., van Duijvenboden, K., de Bakker, D. E. M., Hooijkaas, I. B., Bakkers, J., Barnett, P., & Christoffels, V. M. (2021) · Journal of Cardiovascular Development and Disease · doi:10.3390/jcdd8110134 · Cited by 9
Neddylation drives myofibrillogenesis in the developing heart
Littlejohn, R., Zambrano-Carrasco, J., Zou, J., Lu, Y., Liu, E., Kim, I., Jiao, K., Weintraub, N. L., Zhou, J., Li, J., et al. (2024) · The FASEB Journal · doi:10.1096/fj.202401380r · Cited by 8
Molecular Regulation of Cardiomyocyte Maturation
Shewale, B., Ebrahim, T. A. M., Samal, A., & Dubois, N. C. (2025) · Current Cardiology Reports · doi:10.1007/s11886-024-02189-1 · Cited by 8
PGC-1β-expressing POMC neurons mediate the effect of leptin on thermoregulation in the mouse
Delezie, J., Gill, J. F., Santos, G., Karrer‐Cardel, B., & Handschin, C. (2020) · Scientific Reports · doi:10.1038/s41598-020-73794-7 · Cited by 9
McCombie, G., Medina‐Gómez, G., Lelliott, C. J., Vidal‐Puig, A., & Griffin, J. L. (2012) · Metabolites · doi:10.3390/metabo2020366 · Cited by 7
Benefield, D., Abdelmageed, Y., Fowler, J. A., Smith, S., Arias-Parbul, K., Dunning, C., & Rowe, G. C. (2023) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00241.2022 · Cited by 8
Failed Power Plant Turns Into Mass Murder
Lee, C. F., Cao, Y., & Tian, R. (2018) · Circulation Research · doi:10.1161/circresaha.117.312288 · Cited by 6
Shi, L., Zhang, M., Yang, H., Li, X., He, S., Chu, Y., Gao, M., Zhang, Z., Zhang, J. Z., Li, Z., et al. (2025) · Cell Death and Differentiation · doi:10.1038/s41418-025-01577-6 · Cited by 5
Tissue-specific implications of mitochondrial alterations in aging
Liu, D. (2012) · Frontiers in Bioscience-Elite · doi:10.2741/e654 · Cited by 5
Mitochondrial Biogenesis and Dynamics in Health and Disease
Campos, J. C., Bozi, L. H. M., & Ferreira, J. C. B. (2021) · Springer eBooks · doi:10.1007/978-3-030-86684-6_3 · Cited by 4
Life Course Impact of Glucocorticoids During Pregnancy on Muscle Development and Function
Liu, Y., Ding, Q., & Guo, W. (2021) · Frontiers in Animal Science · doi:10.3389/fanim.2021.788930 · Cited by 5
Molecular Control of Cardiac Fetal/Neonatal Remodeling
Breckenridge, R. A. (2014) · Journal of Cardiovascular Development and Disease · doi:10.3390/jcdd1010029 · Cited by 6
Maturation of Stem Cell-Derived Cardiomyocytes: Foe in Translation Medicine
Liao, Y., Zhu, L., & Wang, Y. (2021) · International Journal of Stem Cells · doi:10.15283/ijsc21077 · Cited by 5
Mahiny-Shahmohammady, D., Hauck, L., Premsingh, B., Grothe, D., & Billia, F. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms251910824 · Cited by 4
Inhibition of Adhesion Molecule Gene Expression and Cell Adhesion by the Metabolic Regulator PGC-1α
Minsky, N., & Roeder, R. G. (2016) · PLoS ONE · doi:10.1371/journal.pone.0165598 · Cited by 6
Gidlund, E. (2019) · Springer eBooks · doi:10.1007/978-3-030-04816-7_3 · Cited by 4
Transcriptional dynamics of the murine heart during perinatal development at single-cell resolution
Feulner, L., Wünnemann, F., Rafatian, N., Liang, J., Medouni, A., Hofmann, P., Hitz, M.-P., Schapiro, D., Leclerc, S., Vliet, P. P. V., et al. (2026) · Biology Open · doi:10.1242/bio.062493 · Cited by 5
Transcriptional Control of Striated Muscle Mitochondrial Biogenesis and Function
Kelly, D. P., & Scarpulla, R. C. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-381510-1.00016-8 · Cited by 4
Self-citationTissue specificity of energy metabolism in mitochondria
Moreno‐Loshuertos, R., & Fernández‐Silva, P. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819621-2.00001-2 · Cited by 4
3.3 Mitochondrial Energy Production
Yalçınkaya, B. H., Genç, S., Çatak, J., Özilgen, M., & Yılmaz, B. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-809597-3.00308-4 · Cited by 4
Vertebrates show coordinated elevated expression of mitochondrial and nuclear genes after birthPreprint
Medini, H., & Mishmar, D. (2025) · Genome Research · doi:10.1101/gr.279700.124 · Cited by 4
Schmid, S., Kupr, B., Pérez‐Schindler, J., Mansingh, S., Beer, M., Mittal, N., Ehrenfeuchter, N., & Handschin, C. (2022) · Molecular Metabolism · doi:10.1016/j.molmet.2022.101643 · Cited by 3
Roy, S. D., Nagarajan, S., Jalal, M. S., Basar, M. A., & Duttaroy, A. (2023) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkad142 · Cited by 3
Mitochondrial non-energetic function and embryonic cardiac development
Shi, J., Jin, Y., Lin, S., Li, X., Zhang, D., Wu, J., Qi, Y., & Li, Y. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1475603 · Cited by 4
Wan, Y. (2010) · Cited by 3
Recent developments in mitochondrial medicine (part 2)
Weissig, V., & Edeas, M. A. (2022) · 4open · doi:10.1051/fopen/2022002 · Cited by 3
Le, Z., Dong, S., Zhang, R., Cai, X.-P., Gao, A., Xiao, R., & Yu, H. (2018) · Journal of Developmental Origins of Health and Disease · doi:10.1017/s2040174418000077 · Cited by 3
Allostatic hypermetabolic response in PGC1α/β heterozygote mouse despite mitochondrial defects
Rodríguez‐Cuenca, S., Lelliott, C. J., Campbell, M., Gopalacharyulu, P. V., Martinez‐Uña, M., Ingvorsen, C., Dias, A. R., Relat, J., Mora, S., Hyötyläinen, T., et al. (2021) · The FASEB Journal · doi:10.1096/fj.202100262rr · Cited by 3
PPAR/PGC-1 Regulation of Metabolism in Cardiac Disease
Duncan, J. G., & Finck, B. N. (2012) · Humana Press eBooks · doi:10.1007/978-1-61779-891-7_4 · Cited by 2
Schillemans, T., Tragante, V., Maitusong, B., Gigante, B., Cresci, S., Laguzzi, F., Vikström, M., Richards, M., Pilbrow, A. P., Cameron, V. A., et al. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.909870 · Cited by 3
FULMINANT MYOCARDITIS-A UNIQUE COMPLICATION OF COVID-19
Ahmed, A., Young, S. K., & Lantz, R. H. (2021) · Journal of the American College of Cardiology · doi:10.1016/s0735-1097(21)03378-7 · Cited by 2
Perturbed Brain Energy Metabolism in Alzheimer’s Disease and Diabetes
Wu, L. (2017) · KU ScholarWorks (University of Kansas) · Cited by 2
Interaction of PGC-1α and GDF15 in the stressed heart
Tian, R. (2025) · Nature Cardiovascular Research · doi:10.1038/s44161-025-00729-8 · Cited by 1
Vinarský, V., Pagliari, S., Aldabash, B., Martino, F., Mazzotti, C., Jirakova, K., Garlíková, Z., Iuri, E. D., Kytýř, D., Benzoni, P., et al. (2025) · Cell Death Discovery · doi:10.1038/s41420-025-02793-2 · Cited by 2
A Functionally Conserved Enhancer is Critical for PGC1A Expression and Thermogenesis in Brown Fat
Su, D., Yang, H., Li, X., Jiang, T., Zhan, S., Zhong, T., Guo, J., Wang, Y., Li, L., Zhang, H., et al. (2026) · Advanced Science · doi:10.1002/advs.202518153 · Cited by 2
Rumyantseva, A., Tippetts, T. S., Wilhalm, A., Carter, W., Moedas, M. F., Rosenberger, F. A., Moore, D., Végvári, Á., Hinze, Y., Muellner-Wong, L., et al. (2026) · Science Advances · doi:10.1126/sciadv.aeg8792 · Cited by 3
Targeting Oxidative Stress in Heart Failure
Li, J. W. Y., & Tang, W. H. W. (2014) · Springer eBooks · doi:10.1007/978-3-642-30018-9_184 · Cited by 1
Transcriptional Control of Mitochondrial Biogenesis and Maturation
Vega, R. B., Leone, T. C., & Kelly, D. P. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1227-8_6 · Cited by 1
Self-citationAlterations in Cardiac Metabolism
Peterson, L. R., Schilling, J. D., & Taegtmeyer, H. (2010) · Elsevier eBooks · doi:10.1016/b978-1-4160-5895-3.10020-8 · Cited by 1
Metabolic Flexibility and Mitochondrial Bioenergetics in the Failing Heart. Therapeutic Approaches
Rosca, M. G. (2021) · Romanian Journal of Cardiology · doi:10.47803/rjc.2021.31.2.269 · Cited by 1
Marín-García, J. (2012) · Springer eBooks · doi:10.1007/978-1-4614-4599-9_4 · Cited by 1
Pioneering PGC-1α–boosted secretome: a novel approach to combating liver fibrosis
Seo, C. H., Na, G. H., Lee, D., Park, J. H., Hong, T. H., Kim, O., Lee, S. C., Kim, K., Choi, H. J., & Kim, S. (2024) · Annals of Surgical Treatment and Research · doi:10.4174/astr.2024.106.3.155 · Cited by 1
Post-Genomic Analysis of Fatty Acid and Glucose Metabolism in Cardiovascular Disease
Marín-García, J. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-404599-6.00016-0 · Cited by 1
Energy Metabolism in Cellular Regenerative Processes: Focus on PPARα
Kulikova, T. G., Stepanova, O. V., Voronova, A. D., Valikhov, M. P., Kuznetsova, T. V., Kurilina, E. V., Akchurin, R. S., Reshetov, I. V., & Sukhikh, G. T. (2020) · Bulletin of Experimental Biology and Medicine · doi:10.1007/s10517-020-04774-0 · Cited by 1
Olanlokun, J. O., Babarinde, C. O., & Olorunsogo, O. O. (2023) · Research Square · doi:10.21203/rs.3.rs-3210506/v1 · Cited by 1
MittoSAM-dependent lipoylation controls postnatal heart development via metabolic remodelingPreprint
Rumyantseva, A., Wilhalm, A., Carter, W., Tippetts, T. S., Moedas, M., Rosenberger, F., Moore, D., Végvári, Á., Hinze, Y., Muellner-Wong, L. S., et al. (2026) · bioRxiv · doi:10.64898/2026.04.20.719537 · Cited by 1
Nuclear Genes Causing Mitochondrial Cardiomyopathy
Ware, S. M., & Towbin, J. A. (2012) · Springer eBooks · doi:10.1007/978-1-4614-3722-2_20
The Role of Altered Lipid Metabolism in Septic Myocardial Dysfunction
Siracusano, L., & Girasole, V. (2013) · InTech eBooks · doi:10.5772/51001
The Drosophila PGC-1 homologue Spargel coordinates mitochondrial biogenesis to insulin-signalling
Tiefenböck, S. K. (2009) · Repository for Publications and Research Data (ETH Zurich) · doi:10.3929/ethz-a-005831335
Special Issue: The evolving role of mitochondria in metabolism
Scarpulla, R. C., Vega, R. B., & Kelly, D. P. (2012)
Self-citationSignal Transduction Pathways That Regulate Mitochondrial Gene Expression
Chen, C., Chen, J., Debebe, A., Yang, L., & Stiles, B. L. (2015) · Oxidative stress and disease · doi:10.1201/b19420-5
Molecular Mechanisms of Cardiovascular Aging
Tarantini, F., Serio, C. D., & Ferrucci, L. (2017) · Springer eBooks · doi:10.1007/978-3-319-43468-1_3
Glucocorticoids promote structural and functional maturation of foetal cardiomyocytes
Rog-Zielinska, E., Craig, M., Manning, J., Richardson, R., Gowans, G. J., Dunbar, Gharbi, K., Kenyon, C., Holmes, M., Hardie, D. G., et al. (2016)
RESEARCH ARTICLE Integrative Cardiovascular Physiology and Pathophysiology
Ribeiro, J. C. (2018)
Role of Mitochondria in Cardiovascular Comorbidities Associated with Obesity and Type 2 Diabetes
Boudina, S. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-811752-1.00011-0
The Evolving Concept of Mitochondrial Dynamics in Heart: Interventional Opportunities
Ashok, S., Ganjoo, M., Panicker, V. T., Pillai, V. V., & Gopala, S. (2019) · Springer eBooks · doi:10.1007/978-981-13-8946-7_25
Metadata
- Authors
- Lai, L., Leone, T. C., Zechner, C., Schaeffer, P. J., Kelly, S. M., Flanagan, D. P., Medeiros, D. M., Kovacs, A., & Kelly, D. P.
- Affiliations
- Washington University in St. Louis (US)
- Kansas State University (US)
- Venue
- Genes & Development
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2008-07-15
- Volume
- 22
- Issue
- 14
- Pages
- 1948-1961
- ISSN
- 0890-9369 (ISSN-L)
- 1549-5477
- PMC
- PMC2492740
- OpenAlex
- W2146878987
- Cited by
- 326
- References
- 59
- Citations by year
- 2026: 15 · 2025: 8 · 2024: 14 · 2023: 18 · 2022: 17 · 2021: 31 · 2020: 16 · 2019: 20 · 2018: 16 · 2017: 14 · 2016: 17 · 2015: 19 · 2014: 18 · 2013: 21 · 2012: 26
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Genes & Development (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- HighWire Press Open Archive (submittedVersion)
- Funders
- American Heart Association
- Alvin J. Siteman Cancer Center (CA91842, #P30 CA91842)
- Deutsche Forschungsgemeinschaft
- National Institutes of Health (5p60dk020579-35, DK-052574, DK56341, DK020579, CA91842)
- National Heart, Lung, and Blood Institute (R01HL058427)
- National Cancer Institute (P30CA091842)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK045416, P60-DK-020579, P30DK056341, P30DK052574)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Adipose Tissue and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Peroxisome Proliferator-Activated Receptors
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Congenital heart defects research
- Keywords
- PGC-1α, PGC-1β, mitochondrial biogenesis, cardiac output, atrioventricular block, brown adipose tissue, fetal gene expression, postnatal heart development, energy metabolism
- MeSH terms
- Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha, Animals, Adipose Tissue, Brown, Female, Heart, Male, Mice, Inbred C57BL, Mitochondria, Heart, Transcription Factors, Blotting, Southern, Trans-Activators, Polymerase Chain Reaction, Mice, Knockout, Integrases, Oligonucleotide Array Sequence Analysis, Gene Expression Profiling, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review