☰

Sarika Srivastava, Ph.D. - Publications

Affiliations: 
2005 University of Miami, Coral Gables, FL 
Area:
Cell Biology, Molecular Biology
Tree Info Grants Similar researchers Related pubs Distance to... Nearest Nobel PubMed Report error

17 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Patel PA, Liang C, Arora A, Vijayan S, Ahuja S, Wagley PK, Settlage R, Lew L, Goodkin HP, Lazar I, Srivastava S, Mukherjee K. Haploinsufficiency of X-linked intellectual disability gene CASK induces post-transcriptional changes in synaptic and cellular metabolic pathways. Experimental Neurology. 113319. PMID 32305418 DOI: 10.1016/J.Expneurol.2020.113319  0.336
2019 McMillan RP, Stewart S, Budnick JA, Caswell CC, Hulver MW, Mukherjee K, Srivastava S. Quantitative Variation in m.3243A > G Mutation Produce Discrete Changes in Energy Metabolism. Scientific Reports. 9: 5752. PMID 30962477 DOI: 10.1038/S41598-019-42262-2  0.493
2018 LaConte LEW, Chavan V, Elias AF, Hudson C, Schwanke C, Styren K, Shoof J, Kok F, Srivastava S, Mukherjee K. Two microcephaly-associated novel missense mutations in CASK specifically disrupt the CASK-neurexin interaction. Human Genetics. PMID 29426960 DOI: 10.1007/S00439-018-1874-3  0.306
2017 Srivastava S. The Mitochondrial Basis of Aging and Age-Related Disorders. Genes. 8. PMID 29257072 DOI: 10.3390/Genes8120398  0.54
2017 Chavan V, Willis J, Walker SK, Clark HR, Liu X, Fox MA, Srivastava S, Mukherjee K. Correction: Central Presynaptic Terminals Are Enriched in ATP but the Majority Lack Mitochondria. Plos One. 12: e0181140. PMID 28700683 DOI: 10.1371/Journal.Pone.0181140  0.35
2016 Mukherjee K, Clark HR, Chavan V, Benson EK, Kidd GJ, Srivastava S. Analysis of Brain Mitochondria Using Serial Block-Face Scanning Electron Microscopy. Journal of Visualized Experiments : Jove. PMID 27501303 DOI: 10.3791/54214  0.493
2016 Srivastava S. Emerging therapeutic roles for NAD(+) metabolism in mitochondrial and age-related disorders. Clinical and Translational Medicine. 5: 25. PMID 27465020 DOI: 10.1186/S40169-016-0104-7  0.464
2016 Srivastava S, McMillan R, Willis J, Clark H, Chavan V, Liang C, Zhang H, Hulver M, Mukherjee K. X-linked intellectual disability gene CASK regulates postnatal brain growth in a non-cell autonomous manner. Acta Neuropathologica Communications. 4: 30. PMID 27036546 DOI: 10.1186/S40478-016-0295-6  0.335
2015 Chavan V, Willis J, Walker SK, Clark HR, Liu X, Fox MA, Srivastava S, Mukherjee K. Central presynaptic terminals are enriched in ATP but the majority lack mitochondria. Plos One. 10: e0125185. PMID 25928229 DOI: 10.1371/Journal.Pone.0125185  0.398
2012 Srivastava S, Gonzalez Herrera KN, Proacccio V, Wallace DC, Haigis MC. Low level of MtDNA mutation promotes mitochondrial bioenergetics and oxidative metabolism via retrograde signaling Mitochondrion. 12: 553. DOI: 10.1016/J.Mito.2012.07.009  0.432
2009 Srivastava S, Diaz F, Iommarini L, Aure K, Lombes A, Moraes CT. PGC-1alpha/beta induced expression partially compensates for respiratory chain defects in cells from patients with mitochondrial disorders. Human Molecular Genetics. 18: 1805-12. PMID 19297390 DOI: 10.1093/Hmg/Ddp093  0.679
2009 Srivastava S, Moraes CT. Cellular adaptations to oxidative phosphorylation defects in cancer Cellular Respiration and Carcinogenesis. 55-72. DOI: 10.1007/978-1-59745-435-3_5  0.601
2007 Srivastava S, Barrett JN, Moraes CT. PGC-1alpha/beta upregulation is associated with improved oxidative phosphorylation in cells harboring nonsense mtDNA mutations. Human Molecular Genetics. 16: 993-1005. PMID 17341490 DOI: 10.1093/Hmg/Ddm045  0.61
2006 Srivastava S, Moraes CT. Nuclear adaptation mechanism associated with PGC-1α/β upregulation preserves oxidative phosphorylation in a human colorectal cancer cell line harboring nonsense mtDNA mutations Mitochondrion. 6: 271. DOI: 10.1016/J.Mito.2006.08.020  0.532
2005 Srivastava S, Moraes CT. Double-strand breaks of mouse muscle mtDNA promote large deletions similar to multiple mtDNA deletions in humans. Human Molecular Genetics. 14: 893-902. PMID 15703189 DOI: 10.1093/Hmg/Ddi082  0.639
2002 Moraes CT, Srivastava S, Kirkinezos I, Oca-Cossio J, van Waveren C, Woischnick M, Diaz F. Mitochondrial DNA structure and function. International Review of Neurobiology. 53: 3-23. PMID 12512335 DOI: 10.1016/S0074-7742(02)53002-6  0.519
2001 Srivastava S, Moraes CT. Manipulating mitochondrial DNA heteroplasmy by a mitochondrially targeted restriction endonuclease. Human Molecular Genetics. 10: 3093-9. PMID 11751691 DOI: 10.1093/Hmg/10.26.3093  0.685
Show low-probability matches.