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Mahtab Tavasoli
Mahtab Tavasoli
postdoctoral fellow at Dalhousie University
在 dal.ca 的电子邮件经过验证
标题
引用次数
引用次数
年份
Post‐training intrahippocampal infusion of nicotine prevents spatial memory retention deficits induced by the cyclo‐oxygenase‐2‐specific inhibitor celecoxib in rats
M Sharifzadeh, M Tavasoli, N Naghdi, A Ghanbari, M Amini, A Roghani
Journal of neurochemistry 95 (4), 1078-1090, 2005
602005
A time course analysis of cyclooxygenase-2 suggests a role in spatial memory retrieval in rats
M Sharifzadeh, M Tavasoli, M Soodi, S Mohammadi-Eraghi, ...
Neuroscience research 54 (3), 171-179, 2006
382006
Inflammation alters angiotensin converting enzymes (ACE and ACE-2) balance in rat heart
S Hanafy, M Tavasoli, F Jamali
Inflammation 34, 609-613, 2011
362011
Genetic diseases of the Kennedy pathways for membrane synthesis
M Tavasoli, S Lahire, T Reid, M Brodovsky, CR McMaster
Journal of Biological Chemistry 295 (51), 17877-17886, 2020
342020
Both CLIC4 and CLIC5A activate ERM proteins in glomerular endothelium
M Tavasoli, A Al-Momany, X Wang, L Li, JC Edwards, BJ Ballermann
American Journal of Physiology-Renal Physiology 311 (5), F945-F957, 2016
232016
The chloride intracellular channel 5A stimulates podocyte Rac1, protecting against hypertension-induced glomerular injury
M Tavasoli, L Li, A Al-Momany, LF Zhu, BA Adam, Z Wang, BJ Ballermann
Kidney international 89 (4), 833-847, 2016
232016
Compact and automated eDNA sampler for in situ monitoring of marine environments
A Hendricks, CM Mackie, E Luy, C Sonnichsen, J Smith, I Grundke, ...
Scientific Reports 13 (1), 5210, 2023
162023
Mechanism of action and therapeutic route for a muscular dystrophy caused by a genetic defect in lipid metabolism
M Tavasoli, S Lahire, S Sokolenko, R Novorolsky, SA Reid, A Lefsay, ...
Nature Communications 13 (1), 1559, 2022
122022
Soluble fms-like tyrosine kinase 1 localization in renal biopsies of CKD
ZK Zsengellér, A Lo, M Tavasoli, E Pernicone, SA Karumanchi, S Rosen
Kidney International Reports 4 (12), 1735-1741, 2019
92019
Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephaly
C Klöckner, JP Fernández-Murray, M Tavasoli, H Sticht, ...
Brain 145 (6), 1916-1923, 2022
62022
A mouse model of inherited choline kinase β-deficiency presents with specific cardiac abnormalities and a predisposition to arrhythmia
M Tavasoli, T Feridooni, H Feridooni, S Sokolenko, A Mishra, A Lefsay, ...
Journal of Biological Chemistry 298 (3), 2022
52022
A miniaturized and automated eDNA sampler: Application to a marine environment
A Hendricks, C Mackie, E Luy, C Sonnichsen, L Miller, M Wright, ...
OCEANS 2022, Hampton Roads, 1-10, 2022
42022
ErbB2/Her2-dependent downregulation of a cell death-promoting protein BLNK in breast cancer cells is required for 3D breast tumor growth
X Liu, S Chipurupalli, P Jiang, M Tavasoli, BH Yoo, M McPhee, ...
Cell Death & Disease 13 (8), 687, 2022
42022
Development and analytical validation of a novel bioavailable 25-hydroxyvitamin D assay
AH Berg, M Tavasoli, AS Lo, SAM Burnett-Bowie, I Bhan, SA Karumanchi, ...
Plos one 16 (7), e0254158, 2021
42021
Atrial natriuretic peptide signaling co-regulates lipid metabolism and ventricular conduction system gene expression in the embryonic heart
A Mishra, M Tavasoli, S Sokolenko, CR McMaster, KBS Pasumarthi
Iscience 27 (1), 2024
12024
The leucine zipper domain of the transcriptional repressor Opi1 underlies a signal transduction mechanism regulating lipid synthesis
JP Fernández-Murray, M Tavasoli, J Williams, CR McMaster
Journal of Biological Chemistry 299 (12), 2023
12023
Choline kinase inhibition promotes ER-phagy
M Tavasoli, S Chipurupalli, CR McMaster
Journal of Lipid Research 63 (8), 2022
12022
Defects in integrin complex formation promote CHKB-mediated muscular dystrophy
M Tavasoli, CR McMaster
Life Science Alliance 7 (8), 2024
2024
Microfluidic chip, systems, and methods for capturing of environmental DNA
JJ Creelman, EA Luy, GCH Beland, SC Morgan, MEJ LaRoche, ...
US Patent 11,964,278, 2024
2024
Heterozygous and homozygous Chkb (Choline kinase beta) deficiencies are associated with cardiomyopathy: Insights from a mouse model
M Tavasoli, T Feridooni, H Feridooni, S Sokolenko, A Mishra, A Lefsay, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 27-27, 2022
2022
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