A novel genetic locus modulates infarct volume independently of the extent of collateral circulation.
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Natural genetic variation of integrin alpha L (Itgal) modulates ischemic brain injury in strokeCollaterals: Implications in cerebral ischemic diseases and therapeutic interventionsGenetic Dissection of Cardiac Remodeling in an Isoproterenol-Induced Heart Failure Mouse Model.Natural allelic variation of the IL-21 receptor modulates ischemic stroke infarct volume.Congenic fine-mapping identifies a major causal locus for variation in the native collateral circulation and ischemic injury in brain and lower extremity.Animal models of ischemic stroke and their application in clinical researchRobust effects of genetic background on responses to subarachnoid hemorrhage in mice.Embracing Biological and Methodological Variance in a New Approach to Pre-Clinical Stroke Testing.Electro-acupuncture at Neiguan pretreatment alters genome-wide gene expressions and protects rat myocardium against ischemia-reperfusion.Left-Biased Spermatogenic Failure in 129/SvJ Dnd1Ter/+ Mice Correlates with Differences in Vascular Architecture, Oxygen Availability, and Metabolites.
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A novel genetic locus modulates infarct volume independently of the extent of collateral circulation.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 25 June 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
A novel genetic locus modulate ...... ent of collateral circulation.
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A novel genetic locus modulate ...... ent of collateral circulation.
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type
label
A novel genetic locus modulate ...... ent of collateral circulation.
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A novel genetic locus modulate ...... ent of collateral circulation.
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prefLabel
A novel genetic locus modulate ...... ent of collateral circulation.
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A novel genetic locus modulate ...... ent of collateral circulation.
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P2093
P2860
P1476
A novel genetic locus modulate ...... ent of collateral circulation.
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Douglas A Marchuk
Pei-Lun Chu
Sehoon Keum
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P304
P356
10.1152/PHYSIOLGENOMICS.00063.2013
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2013-06-25T00:00:00Z