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10.1007/s10577-018-9573-4 http://scihub22266oqcxt.onion/10.1007/s10577-018-9573-4 C5857278!5857278!29460123     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Chromosome+Res 2018 ; 26 (1): 93-111 Nephropedia Template TP {{tp|p=29460123|t=2018. Warning SINEs: Alu elements, evolution of the human brain, and the spectrum of neurological disease |pdf=|usr=}}{{29460123}} gab.com Text Warning SINEs: Alu elements, evolution of the human brain, and the spectrum of neurological disease JO: Chromosome Res http://www.kidney.de/pget.php?&tw=1&pmid=29460123 #FOAvip Alu elements are a highly successful family of primate-specific retrotransposons that have fundamentally shaped primate evolution, including the evolution of our own species. Alus play critical roles in the formation of neurological networks and the epigenetic regulation of biochemical processes throughout the central nervous system (CNS), and thus are hypothesized to have contributed to the origin of human cognition. Despite the benefits that Alus provide, deleterious Alu activity is associated with a number of neurological and neurodegenerative disorders. In particular, neurological networks are potentially vulnerable to the epigenetic dysregulation of Alu elements operating across the suite of nuclear-encoded mitochondrial genes that are critical for both mitochondrial and CNS function. Here, we highlight the beneficial neurological aspects of Alu elements as well as their potential to cause disease by disrupting key cellular processes across the CNS. We identify at least 37 neurological and neurodegenerative disorders wherein deleterious Alu activity has been implicated as a contributing factor for the manifestation of disease, and for many of these disorders, this activity is operating on genes that are essential for proper mitochondrial function. We conclude that the epigenetic dysregulation of Alu elements can ultimately disrupt mitochondrial homeostasis within the CNS. This mechanism is a plausible source for the incipient neuronal stress that is consistently observed across a spectrum of sporadic neurological and neurodegenerative disorders.Electronic supplementary material: The online version of this article (10.1007/s10577-018-9573-4) contains supplementary material, which is available to authorized users. Twit Text FOAVip Warning SINEs: Alu elements, evolution of the human brain, and the spectrum of neurological disease ????Chromosome Res http://www.kidney.de/pget.php?&tw=1&pmid=29460123 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=29460123 #FOAvip English Wikipedia <ref>{{Cite pmid|29460123}}</ref> Warning SINEs: Alu elements, evolution of the human brain, and the spectrum of neurological disease #MMPMID29460123 Larsen PA; Hunnicutt KE; Larsen RJ; Yoder AD; Saunders AM Chromosome Res 2018[]; 26 (1): 93-111 PMID29460123show ga Alu elements are a highly successful family of primate-specific retrotransposons that have fundamentally shaped primate evolution, including the evolution of our own species. Alus play critical roles in the formation of neurological networks and the epigenetic regulation of biochemical processes throughout the central nervous system (CNS), and thus are hypothesized to have contributed to the origin of human cognition. Despite the benefits that Alus provide, deleterious Alu activity is associated with a number of neurological and neurodegenerative disorders. In particular, neurological networks are potentially vulnerable to the epigenetic dysregulation of Alu elements operating across the suite of nuclear-encoded mitochondrial genes that are critical for both mitochondrial and CNS function. Here, we highlight the beneficial neurological aspects of Alu elements as well as their potential to cause disease by disrupting key cellular processes across the CNS. We identify at least 37 neurological and neurodegenerative disorders wherein deleterious Alu activity has been implicated as a contributing factor for the manifestation of disease, and for many of these disorders, this activity is operating on genes that are essential for proper mitochondrial function. We conclude that the epigenetic dysregulation of Alu elements can ultimately disrupt mitochondrial homeostasis within the CNS. This mechanism is a plausible source for the incipient neuronal stress that is consistently observed across a spectrum of sporadic neurological and neurodegenerative disorders.Electronic supplementary material: The online version of this article (10.1007/s10577-018-9573-4) contains supplementary material, which is available to authorized users. äWarning SINEs: Alu elements, evolution of the human brain, and the spe(epmc).pdf DeepDyve Pubget Overpricing