Results 11 to 20 of about 428,092 (271)

Knockout Corner: Knockout mice for monoamine oxidase A [PDF]

open access: yesThe International Journal of Neuropsychopharmacology, 1999
A line of transgenic mice was isolated in which transgene integration had caused a deletion in the gene encoding monoamine oxidase A, an enzyme that degrades serotonin and norepinephrine. This has provided an animal model of MAOA deficiency in humans, a condition characterized by borderline mental retardation and impulsive aggression.
Isabelle Seif, Edward De Maeyer
openaire   +3 more sources

Altered reward circuitry in the norepinephrine transporter knockout mouse. [PDF]

open access: yesPLoS ONE, 2013
Synaptic levels of the monoamine neurotransmitters dopamine, serotonin, and norepinephrine are modulated by their respective plasma membrane transporters, albeit with a few exceptions.
Joseph J Gallagher   +5 more
doaj   +1 more source

The Endogenous Alterations of the Gut Microbiota and Feces Metabolites Alleviate Oxidative Damage in the Brain of LanCL1 Knockout Mice

open access: yesFrontiers in Microbiology, 2020
Altered composition of the gut microbiota has been observed in many neurodegenerative diseases. LanCL1 has been proven to protect neurons and reduce oxidative stress.
Fangxing Zhang   +30 more
doaj   +1 more source

Direct Comparison of a Natural Loss-Of-Function Single Nucleotide Polymorphism with a Targeted Deletion in the Ncf1 Gene Reveals Different Phenotypes. [PDF]

open access: yesPLoS ONE, 2015
The genetic targeting of mouse models has given insight into complex processes. However, phenotypes of genetically targeted mice are susceptible to artifacts due to gene manipulation, which may lead to misinterpretation of the observations.
Outi Sareila   +4 more
doaj   +1 more source

Erythropoiesis and Blood Pressure Are Regulated via AT1 Receptor by Distinctive Pathways. [PDF]

open access: yesPLoS ONE, 2015
The renin-angiotensin system (RAS) plays a central role in blood pressure regulation. Although clinical and experimental studies have suggested that inhibition of RAS is associated with progression of anemia, little evidence is available to support this ...
Hideki Kato   +8 more
doaj   +1 more source

NoxO1 Knockout Promotes Longevity in Mice [PDF]

open access: yesAntioxidants, 2020
According to the free radical theory of aging, reactive oxygen species (ROS) have been proposed to be a major cause of aging for a long time. Meanwhile, it became clear that ROS have diverse functions in a healthy organism. They act as second messengers, and as transient inhibitors of phosphatases and others.
Tim Schader   +5 more
openaire   +6 more sources

Ppp2ca knockout in mice spermatogenesis [PDF]

open access: yesREPRODUCTION, 2015
Protein phosphatase 2A (PP2A) is a ubiquitous serine/threonine phosphatase involved in meiosis, mitosis, sperm capacitation, and apoptosis. Abberant activity of PP2A has been associated with a number of diseases. The homolog PPP2CA and PPP2CB can each function as the phosphatase catalytic subunit generally referred to as PP2AC.
Jianmin Li   +4 more
openaire   +2 more sources

Functional Genomics for the Identification of Modulators of Platelet-Dependent Thrombus Formation

open access: yesTH Open, 2018
Despite the absence of the genome in platelets, transcription profiling provides important insights into platelet function and can help clarify abnormalities in platelet disorders.
Elien Vermeersch   +6 more
doaj   +1 more source

Remyelination in experimentally demyelinated connexin 32 KnockOut mice Remielinização em camundongos KnockOut para conexina 32 desmielinizados experimentalmente

open access: yesArquivos de Neuro-Psiquiatria, 2009
The aim of this study was to evaluate the role of connexin 32 (Cx 32) during remyelination of the peripheral nervous system, through a local injection of either 0,1% ethidium bromide solution or saline in the sciatic nerve of Cx 32 knockout mice ...
Adriano Tony Ramos   +10 more
doaj   +1 more source

Evolutionarily conserved human targets of adenosine to inosine RNA editing [PDF]

open access: yesNucleic Acids Research, Vol. 33, 1162-1168 (2005), 2005
A-to-I RNA editing by ADARs is a post-transcriptional mechanism for expanding the proteomic repertoire. Genetic recoding by editing was so far observed for only a few mammalian RNAs that are predominantly expressed in nervous tissues. However, as these editing targets fail to explain the broad and severe phenotypes of ADAR1 knockout mice, additional ...
arxiv   +1 more source

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