| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/DVG.20601 |
| P8608 | Fatcat ID | release_wm6dxzu7erco3ckaehurj4xp7a |
| P698 | PubMed publication ID | 20140888 |
| P2093 | author name string | Mikhail A Filippov | |
| Meike Hick | |||
| Ulrike C Müller | |||
| Jakob-Andreas Tschäpe | |||
| Jan-Philipp Mallm | |||
| P2860 | cites work | Cortical dysplasia resembling human type 2 lissencephaly in mice lacking all three APP family members | Q28504488 |
| Copper levels are increased in the cerebral cortex and liver of APP and APLP2 knockout mice | Q28505777 | ||
| Age-related cognitive deficits, impaired long-term potentiation and reduction in synaptic marker density in mice lacking the beta-amyloid precursor protein | Q28513133 | ||
| Neurobehavioral development, adult openfield exploration and swimming navigation learning in mice with a modified beta-amyloid precursor protein gene | Q28513269 | ||
| Behavioral and anatomical deficits in mice homozygous for a modified beta-amyloid precursor protein gene | Q28586800 | ||
| Genetic background changes the pattern of forebrain commissure defects in transgenic mice underexpressing the beta-amyloid-precursor protein | Q28587017 | ||
| Defective neuromuscular synapses in mice lacking amyloid precursor protein (APP) and APP-Like protein 2 | Q28589908 | ||
| Generation of APLP2 KO mice and early postnatal lethality in APLP2/APP double KO mice | Q28590025 | ||
| Mechanisms contributing to the deficits in hippocampal synaptic plasticity in mice lacking amyloid precursor protein | Q28592893 | ||
| beta-Amyloid precursor protein-deficient mice show reactive gliosis and decreased locomotor activity | Q28593175 | ||
| A cre-transgenic mouse strain for the ubiquitous deletion of loxP-flanked gene segments including deletion in germ cells | Q29614542 | ||
| Amyloid precursor protein trafficking, processing, and function | Q29617429 | ||
| Embryonic stem cell-derived neurons as a cellular system to study gene function: lack of amyloid precursor proteins APP and APLP2 leads to defective synaptic transmission | Q34785066 | ||
| Cell biology of protein misfolding: the examples of Alzheimer's and Parkinson's diseases | Q35934211 | ||
| The functions of mammalian amyloid precursor protein and related amyloid precursor-like proteins | Q36626425 | ||
| Bridging physiology and pathology in AD. | Q37518549 | ||
| Generation of mice with a 200-kb amyloid precursor protein gene deletion by Cre recombinase-mediated site-specific recombination in embryonic stem cells | Q37576797 | ||
| The secreted beta-amyloid precursor protein ectodomain APPs alpha is sufficient to rescue the anatomical, behavioral, and electrophysiological abnormalities of APP-deficient mice. | Q40106778 | ||
| Mice with combined gene knock-outs reveal essential and partially redundant functions of amyloid precursor protein family members. | Q42495065 | ||
| Distribution of GABAA receptor subunit mRNAs in rat lumbar spinal cord | Q43968835 | ||
| Activity requires soluble amyloid precursor protein alpha to promote neurite outgrowth in neural stem cell-derived neurons via activation of the MAPK pathway. | Q46418672 | ||
| Regulation of cholesterol and sphingomyelin metabolism by amyloid-beta and presenilin | Q46755710 | ||
| Expression in mouse embryos and in adult mouse brain of three members of the amyloid precursor protein family, of the alpha-2-macroglobulin receptor/low density lipoprotein receptor-related protein and of its ligands apolipoprotein E, lipoprotein li | Q47357147 | ||
| Hypersensitivity to seizures in beta-amyloid precursor protein deficient mice | Q48236519 | ||
| P433 | issue | 3 | |
| P304 | page(s) | 200-206 | |
| P577 | publication date | 2010-03-01 | |
| P1433 | published in | Genesis | Q5532784 |
| P1476 | title | Generation of conditional null alleles for APP and APLP2. | |
| P478 | volume | 48 |
| Q37902514 | APP physiological and pathophysiological functions: insights from animal models. |
| Q36005686 | All in the Family: How the APPs Regulate Neurogenesis |
| Q33622388 | Comparative analysis of single and combined APP/APLP knockouts reveals reduced spine density in APP-KO mice that is prevented by APPsα expression |
| Q33854917 | Comparative transcriptome profiling of amyloid precursor protein family members in the adult cortex |
| Q48186706 | Dysregulation of hypoxia-inducible factor by presenilin/γ-secretase loss-of-function mutations. |
| Q48268002 | Embryonic mosaic deletion of APP results in displaced Reelin-expressing cells in the cerebral cortex |
| Q82467947 | Functional consequences of the lack of amyloid precursor protein in the mouse dentate gyrus in vivo |
| Q37935600 | Functions of the APP gene family in the nervous system: insights from mouse models |
| Q28277658 | Genome-wide nucleosome positioning during embryonic stem cell development |
| Q30666181 | Heterochromatin Protein 1β (HP1β) has distinct functions and distinct nuclear distribution in pluripotent versus differentiated cells |
| Q39134078 | Neurodegenerative Disease Transmission and Transgenesis in Mice. |
| Q37987144 | Physiological functions of APP family proteins |
| Q59137316 | Presenilin-mediated cleavage of APP regulates synaptotagmin-7 and presynaptic plasticity |
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