| scholarly article | Q13442814 |
| P2093 | author name string | U. Müller | |
| C. Weissmann | |||
| Z. W. Li | |||
| D. P. Wolfer | |||
| H. P. Lipp | |||
| F. Magara | |||
| M. Stagljar | |||
| P2860 | cites work | Phenotype of mice lacking functional Deleted in colorectal cancer (Dcc) gene | Q28236533 |
| 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 | ||
| Sek4 and Nuk receptors cooperate in guidance of commissural axons and in palate formation | Q28588287 | ||
| beta-Amyloid precursor protein-deficient mice show reactive gliosis and decreased locomotor activity | Q28593175 | ||
| Netrin-1 is required for commissural axon guidance in the developing vertebrate nervous system | Q29616040 | ||
| A rapid, sensitive histochemical stain for myelin in frozen brain sections | Q30441336 | ||
| Gene-targeting studies of mammalian behavior: is it the mutation or the background genotype? | Q34390023 | ||
| MARCKS deficiency in mice leads to abnormal brain development and perinatal death | Q34666214 | ||
| Impaired fetal T cell development and perinatal lethality in mice lacking the cAMP response element binding protein | Q36475369 | ||
| Generation of mice with a 200-kb amyloid precursor protein gene deletion by Cre recombinase-mediated site-specific recombination in embryonic stem cells | Q37576797 | ||
| Neural tube defects and abnormal brain development in F52-deficient mice | Q37710371 | ||
| Genetic and developmental defects of the mouse corpus callosum | Q38688588 | ||
| Targeting learning | Q40388127 | ||
| Genetic variation among 129 substrains and its importance for targeted mutagenesis in mice | Q40896736 | ||
| Tests of genetic allelism between four inbred mouse strains with absent corpus callosum | Q41149213 | ||
| Heritable aspects of anomalous myelinated fibre tracts in the forebrain of the laboratory mouse | Q41513542 | ||
| Immunocytochemical demonstration of early appearing astroglial structures that form boundaries and pathways along axon tracts in the fetal brain | Q42510213 | ||
| Deficiency of the corpus callosum: incomplete penetrance and substrain differentiation in BALB/c mice | Q43966857 | ||
| The efficiency of systematic sampling in stereology and its prediction. | Q44974729 | ||
| Mutation of the Emx-1 homeobox gene disrupts the corpus callosum | Q46717388 | ||
| Sex and species differences in mouse and rat forebrain commissures depend on the method of adjusting for brain size | Q47273280 | ||
| Genetically modified mice and cognition | Q47946059 | ||
| The fibers which course within the Probst's longitudinal bundle seen in the brain of a congenitally acallosal mouse: a study with the horseradish peroxidase technique | Q48111476 | ||
| Hypersensitivity to seizures in beta-amyloid precursor protein deficient mice | Q48236519 | ||
| Prenatal formation of the normal mouse corpus callosum: a quantitative study with carbocyanine dyes | Q48436769 | ||
| Deficient corpus callosum in hybrids between ddN and three other abnormal mouse strains | Q48527152 | ||
| Mice in utero while their mother is lactating suffer higher frequency of deficient corpus callosum | Q48876153 | ||
| Axonal guidance during development of the great cerebral commissures: descriptive and experimental studies, in vivo, on the role of preformed glial pathways | Q48902697 | ||
| Deficiency of corpus callosum varies with strain and supplier of the mice | Q48944341 | ||
| Retarded formation of the hippocampal commissure in embryos from mouse strains lacking a corpus callosum. | Q52197394 | ||
| Mutant Mice and Neuroscience: Recommendations Concerning Genetic Background | Q57843811 | ||
| Inheritance of retarded forebrain commissure development in fetal mice: results from classical crosses and recombinant inbred strains | Q69955401 | ||
| Mode of inheritance of deficient corpus callosum in mice | Q70430466 | ||
| Cortical axon trajectories and growth cone morphologies in fetuses of acallosal mouse strains | Q71599577 | ||
| A new hybrid mouse model for agenesis of the corpus callosum | Q72495385 | ||
| P433 | issue | 8 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | brain | Q1073 |
| Amyloid beta (A4) precursor protein | Q14865884 | ||
| P304 | page(s) | 4656–4661 | |
| P577 | publication date | 1999-04-13 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Genetic background changes the pattern of forebrain commissure defects in transgenic mice underexpressing the beta-amyloid-precursor protein | |
| P478 | volume | 96 |
| Q52721455 | 7-Deoxy-trans-dihydronarciclasine Reduces β-Amyloid and Ameliorates Memory Impairment in a Transgenic Model of Alzheimer's Disease. |
| Q48156331 | A behavioral and neuroanatomical assessment of an inbred substrain of 129 mice with behavioral comparisons to C57BL/6J mice |
| Q42850436 | A novel locus on proximal chromosome 18 associated with agenesis of the corpus callosum in mice |
| Q57092702 | APP involvement in retinogenesis of mice |
| Q48444707 | Acute function of secreted amyloid precursor protein fragment APPsα in synaptic plasticity. |
| Q35956633 | Agenesis of the Corpus Callosum Due to Defective Glial Wedge Formation in Lhx2 Mutant Mice. |
| Q36005686 | All in the Family: How the APPs Regulate Neurogenesis |
| Q42071665 | Altered sensitivity to excitotoxic cell death and glutamate receptor expression between two commonly studied mouse strains |
| Q30499574 | Alzheimer disease models and human neuropathology: similarities and differences |
| Q37348863 | Amyloid precursor protein maintains constitutive and adaptive plasticity of dendritic spines in adult brain by regulating D-serine homeostasis |
| Q36216011 | Amyloid precursor protein regulates netrin-1-mediated commissural axon outgrowth |
| Q37773826 | Amyloid-modifying therapies for Alzheimer's disease: therapeutic progress and its implications |
| Q41073036 | Amyloid-precursor Like Proteins APLP1 and APLP2 Are Dispensable for Normal Development of the Neonatal Respiratory Network |
| Q48445122 | Axonal pathfinding mechanisms at the cortical midline and in the development of the corpus callosum |
| Q44936841 | Behavioral phenotype of pre-proenkephalin-deficient mice on diverse congenic backgrounds |
| Q43780934 | Behavioural testing of standard inbred and 5HT(1B) knockout mice: implications of absent corpus callosum |
| Q37869935 | Biology and pathophysiology of the amyloid precursor protein |
| Q30492796 | COL25A1 triggers and promotes Alzheimer's disease-like pathology in vivo |
| 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 |
| Q34420664 | Conditioned taste aversion as a learning and memory paradigm. |
| Q28504488 | Cortical dysplasia resembling human type 2 lissencephaly in mice lacking all three APP family members |
| Q34345763 | Daily scheduled high fat meals moderately entrain behavioral anticipatory activity, body temperature, and hypothalamic c-Fos activation. |
| Q35893533 | Deficits in axonal transport in hippocampal-based circuitry and the visual pathway in APP knock-out animals witnessed by manganese enhanced MRI. |
| Q34331096 | Dentate gyrus volume is reduced before onset of plaque formation in PDAPP mice: a magnetic resonance microscopy and stereologic analysis |
| Q30433584 | Differences in memory development among C57BL/6NCrl, 129S2/SvPasCrl, and FVB/NCrl mice after delay and trace fear conditioning |
| Q46959740 | Disruption of axonal transport and neuronal viability by amyloid precursor protein mutations in Drosophila. |
| Q24673147 | Disruption of the murine nuclear factor I-A gene (Nfia) results in perinatal lethality, hydrocephalus, and agenesis of the corpus callosum |
| Q41210086 | Endogenous amyloid-β is necessary for hippocampal synaptic plasticity and memory |
| Q45221632 | Endoproteolytic cleavage of FE65 converts the adaptor protein to a potent suppressor of the sAPPalpha pathway in primates |
| Q48243692 | Enriched early experiences of mice underexpressing the beta-amyloid precursor protein restore spatial learning capabilities but not normal openfield behavior of adult animals |
| Q28506956 | Essential roles for the FE65 amyloid precursor protein-interacting proteins in brain development |
| Q38715222 | Expression of endogenous mouse APP modulates β-amyloid deposition in hAPP-transgenic mice |
| Q35237718 | Finding the most appropriate mouse model of juvenile CLN3 (Batten) disease for therapeutic studies: the importance of genetic background and gender |
| Q33862796 | Function, therapeutic potential and cell biology of BACE proteases: current status and future prospects |
| Q37935600 | Functions of the APP gene family in the nervous system: insights from mouse models |
| Q39324113 | GABAergic hyperinnervation of dentate granule cells in the Ts65Dn mouse model of down syndrome: Exploring the role of App. |
| Q48316010 | Generation of conditional null alleles for APP and APLP2. |
| Q28213654 | Growth-associated protein-43 is required for commissural axon guidance in the developing vertebrate nervous system |
| Q91635058 | Hebbian and Homeostatic Synaptic Plasticity-Do Alterations of One Reflect Enhancement of the Other? |
| Q36673429 | Hippocampal commissure defects in crosses of four inbred mouse strains with absent corpus callosum |
| Q27325718 | Hippocampal network oscillations in APP/APLP2-deficient mice |
| Q48537271 | Histomorphological Phenotyping of the Adult Mouse Brain |
| Q91152867 | In vivo Ca2+ imaging of astrocytic microdomains reveals a critical role of the amyloid precursor protein for mitochondria |
| Q26999922 | Insights into the physiological function of the β-amyloid precursor protein: beyond Alzheimer's disease |
| Q28592685 | Kinesin-mediated axonal transport of a membrane compartment containing beta-secretase and presenilin-1 requires APP |
| Q34134816 | Knockout mice: simple solutions to the problems of genetic background and flanking genes |
| Q51767457 | Locomotor differences in mice expressing wild-type human α-synuclein. |
| Q37026050 | Loss of presenilin function is associated with a selective gain of APP function. |
| Q33183067 | Measuring pain in the (knockout) mouse: big challenges in a small mammal |
| Q42495065 | Mice with combined gene knock-outs reveal essential and partially redundant functions of amyloid precursor protein family members. |
| Q44567921 | Netrin-DCC signaling regulates corpus callosum formation through attraction of pioneering axons and by modulating Slit2-mediated repulsion. |
| Q30503579 | Neuronal untranslated BC1 RNA: targeted gene elimination in mice. |
| Q39209681 | Not just amyloid: physiological functions of the amyloid precursor protein family |
| Q37987144 | Physiological functions of APP family proteins |
| Q92727301 | PlexinA1 is crucial for the midline crossing of callosal axons during corpus callosum development in BALB/cAJ mice |
| Q51653976 | Protein Misfolding in Prion and Prion-Like Diseases: Reconsidering a Required Role for Protein Loss-of-Function. |
| Q48633792 | Recombinant inbreeding in mice reveals thresholds in embryonic corpus callosum development |
| Q47593384 | Regulation of Neurotransmitter Release by Amyloid Precursor Protein Through Synapsin Phosphorylation |
| Q33930287 | Roles of the NFI/CTF gene family in transcription and development |
| Q38706815 | Similar reliability and equivalent performance of female and male mice in the open field and water-maze place navigation task |
| Q42660048 | Standardizing tests of mouse behavior: reasons, recommendations, and reality |
| Q40340003 | Suppression of cyclin-dependent kinase 5 activation by amyloid precursor protein: a novel excitoprotective mechanism involving modulation of tau phosphorylation. |
| Q48337652 | Survey of 21 inbred mouse strains in two laboratories reveals that BTBR T/+ tf/tf has severely reduced hippocampal commissure and absent corpus callosum |
| Q33650414 | Ten years of gene targeting: targeted mouse mutants, from vector design to phenotype analysis |
| Q40874327 | The APP Intracellular Domain Is Required for Normal Synaptic Morphology, Synaptic Plasticity, and Hippocampus-Dependent Behavior. |
| Q21090025 | The Alzheimer's disease-associated amyloid beta-protein is an antimicrobial peptide |
| Q41170054 | The Amyloid Precursor Protein Is a Conserved Receptor for Slit to Mediate Axon Guidance. |
| Q28205749 | The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum |
| Q38766310 | The Role of APP in Structural Spine Plasticity |
| Q37942500 | The gene or not the gene--that is the question: understanding the genetically engineered mouse phenotype |
| Q43988916 | The impact of cholesterol, DHA, and sphingolipids on Alzheimer's disease |
| Q34708261 | The intracellular threonine of amyloid precursor protein that is essential for docking of Pin1 is dispensable for developmental function. |
| Q39414505 | The physiological role of the amyloid precursor protein as an adhesion molecule in the developing nervous system |
| Q36358021 | The protection of acetylcholinesterase inhibitor on β-amyloid-induced the injury of neurite outgrowth via regulating axon guidance related genes expression in neuronal cells |
| Q40106778 | The secreted beta-amyloid precursor protein ectodomain APPs alpha is sufficient to rescue the anatomical, behavioral, and electrophysiological abnormalities of APP-deficient mice. |
| Q47073605 | The zebrafish amyloid precursor protein-b is required for motor neuron guidance and synapse formation |
| Q50244311 | Transcriptomic Analysis of Drosophila Mushroom Body Neurons Lacking Amyloid-β Precursor-Like Protein Activity |
| Q40142134 | Transcriptomic profile analysis of mouse neural tube development by RNA-Seq. |
| Q30390611 | Truncating mutations in APP cause a distinct neurological phenotype. |
| Q37515518 | Understanding the molecular basis of Alzheimer's disease using a Caenorhabditis elegans model system |
| Q52124270 | Wheel running behavior is impaired by both surgical section and genetic absence of the mouse corpus callosum. |
Search more.