| scholarly article | Q13442814 |
| P356 | DOI | 10.1038/NG0995-71 |
| P698 | PubMed publication ID | 7550318 |
| P2093 | author name string | Buzsaki G | |
| Toth M | |||
| Grimsby J | |||
| Donovan GP | |||
| P2860 | cites work | The pogo transposable element family of Drosophila melanogaster | Q42598922 |
| Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region of chromosome 6. | Q43866407 | ||
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| Localization of thyrotropin-releasing hormone receptor and thyrotroph embryonic factor on mouse Chromosome 15 | Q60719569 | ||
| Linkage studies in progressive myoclonus epilepsy: Unverricht-Lundborg and Lafora's diseases | Q68228817 | ||
| The chromosome 6p epilepsy locus: exploring mode of inheritance and heterogeneity through linkage analysis | Q70733535 | ||
| A nonsense mutation in the α4 subunit of the nicotinic acetylcholine receptor (CHRNA4) cosegregates with 20q-linked benign neonatal familial convulsions (EBNI) | Q73497387 | ||
| Localization of a gene for partial epilepsy to chromosome 10q | Q24646776 | ||
| Basic local alignment search tool | Q25938991 | ||
| Characterisation of PDC2, a gene necessary for high level expression of pyruvate decarboxylase structural genes in Saccharomyces cerevisiae | Q27933229 | ||
| Eating disorder and epilepsy in mice lacking 5-HT2c serotonin receptors | Q28119146 | ||
| Modification of seizure activity by electrical stimulation. II. Motor seizure | Q28236678 | ||
| Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2 | Q28295745 | ||
| A single gene error of noradrenergic axon growth synchronizes central neurones | Q28594007 | ||
| Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation | Q34152888 | ||
| Molecular cloning of cDNA for CENP-B, the major human centromere autoantigen | Q34393316 | ||
| Conversion of the lac repressor into an allosterically regulated transcriptional activator for mammalian cells | Q36714470 | ||
| Maps from two interspecific backcross DNA panels available as a community genetic mapping resource | Q36738873 | ||
| Cellular and molecular basis of epilepsy. | Q40764804 | ||
| Differentiation is induced in three-dimensional cultures of brain cells immortalized by the LAP mammalian regulatory system | Q41312412 | ||
| A human centromere protein, CENP-B, has a DNA binding domain containing four potential alpha helices at the NH2 terminus, which is separable from dimerizing activity | Q41954244 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 71-75 | |
| P577 | publication date | 1995-09-01 | |
| P1433 | published in | Nature Genetics | Q976454 |
| P1476 | title | Epileptic seizures caused by inactivation of a novel gene, jerky, related to centromere binding protein-B in transgenic mice | |
| P478 | volume | 11 |
| Q28756289 | A centromere DNA-binding protein from fission yeast affects chromosome segregation and has homology to human CENP-B |
| Q38360406 | A new, expressed multigene family containing a hot spot for insertion of retroelements is associated with polymorphic subtelomeric regions of Trypanosoma brucei |
| Q34499463 | CELF4 regulates translation and local abundance of a vast set of mRNAs, including genes associated with regulation of synaptic function |
| Q52544632 | CENP-B is not critical for meiotic chromosome segregation in male mice. |
| Q34387487 | Childhood absence epilepsy with tonic-clonic seizures and electroencephalogram 3-4-Hz spike and multispike-slow wave complexes: linkage to chromosome 8q24. |
| Q24319948 | Cloning, mapping, and tissue distribution of a human homologue of the mouse jerky gene product |
| Q33293169 | Complex seizure disorder caused by Brunol4 deficiency in mice |
| Q28268659 | Computational neurogenetic modelling: a pathway to new discoveries in genetic neuroscience |
| Q34214621 | Confirmation of multiple seizure susceptibility QTLs on chromosome 15 in C57BL/6J and DBA/2J inbred mice |
| Q28755338 | Convergent domestication of pogo-like transposases into centromere-binding proteins in fission yeast and mammals |
| Q27636485 | Crystal structure of the CENP-B protein-DNA complex: the DNA-binding domains of CENP-B induce kinks in the CENP-B box DNA. |
| Q27642262 | Crystal structure of the human centromere protein B (CENP-B) dimerization domain at 1.65-A resolution |
| Q28263286 | Deficiency in protein L-isoaspartyl methyltransferase results in a fatal progressive epilepsy |
| Q93132175 | Disturbed Prefrontal Cortex Activity in the Absence of Schizophrenia-Like Behavioral Dysfunction in Arc/Arg3.1 Deficient Mice |
| Q31802280 | E1 mice epilepsy shows genetic polymorphism for S-Adenosyl-L-homocysteine hydrolase |
| Q41720371 | Epilepsy genetics: an abundance of riches for biologists. |
| Q28508321 | Etiology of a genetically complex seizure disorder in Celf4 mutant mice |
| Q41365396 | Examining non-LTR retrotransposons in the context of the evolving primate brain |
| Q48098135 | Exclusion of the JRK/JH8 gene as a candidate for human childhood absence epilepsy mapped on 8q24. |
| Q33962852 | Fission yeast homologs of human CENP-B have redundant functions affecting cell growth and chromosome segregation |
| Q28359860 | Functional redundancies, distinct localizations and interactions among three fission yeast homologs of centromere protein-B |
| Q44283571 | Hippocampal network patterns of activity in the mouse. |
| Q34453729 | Human centromere protein B induces translational positioning of nucleosomes on alpha-satellite sequences |
| Q28750162 | Inherent promoter bidirectionality facilitates maintenance of sequence integrity and transcription of parasitic DNA in mammalian genomes |
| Q29615764 | Interspersed repeats and other mementos of transposable elements in mammalian genomes |
| Q38678867 | Intestinal stem cell overproliferation resulting from inactivation of the APC tumor suppressor requires the transcription cofactors Earthbound and Erect wing. |
| Q28592221 | Jerky, a protein deficient in a mouse epilepsy model, is associated with translationally inactive mRNA in neurons |
| Q24296922 | Jerky/Earthbound facilitates cell-specific Wnt/Wingless signalling by modulating β-catenin-TCF activity |
| Q42643929 | Members of the pogo superfamily of DNA-mediated transposons in the human genome |
| Q73473447 | Mutation analysis of the inwardly rectifying K(+) channels KCNJ6 (GIRK2) and KCNJ3 (GIRK1) in juvenile myoclonic epilepsy |
| Q24548219 | PCNA binding proteins in Drosophila melanogaster : the analysis of a conserved PCNA binding domain |
| Q34192362 | Perspective: transposable elements, parasitic DNA, and genome evolution |
| Q42655007 | Polymorphism analysis of JRK/JH8, the human homologue of mouse jerky, and description of a rare mutation in a case of CAE evolving to JME. |
| Q36541953 | Purification and characterization of a CENP-B homologue protein that binds to the centromeric K-type repeat DNA of Schizosaccharomyces pombe |
| Q38330346 | Putative CENP-B paralogues are not present at mammalian centromeres |
| Q33755692 | Recent advances in the genetics of epilepsy: insights from human and animal studies |
| Q33680929 | Seizure disorders in mutant mice: relevance to human epilepsies |
| Q38345013 | Sensitivity to jerky gene dosage underlies epileptic seizures in mice |
| Q41098512 | Targeting epilepsy genes |
| Q35019591 | The RNA binding domain of Jerky consists of tandemly arranged helix-turn-helix/homeodomain-like motifs and binds specific sets of mRNAs |
| Q33320829 | Transposable elements as drivers of genomic and biological diversity in vertebrates |
| Q73222839 | Ultra-slow oscillation (0.025 Hz) triggers hippocampal afterdischarges in Wistar rats |
| Q54206333 | Wingless/Wnt Signaling in Intestinal Development, Homeostasis, Regeneration and Tumorigenesis: A Drosophila Perspective. |
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