scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0079-6123(08)64028-5 |
P698 | PubMed publication ID | 9932421 |
P2093 | author name string | A Neubauer | |
D P de Kleijn | |||
F W van Leeuwen | |||
E M Hol | |||
J A Sluijs | |||
M A Sonnemans | |||
R D Ramdjielal | |||
P2860 | cites work | Molecular cloning of the cDNA for a human amyloid precursor protein homolog: evidence for a multigene family | Q24328904 |
The human ubiquitin gene family: structure of a gene and pseudogenes from the Ub B subfamily | Q24629813 | ||
The human ubiquitin-52 amino acid fusion protein gene shares several structural features with mammalian ribosomal protein genes | Q24632736 | ||
Frameshift mutants of beta amyloid precursor protein and ubiquitin-B in Alzheimer's and Down patients | Q28258349 | ||
Sequence identification of 2,375 human brain genes | Q28283772 | ||
GAP-43: an intrinsic determinant of neuronal development and plasticity | Q28303146 | ||
Peptides containing the RERMS sequence of amyloid beta/A4 protein precursor bind cell surface and promote neurite extension | Q28513050 | ||
The ubiquitin system | Q29618565 | ||
Possible factors in the etiology of Alzheimer's disease | Q30419530 | ||
Genomic organization of the human amyloid beta-protein precursor gene | Q34151473 | ||
Age-related development of a heterozygous phenotype in solitary neurons of the homozygous Brattleboro rat | Q34298676 | ||
Regulation and expression of the Alzheimer's beta/A4 amyloid protein precursor in health, disease, and Down's syndrome | Q34344488 | ||
DNA repair and Alzheimer's disease | Q35515165 | ||
Frameshift mutations at two hotspots in vasopressin transcripts in post-mitotic neurons | Q35550396 | ||
Molecular biology's impact on our understanding of aging | Q36246851 | ||
Ubiquitin in health and disease. | Q36393421 | ||
Pseudo-templated transcription in prokaryotic and eukaryotic organisms | Q37712233 | ||
Discordant expression and variable numbers of neighboring GGA- and GAA-rich triplet repeats in the 3' untranslated regions of two groups of messenger RNAs encoded by the rat polymeric immunoglobulin receptor gene | Q40393541 | ||
Somatic mutations in the brain: relationship to aging? | Q40416494 | ||
Molecular genetics of Alzheimer disease: identification of genes and gene mutations | Q40517536 | ||
Transcription-coupled repair and human disease | Q40556402 | ||
Genomic damage and its repair in young and aging brain | Q40819236 | ||
Endosome-lysosomes, ubiquitin and neurodegeneration. | Q41154900 | ||
Alzheimer's disease: genotypes, phenotypes, and treatments | Q41340438 | ||
Amyloid, the presenilins and Alzheimer's disease | Q41433661 | ||
Life and death of neurons in the aging brain | Q41614205 | ||
Accumulation of amyloid precursor fragment in Alzheimer plaques | Q43713988 | ||
An antiserum against amyloid beta-protein precursor detects a unique peptide in Alzheimer brain | Q46153889 | ||
No global neocortical nerve cell loss in brains from patients with senile dementia of Alzheimer's type | Q48134637 | ||
Differential neurophysin immunoreactivities in solitary magnocellular neurons of the homozygous Brattleboro rat indicate an altered neurophysin moiety | Q48188201 | ||
Mutations in RNA: a first example of molecular misreading in Alzheimer's disease | Q48404361 | ||
Limits of neurogenesis in primates | Q48513691 | ||
Occurrence of neuropathological changes and dementia of Alzheimer's disease in Down's syndrome | Q48516987 | ||
Possible new cause of Alzheimer's disease found | Q48553732 | ||
Amyloid precursor-like protein 1 accumulates in neuritic plaques in Alzheimer's disease | Q48554980 | ||
Mutant vasopressin precursors in the human hypothalamus: evidence for neuronal somatic mutations in man. | Q49039426 | ||
Amyloid A4 protein and its precursor in Down's syndrome and Alzheimer's disease. | Q53187594 | ||
Expression of the Alzheimer amyloid precursor gene transcripts in the human brain. | Q53190283 | ||
Hypersensitivity to ionizing radiation in cultured cells from Down syndrome patients. | Q53191598 | ||
Ubiquitin is a component of paired helical filaments in Alzheimer's disease. | Q53303482 | ||
Phosphorolytic error correction during transcription. | Q54637178 | ||
Estimation of the Genetic Contribution of Presenilin-1 and -2 Mutations in a Population-Based Study of Presenile Alzheimer Disease | Q57419118 | ||
Impact of altered protein structures on the intracellular traffic of a mutated vasopressin precursor from Brattleboro rats | Q69216174 | ||
Alzheimer disease fibroblasts are hypersensitive to the lethal effects of a DNA-damaging chemical | Q69991472 | ||
Ubiquitin is conjugated with amino-terminally processed tau in paired helical filaments | Q70462570 | ||
Immunocytochemical evidence for the presence of vasopressin in intermediate sized neurosecretory granules of solitary neurohypophyseal terminals in the homozygous Brattleboro rat | Q71323736 | ||
Production of amyloid-beta-peptide by cultured cells: no evidence for internal initiation of translation at Met596 | Q72743932 | ||
P921 | main subject | Alzheimer's disease | Q11081 |
Down syndrome | Q47715 | ||
P304 | page(s) | 379-395 | |
P577 | publication date | 1998-01-01 | |
P1433 | published in | Progress in Brain Research | Q15800382 |
P1476 | title | Dinucleotide deletions in neuronal transcripts: a novel type of mutation in non-familial Alzheimer's disease and Down syndrome patients | |
P478 | volume | 117 |
Q34401966 | Biological ageing research in the Netherlands |
Q47713062 | Frameshifted beta-amyloid precursor protein (APP+1) is a secretory protein, and the level of APP+1 in cerebrospinal fluid is linked to Alzheimer pathology |
Q44557854 | Neuronal expression of GFAP in patients with Alzheimer pathology and identification of novel GFAP splice forms |
Q73348432 | Novel frameshift mutations near short simple repeats |
Q28349567 | Translational misreading: a tRNA modification counteracts a +2 ribosomal frameshift |