| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| K L Kwong, V Won. Neurodevelopmental profile of Down syndrome in Chinese children. Journal of paediatrics and child health. vol 32. issue 2. 1997-05-16. PMID:9156526. |
to give an overall appraisal of the clinical features of down syndrome (ds) in chinese children with emphasis on the neurodevelopmental outcome, and to compare the related complications with that of other races. |
1997-05-16 |
2023-08-12 |
Not clear |
| Q P Qin, M Christiansen, T H Nguyen, S Sørensen, S O Larsen, B Nørgaard-Pederse. Schwangerschaftsprotein 1 (SP1) as a maternal serum marker for Down syndrome in the first and second trimesters. Prenatal diagnosis. vol 17. issue 2. 1997-05-15. PMID:9061756. |
the potential of the maternal serum concentration of schwangerschaftsprotein 1 (mssp1) as a marker for down syndrome (ds) pregnancies was evaluated in the fifth to the 20th gestational week using 156 ds pregnancies and 546 unaffected control pregnancies. |
1997-05-15 |
2023-08-12 |
Not clear |
| M Ohira, N Seki, T Nagase, E Suzuki, N Nomura, O Ohara, M Hattori, Y Sakaki, T Eki, Y Murakami, T Saito, H Ichikawa, M Ohk. Gene identification in 1.6-Mb region of the Down syndrome region on chromosome 21. Genome research. vol 7. issue 1. 1997-05-14. PMID:9037601. |
the down syndrome (ds) region has been defined by analyses of partial trisomy 21. |
1997-05-14 |
2023-08-12 |
human |
| G Bernert, M Nemethova, M Herrera-Marschitz, N Cairns, G Lube. Decreased cyclin dependent kinase in brain of patients with Down syndrome. Neuroscience letters. vol 216. issue 1. 1997-05-12. PMID:8892394. |
in order to study whether phosphokinases might be involved in the neuropathology of down syndrome (ds) and alzheimer disease (ad), cyclin dependent kinase (cdk) activity and protein, phosphokinase c (pkc) and phosphokinase a (pka) activities have been determined in frontal lobes of ds, ad and control brains. |
1997-05-12 |
2023-08-12 |
Not clear |
| C Schneider, D Risser, L Kirchner, E Kitzmüller, N Cairns, H Prast, N Singewald, G Lube. Similar deficits of central histaminergic system in patients with Down syndrome and Alzheimer disease. Neuroscience letters. vol 222. issue 3. 1997-05-09. PMID:9148245. |
in order to study whether alzheimer-like neuropathological changes involve the central histaminergic system we measured the concentration of histamine, its precursor histidine as well as the activity of histidine decarboxylase (hdc) and histamine-n-methyl-transferase (hmt) in frontal cortex of aging down syndrome (ds) patients, alzheimer patients and control individuals. |
1997-05-09 |
2023-08-12 |
Not clear |
| G E Demas, R J Nelson, B K Krueger, P J Yarowsk. Spatial memory deficits in segmental trisomic Ts65Dn mice. Behavioural brain research. vol 82. issue 1. 1997-04-25. PMID:9021073. |
spatial memory was assessed in the segmental trisomic 16 mouse (ts65dn), a potential model for down syndrome (ds), using the 12-arm radial maze (ram). |
1997-04-25 |
2023-08-12 |
mouse |
| E C Jenkins, N Schupf, M Genovese, L L Ye, D Kapell, B Canto, M Harris, D Devenny, J H Lee, W T Brow. Increased low-level chromosome 21 mosaicism in older individuals with Down syndrome. American journal of medical genetics. vol 68. issue 2. 1997-04-25. PMID:9028448. |
during a study of the familial aggregation of down syndrome (ds) and alzheimer disease (ad), we observed an increase in mosaicism for disomy 21 in older individuals with ds. |
1997-04-25 |
2023-08-12 |
human |
| C Toledo, Y Alembik, B Dott, S Finck, C Stol. [Anomalies of thyroid function in children with Down syndrome]. Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. vol 4. issue 2. 1997-04-25. PMID:9097820. |
abnormal thyroid function was shown in children with down syndrome (ds). |
1997-04-25 |
2023-08-12 |
Not clear |
| A Dani, P Pietrini, M L Furey, A R McIntosh, C L Grady, B Horwitz, U Freo, G E Alexander, M B Schapir. Brain cognition and metabolism in Down syndrome adults in association with development of dementia. Neuroreport. vol 7. issue 18. 1997-04-18. PMID:9116213. |
to identify changes in brain functions associated with the development of dementia, brain metabolism and cognition were assessed repeatedly in 12 adults with down syndrome (ds) using positron emission tomography and neuropsychological tests. |
1997-04-18 |
2023-08-12 |
human |
| D Risser, G Lubec, N Cairns, M Herrera-Marschit. Excitatory amino acids and monoamines in parahippocampal gyrus and frontal cortical pole of adults with Down syndrome. Life sciences. vol 60. issue 15. 1997-04-17. PMID:9096240. |
aspartate (asp), glutamate (glu), noradrenaline (na), dopamine (da) and its acidic metabolites dopac and hva, serotonin (5-ht) and its metabolite 5-hiaa were simultaneously investigated in post-mortem tissue samples from right parahippocampal gyrus (temporal cortex) and frontal cortical pole (frontal cortex) of adults with down syndrome (ds), and of neurologically healthy controls by use of high performance liquid chromatography (hplc). |
1997-04-17 |
2023-08-12 |
human |
| M Nadal, S Moreno, M Pritchard, M A Preciado, X Estivill, M A Ramos-Arroy. Down syndrome: characterisation of a case with partial trisomy of chromosome 21 owing to a paternal balanced translocation (15;21) (q26;q22.1) by FISH. Journal of medical genetics. vol 34. issue 1. 1997-04-10. PMID:9032650. |
a patient with a typical down syndrome (ds) phenotype and a normal karyotype was studied by fish. |
1997-04-10 |
2023-08-12 |
Not clear |
| M Bonamico, A Rasore-Quartino, P Mariani, P Scartezzini, P Cerruti, M C Tozzi, M Cingolani, G Gemm. Down syndrome and coeliac disease: usefulness of antigliadin and antiendomysium antibodies. Acta paediatrica (Oslo, Norway : 1992). vol 85. issue 12. 1997-04-03. PMID:9001668. |
the usefulness of antigliadin (aga) and antiendomysium antibodies (ema) as a screening test for coeliac disease (cd) in 113 down syndrome (ds) patients (61 children) was evaluated. |
1997-04-03 |
2023-08-12 |
human |
| B E Ahlbom, P Goetz, J R Korenberg, U Pettersson, E Seemanova, C Wadelius, L Zech, G Anneré. Molecular analysis of chromosome 21 in a patient with a phenotype of Down syndrome and apparently normal karyotype. American journal of medical genetics. vol 63. issue 4. 1997-03-20. PMID:8826436. |
down syndrome (ds) is caused in most cases by the presence of an extra chromosome 21. |
1997-03-20 |
2023-08-12 |
Not clear |
| H Chen, C Rossier, S E Antonaraki. Cloning of a human homolog of the Drosophila enhancer of zeste gene (EZH2) that maps to chromosome 21q22.2. Genomics. vol 38. issue 1. 1997-03-17. PMID:8954776. |
to identify genes that map on human chromosome 21 (hc21) and that may contribute to the phenotype of down syndrome (ds), exon trapping was applied to cosmid dna from an hc21-specific library ll21nco2-q. |
1997-03-17 |
2023-08-12 |
human |
| E H Aylward, R Habbak, A C Warren, M B Pulsifer, P E Barta, M Jerram, G D Pearlso. Cerebellar volume in adults with Down syndrome. Archives of neurology. vol 54. issue 2. 1997-03-13. PMID:9041863. |
to determine the effects of aging on cerebellar volume in individuals with down syndrome (ds). |
1997-03-13 |
2023-08-12 |
Not clear |
| R Gaggero, P T Donati, R Curia, M De Negr. Occlusion of unilateral carotid artery in Down syndrome. Brain & development. vol 18. issue 1. 1997-03-07. PMID:8907351. |
the association between moyamoya phenomena and down syndrome (ds) is reported in the literature. |
1997-03-07 |
2023-08-12 |
Not clear |
| C L Olsen, P K Cross, L J Gensburg, J P Hughe. The effects of prenatal diagnosis, population ageing, and changing fertility rates on the live birth prevalence of Down syndrome in New York State, 1983-1992. Prenatal diagnosis. vol 16. issue 11. 1997-03-06. PMID:8953632. |
the incidence of down syndrome (ds) at conception is highly dependent on the maternal age distribution and age-specific pregnancy rates. |
1997-03-06 |
2023-08-12 |
Not clear |
| B Källén, P Mastroiacovo, E Rober. Major congenital malformations in Down syndrome. American journal of medical genetics. vol 65. issue 2. 1997-02-19. PMID:8911611. |
we studied major malformations in 5,581 infants with down syndrome (ds) from three registers of congenital malformations. |
1997-02-19 |
2023-08-12 |
Not clear |
| J Kuromitsu, H Yamashita, H Kataoka, T Takahara, M Muramatsu, T Sekine, N Okamoto, Y Furuichi, Y Hayashizak. A unique downregulation of h2-calponin gene expression in Down syndrome: a possible attenuation mechanism for fetal survival by methylation at the CpG island in the trisomic chromosome 21. Molecular and cellular biology. vol 17. issue 2. 1997-02-18. PMID:9001224. |
to understand the effect of trisomic chromosome 21 on the cause of down syndrome (ds), dna methylation in the cpg island, which regulates the expression of adjacent genes, was investigated with the dnas of chromosome 21 isolated from ds patients and their parents. |
1997-02-18 |
2023-08-12 |
Not clear |
| S L Klein, L J Kriegsfeld, J E Hairston, V Rau, R J Nelson, P J Yarowsk. Characterization of sensorimotor performance, reproductive and aggressive behaviors in segmental trisomic 16 (Ts65Dn) mice. Physiology & behavior. vol 60. issue 4. 1997-02-05. PMID:8884947. |
in the present study, segmental trisomy 16 (ts65dn) mice, an animal model of down syndrome (ds), were examined for sensorimotor, reproductive, and aggression abnormalities associated with ds. |
1997-02-05 |
2023-08-12 |
mouse |