| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| B R Fruen, B R Leste. Inositol and inositol 1,4,5-trisphosphate content of Down syndrome fibroblasts exhibiting enhanced inositol uptake. FEBS letters. vol 295. issue 1-3. 1992-02-20. PMID:1837274. |
fibroblasts from individuals with down syndrome (ds; trisomy 21) exhibit increased inositol uptake. |
1992-02-20 |
2023-08-11 |
human |
| E K Khandogina, G R Mutovich, S V Zvereva, D O Zverev, E V Neudakhin, B A Arkhipov, A P Akif'e. [Absence of radiation-induced adaptive response in lymphocytes of patients with Down's syndrome]. Biulleten' eksperimental'noi biologii i meditsiny. vol 112. issue 9. 1992-01-23. PMID:1836143. |
the adaptive syndrome and response (ar) in lymphocytes from 6 patients with down syndrome (ds) were investigated. |
1992-01-23 |
2023-08-11 |
Not clear |
| E D Ruchelli, A Uri, J E Dimmick, K E Bove, D S Huff, L M Duncan, J B Jennings, C L Witzlebe. Severe perinatal liver disease and Down syndrome: an apparent relationship. Human pathology. vol 22. issue 12. 1992-01-23. PMID:1836197. |
down syndrome (ds) is not usually thought of in association with significant infantile liver disease. |
1992-01-23 |
2023-08-11 |
Not clear |
| G Barkai, R Chaki, M Sochat, B Goldma. Human chorionic gonadotrophin and trisomy 18. American journal of medical genetics. vol 41. issue 1. 1991-12-23. PMID:1719814. |
estimation of maternal serum beta-hcg is used in conjunction with alpha-fetoprotein (afp) and estriol (e3) for estimating the risk of down syndrome (ds) affected fetuses. |
1991-12-23 |
2023-08-11 |
human |
| G Van Camp, H Backhovens, M Cruts, A Wehnert, W Van Hul, P Stinissen, C Van Broeckhove. Identification of chromosome 21 DNA polymorphisms for genetic studies in Alzheimer's disease and Down syndrome. Human genetics. vol 87. issue 6. 1991-12-03. PMID:1682232. |
in addition, we used the (ca)n dinucleotide polymorphism to reconstruct the non-disjunction event in a down syndrome (ds) patient whose mother died of familial ad. |
1991-12-03 |
2023-08-11 |
Not clear |
| H Nakagawa, K Iinum. [Photoelasticity study of feet in Down syndrome]. No to hattatsu = Brain and development. vol 23. issue 5. 1991-12-02. PMID:1834104. |
children with down syndrome (ds) (n = 18) known to have marked muscular hypotonicity were examined as a clinical model for functional evaluation of plantar arches in respect to body-weight-loading distribution. |
1991-12-02 |
2023-08-11 |
Not clear |
| H Suzuki, K Kodam. [Incidence rate of cerebral palsy, severe mental and motor retardation, and mental retardation in a suburban Tokyo area]. No to hattatsu = Brain and development. vol 23. issue 5. 1991-12-02. PMID:1834106. |
the number of patients with down syndrome (ds) was 9 and the incidence rate was 1.3/1,000. |
1991-12-02 |
2023-08-11 |
Not clear |
| O R Gonzalez, I G Gomez, A L Recalde, B H Landin. Postnatal development of the cystic lung lesion of Down syndrome: suggestion that the cause is reduced formation of peripheral air spaces. Pediatric pathology. vol 11. issue 4. 1991-11-25. PMID:1835001. |
the incidence of small subpleural lung cysts was analyzed for autopsies of 98 patients with down syndrome (ds): 9 fetuses or stillborns and 89 liveborns. |
1991-11-25 |
2023-08-11 |
Not clear |
| K A Loveland, B Tunal. Social scripts for conversational interactions in autism and Down syndrome. Journal of autism and developmental disorders. vol 21. issue 2. 1991-09-12. PMID:1830877. |
the ability of high-functioning verbal individuals with autism or down syndrome (ds) to respond appropriately to conversational "social scripts" involving responding to another person's distress was investigated. |
1991-09-12 |
2023-08-11 |
human |
| T Shara. Aging gametes in relation to incidence, gender, and twinning in Down syndrome. American journal of medical genetics. vol 39. issue 1. 1991-09-12. PMID:1831008. |
sexual practices have been implicated in the causation of down syndrome (ds). |
1991-09-12 |
2023-08-11 |
Not clear |
| N Bunin, P C Nowell, J Belasco, N Shah, M Willoughby, P A Farber, B Lang. Chromosome 7 abnormalities in children with Down syndrome and preleukemia. Cancer genetics and cytogenetics. vol 54. issue 1. 1991-08-13. PMID:1829646. |
three children, two boys and one girl, with down syndrome (ds) who presented with preleukemia and loss of all or part of chromosome 7 were studied. |
1991-08-13 |
2023-08-11 |
Not clear |
| J E Myrick, S P Caudill, I L Hubert, M K Robinson, M J Adams, S M Puesche. Identification of haptoglobin alpha-2FF variants in mid-trimester maternal serum as potential markers for Down syndrome. Applied and theoretical electrophoresis : the official journal of the International Electrophoresis Society. vol 1. issue 5. 1991-08-08. PMID:2151560. |
exploratory protein analysis in mid-trimester maternal sera by 2-dimensional electrophoresis and image analysis was performed to determine the differences between mothers carrying fetuses with down syndrome (ds) and control mothers. |
1991-08-08 |
2023-08-11 |
Not clear |
| W M Pardridge, J L Buciak, J Yang, B L Miller, H V Vinter. Measurement of amyloid peptide precursor of Alzheimer disease in human blood by double antibody immunoradiometric assay. Alzheimer disease and associated disorders. vol 5. issue 1. 1991-06-07. PMID:2025420. |
results of the irma showed that the app is present in human plasma (mean +/- se concentration = 32 +/- 6 pm, n = 25), and there was no significant difference in the app concentration in 25 controls, 19 patients with ad, and 10 individuals with down syndrome (ds). |
1991-06-07 |
2023-08-11 |
human |
| S Jacobs, W Gile. Down syndrome and low maternal serum alpha fetoprotein. The Australian & New Zealand journal of obstetrics & gynaecology. vol 30. issue 4. 1991-05-09. PMID:1707270. |
the early pregnancy maternal serum alpha-fetoprotein (msafp) results for 35 patients who delivered a baby with down syndrome (ds) were analysed. |
1991-05-09 |
2023-08-11 |
Not clear |
| G Annerén, K H Gustavson, V R Sara, T Tuvem. Growth retardation in Down syndrome in relation to insulin-like growth factors and growth hormone. American journal of medical genetics. Supplement. vol 7. 1991-04-16. PMID:1963538. |
growth retardation is a cardinal characteristic of down syndrome (ds). |
1991-04-16 |
2023-08-11 |
human |
| L Perroni, F Dagna Bricarelli, M Grasso, M Pierluigi, M Baldi, C Pedemonte, P Strigin. Crossing over and chromosome 21 nondisjunction: a study of 60 families. American journal of medical genetics. Supplement. vol 7. 1991-04-16. PMID:1981474. |
to test the hypothesis that meiotic nondisjunction may be caused by reduced chiasma frequency, hence recombination, we investigated 60 families with a trisomic child affected with down syndrome (ds). |
1991-04-16 |
2023-08-11 |
Not clear |
| A Serra, C Brahe, A Millington-Ward, G Neri, B Tedeschi, F Tassone, R Bov. Pericentric inversion of chromosome 9: prevalence in 300 Down syndrome families and molecular studies of nondisjunction. American journal of medical genetics. Supplement. vol 7. 1991-04-16. PMID:1981475. |
the incidence of down syndrome (ds) families where one of the parents is an heterozygous carrier of pericentric inversion of the heterochromatic region of chromosome 9-inv(9) (qh) - was determined in 3 independent groups of 100 families each. |
1991-04-16 |
2023-08-11 |
Not clear |
| M B Petersen, L Tranebjaerg, M K McCormick, N Michelsen, M Mikkelsen, S E Antonaraki. Clinical, cytogenetic, and molecular genetic characterization of two unrelated patients with different duplications of 21q. American journal of medical genetics. Supplement. vol 7. 1991-04-16. PMID:2149934. |
patient mp01 had mild mental retardation, facial findings characteristic of down syndrome (ds), and a terminal duplication of chromosome 21. |
1991-04-16 |
2023-08-11 |
Not clear |
| A Serra, G Ner. Trisomy 21: conference report and 1990 update. American journal of medical genetics. Supplement. vol 7. 1991-04-16. PMID:2149935. |
they centered around four major foci: the genotype, the phenotype, the pathogenesis of down syndrome (ds), and the down person. |
1991-04-16 |
2023-08-11 |
human |
| C Brahe, F Tassone, A Moscetti, A Millington-Ward, R Bova, A Serr. Molecular study of parental origin of extra chromosome 21 in regular and de novo translocation trisomies. American journal of medical genetics. Supplement. vol 7. 1991-04-16. PMID:2149938. |
the parental origin of the extra chromosome 21 (or extra 21q) was determined in seven informative families with a down syndrome (ds) child by using molecular polymorphisms. |
1991-04-16 |
2023-08-11 |
Not clear |