| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Mette Hansen Viuff, Kirstine Stochholm, Niels Uldbjerg, Birgitte Bruun Nielsen, Claus Højbjerg Gravhol. Only a minority of sex chromosome abnormalities are detected by a national prenatal screening program for Down syndrome. Human reproduction (Oxford, England). vol 30. issue 10. 2016-07-27. PMID:26251461. |
how does a national prenatal screening program for down syndrome (ds) perform in detecting sex chromosome abnormalities (scas)-turner syndrome (ts), klinefelter syndrome, 47,xxx and 47,xyy syndromes. |
2016-07-27 |
2023-08-13 |
Not clear |
| Danyal Thaver, Mirza Be. Pulmonary Crohn's Disease in Down Syndrome: A Link or Linkage Problem. Case reports in gastroenterology. vol 10. issue 2. 2016-07-27. PMID:27462187. |
down syndrome (ds) has been associated with increased frequency of autoimmune diseases. |
2016-07-27 |
2023-08-13 |
Not clear |
| Avery H Weiss, John P Kelly, James O Phillip. Infantile Nystagmus and Abnormalities of Conjugate Eye Movements in Down Syndrome. Investigative ophthalmology & visual science. vol 57. issue 3. 2016-07-26. PMID:26998716. |
subjects with down syndrome (ds) have an anatomical defect within the cerebellum that may impact downstream oculomotor areas. |
2016-07-26 |
2023-08-13 |
human |
| Ellen Ternby, Ove Axelsson, Göran Annerén, Peter Lindgren, Charlotta Ingvoldsta. Why do pregnant women accept or decline prenatal diagnosis for Down syndrome? Journal of community genetics. vol 7. issue 3. 2016-07-26. PMID:27438596. |
to investigate if actual knowledge of down syndrome (ds), influences the decision to accept or decline prenatal diagnosis (pnd). |
2016-07-26 |
2023-08-13 |
Not clear |
| Joseph W Goodliffe, Jose Luis Olmos-Serrano, Nadine M Aziz, Jeroen L A Pennings, Faycal Guedj, Diana W Bianchi, Tarik F Hayda. Absence of Prenatal Forebrain Defects in the Dp(16)1Yey/+ Mouse Model of Down Syndrome. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 36. issue 10. 2016-07-19. PMID:26961948. |
studies in humans with down syndrome (ds) show that alterations in fetal brain development are followed by postnatal deficits in neuronal numbers, synaptic plasticity, and cognitive and motor function. |
2016-07-19 |
2023-08-13 |
mouse |
| Xavier Bofill-De Ros, Mónica Santos, Maria Vila-Casadesús, Eneko Villanueva, Nuria Andreu, Mara Dierssen, Cristina Filla. Genome-wide miR-155 and miR-802 target gene identification in the hippocampus of Ts65Dn Down syndrome mouse model by miRNA sponges. BMC genomics. vol 16. 2016-07-18. PMID:26546125. |
down syndrome (ds) or trisomy 21 is the result of a genetic dosage imbalance that translates in a broad clinical spectrum. |
2016-07-18 |
2023-08-13 |
mouse |
| Susan J Loveall, Frances A Conner. Reading Skills in Down Syndrome: An Examination of Orthographic Knowledge. American journal on intellectual and developmental disabilities. vol 121. issue 2. 2016-07-15. PMID:26914465. |
the primary goal of this study was to examine the word identification domain of the simple view of reading in participants with down syndrome (ds) by comparing them to participants with typical development (td) matched on word identification ability. |
2016-07-15 |
2023-08-13 |
human |
| Grace Kee See Lam, Alex Wing Kwan Leung, Shau Yin Ha, Chung Wing Luk, Chak Ho Li, Siu Cheung Ling, Alan Kwok Shing Chiang, Chi Kong L. Acute Leukemia in Down Syndrome Children in Hong Kong: Retrospective Review. Journal of pediatric hematology/oncology. vol 38. issue 2. 2016-07-14. PMID:26808367. |
children with down syndrome (ds) are at higher risk of developing acute leukemia. |
2016-07-14 |
2023-08-13 |
Not clear |
| Joshua D Blazek, Irushi Abeysekera, Jiliang Li, Randall J Rope. Rescue of the abnormal skeletal phenotype in Ts65Dn Down syndrome mice using genetic and therapeutic modulation of trisomic Dyrk1a. Human molecular genetics. vol 24. issue 20. 2016-07-12. PMID:26206885. |
trisomy 21 causes skeletal alterations in individuals with down syndrome (ds), but the causative trisomic gene and a therapeutic approach to rescue these abnormalities are unknown. |
2016-07-12 |
2023-08-13 |
mouse |
| Denghong Chen, Zhenhua Zhang, Yuxiu Men. Systematic Tracking of Disrupted Modules Identifies Altered Pathways Associated with Congenital Heart Defects in Down Syndrome. Medical science monitor : international medical journal of experimental and clinical research. vol 21. 2016-07-11. PMID:26524729. |
this work aimed to identify altered pathways in congenital heart defects (chd) in down syndrome (ds) by systematically tracking the dysregulated modules of reweighted protein-protein interaction (ppi) networks. |
2016-07-11 |
2023-08-13 |
Not clear |
| Bruno Henrique Silva Araujo, Laila Brito Torres, Laura Maria F F Guilhot. Cerebal overinhibition could be the basis for the high prevalence of epilepsy in persons with Down syndrome. Epilepsy & behavior : E&B. vol 53. 2016-07-11. PMID:26558714. |
down syndrome (ds) is the most common cause of genetic intellectual disability, and the trisomy 21 is associated with more than 80 clinical traits, including higher risk for epilepsy. |
2016-07-11 |
2023-08-13 |
mouse |
| Annan Yang, Duane Currier, Jennifer L Poitras, Roger H Reeve. Increased Skin Tumor Incidence and Keratinocyte Hyper-Proliferation in a Mouse Model of Down Syndrome. PloS one. vol 11. issue 1. 2016-07-11. PMID:26752700. |
down syndrome (ds) is a genetic disorder caused by the presence of an extra copy of human chromosome 21 (hsa21). |
2016-07-11 |
2023-08-13 |
mouse |
| Vincenzo Borelli, Valerie Vanhooren, Emanuela Lonardi, Karli R Reiding, Miriam Capri, Claude Libert, Paolo Garagnani, Stefano Salvioli, Claudio Franceschi, Manfred Wuhre. Plasma N-Glycome Signature of Down Syndrome. Journal of proteome research. vol 14. issue 10. 2016-07-08. PMID:26334954. |
here, we studied n-glycomic changes in down syndrome (ds). |
2016-07-08 |
2023-08-13 |
Not clear |
| Jamie R K Marland, Karen J Smillie, Michael A Cousi. Synaptic Vesicle Recycling Is Unaffected in the Ts65Dn Mouse Model of Down Syndrome. PloS one. vol 11. issue 1. 2016-07-08. PMID:26808141. |
down syndrome (ds) is the most common genetic cause of intellectual disability, and arises from trisomy of human chromosome 21. |
2016-07-08 |
2023-08-13 |
mouse |
| Jennifer N Vega, Timothy J Hohman, Jennifer R Pryweller, Elisabeth M Dykens, Tricia A Thornton-Well. Resting-State Functional Connectivity in Individuals with Down Syndrome and Williams Syndrome Compared with Typically Developing Controls. Brain connectivity. vol 5. issue 8. 2016-07-07. PMID:25712025. |
this study examined rsfc in down syndrome (ds) compared with another neurodevelopmental disorder, williams syndrome (ws), and td. |
2016-07-07 |
2023-08-13 |
human |
| A Matute-Llorente, A González-Agüero, A Gómez-Cabello, H Olmedillas, G Vicente-Rodríguez, J A Casajú. Effect of whole body vibration training on bone mineral density and bone quality in adolescents with Down syndrome: a randomized controlled trial. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA. vol 26. issue 10. 2016-07-06. PMID:25994905. |
adolescents with down syndrome (ds) have poorer bone health than their peers without ds. |
2016-07-06 |
2023-08-13 |
Not clear |
| Alison Downes, Julia S Anixt, Anna J Esbensen, Susan Wiley, Jareen Meinzen-Der. Psychotropic Medication Use in Children and Adolescents With Down Syndrome. Journal of developmental and behavioral pediatrics : JDBP. vol 36. issue 8. 2016-07-06. PMID:26035141. |
to estimate the rate of psychotropic medication use in children and adolescents with down syndrome (ds) and to describe age-related trends. |
2016-07-06 |
2023-08-13 |
Not clear |
| Maite Mendioroz, Catherine Do, Xiaoling Jiang, Chunhong Liu, Huferesh K Darbary, Charles F Lang, John Lin, Anna Thomas, Sayeda Abu-Amero, Philip Stanier, Alexis Temkin, Alexander Yale, Meng-Min Liu, Yang Li, Martha Salas, Kristi Kerkel, George Capone, Wayne Silverman, Y Eugene Yu, Gudrun Moore, Jerzy Wegiel, Benjamin Tyck. Trans effects of chromosome aneuploidies on DNA methylation patterns in human Down syndrome and mouse models. Genome biology. vol 16. 2016-07-06. PMID:26607552. |
trisomy 21 causes down syndrome (ds), but the mechanisms by which the extra chromosome leads to deficient intellectual and immune function are not well understood. |
2016-07-06 |
2023-08-13 |
mouse |
| Arnaud Duchon, Yann Heraul. DYRK1A, a Dosage-Sensitive Gene Involved in Neurodevelopmental Disorders, Is a Target for Drug Development in Down Syndrome. Frontiers in behavioral neuroscience. vol 10. 2016-07-04. PMID:27375444. |
down syndrome (ds) is one of the leading causes of intellectual disability, and patients with ds face various health issues, including learning and memory deficits, congenital heart disease, alzheimer's disease (ad), leukemia, and cancer, leading to huge medical and social costs. |
2016-07-04 |
2023-08-13 |
mouse |
| Pankaj D Mehta, Bruce A Patrick, Marc Barshatzky, Sangita P Mehta, Janusz Frackowiak, Bozena Mazur-Kolecka, David L Mille. Generation of Rabbit Monoclonal Antibody to Amyloid-β38 (Aβ38): Increased Plasma Aβ38 Levels in Down Syndrome. Journal of Alzheimer's disease : JAD. vol 46. issue 4. 2016-06-30. PMID:26402629. |
our second aim was to quantitate aβ38 levels in plasma from older down syndrome (ds) persons and age-matched controls. |
2016-06-30 |
2023-08-13 |
rabbit |