| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Maria Michela Del Viva, Arianna Tozzi, Stefania Bargagna, Giovanni Cion. Motion perception deficit in Down Syndrome. Neuropsychologia. vol 75. 2016-05-16. PMID:26057435. |
overall, our results show a selective and substantial deficit in the perception of optic flow motion and a corresponding suppression of electroencephalographic activity in ds individuals, thus establishing a further common trait between down syndrome and alzheimer's disease. |
2016-05-16 |
2023-08-13 |
human |
| Marwan N Sabbagh, Kewei Chen, Joseph Rogers, Adam S Fleisher, Carolyn Liebsack, Dan Bandy, Christine Belden, Hillary Protas, Pradeep Thiyyagura, Xiaofen Liu, Auttawut Roontiva, Ji Luo, Sandra Jacobson, Michael Malek-Ahmadi, Jessica Powell, Eric M Reima. Florbetapir PET, FDG PET, and MRI in Down syndrome individuals with and without Alzheimer's dementia. Alzheimer's & dementia : the journal of the Alzheimer's Association. vol 11. issue 8. 2016-05-05. PMID:25849033. |
down syndrome (ds) is associated with amyloid b (ab) deposition. |
2016-05-05 |
2023-08-13 |
Not clear |
| Roberto A Abreu-Mendoza, Natalia Arias-Trej. Numerical and area comparison abilities in Down syndrome. Research in developmental disabilities. vol 41-42. 2016-05-05. PMID:26057838. |
individuals with down syndrome (ds) have great difficulty in learning mathematics. |
2016-05-05 |
2023-08-13 |
human |
| b' Maria Esther Leiva Portocarrero, Mirjam M Garvelink, Maria Margarita Becerra Perez, Anik Gigu\\xc3\\xa8re, Hubert Robitaille, Brenda J Wilson, Fran\\xc3\\xa7ois Rousseau, France L\\xc3\\xa9gar\\xc3\\xa. Decision aids that support decisions about prenatal testing for Down syndrome: an environmental scan. BMC medical informatics and decision making. vol 15. 2016-05-05. PMID:26404088.' |
prenatal screening tests for down syndrome (ds) are routine in many developed countries and new tests are rapidly becoming available. |
2016-05-05 |
2023-08-13 |
Not clear |
| Ashley P Ng, Yifang Hu, Donald Metcalf, Craig D Hyland, Helen Ierino, Belinda Phipson, Di Wu, Tracey M Baldwin, Maria Kauppi, Hiu Kiu, Ladina Di Rago, Douglas J Hilton, Gordon K Smyth, Warren S Alexande. Early lineage priming by trisomy of Erg leads to myeloproliferation in a Down syndrome model. PLoS genetics. vol 11. issue 5. 2016-04-27. PMID:25973911. |
down syndrome (ds), with trisomy of chromosome 21 (hsa21), is the commonest human aneuploidy. |
2016-04-27 |
2023-08-13 |
mouse |
| Utano Tomaru, Takahiro Tsuji, Shizuka Kiuchi, Akihiro Ishizu, Akira Suzuki, Noriyuki Otsuka, Tomoki Ito, Hitoshi Ikeda, Yuichiro Fukasawa, Masanori Kasahar. Decreased expression of thymus-specific proteasome subunit β5t in Down syndrome patients. Histopathology. vol 67. issue 2. 2016-04-26. PMID:25556590. |
the majority of patients with down syndrome (ds), trisomy 21, have morphologically abnormal thymuses and present with intrinsic immunological abnormalities affecting mainly the cellular immune response. |
2016-04-26 |
2023-08-13 |
Not clear |
| Cahide Yılmaz, Murat Doğan, Fatmagül Başarslan, Nebi Yılmaz, Sevil Yuca, Keziban Bulan, Avni Kaya, Hüseyin Çakse. Evaluation of Lymphocyte Subgroups in Children With Down Syndrome. Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis. vol 21. issue 6. 2016-04-25. PMID:24243939. |
in this study, lymphocyte subgroups including blood cd3, cd4, cd8, cd4/cd8, cd19, and cd16.56 values were analyzed in children with down syndrome (ds). |
2016-04-25 |
2023-08-12 |
human |
| Tahyna Duda Deps, Gabriela Lopes Angelo, Carolina Castro Martins, Saul Martins Paiva, Isabela Almeida Pordeus, Ana Cristina Borges-Oliveir. Association between Dental Caries and Down Syndrome: A Systematic Review and Meta-Analysis. PloS one. vol 10. issue 6. 2016-04-25. PMID:26086498. |
scientific evidence of susceptibility to dental caries in the population with down syndrome (ds) is limited and conflicting, making it difficult to establish firm conclusions. |
2016-04-25 |
2023-08-13 |
Not clear |
| Donna M Wilcock, Jennifer Hurban, Alex M Helman, Tiffany L Sudduth, Katie L McCarty, Tina L Beckett, Joshua C Ferrell, M Paul Murphy, Erin L Abner, Frederick A Schmitt, Elizabeth Hea. Down syndrome individuals with Alzheimer's disease have a distinct neuroinflammatory phenotype compared to sporadic Alzheimer's disease. Neurobiology of aging. vol 36. issue 9. 2016-04-25. PMID:26103884. |
down syndrome (ds) is the most common genetic cause of intellectual disability and is primarily caused by the triplication of chromosome 21. |
2016-04-25 |
2023-08-13 |
Not clear |
| Pavel V Belichenko, Alexander M Kleschevnikov, Ann Becker, Grant E Wagner, Larisa V Lysenko, Y Eugene Yu, William C Moble. Down Syndrome Cognitive Phenotypes Modeled in Mice Trisomic for All HSA 21 Homologues. PloS one. vol 10. issue 7. 2016-04-25. PMID:26230397. |
down syndrome (ds), trisomy for chromosome 21, is the most common genetic cause of intellectual disability. |
2016-04-25 |
2023-08-13 |
mouse |
| Bin Yu, Bin Zhang, Wen-Bo Zhou, Qiu-Wei Wang, Pei Yuan, Yu-Qi Yang, Jing Kon. Assessing apoptosis gene expression profiling with a PCR array in the hippocampus of Ts65Dn mice. BioMed research international. vol 2015. 2016-04-22. PMID:26075220. |
it is well known that down syndrome (ds) is a condition in which extra genetic material causes delays in the way a child develops, both mentally and physically. |
2016-04-22 |
2023-08-13 |
mouse |
| Weiwei Zhao, Fan Chen, Menghua Wu, Shuai Jiang, Binbin Wu, Huali Luo, Jingyi Wen, Chaohui Hu, Shihui Y. Postnatal Identification of Trisomy 21: An Overview of 7,133 Postnatal Trisomy 21 Cases Identified in a Diagnostic Reference Laboratory in China. PloS one. vol 10. issue 7. 2016-04-22. PMID:26176847. |
the male/female (m/f ratio) for the total 7,133 tri21 cases and for the 6,671 cases with non-mosaic standard tri21 are 1.50 and 1.53 respectively, significantly higher than the 0.93 for all the 247,818 cases we karyotyped, the 1.30 for the down syndrome (ds) identified during perinatal period in china, and the 1.20 for the livebirth in chinese population. |
2016-04-22 |
2023-08-13 |
Not clear |
| Hyunkyung Cho. [Adaptation in Families of Children with Down Syndrome: A Mixed-methods Design]. Journal of Korean Academy of Nursing. vol 45. issue 4. 2016-04-21. PMID:26364525. |
the purpose of this study, which was guided by the resiliency model of family stress, adjustment, and adaptation, was twofold: (a) to explore family and parental adaptation and factors influencing family adaptation in korean families of children with down syndrome (ds) through a quantitative methodology and (b) to understand the life with a korean child with ds through a qualitative method. |
2016-04-21 |
2023-08-13 |
Not clear |
| Linlin Wang, John M Peters, Franklin Fuda, Long Li, Nitin J Karandikar, Prasad Koduru, Huan-You Wang, Weina Che. Acute megakaryoblastic leukemia associated with trisomy 21 demonstrates a distinct immunophenotype. Cytometry. Part B, Clinical cytometry. vol 88. issue 4. 2016-04-19. PMID:25361478. |
acute megakaryoblastic leukemia (amkl) is a rare form of acute myeloid leukemia that encompasses three distinct subgroups: children with down syndrome (ds-amkl), children without ds (non-ds-amkl), and adults (adult-amkl). |
2016-04-19 |
2023-08-13 |
Not clear |
| Julia L Bassell, Han Phan, Roberta Leu, Rebecca Kronk, Jeannie Visootsa. Sleep profiles in children with Down syndrome. American journal of medical genetics. Part A. vol 167A. issue 8. 2016-04-19. PMID:26105013. |
down syndrome (ds) is the most common genetic cause of intellectual disability and results from an extra chromosome 21 (trisomy 21). |
2016-04-19 |
2023-08-13 |
Not clear |
| Carlos Campos, Ángela Casad. Oxidative stress, thyroid dysfunction & Down syndrome. The Indian journal of medical research. vol 142. issue 2. 2016-04-18. PMID:26354208. |
down syndrome (ds) is one of the most common chromosomal disorders, occurring in one out of 700-1000 live births, and the most common cause of mental retardation. |
2016-04-18 |
2023-08-13 |
Not clear |
| Roksana Malak, Anna Kostiukow, Agnieszka Krawczyk-Wasielewska, Ewa Mojs, Włodzimierz Samborsk. Delays in Motor Development in Children with Down Syndrome. Medical science monitor : international medical journal of experimental and clinical research. vol 21. 2016-04-15. PMID:26132100. |
children with down syndrome (ds) present with delays in motor development. |
2016-04-15 |
2023-08-13 |
Not clear |
| K K Sukla, S K Jaiswal, A K Rai, O P Mishra, V Gupta, A Kumar, R Rama. Role of folate-homocysteine pathway gene polymorphisms and nutritional cofactors in Down syndrome: A triad study. Human reproduction (Oxford, England). vol 30. issue 8. 2016-04-13. PMID:26040482. |
do gene-gene and gene-environment interactions in folate-homocysteine (hcy) pathway have a predisposing role for down syndrome (ds)? |
2016-04-13 |
2023-08-13 |
Not clear |
| I Albizua, B L Rambo-Martin, E G Allen, W He, A S Amin, S L Sherma. Association between telomere length and chromosome 21 nondisjunction in the oocyte. Human genetics. vol 134. issue 11-12. 2016-04-12. PMID:26407969. |
chromosome 21 nondisjunction in oocytes is the most common cause of trisomy 21, the primary chromosomal abnormality responsible for down syndrome (ds). |
2016-04-12 |
2023-08-13 |
Not clear |
| A Urumova, Velibor Tasic, E Bojadjieva, M G Pomponi, G Neri, Z Guce. Identical monochorionic twins with down syndrome and paternal origin of the extra chromosome 21. Prilozi. vol 33. issue 2. 2016-04-08. PMID:23425868. |
trisomy 21, the cause of down syndrome (ds), is the most frequent trisomy in humans. |
2016-04-08 |
2023-08-12 |
Not clear |