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1. Full Text TFH lymphomas: the times they aza-changin'?
by Weinstock, DM and Horwitz, SM
BLOOD, ISSN 0006-4971, 10/2019, Volume 134, Issue 17, pp. 1364 - 1365
In this issue of Blood, O'Connor and colleagues(1) report a phase 1 study of romidepsin combined with oral azacytidine in patients with relapsed/refractory... 
HEMATOLOGY | PERIPHERAL T-CELL
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2. Full Text Identification of Circulating Serum Multi-MicroRNA Signatures in Human DLBCL Models
by Beheshti, Afshin and Stevenson, Kristen and Vanderburg, Charles and Ravi, Dashnamoorthy and McDonald, J. Tyson and Christie, Amanda L and Shigemori, Kay and Jester, Hallie and Weinstock, David M and Evens, Andrew M
Scientific Reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 1 - 11
There remains a need to identify new sensitive diagnostic and predictive blood-based platforms in lymphoma. We previously discovered a novel circulating... 
Cell culture | Animal models | MiRNA | Myc protein | Tumor cell lines | Patients | Lysates | Lymphocytes B | MicroRNAs | Xenografts | Cell lines | Lymphomas | B-cell lymphoma
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3. Full Text A map of human genome variation from population-scale sequencing
by Altshuler, David L and Durbin, Richard M and Abecasis, Gonçalo R and Bentley, David R and Chakravarti, Aravinda and Clark, Andrew G and Collins, Francis S and De La Vega, Francisco M and Donnelly, Peter and Egholm, Michael and Flicek, Paul and Gabriel, Stacey B and Gibbs, Richard A and Knoppers, Bartha M and Lander, Eric S and Lehrach, Hans and Mardis, Elaine R and McVean, Gil A and Nickerson, Debbie A and Peltonen, Leena and Schafer, Alan J and Sherry, Stephen T and Wang, Jun and Wilson, Richard K and Deiros, David and Metzker, Mike and Muzny, Donna and Reid, Jeff and Wheeler, David and Wang, Shenzhen Jun and Li, Jingxiang and Jian, Min and Li, Guoqing and Li, Ruiqiang and Liang, Huiqing and Tian, Geng and Wang, Bo and Wang, Jian and Wang, Wei and Yang, Huanming and Zhang, Xiuqing and Zheng, Huisong and Ambrogio, Lauren and Bloom, Toby and Cibulskis, Kristian and Fennell, Tim J and Jaffe, David B and Shefler, Erica and Sougnez, Carrie L and Bentley, Illumina David R and Gormley, Niall and Humphray, Sean and Kingsbury, Zoya and Koko-Gonzales, Paula and Stone, Jennifer and Mc Kernan, Kevin J and Costa, Gina L and Ichikawa, Jeffry K and Lee, Clarence C and Sudbrak, Ralf and Borodina, Tatiana A and Dahl, Andreas and Davydov, Alexey N and Marquardt, Peter and Mertes, Florian and Nietfeld, Wilfiried and Rosenstiel, Philip and Schreiber, Stefan and Soldatov, Aleksey V and Timmermann, Bernd and Tolzmann, Marius and Affourtit, Jason and Ashworth, Dana and Attiya, Said and Bachorski, Melissa and Buglione, Eli and Burke, Adam and Caprio, Amanda and Celone, Christopher and Clark, Shauna and Conners, David and Desany, Brian and Gu, Lisa and Guccione, Lorri and Kao, Kalvin and Kebbel, Andrew and Knowlton, Jennifer and Labrecque, Matthew and McDade, Louise and Mealmaker, Craig and Minderman, Melissa and Nawrocki, Anne and Niazi, Faheem and Pareja, Kristen and Ramenani, Ravi and Riches, David and Song, Wanmin and Turcotte, Cynthia and Wang, Shally and Dooling, David and ... and 1000 Genomes Project Consortium and The 1000 Genomes Project Consortium
Nature, ISSN 0028-0836, 10/2010, Volume 467, Issue 7319, pp. 1061 - 1073
The 1000 Genomes Project aims to provide a deep characterization of human genome sequence variation as a foundation for investigating the relationship between... 
NUCLEOTIDE | IMPUTATION | PRDM9 | RARE VARIANTS | GENE | MULTIDISCIPLINARY SCIENCES | WIDE ASSOCIATION | MOTIF | Humans | Male | Selection, Genetic - genetics | Haplotypes - genetics | DNA, Mitochondrial - genetics | DNA Mutational Analysis | Recombination, Genetic - genetics | Female | Genomics - methods | Genome-Wide Association Study | Genetic Association Studies | Computational Biology | Genotype | Calibration | Mutation - genetics | Genome, Human - genetics | Chromosomes, Human, Y - genetics | Pilot Projects | Sample Size | Sequence Alignment | Genetics, Population - methods | Polymorphism, Single Nucleotide - genetics | Genetic Variation - genetics | Sequence Analysis, DNA - methods | Evolution, Molecular | Research | Nucleotide sequencing | Human genome | Human population genetics | Identification and classification | Methods | Studies | Design | Pilot projects | Genomics | Genetics | Mutation | Deoxyribonucleic acid--DNA | Life Sciences
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4. Full Text Demographic history and rare allele sharing among human populations
by Simon Gravel and Brenna M. Henn and Ryan N. Gutenkunst and Amit R. Indap and Gabor T. Marth and Andrew G. Clark and Fuli Yu and Richard A. Gibbs and Carlos D. Bustamante and 1000 Genomes Project and The 1000 Genomes Project
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 7/2011, Volume 108, Issue 29, pp. 11983 - 11988
High-throughput sequencing technology enables population-level surveys of human genomic variation. Here, we examine the joint allele frequency distributions... 
Demography | Population growth | Exons | Population estimates | Population size | Genomes | Sequencing | Population genetics | Parametric models | Human genetics | Human evolution | Genetic drift | Demographic inference | ANIMALS | population genetics | NUMBER | VARIANTS | genetic drift | SIZES | MULTIDISCIPLINARY SCIENCES | demographic inference | CAPTURE PROBABILITIES VARY | RATES | HUMAN GENOME | human evolution | FREQUENCY-SPECTRUM | DIVERGENCE | SELECTION | Genetic Variation | Genetics, Population | Genetic Drift | Gene Frequency | Humans | Genes - genetics | Models, Genetic | Continental Population Groups - genetics | Genomics - methods | Sequence Analysis, DNA | Evolution, Molecular | Genetic aspects | Research | Genetic variation | Biological Sciences
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5. Full Text The next best thing
by Murakami, Mark A and Weinstock, David M
Nature, ISSN 0028-0836, 09/2017, Volume 549, Issue 7670, pp. 39 - 41
Recent advances have enabled human tumour cells to be transplanted into immunodeficient mice with a high success rate. On page 96, Stewart et al.1 present a... 
Studies | Chemotherapy | Animal models | Laboratories | Immunodeficiency | Models | Mice | Cancer therapies | Tumors | Cancer
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6. Full Text An integrated map of genetic variation from 1,092 human genomes
by Altshuler, David M and Durbin, Richard M and Abecasis, Gonçalo R and Bentley, David R and Chakravarti, Aravinda and Clark, Andrew G and Donnelly, Peter and Eichler, Evan E and Flicek, Paul and Gabriel, Stacey B and Gibbs, Richard A and Green, Eric D and Hurles, Matthew E and Knoppers, Bartha M and Korbel, Jan O and Lander, Eric S and Lee, Charles and Lehrach, Hans and Mardis, Elaine R and Marth, Gabor T and McVean, Gil A and Nickerson, Deborah A and Schmidt, Jeanette P and Sherry, Stephen T and Wang, Jun and Wilson, Richard K and Dinh, Huyen and Kovar, Christie and Lee, Sandra and Lewis, Lora and Muzny, Donna and Reid, Jeff and Wang, Min and Fang, Xiaodong and Guo, Xiaosen and Jian, Min and Jiang, Hui and Jin, Xin and Li, Guoqing and Li, Jingxiang and Li, Yingrui and Li, Zhuo and Liu, Xiao and Lu, Yao and Ma, Xuedi and Su, Zhe and Tai, Shuaishuai and Tang, Meifang and Wang, Bo and Wang, Guangbiao and Wu, Honglong and Wu, Renhua and Yin, Ye and Zhang, Wenwei and Zhao, Jiao and Zhao, Meiru and Zheng, Xiaole and Zhou, Yan and Gupta, Namrata and Clarke, Laura and Leinonen, Rasko and Smith, Richard E and Zheng-Bradley, Xiangqun and Grocock, Russell and Humphray, Sean and James, Terena and Kingsbury, Zoya and Sudbrak, Ralf and Albrecht, Marcus W and Amstislavskiy, Vyacheslav S and Borodina, Tatiana A and Lienhard, Matthias and Mertes, Florian and Sultan, Marc and Timmermann, Bernd and Yaspo, Marie-Laure and Fulton, Lucinda and Fulton, Robert and Weinstock, George M and Balasubramaniam, Senduran and Burton, John and Danecek, Petr and Keane, Thomas M and Kolb-Kokocinski, Anja and McCarthy, Shane and Stalker, James and Quail, Michael and Davies, Christopher J and Gollub, Jeremy and Webster, Teresa and Wong, Brant and Zhan, Yiping and Auton, Adam and Yu, Fuli and Bainbridge, Matthew and Challis, Danny and Evani, Uday S and Lu, James and Nagaswamy, Uma and Sabo, Aniko and ... and 1000 Genomes Project Consortium and The 1000 Genomes Project Consortium
Nature, ISSN 0028-0836, 11/2012, Volume 491, Issue 7422, pp. 56 - 65
By characterizing the geographic and functional spectrum of human genetic variation, the 1000 Genomes Project aims to build a resource to help to understand... 
RARE | VARIANTS | MULTIDISCIPLINARY SCIENCES | MUTATION | POPULATION-STRUCTURE | RISK | LOCI | WIDE ASSOCIATION | COPY NUMBER VARIATION | Genetics, Population | Conserved Sequence - genetics | Genome-Wide Association Study | Genomics | Humans | Binding Sites - genetics | Continental Population Groups - genetics | Genome, Human - genetics | Transcription Factors - metabolism | Haplotypes - genetics | Genetics, Medical | Nucleotide Motifs | Alleles | Polymorphism, Single Nucleotide - genetics | Genetic Variation - genetics | Evolution, Molecular | Sequence Deletion - genetics | Chromosome mapping | Human genome | Genetic variation | Identification and classification | Methods | Studies | Haplotypes | Accuracy | Algorithms | Genealogy | Genetics | Data processing | Principal components analysis | Statistical methods | Genomes | Genoma humà
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