Institution
Biomedical Primate Research Centre
Nonprofit•Rijswijk, Netherlands•
About: Biomedical Primate Research Centre is a nonprofit organization based out in Rijswijk, Netherlands. It is known for research contribution in the topics: Antigen & Virus. The organization has 354 authors who have published 986 publications receiving 45748 citations.
Topics: Antigen, Virus, Immune system, Experimental autoimmune encephalomyelitis, Plasmodium falciparum
Papers published on a yearly basis
Papers
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Anthony Nolan1, University of Oxford2, Biomedical Primate Research Centre3, Kettering University4, Hoffmann-La Roche5, University of Texas MD Anderson Cancer Center6, Fred Hutchinson Cancer Research Center7, University of Washington8, University of California, Los Angeles9, Hallym University10, University of Geneva11, National Marrow Donor Program12, Medical University of Vienna13, Stanford University14, Harvard University15, University of Cambridge16
TL;DR: This report documents the additions and revisions to the nomenclature of HLA specificities following the principles established in previous reports.
Abstract: The WHO Nomenclature Committee for Factors of the HLA System met following the 14th International HLA and Immunogenetics Workshop in Melbourne, Australia in December 2005 and Buzios, Brazil during the 15th International HLA and Immunogenetics Workshop in September 2008. This report documents the additions and revisions to the nomenclature of HLA specificities following the principles established in previous reports (1–18).
2,390 citations
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TL;DR: In this article, the small subunit ribosomal RNA and the circumsporozoite protein genes were sequenced for eight isolates that had been microscopically identified as P knowlesi by microscopy.
1,100 citations
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TL;DR: It is shown that the patients had strong immune responses against the viral spike protein, a complex that binds to receptors on the host cell, and monoclonal antibodies isolated here are promising candidates for COVID-19 treatment and prevention.
Abstract: The rapid spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has had a large impact on global health, travel, and economy. Therefore, preventative and therapeutic measures are urgently needed. Here, we isolated monoclonal antibodies from three convalescent coronavirus disease 2019 (COVID-19) patients using a SARS-CoV-2 stabilized prefusion spike protein. These antibodies had low levels of somatic hypermutation and showed a strong enrichment in VH1-69, VH3-30-3, and VH1-24 gene usage. A subset of the antibodies was able to potently inhibit authentic SARS-CoV-2 infection at a concentration as low as 0.007 micrograms per milliliter. Competition and electron microscopy studies illustrate that the SARS-CoV-2 spike protein contains multiple distinct antigenic sites, including several receptor-binding domain (RBD) epitopes as well as non-RBD epitopes. In addition to providing guidance for vaccine design, the antibodies described here are promising candidates for COVID-19 treatment and prevention.
1,070 citations
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TL;DR: Three mouse species that are approximately as related to each other as are humans, chimpanzees, and orangutans are studied, and species-specific gene expression patterns indicating that changes in protein and gene expression have been particularly pronounced in the human brain are identified.
Abstract: Although humans and their closest evolutionary relatives, the chimpanzees, are 98.7% identical in their genomic DNA sequences, they differ in many morphological, behavioral, and cognitive aspects. The underlying genetic basis of many of these differences may be altered gene expression. We have compared the transcriptome in blood leukocytes, liver, and brain of humans, chimpanzees, orangutans, and macaques using microarrays, as well as protein expression patterns of humans and chimpanzees using two-dimensional gel electrophoresis. We also studied three mouse species that are approximately as related to each other as are humans, chimpanzees, and orangutans. We identified species-specific gene expression patterns indicating that changes in protein and gene expression have been particularly pronounced in the human brain.
867 citations
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Pompeu Fabra University1, University of Washington2, Stanford University3, University of Michigan4, Harvard University5, University of Arizona6, Max Planck Society7, Aarhus University8, Bilkent University9, University of Minnesota10, University of California, San Francisco11, Autonomous University of Barcelona12, Biomedical Primate Research Centre13, Duke University14, Washington State University15, Franklin & Marshall College16, University of Oxford17, University of Bari18, University of California, San Diego19, University of Copenhagen20, Washington University in St. Louis21, University of Pennsylvania22, National Institutes of Health23, State University of New York System24, Catalan Institution for Research and Advanced Studies25, Copenhagen Zoo26, Howard Hughes Medical Institute27
TL;DR: This comprehensive catalogue of great ape genome diversity provides a framework for understanding evolution and a resource for more effective management of wild and captive great ape populations.
Abstract: Most great ape genetic variation remains uncharacterized; however, its study is critical for understanding population history, recombination, selection and susceptibility to disease. Here we sequence to high coverage a total of 79 wild- and captive-born individuals representing all six great ape species and seven subspecies and report 88.8 million single nucleotide polymorphisms. Our analysis provides support for genetically distinct populations within each species, signals of gene flow, and the split of common chimpanzees into two distinct groups: Nigeria-Cameroon/western and central/eastern populations. We find extensive inbreeding in almost all wild populations, with eastern gorillas being the most extreme. Inferred effective population sizes have varied radically over time in different lineages and this appears to have a profound effect on the genetic diversity at, or close to, genes in almost all species. We discover and assign 1,982 loss-of-function variants throughout the human and great ape lineages, determining that the rate of gene loss has not been different in the human branch compared to other internal branches in the great ape phylogeny. This comprehensive catalogue of great ape genome diversity provides a framework for understanding evolution and a resource for more effective management of wild and captive great ape populations.
807 citations
Authors
Showing all 357 results
Name | H-index | Papers | Citations |
---|---|---|---|
Hans Lassmann | 155 | 724 | 79933 |
James I. Mullins | 100 | 404 | 33038 |
Alan L. Landay | 92 | 556 | 32794 |
Robin F. Anders | 74 | 255 | 16107 |
Andrew P. Waters | 70 | 226 | 17816 |
Chris J. Janse | 70 | 276 | 18120 |
Jon D. Laman | 68 | 261 | 18364 |
Leann Tilley | 65 | 223 | 12292 |
Ronald E. Bontrop | 61 | 243 | 16393 |
Michael J. Blackman | 60 | 166 | 11263 |
Jonathan L. Heeney | 59 | 330 | 11916 |
Alan W. Thomas | 59 | 164 | 12039 |
Michael Foley | 54 | 194 | 9434 |
A. van Belkum | 53 | 178 | 12800 |
Sandra Amor | 53 | 148 | 8596 |