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Institution

Rockefeller University

EducationNew York, New York, United States
About: Rockefeller University is a education organization based out in New York, New York, United States. It is known for research contribution in the topics: Population & Gene. The organization has 15867 authors who have published 32938 publications receiving 2940261 citations. The organization is also known as: Rockefeller University & Rockefeller Institute.
Topics: Population, Gene, Virus, RNA, Antigen


Papers
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Journal ArticleDOI
TL;DR: A sensitive calorimetric method for the quantitative determination of SAL is described and 6AL has been found in urine of a patient with acute porphyria and also in normal urine.

1,428 citations

Journal ArticleDOI
Mark Kac1
TL;DR: Can one hear the shape of a drum? as discussed by the authors, 1966; The American Mathematical Monthly: Vol. 73, No. 4P2, pp. 1-23.
Abstract: (1966). Can One Hear the Shape of a Drum? The American Mathematical Monthly: Vol. 73, No. 4P2, pp. 1-23.

1,427 citations

Journal ArticleDOI
TL;DR: The feasibility of antigen-specific inhibition of effector T cell function in vivo in humans is demonstrated and caution is urged with the use of immature DCs when trying to enhance tumor or microbial immunity.
Abstract: Immunostimulatory properties of dendritic cells (DCs) are linked to their maturation state. Injection of mature DCs rapidly enhances antigen-specific CD4+ and CD8+ T cell immunity in humans. Here we describe the immune response to a single injection of immature DCs pulsed with influenza matrix peptide (MP) and keyhole limpet hemocyanin (KLH) in two healthy subjects. In contrast to prior findings using mature DCs, injection of immature DCs in both subjects led to the specific inhibition of MP-specific CD8+ T cell effector function in freshly isolated T cells and the appearance of MP-specific interleukin 10–producing cells. When pre- and postimmunization T cells were boosted in culture, there were greater numbers of MP-specific major histocompatibility complex tetramer-binding cells after immunization, but these had reduced interferon γ production and lacked killer activity. These data demonstrate the feasibility of antigen-specific inhibition of effector T cell function in vivo in humans and urge caution with the use of immature DCs when trying to enhance tumor or microbial immunity.

1,426 citations

Journal ArticleDOI
TL;DR: In animal models, neurons in the hippocampus and prefrontal cortex respond to repeated stress by showing atrophy, whereas neurons in amygdala show a growth response, yet these are not necessarily “damaged” and may be treatable with the right medications.
Abstract: Stress promotes adaptation, but prolonged stress leads over time to wear-and-tear on the body (allostatic load). Neural changes mirror the pattern seen in other body systems, that is, short-term adaptation vs. long-term damage. Allostatic load leads to impaired immunity, atherosclerosis, obesity, bone demineralization, and atrophy of nerve cells in the brain. Many of these processes are seen in major depressive illness and may be expressed also in other chronic anxiety disorders. The brain controls the physiological and behavioral coping responses to daily events and stressors. The hippocampal formation expresses high levels of adrenal steroid receptors and is a malleable brain structure that is important for certain types of learning and memory. It is also vulnerable to the effects of stress and trauma. The amygdala mediates physiological and behavioral responses associated with fear. The prefrontal cortex plays an important role in working memory and executive function and is also involved in extinction of learning. All three regions are targets of stress hormones. In animal models, neurons in the hippocampus and prefrontal cortex respond to repeated stress by showing atrophy, whereas neurons in amygdala show a growth response. Yet, these are not necessarily "damaged" and may be treatable with the right medications.

1,415 citations

Journal ArticleDOI
TL;DR: In this article, the authors performed immunohistochemistry for cell-specific markers and the thymidine analog bromodeoxyuridine (BrdU), a marker of DNA synthesis, on the brains of adult tree shrews subjected to psychosocial stress or NMDA receptor antagonist treatment.
Abstract: These studies were designed to determine whether adult neurogenesis occurs in the dentate gyrus of the tree shrew, an animal phylogenetically between insectivores and primates, and to explore the possibility that this process is regulated by stressful experiences and NMDA receptor activation. We performed immunohistochemistry for cell-specific markers and the thymidine analog bromodeoxyuridine (BrdU), a marker of DNA synthesis that labels proliferating cells and their progeny, on the brains of adult tree shrews subjected to psychosocial stress or NMDA receptor antagonist treatment. Cells that incorporated BrdU in the dentate gyrus of adult tree shrews were primarily located in the subgranular zone, had morphological characteristics of granule neuron precursors, and appeared to divide within 24 hr after BrdU injection. Three weeks after BrdU injection, BrdU-labeled cells had neuronal morphology, expressed the neuronal marker neuron specific enolase, and were incorporated into the granule cell layer. Vimentin-immunoreactive radial glia were observed in the dentate gyrus with cell bodies in the subgranular zone and processes extending into the granule cell layer. Exposure to acute psychosocial stress resulted in a rapid decrease in the number of BrdU-labeled cells in the dentate gyrus. In contrast, blockade of NMDA receptors, with the NMDA receptor antagonist MK-801, resulted in an increase in the number of BrdU-labeled cells in the dentate gyrus. These results indicate that adult neurogenesis occurs in the tree shrew dentate gyrus and is regulated by a stressful experience and NMDA receptor activation. Furthermore, we suggest that these characteristics may be common to most mammalian species.

1,415 citations


Authors

Showing all 15925 results

NameH-indexPapersCitations
Bruce S. McEwen2151163200638
David Baltimore203876162955
Ronald M. Evans199708166722
Lewis C. Cantley196748169037
Ronald Klein1941305149140
Scott M. Grundy187841231821
Jie Zhang1784857221720
Andrea Bocci1722402176461
Ralph M. Steinman171453121518
Masayuki Yamamoto1711576123028
Zena Werb168473122629
Nahum Sonenberg167647104053
Michel C. Nussenzweig16551687665
Harvey F. Lodish165782101124
Dennis R. Burton16468390959
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202314
202284
2021873
2020792
2019716
2018767