Search Results - (Author, Cooperation:C. Dunn)
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1Zhao, F. L., Ahn, J. J., Chen, E. L. Y., Yi, T. J., Stickle, N. H., Spaner, D., Zuniga-Pflücker, J. C., Dunn, S. E.
The American Association of Immunologists (AAI)
Published 2018Staff ViewPublication Date: 2018-10-23Publisher: The American Association of Immunologists (AAI)Print ISSN: 0022-1767Electronic ISSN: 1550-6606Topics: MedicinePublished by: -
2M. Thompson ; C. Dunn ; D. Calkin
American Association for the Advancement of Science (AAAS)
Published 2015Staff ViewPublication Date: 2015-11-21Publisher: American Association for the Advancement of Science (AAAS)Print ISSN: 0036-8075Electronic ISSN: 1095-9203Topics: BiologyChemistry and PharmacologyComputer ScienceMedicineNatural Sciences in GeneralPhysicsKeywords: *Environmental Policy ; Fires/*legislation & jurisprudence ; *ForestsPublished by: -
3Staff View
Publication Date: 2016-05-14Publisher: American Association for the Advancement of Science (AAAS)Print ISSN: 0036-8075Electronic ISSN: 1095-9203Topics: BiologyChemistry and PharmacologyComputer ScienceMedicineNatural Sciences in GeneralPhysicsPublished by: -
4D. Gordon ; J. Huddleston ; M. J. Chaisson ; C. M. Hill ; Z. N. Kronenberg ; K. M. Munson ; M. Malig ; A. Raja ; I. Fiddes ; L. W. Hillier ; C. Dunn ; C. Baker ; J. Armstrong ; M. Diekhans ; B. Paten ; J. Shendure ; R. K. Wilson ; D. Haussler ; C. S. Chin ; E. E. Eichler
American Association for the Advancement of Science (AAAS)
Published 2016Staff ViewPublication Date: 2016-04-02Publisher: American Association for the Advancement of Science (AAAS)Print ISSN: 0036-8075Electronic ISSN: 1095-9203Topics: BiologyChemistry and PharmacologyComputer ScienceMedicineNatural Sciences in GeneralPhysicsKeywords: Animals ; Contig Mapping ; Evolution, Molecular ; Expressed Sequence Tags ; Female ; Genetic Variation ; Genome, Human ; Genomics ; Gorilla gorilla/*genetics ; Humans ; Sequence Alignment ; Sequence Analysis, DNA/*methodsPublished by: -
5Caenorhabditis elegans DBL-1/BMP Regulates Lipid Accumulation via Interaction with Insulin SignalingClark, J. F., Meade, M., Ranepura, G., Hall, D. H., Savage-Dunn, C.
Genetics Society of America (GSA)
Published 2018Staff ViewPublication Date: 2018-01-05Publisher: Genetics Society of America (GSA)Electronic ISSN: 2160-1836Topics: BiologyPublished by: -
6Madaan, U., Yzeiraj, E., Meade, M., Clark, J. F., Rushlow, C. A., Savage-Dunn, C.
Genetics Society of America (GSA)
Published 2018Staff ViewPublication Date: 2018-12-07Publisher: Genetics Society of America (GSA)Print ISSN: 0016-6731Topics: BiologyPublished by: -
7RICHARDS, I. M. ; SHIELDS, S. K. ; GRIFFIN, R. L. ; FIDLER, S. F. ; DUNN, C. J.
Oxford, UK : Blackwell Publishing Ltd
Published 1992Staff ViewISSN: 1365-2222Source: Blackwell Publishing Journal Backfiles 1879-2005Topics: MedicineType of Medium: Electronic ResourceURL: -
8Staff View
ISSN: 0030-851XTopics: Political ScienceSociologyEconomicsNotes: Book ReviewsURL: -
9Staff View
ISSN: 0030-851XTopics: Political ScienceSociologyEconomicsNotes: BOOKS REVIEWED IN THIS NUMBERURL: -
10Staff View
ISSN: 0030-851XTopics: Political ScienceSociologyEconomicsNotes: BOOK REVIEWSURL: -
11Staff View
ISSN: 0030-851XTopics: Political ScienceSociologyEconomicsNotes: BOOK REVIEWSURL: -
12Staff View
ISSN: 0025-8385Topics: Linguistics and Literary StudiesNotes: REVIEWSURL: -
13MACKAY, A. R. ; SEDGWICK, A. D. ; DUNN, C. J. ; FLEMING, W. E. ; WILLOUGHBY, D. A.
Oxford, UK : Blackwell Publishing Ltd
Published 1985Staff ViewISSN: 1365-2133Source: Blackwell Publishing Journal Backfiles 1879-2005Topics: MedicineType of Medium: Electronic ResourceURL: -
14Bowcock, A. ; Osborne-Lawrence, S. ; Barnes, R. ; Chakravarti, A. ; Washington, S. ; Dunn, C.
Amsterdam : ElsevierStaff ViewISSN: 0888-7543Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: BiologyMedicineType of Medium: Electronic ResourceURL: -
15Staff View
ISSN: 0022-4405Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: PsychologyType of Medium: Electronic ResourceURL: -
16Staff View
ISSN: 0550-3213Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: PhysicsType of Medium: Electronic ResourceURL: -
17Staff View
ISSN: 0260-9827Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: GeographyPolitical ScienceType of Medium: Electronic ResourceURL: -
18Staff View
ISSN: 1432-0827Keywords: Osteoclast ; Motility ; Calcitonin ; Prostacyclin ; Cyclic AMPSource: Springer Online Journal Archives 1860-2000Topics: BiologyMedicinePhysicsNotes: Summary We separated osteoclasts from bone and observed the effect of several known and potential mediators of the control of bone resorption on their cytoplasmic motility. We already found that calcitonin (CT), a hormone that inhibits bone resorption, regularly causes complete inhibition of cytoplasmic motility, specific for osteoclasts, through a trypsin-sensitive membrane receptor [1]. We report here that prostaglandin I2 (PGI2) and dibutyryl cyclic AMP induce an identical change in osteoclastic behavior. We found that theophylline, which inhibits intracellular cyclic AMP degradation, and which itself had no effect on osteoclastic motility, potentiated the cytoplasmic inhibition casued by CT, PGI2, and cyclic AMP. This suggests that PGI2 and CT cause cytoplasmic quiescence by increasing the intracellular level of cyclic AMP, a view compatible with the known ability of CT to increase cyclic AMP in bone [2]. Parathyroid hormone (PTH), PGE2, and 1,25 dihydroxycholecalciferol (1,25 (OH)2D3), hormones known to stimulate osteoclasts, did not stimulate the activity of either active or quiescent isolated osteoclasts. The undoubted ability of these hormones to stimulate osteoclastic activityin vivo may therefore be mediated through a primary hormonal interaction with another cell type.Type of Medium: Electronic ResourceURL: -
19Staff View
ISSN: 0160-9327Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: Natural Sciences in GeneralType of Medium: Electronic ResourceURL: -
20Staff View
ISSN: 1432-0584Keywords: Prostaglandins ; Erythropoiesis ; Cell separationSource: Springer Online Journal Archives 1860-2000Topics: MedicineNotes: Summary Ten prostaglandin derivatives have been investigated for their ability to stimulate heme synthesis in serum-free cultures of fetal mouse liver cells in an attempt to define the structural requirements of the prostaglandin molecule necessary for erythrostimulation. In descending order of potency, only PGE2, PGF2α and PGB1produced at least 50% stimulation of endogenous heme synthesis. Seven of the ten prostaglandin derivatives tested were inhibitory at high concentrations. The PGE2 effect was pharmacologically distinct from that of Ep and could be antagonized by 15epi PGF2α. Unit gravity cell sedimentation studies demonstrated that PGE2 stimulated only the larger cells within the erythropoietin responsive cell population.Type of Medium: Electronic ResourceURL: