1,894,799 research outputs found
People going to Rara
No full textGroup of people going to Rara; maypole in background.Print size: 3 1/4 x 2 1/8 inches.Credit: Erika Bourguignon Haiti Photograph Collection at The Ohio State University
PML-nuclear body formation is impaired in deletion mutant PML-RARA-expressing cells.
No full text(A) PML/RARA degradation upon RA treatment in Wt-PML-RARA- and mutant-PML-RARA-transduced cells was analyzed by Western blot using anti-FLAG antibody. The cells were treated with 1 μM of ATRA or tamibarotene for 12 hours. (B) Localization of PML and PML-nuclear body formation was evaluated by immunofluorescence staining in Wt-PML-RARA- and mutated- PML-RARA-transduced HL-60 cells. The cells were treated with 1 μM of ATRA or tamibarotene for seven days.</p
Swara Suling: Javanisches Gamelan
No full textStück: Swara Suling
Leiterin: Sarah Weiss
Instrument: Javanisches Gamelan
Gruppe: Nyai Rara Saraswat
RarA-mV H202
No full textFluorescence microscopy, B. subtiliscells were grown in S750minimal medium at 30ºC under shaking conditions until exponential growth. Three microliters of cells were transferred on an agarose slide – a glass slide (microscope slides standard, Roth) coated with an agarose layer (S750minimal medium, 10 mg/mL agarose) – and covered with a cover slip (Roth). Conventional light microscopy was performed using a Zeiss Observer Z1 (Carl Zeiss) with an oil immersion objective (100 x magnification, 1.45 numerical aperture, alpha Plan-FLUAR, Carl Zeiss) and a CCD camera (CoolSNAP EZ, Photometrics), or with a BX51 microscope (Olympus) with a Cool Snap EZ camera (Photometrics) and a xenon light source (Olympus). Electronic data were processed using Metamorph 7.5.5.0 software (Molecular Devices, Sunnyvale, CA, USA), which also allows the calibration of the fluorescence intensity and pixel size to determine the cell length, time-lapse epifluorescence microscopy of RarA-mV were collected every 3min.</p
RarA-mV MMS
No full textFluorescence microscopy time-lapse, B. subtilis cells were grown in S750minimal medium at 30ºC under shaking conditions until exponential growth. Three microliters of cells were transferred on an agarose slide – a glass slide (microscope slides standard, Roth) coated with an agarose layer (S750minimal medium, 10 mg/mL agarose) – and covered with a cover slip (Roth). Conventional light microscopy was performed using a Zeiss Observer Z1 (Carl Zeiss) with an oil immersion objective (100 x magnification, 1.45 numerical aperture, alpha Plan-FLUAR, Carl Zeiss) and a CCD camera (CoolSNAP EZ, Photometrics), or with a BX51 microscope (Olympus) with a Cool Snap EZ camera (Photometrics) and a xenon light source (Olympus). Electronic data were processed using Metamorph 7.5.5.0 software (Molecular Devices, Sunnyvale, CA, USA), which also allows the calibration of the fluorescence intensity and pixel size to determine the cell length, time-lapse epifluorescence microscopy of RarA-mV were collected every 3min
Eutrombicula rara
No full textEutrombicula rara (Walch, 1924) Trombicula rara Walch, 1924: 527, figs. 23–26; Womersley & Heaslip 1943: 90, pl. IV (5); Gunther 1952: 17. Trombicula (Eutrombicula) rara: Thor & Willmann 1947: 283, fig. 341. Trombicula (Trombicula) rara: Wharton & Fuller 1952: 69. Trombicula (Neotrombicula) rara: Womersley 1952: 80, pl. 13 (A–D). Neotrombicula rara: Radford 1954: 259. Siseca rara: Womersley & Audy, 1957: 237, figs. 4, 5 (nymph), 268; Audy 1957: 247; Nadchatram 1972: 190; Lakshana 1973: 13; Brown & Goff 1988a: 222; Goff & Easton 1989: 239; Chau et al. 2007: 89, fig. 42. Eutrombicula (Siseca) rara: Vercammen-Grandjean 1965b: 34; 1968b: 65. Eutrombicula rara: Domrow & Lester 1985: 11, fig. 23. Type deposition. Possibly in KWI (Domrow & Lester 1985). Type data. Ex man, Sumatra, Deli (Indonesia, North Sumatra Province, Deli Serdang Regency). Hosts. RODENTIA: Callosciurus caniceps, C. erythraeus, C. erythraeus flavimanus, C. finlaysoni, C. samarensis, Dremomys rufigenis, Hylopetes phayrei, Menetes berdmorei, Niviventer fulvescens, Rattus andamanensis, R. rattus, Sundamys muelleri; SCANDENTIA: Tupaia glis; PRIMATES: Homo sapiens; SQUAMATA: Carlia rhomboidalis, Concinnia tenuis, Eutropis multicarinata, E. multifasciata, Sphenomorphus jobiensis, S. variegatus; AVES: Cyornis tickelliae, Pitta moluccensis, P. sordida. Distribution. Australia, Indonesia, Malaysia, Papua New Guinea, Philippines, Thailand, Vietnam.Published as part of Stekolnikov, Alexandr A., 2021, A checklist of chigger mites (Acariformes: Trombiculidae) of Southeast Asia, pp. 1-163 in Zootaxa 4913 (1) on page 107, DOI: 10.11646/zootaxa.4913.1.1, http://zenodo.org/record/444891
Going Beyond Counting First Authors in Author Co-citation Analysis
Full text linkThe present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
RarA-mV WT
No full textFluorescence microscopy time-lapse, B. subtilis cells were grown in S750minimal medium at 30ºC under shaking conditions until exponential growth. Three microliters of cells were transferred on an agarose slide – a glass slide (microscope slides standard, Roth) coated with an agarose layer (S750minimal medium, 10 mg/mL agarose) – and covered with a cover slip (Roth). Conventional light microscopy was performed using a Zeiss Observer Z1 (Carl Zeiss) with an oil immersion objective (100 x magnification, 1.45 numerical aperture, alpha Plan-FLUAR, Carl Zeiss) and a CCD camera (CoolSNAP EZ, Photometrics), or with a BX51 microscope (Olympus) with a Cool Snap EZ camera (Photometrics) and a xenon light source (Olympus). Electronic data were processed using Metamorph 7.5.5.0 software (Molecular Devices, Sunnyvale, CA, USA), which also allows the calibration of the fluorescence intensity and pixel size to determine the cell length, time-lapse epifluorescence microscopy of RarA-mV were collected every 3min. </p
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