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Journal articles on the topic 'Habry'

Author: Grafiati

Published: 4 June 2021

Last updated: 16 February 2022

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1

Khalekuzzaman, Md, Muhammed Alamgir, Mehedi Hasan, and Md Nahid Hasan. "Performance comparison of uninsulated and insulated hybrid anaerobic baffled reactor (HABR) operating at warm temperature." Water Science and Technology 78, no. 9 (2018): 1879–92. http://dx.doi.org/10.2166/wst.2018.401.

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Abstract In this research, a hybrid anaerobic baffled reactor (HABR) configuration was proposed consisting of a front sedimentation chamber and four regular baffled chambers followed by two floated filter media chambers for the treatment of domestic wastewater. Performance comparison of uninsulated and insulated HABRs was carried out operating at warm temperature (18.6–37.6 °C) under variable HRTs (30 h and 20 h). The study suggests that almost similar chemical oxygen demand (91% vs 88%), total suspended solids (90% vs 95%), turbidity (98% vs 97%), and volatile suspended solids (90% vs 93%) re

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2

Habr, Fadlallah. "Role of endoscopic ultrasound in the diagnosis and staging of pancreatic cancer." Frontiers in Bioscience 5, no. 1 (2000): e30. http://dx.doi.org/10.2741/habr.

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3

Haberal, Mehmet. "In Memoriam : Dr. Pekka Juha Häyry." Experimental and Clinical Transplantation 18, no. 3 (2020): 269. http://dx.doi.org/10.6002/ect.2020.hayry.

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4

ÇELİK, Hatice, Sevim Aslan FELEK, Ahmet İSLAM, and Mehmet Alpaslan GÖNÜLTAŞ. "Congenital Hairy Polyp of Eustachian Tube in an Adult: An Unusual Case." Turkiye Klinikleri Journal of Medical Sciences 30, no. 5 (2010): 1742–44. http://dx.doi.org/10.5336/medsci.2008-9647.

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5

Husted, Bette. "Harry." English Journal 74, no. 6 (1985): 46. http://dx.doi.org/10.2307/816893.

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6

Czerwiec, MK. "“Harry”." Configurations 22, no. 2 (2014): 205–6. http://dx.doi.org/10.1353/con.2014.0016.

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7

Haines, Joe D. "Harry." Postgraduate Medicine 84, no. 5 (1988): 306–7. http://dx.doi.org/10.1080/00325481.1988.11700453.

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8

Hofmann, Janine. "Harry." Lebensmittel Zeitung 73, no. 26 (2021): 84. http://dx.doi.org/10.51202/0947-7527-2021-26-084.

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9

Hofmann, Janine. "Harry." Lebensmittel Zeitung 73, no. 26 (2021): 86. http://dx.doi.org/10.51202/0947-7527-2021-26-086.

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10

Drobot, K. O. "TARRAGON (Artemisia dracunculus L.) “HAIRY” ROOT CULTURE PRODUCTION." Biotechnologia Acta 9, no. 2 (2016): 55–60. http://dx.doi.org/10.15407/biotech9.02.055.

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11

Teasdale, John R., and Craig S. T. Daughtry. "Weed Suppression by Live and Desiccated Hairy Vetch (Vicia villosa)." Weed Science 41, no. 2 (1993): 207–12. http://dx.doi.org/10.1017/s0043174500076074.

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Hairy vetch was grown as a winter annual cover crop and evaluated for weed suppression when desiccated by paraquat or left alive until natural senescence in a 3-yr field experiment. Total weed density and biomass were variable in the desiccated hairy vetch treatment relative to a bare soil treatment but were consistently lower in the live hairy vetch treatment relative to the desiccated or bare soil treatments. An average of 87% of sites under live hairy vetch compared to 8% of sites under desiccated hairy vetch transmitted less than 1% of unobstructed sunlight. The red (660 nm) to far-red (73

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12

Hoffman, Melinda L., Emilie E. Regnier, and John Cardina. "Weed and Corn (Zea mays) Responses to a Hairy Vetch (Vicia villosa) Cover Crop." Weed Technology 7, no. 3 (1993): 594–99. http://dx.doi.org/10.1017/s0890037x00037398.

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Field studies were conducted in 1990 and 1991 to determine the effects of corn planting date and hairy vetch control method on the efficacy of fall-planted hairy vetch as a weedsuppressive cover crop for no-till corn. Glyphosate controlled hairy vetch when applied at the early bud growth stage (April), but hairy vetch residue provided no weed control compared to the weedy check. Mowing was not an effective means of suppressing hairy vetch at the early bud stage. Untreated hairy vetch reduced weed biomass 96% in 1990 and 58% in 1991 but reduced yield over 76% in April-planted corn. There was no

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13

Patel, Kazoomi, Rupal Shah, Biren Parikh, Jyoti Sawhney, and Bina Brahmbhatt. "Hairy cell leukemia: A clinicopathological study of 18 cases." Annals of Pathology and Laboratory Medicine 5, no. 3 (2018): A256–261. http://dx.doi.org/10.21276/apalm.1660.

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14

Rahman, Mukhlesur. "Independent assortment of seed color and hairy leaf genes in Brassica rapa L." Canadian Journal of Plant Science 94, no. 4 (2014): 615–20. http://dx.doi.org/10.4141/cjps2012-323.

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Rahman, M. 2014. Independent assortment of seed color and hairy leaf genes in Brassica rapa L. Can. J. Plant Sci. 94: 615–620. A genetic study of seed color and hairy leaf in Brassica rapa was conducted in progeny originating from the brown-seeded, hairy leaf B. rapa subsp. chinensis line and the Bangladeshi B. rapa var. trilocularis line. A joint segregation of both traits was also examined in the F2 and backcross populations. Seed color segregated into brown, yellow–brown, and yellow, which suggests that digenic control of brown or yellow–brown color was dominant over yellow seed color. Hair

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15

Wu, Mark L., Hau C. Kwaan, and Charles L. Goolsby. "Atypical Hairy Cell Leukemia." Archives of Pathology & Laboratory Medicine 124, no. 11 (2000): 1710–13. http://dx.doi.org/10.5858/2000-124-1710-ahcl.

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Abstract The morphologic differential diagnosis of mature B-cell neoplasms with cytoplasmic projections includes splenic lymphoma with villous lymphocytes and hairy cell leukemia. Although the classification of hairy cell leukemia is not universally recognized, 3 variants have been described, namely, classic, variant, and Japanese variant, each of which has different clinical and immunophenotypic features. Classic hairy cell leukemia is virtually always CD11c+, CD25+, and CD103+. Variant and Japanese variant hairy cell leukemias are usually CD11c+, always CD25−, and occasionally CD103+. Each v

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16

SAMADI, Afsaneh, Jirair CARAPETIAN, Reza HEIDARI, Morad JAFARI, and Abdollah HASSANZADEH GORTTAPEH. "Hairy Root Induction in Linum mucronatum ssp. mucronatum, an Anti-Tumor Lignans Producing Plant." Notulae Botanicae Horti Agrobotanici Cluj-Napoca 40, no. 1 (2012): 125. http://dx.doi.org/10.15835/nbha4017312.

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Transgenic hairy root system is a promising source of secondary metabolites in medicinal plants with high pharmaceutical value.For the first time, hairy roots were established in different explants of Linum mucronatum, an anti-cancer agent producing plant, via amikimopine type strain of Agrobacterium rhizogenes, â€˜A13â€™. The percentage of hairy root induction varied from 0 to 60% depended onthe explants and hypocotyl (including cotyledonary node) explants were found to be highly susceptible to A. rhizogenes infection withthe highest (60%) rate of hairy root induction. four different Murashig

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17

Siefkes-Boer, H. J., M. J. Noonan, D. W. Bullock, and A. J. Conner. "HAIRY ROOT TRANSFORMATION SYSTEM IN LARGE-SEEDED GRAIN LEGUMES." Israel Journal of Plant Sciences 43, no. 1 (1995): 1–5. http://dx.doi.org/10.1080/07929978.1995.10676585.

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Hairy roots were produced on faba bean (Vicia faba L.) and chickpea (Cicer arietinum L.) plants by inoculation with Agrobacterium root-inducing strains. Examination of 14 plant genotypes and eight Agrobacterium strains in all possible combinations revealed specific strain/genotype interactions. Hairy root size and morphology differed substantially between faba bean and chickpea hairy roots. Sixty percent of chickpea hairy roots were 10–15 mm in length and forty percent, 15–25 mm. All were <1.0 mm in thickness. Sixty-three percent of faba bean hairy roots were 15–25 mm long and thirty-seven

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18

Blackshaw, Robert E. "Hairy Nightshade (Solanum sarrachoides) Interference in Dry Beans (Phaseolus vulgaris)." Weed Science 39, no. 1 (1991): 48–53. http://dx.doi.org/10.1017/s0043174500057854.

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Field studies were conducted to determine the effect of varying densities of hairy nightshade and varying durations of interference on the biomass and seed yield of dry beans. As few as two hairy nightshade plants per meter of row reduced bean seed yield by an average of 13% over the 2 yr of the study. Increasing the density of hairy nightshade to 100 plants per meter resulted in bean yield losses of 77%. Hairy nightshade interference during the first 3 weeks after crop emergence was sufficient to reduce bean yields. Up to 9 weeks of hairy nightshade-free maintenance after crop emergence was r

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19

Wang, Jung-Hao, Hsiao-Han Lin, Chi-Te Liu, Ta-Chung Lin, Li-yu Daisy Liu, and Kung-Ta Lee. "Transcriptomic Analysis Reveals That Reactive Oxygen Species and Genes Encoding Lipid Transfer Protein Are Associated with Tobacco Hairy Root Growth and Branch Development." Molecular Plant-Microbe Interactions® 27, no. 7 (2014): 678–87. http://dx.doi.org/10.1094/mpmi-12-13-0369-r.

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The hairy root, a specialized plant tissue that emerges from a cell transformed with transfer DNA (T-DNA) from Agrobacterium rhizogenes, can be used to study root biology and utilized in biotechnological applications. The rol genes are known to participate in the generation of hairy roots; however, the means by which the rol genes contribute to the initiation and the maintenance of hairy roots remains largely unknown. We demonstrated that tobacco hairy roots lacking either rolB or rolC exhibited fewer branch roots and lost their growth ability in long-term subculture. Additionally, a microarra

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20

Saha, Tusar T., Sang Woon Shin, Wei Dou, et al. "Hairy and Groucho mediate the action of juvenile hormone receptor Methoprene-tolerant in gene repression." Proceedings of the National Academy of Sciences 113, no. 6 (2016): E735—E743. http://dx.doi.org/10.1073/pnas.1523838113.

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The arthropod-specific juvenile hormone (JH) controls numerous essential functions. Its involvement in gene activation is known to be mediated by the transcription factor Methoprene-tolerant (Met), which turns on JH-controlled genes by directly binding to E-box–like motifs in their regulatory regions. However, it remains unclear how JH represses genes. We used the Aedes aegypti female mosquito, in which JH is necessary for reproductive maturation, to show that a repressor, Hairy, is required for the gene-repressive action of JH and Met. The RNA interference (RNAi) screen for Met and Hairy in t

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21

Robertson, Ivan. "Harry Truman." Books Ireland, no. 230 (2000): 113. http://dx.doi.org/10.2307/20632075.

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22

Naylor, John F., and Kevin Morgan. "Harry Pollitt." American Historical Review 100, no. 1 (1995): 166. http://dx.doi.org/10.2307/2168036.

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23

Mullins, PhiI, and Marty Moleski. "Harry Prosch." Tradition and Discovery: The Polanyi Society Periodical 32, no. 2 (2005): 8–24. http://dx.doi.org/10.5840/traddisc2005/200632221.

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24

Lindop, Clive. "Harry 17." Thinking: The Journal of Philosophy for Children 8, no. 3 (1989): 39–40. http://dx.doi.org/10.5840/thinking19898313.

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25

Drew, Stephen. "Potter: Hairy." Annals of Improbable Research 11, no. 5 (2005): 8. http://dx.doi.org/10.3142/107951405781388463.

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26

Simms, Colin. "For Harry." Chicago Review 44, no. 2 (1998): 16. http://dx.doi.org/10.2307/25304271.

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27

Cohen, Leslie G. "Harry James." Annals of Internal Medicine 131, no. 9 (1999): 710. http://dx.doi.org/10.7326/0003-4819-131-9-199911020-00014.

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28

Sekar, ShanmugaC, SwethaSunny Kurian, and P. Surendran. "Hairy Mouth." International Journal of Trichology 4, no. 4 (2012): 289. http://dx.doi.org/10.4103/0974-7753.111218.

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29

Despret, Vinciane, and Serge Gutwirth. "L’affaire Harry." Terrain, no. 52 (March 5, 2009): 142–51. http://dx.doi.org/10.4000/terrain.13628.

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30

Montabone, Benoît. "Harry Potter." Géographie et cultures, no. 68 (December 10, 2008): 99–114. http://dx.doi.org/10.4000/gc.862.

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31

Strassmann, Steve. "Hairy brushes." ACM SIGGRAPH Computer Graphics 20, no. 4 (1986): 225–32. http://dx.doi.org/10.1145/15886.15911.

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32

Watts, Geoff. "Harry Keen." Lancet 381, no. 9879 (2013): 1714. http://dx.doi.org/10.1016/s0140-6736(13)61066-1.

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33

Choi, Jae. "Harry Houdini." Iowa Review 40, no. 3 (2010): 76. http://dx.doi.org/10.17077/0021-065x.6948.

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34

Shapiro, Michael J. "Harry Friedman." PS: Political Science & Politics 30, no. 02 (1997): 226–27. http://dx.doi.org/10.1017/s1049096500043456.

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35

Gale, E. "Harry Keen." BMJ 346, may07 1 (2013): f2852. http://dx.doi.org/10.1136/bmj.f2852.

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36

Lewis, William B. "Heinous Harry:." Child & Youth Services 11, no. 2 (1989): 95–104. http://dx.doi.org/10.1300/j024v11n02_11.

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37

Shimizu, T., and Y. Tokuda. "Hairy tongue." Case Reports 2012, oct04 1 (2012): bcr0220125755. http://dx.doi.org/10.1136/bcr-02-2012-5755.

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38

Bakry, Mohamed B., Saarah Arshad, Salman Haq, et al. "Hairy Hoarseness." Chest 126, no. 4 (2004): 943S. http://dx.doi.org/10.1378/chest.126.4_meetingabstracts.943s-a.

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39

Arovas, Daniel, M. Brian Maple, and Pradeep Kumar. "Harry Suhl." Physics Today 73, no. 12 (2020): 64. http://dx.doi.org/10.1063/pt.3.4641.

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40

Bush, Tony. "Harry Tomlinson." Educational Management Administration & Leadership 34, no. 1 (2006): 8. http://dx.doi.org/10.1177/174114320603400103.

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41

Patten, Brian. "For Harry." Self & Society 39, no. 2 (2011): 17. http://dx.doi.org/10.1080/03060497.2011.11084194.

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42

Beckman, M. "Hairy Breakup." Science of Aging Knowledge Environment 2005, no. 33 (2005): nf66. http://dx.doi.org/10.1126/sageke.2005.33.nf66.

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43

Lucas, S. "Hairy leukoplakia." Histopathology 20, no. 4 (1992): 365. http://dx.doi.org/10.1111/j.1365-2559.1992.tb00998.x.

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44

Southam, J. C. "Hairy leukoplakia." Histopathology 20, no. 4 (1992): 365. http://dx.doi.org/10.1111/j.1365-2559.1992.tb00999.x.

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45

Pultz, John. "Harry Callahan." History of Photography 15, no. 3 (1991): 222–27. http://dx.doi.org/10.1080/03087298.1991.10443177.

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46

No authorship indicated. "Harry Levinson." American Psychologist 48, no. 4 (1993): 355–56. http://dx.doi.org/10.1037/h0090735.

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47

Davies, S. J. J. F. "Harry Frith." Emu - Austral Ornithology 92, no. 2 (1992): 123–24. http://dx.doi.org/10.1071/mu9920123.

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48

Proubasta, Dolores. "Harry Mayne." Leading Edge 4, no. 7 (1985): 18–24. http://dx.doi.org/10.1190/1.1439157.

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49

Lechner, Stefan G., and Gary R. Lewin. "Hairy Sensation." Physiology 28, no. 3 (2013): 142–50. http://dx.doi.org/10.1152/physiol.00059.2012.

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The hairs of the skin not only function to prevent heat loss but also have important sensory functions. Recent work has now established that each hair of the skin is innervated by one or more of three types of mechanoreceptor ending. Each of these three mechanoreceptor types possesses distinct molecular features and detects distinctive information about skin touch, which is relayed to specific brain locations in a somatotopic fashion.

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50

Duncan, A. W. C. D. K. "Harry Williams." BMJ 350, jun12 18 (2015): h3107. http://dx.doi.org/10.1136/bmj.h3107.

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