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Journal articles on the topic 'Hatry'

Author: Grafiati

Published: 4 June 2021

Last updated: 6 February 2022

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1

Hatry, Heide. "Imagine It Thick In Your Own Skin: Sculptures and a Unique Artist’s Book." MediaTropes 7, no. 2 (February 6, 2020): 120–37. http://dx.doi.org/10.33137/mt.v7i2.33674.

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In this artistic contribution, New York-based German artist Heide Hatry offers pictures of her sculpture series Imagine It Thick In Your Own Hair. According to Hatry, the project was intended to make people aware of the tragedy and motivate them to help clean up the disaster BP created in 2010 with the Deepwater Horizon spill. Hatry is best known for her body-related performances and her work employing animal flesh and organs, and cremated remains. Among her fundamental preoccupations are identity, death, the nature of aesthetic experience and the meaning of beauty, the effects of knowledge upon perception, the human exploitation of the natural world, and the social oblivion that permits atrocity to persist in our midst.

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2

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

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3

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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4

KARATAŞLI, Muhammet. "Measurement of Environmental Gamma Radiation in and Around The Hatay Province, Turkey." Afyon Kocatepe University Journal of Sciences and Engineering 18, no. 3 (December 1, 2018): 780–85. http://dx.doi.org/10.5578/fmbd.67766.

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5

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

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6

DIRVEN, Lucinda. "Hatra." ARAM Periodical 19 (June 30, 2007): 363–80. http://dx.doi.org/10.2143/aram.19.0.2020735.

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7

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

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8

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

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9

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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10

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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11

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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12

Teasdale, John R., and Craig S. T. Daughtry. "Weed Suppression by Live and Desiccated Hairy Vetch (Vicia villosa)." Weed Science 41, no. 2 (June 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 (730 nm) ratio of transmitted light was reduced by 70% under live hairy vetch compared to 17% under desiccated hairy vetch. Daily maximum soil temperature and diurnal soil temperature amplitude were reduced by live hairy vetch > desiccated hairy vetch > bare soil. Soil moisture content was greater under both live and desiccated hairy vetch compared to bare soil during droughty periods. Changes in light extinction, red to far-red ratio, and diurnal soil temperature amplitude were sufficient to explain greater weed suppression by live than desiccated hairy vetch.

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13

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 (September 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 competition of untreated hairy vetch with corn when corn planting was delayed until May or June (mid- or late-bloom growth stages of hairy vetch). Corn planted in May into untreated hairy vetch yielded similarly to corn planted in a no-cover weed-free check.

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14

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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15

Rahman, Mukhlesur. "Independent assortment of seed color and hairy leaf genes in Brassica rapa L." Canadian Journal of Plant Science 94, no. 4 (May 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. Hairy leaves were found to be under monogenic control, and hairy leaf was dominant over non-hairy leaf. The data show that genes controlling seed color and hairy leaf are inherited independently.

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16

Wu, Mark L., Hau C. Kwaan, and Charles L. Goolsby. "Atypical Hairy Cell Leukemia." Archives of Pathology & Laboratory Medicine 124, no. 11 (November 1, 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 variant is characteristically CD10−. We present a case of hairy cell leukemia with a unique immunoprofile in that the cells were CD10+, CD25+, and CD103−, and we review the criteria helpful in differentiating “hairy” B-cell neoplasms. This case emphasizes the variability of hairy cell leukemia and the need to correlate all clinical and pathologic data in reaching a diagnosis.

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17

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 (May 14, 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 Murashige and Skoog (MS)-based liquid culture media were used for wellestablishment of hairy roots. Hairy root growth medium D (HRGM-D) containing hormone-free MS basal medium with an extra oneday pre-incubation period at 35Â°C was found to be more efficient for profuse growth (fresh weight; 8500 mg per 25 ml culture medium)of hairy roots. Hairy root system presented in this study may offer a suitable platform for optimization and production of satisfactorylevel of aryltetralin lignans like podophyllotoxin and its derivatives from L. mucronatum.

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18

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 (May 13, 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 percent, 25–40 mm. All faba bean hairy roots were between 1.0 and 1.5 mm in thickness.

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19

Blackshaw, Robert E. "Hairy Nightshade (Solanum sarrachoides) Interference in Dry Beans (Phaseolus vulgaris)." Weed Science 39, no. 1 (March 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 required to prevent bean yield losses. Hairy nightshade was a prolific seed producer. At low infestation densities, over 45 000 seeds per plant were produced. Hairy nightshade seed production peaked at over 300 000 seeds m–1at about 30 plants per m of row. Depending on the length of the growing season, 6 to 9 weeks of weed-free conditions after crop emergence were required to prevent hairy nightshade from producing viable seeds before the first killing frost in the fall. Results are discussed in terms of timing and longevity of control required to reduce hairy nightshade interference in dry beans.

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20

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 (July 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 microarray analysis revealed that the expression of several genes encoding lipid transfer proteins (LTP) and reactive oxygen species (ROS)-related genes was significantly suppressed in rolB- or rolC-deficient hairy roots. We found that hairy root clones that exhibited greater branching expressed higher levels of RolB or RolC and the genes encoding LTP identified from the microarray. When hairy roots were compared with intact roots, the expression levels of LTP-encoding genes were dramatically different. In addition, ROS were present at lower levels in rolB- and rolC-deficient hairy roots. We therefore suggest that upregulating LTP and increasing the level of ROS is important for hairy root growth.

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21

Saha, Tusar T., Sang Woon Shin, Wei Dou, Sourav Roy, Bo Zhao, Yuan Hou, Xue-Li Wang, Zhen Zou, Thomas Girke, and Alexander S. Raikhel. "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 (January 7, 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 the Aedes female fat body revealed a large cohort of Met- and Hairy-corepressed genes. Analysis of selected genes from this cohort demonstrated that they are repressed by JH, but RNAi of either Met or Hairy renders JH ineffective in repressing these genes in an in vitro fat-body culture assay. Moreover, this JH action was prevented by the addition of the translational inhibitor cycloheximide (CHX) to the culture, indicating the existence of an indirect regulatory hierarchy. The lack of Hairy protein in the CHX-treated tissue was verified using immunoblot analysis, and the upstream regions of Met/Hairy-corepressed genes were shown to contain common binding motifs that interact with Hairy. Groucho (gro) RNAi silencing phenocopied the effect of Hairy RNAi knockdown, indicating that it is involved in the JH/Met/Hairy hierarchy. Finally, the requirement of Hairy and Gro for gene repression was confirmed in a cell transfection assay. Thus, our study has established that Hairy and its cofactor Gro mediate the repressive function of JH and Met.

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22

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

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23

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

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24

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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25

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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26

Drew, Stephen. "Potter: Hairy." Annals of Improbable Research 11, no. 5 (September 1, 2005): 8. http://dx.doi.org/10.3142/107951405781388463.

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27

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

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28

Cohen, Leslie G. "Harry James." Annals of Internal Medicine 131, no. 9 (November 2, 1999): 710. http://dx.doi.org/10.7326/0003-4819-131-9-199911020-00014.

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29

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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30

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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31

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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32

Strassmann, Steve. "Hairy brushes." ACM SIGGRAPH Computer Graphics 20, no. 4 (August 31, 1986): 225–32. http://dx.doi.org/10.1145/15886.15911.

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33

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

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34

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

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35

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

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36

Gale, E. "Harry Keen." BMJ 346, may07 1 (May 7, 2013): f2852. http://dx.doi.org/10.1136/bmj.f2852.

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37

Lewis, William B. "Heinous Harry:." Child & Youth Services 11, no. 2 (August 7, 1989): 95–104. http://dx.doi.org/10.1300/j024v11n02_11.

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38

Shimizu, T., and Y. Tokuda. "Hairy tongue." Case Reports 2012, oct04 1 (October 6, 2012): bcr0220125755. http://dx.doi.org/10.1136/bcr-02-2012-5755.

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39

Bakry, Mohamed B., Saarah Arshad, Salman Haq, Frew Gebreab, Louis Voigt, Suhail Raoof, and Gerard Lombardo. "Hairy Hoarseness." Chest 126, no. 4 (October 2004): 943S. http://dx.doi.org/10.1378/chest.126.4_meetingabstracts.943s-a.

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40

Arovas, Daniel, M. Brian Maple, and Pradeep Kumar. "Harry Suhl." Physics Today 73, no. 12 (December 1, 2020): 64. http://dx.doi.org/10.1063/pt.3.4641.

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41

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

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42

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

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43

Beckman, M. "Hairy Breakup." Science of Aging Knowledge Environment 2005, no. 33 (August 17, 2005): nf66. http://dx.doi.org/10.1126/sageke.2005.33.nf66.

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44

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

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45

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

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46

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

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47

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

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48

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

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49

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

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50

Lechner, Stefan G., and Gary R. Lewin. "Hairy Sensation." Physiology 28, no. 3 (May 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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