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Evaluation of CGA 64251 for postharvest disease control of papaya, 1980


, : Evaluation of CGA 64251 for postharvest disease control of papaya, 1980. Fungicide and nematicide tests results American Phytopathological Society6(36): 50


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Ridsdill Smith Tom; Flynn Des; Darling Stuart, 2008: Benefits of two-boat 4D acquisition, an Australian case study. In February 2007, Woodside acquired a two-boat, push reverse 4D monitor survey over the Enfield oil field offshore Western Australia (Figure 1). Two-boat push reverse acquisition maximizes 4D repeatability and minimizes 4D infill in a survey area...

Anonymous, 1970: Revolution in nurses' uniforms. Kangogaku Zasshi 34(4): 26-31

Wu, L.A.; Kanitz, E.; Crumly, J.; D'Ancona, F.; Strikas, R.A., 2014: Adult immunization policies in advanced economies: vaccination recommendations, financing, and vaccination coverage. While many countries have robust child immunization programs and high child vaccination coverage, vaccination of adults has received less attention. The objective of this study was to describe the adult vaccination policies in developed countries....

Larsen, J.; Stubbings, V.; Møller, R.Steensbjerre.; Hjalgrim, H., 2016: Glucose transporter-1 deficiency syndrome can cause various clinical symptoms. Glucose transporter-1 deficiency syndrome (GLUT1-DS) is caused by a decreased function of the glucose transporter GLUT1 protein, which is located in the blood brain barrier. This leads to inadequate glucose levels for brain metabolism and can caus...

Brewer, D.; Greenwell, M.; Taylor, A., 1993: Studies on Trichoderma isolates from Mytilus edulis collected on the shores of Cape Breton and Prince Edward Islands. Samples of Mytilis edulis (mussel) were collected from coastal sites, randomly selected on the south-eastern shores of Prince Edward Island and from similar locations on the southern shore of Cape Breton Island. Cultivation of aliquots of tissue f...

Suri, T.; Dixit, A., 2017: The phenotype of EZH2 haploinsufficiency-1.2-Mb deletion at 7q36.1 in a child with tall stature and intellectual disability. Weaver syndrome is a rare overgrowth syndrome with distinct facial features in young children and variable learning disability. Heterozygous missense mutations in EZH2 are present in over 90% of patients with Weaver syndrome but the exact mechanis...

Virk, R.S.; Arora, P., 2007: Chronic sinonasal aspergillosis with associated mucormycosis. Ear, Nose, & Throat Journal 86(1): 22-22

Heath D.; Cleary P., 1989: Potential chromosomal linkage of the fc receptor and m protein genes in the m type 76 strain cs110 of group a streptococci. Abstracts of the Annual Meeting of the American Society for Microbiology 89: 82

Zekanowski, C.; Cabalska, B.; Borsuk, P.; Bal, J., 1997: Mutations of the phenylalanine hydroxylase gene in mild hyperphenylalaninemia: a novel mutation in exon 3. Mutation analysis of the N-acetylgalactosamine-6-sulfate sulfatase gene was performed in a group of 35 patients with mucopolysaccharidosis type IVA from 33 families, mainly of European origin. By nonradioactive SSCP screening, 35 different gene mu...