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1.
Sci Rep ; 13(1): 12705, 2023 08 05.
Article in English | MEDLINE | ID: mdl-37543669

ABSTRACT

Water/drought stress experiments are frequently conducted under imposed stress or rainout shelters, while natural drought hot-spot investigations are rare. The "drought hot spot" in Anantapur, Andhra Pradesh, India, is appropriate for drought stress evaluation due to its hot, arid environment, limited rainfall, with over 50% rainfall variability. According to reports, 30 out of 200 groundnut cultivars in India are supposed to possess drought-tolerant characteristics. However, these cultivars are yet to be evaluated in areas that are prone to drought. This study tested these drought-tolerant genotypes in naturally drought-prone areas of Anantapur under rainfed conditions from Kharif 2017 to 2019. Pod yield and rainfall-use-efficiency (RUE) were measured for these genotypes. Genotype and genotype*environment interactions affected pod yield and RUE (GEI). The AMMI model exhibits significant season-to-season variability within the same area with environmental vectors > 90° angles. GGE biplot suggested the 2018 wet season for drought-resistant cultivar identification. Kadiri5 and GPBD5 were the most drought-tolerant cultivars for cultivation in Anantapur and adjacent regions. These types could also be used to generate drought-tolerant groundnut variants for drought-prone regions.


Subject(s)
Droughts , Genotype , Seasons , Base Sequence , India
2.
Food Chem ; 248: 210-216, 2018 May 15.
Article in English | MEDLINE | ID: mdl-29329846

ABSTRACT

An enzymatic process was developed for the preparation of a nutritionally enriched 1,3-diacylglycerol(DAG)-rich oil from a blend of refined sunflower and rice bran oils. The process involves hydrolysis of vegetable oil blend using Candida cylindracea followed by esterification with glycerol using Lipozyme RM1M. The resultant DAG-rich oil contains 84% of DAG (66% of 1,3-DAG, 18% of 1,2-DAG) and 16% of triacylglycerol (TAG) along with micro nutrients like γ-oryzanol, tocotrienols, tocopherols and phytosterols. Nutritional studies of the DAG-rich oil were conducted in Wistar rats and compared with sunflower oil (SFO). The calorific value of the DAG-rich oil was estimated to be 6.45 Kcals/g as against 9.25 Kcals/g for SFO. The serum and liver cholesterol and TAG levels in rats fed with 1,3-DAG-rich oil were found to be significantly reduced as compared to rats fed diet containing SFO. We conclude that 1,3-DAG-rich oil is a low calorie fat and exhibits hypolipidemic effects.


Subject(s)
Diglycerides/chemistry , Hypolipidemic Agents/chemistry , Hypolipidemic Agents/pharmacology , Rice Bran Oil/chemistry , Sunflower Oil/chemistry , Animals , Caloric Restriction , Candida , Cholesterol/blood , Cholesterol/metabolism , Esterification , Lipase/chemistry , Lipase/metabolism , Liver/drug effects , Liver/metabolism , Male , Phytosterols/analysis , Rats , Rats, Wistar , Tocopherols/analysis , Triglycerides/analysis , Triglycerides/metabolism
3.
Indian J Psychol Med ; 38(1): 78-80, 2016.
Article in English | MEDLINE | ID: mdl-27011411

ABSTRACT

Transvestism, commonly termed as cross-dressing, means to dress in the clothing of opposite sex. We describe a series of three cases with transvestism as one of their primary complaints. The discussion sheds light on the various ways in which transvestism as a symptom can present in Psychiatry. In the first two cases, there was lower intelligence. In first and third case, there were other paraphilia along with transvestism. Second case had co-morbid obsessive-compulsive disorder (OCD) and had good response to selective serotonin reuptake inhibitor (SSRI).

4.
Case Rep Med ; 2014: 267913, 2014.
Article in English | MEDLINE | ID: mdl-24822068

ABSTRACT

Budd-Chiari syndrome refers to hepatic pathology secondary to diminished venous outflow, most commonly associated with venothrombotic disease. Clinically, patients with Budd-Chiari present with hepatomegaly, ascites, abdominal distension, and pain. On imaging, Budd-Chiari syndrome is hallmarked by occluded IVC and or hepatic veins, caudate lobe enlargement, heterogeneous liver enhancement, intrahepatic collaterals, and hypervascular nodules. Etiopathological factors for Budd-Chiari syndrome include several systemic thrombotic and nonthrombotic conditions that can cause venous outflow obstruction at hepatic veins and/or IVC. While the transjugular intrahepatic portosystemic shunt (TIPS) is used as a treatment option for Budd-Chiari syndrome, Budd-Chiari syndrome is not a well-known complication of TIPS procedure. We report a case of Budd-Chiari syndrome that occurred in a transplanted cirrhotic liver from malpositioned proximal portion of the TIPS in IVC causing occlusion of the ostia of hepatic veins which was subsequently diagnosed on contrast-enhanced CT.

6.
Neuroradiol J ; 25(2): 188-92, 2012 May.
Article in English | MEDLINE | ID: mdl-24028913

ABSTRACT

Osteosarcomas are typically long bone tumors and rarely affect the skull, with most articles reporting single cases. As elsewhere in the body, these lesions may be classified as primary or secondary, chiefly post-Paget and post-radiation therapy. We describe two cases of primary osteosarcoma of skull one presenting with cerebellar symptoms and another with giant skull swelling. Complete evaluation with 64 slice CT and histopathological correlation was carried out.

7.
Neuroradiol J ; 25(2): 200-5, 2012 May.
Article in English | MEDLINE | ID: mdl-24028915

ABSTRACT

Disseminated cysticercosis is a rare form of cysticercosis in which the cysticerci spread throughout the body. We describe the case of a seven-year-old child with disseminated cysticercosis. He presented with a one month history of swelling of the whole body, unable to walk for one month and swelling of both eyes for 20 days. After extensive investigation from superficial musculoskeletal ultrasound B-scan of eye, brain computed tomography, brain magnetic resonance imaging (MRI), whole body MRI and pathologic biopsy, the child was diagnosed as having cysticercosis involving the brain, retina and skeletal muscles throughout the whole body.

8.
Neuroradiol J ; 25(3): 374-8, 2012 Jul.
Article in English | MEDLINE | ID: mdl-24028993

ABSTRACT

True solitary plasmacytoma of the skull without signs of systemic myelomatosis is very rare as is orbital involvement. It can be part of generalized disease (multiple myeloma) or localized disease, presenting as orbital tumor. We describe a case of solitary osseous plasmacytoma of the orbit. This 40-year-old man presented with a four month history of proptosis of the left eye, swelling in the left orbito-temporal region with a mild decrease in visual acuity. Multidetector row computed tomography scan showed a geographic osteolytic, well-demarcated lesion involving the greater wing of the sphenoid bone showing homogeneous contrast enhancement with extra-axial extension to the middle and anterior cranial fossa extension with extraconal extension into the orbit at the right side. Fine needle and later biopsy of the lesion revealed plasmacytoma.

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