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  • 1
    In: Antonie van Leeuwenhoek, Springer Science and Business Media LLC, Vol. 110, No. 10 ( 2017-10), p. 1357-1371
    Type of Medium: Online Resource
    ISSN: 0003-6072 , 1572-9699
    RVK:
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2017
    detail.hit.zdb_id: 1478112-8
    SSG: 12
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  • 2
    Online Resource
    Online Resource
    Wiley ; 2021
    In:  Physiologia Plantarum Vol. 173, No. 4 ( 2021-12), p. 1535-1555
    In: Physiologia Plantarum, Wiley, Vol. 173, No. 4 ( 2021-12), p. 1535-1555
    Abstract: Salt stress is a globally increasing environmental detriment to crop growth and productivity. Exposure to salt stress evokes a complex medley of cellular signals, which rapidly reprogram transcriptional and metabolic networks to shape plant phenotype. To date, genetic engineering approaches were used with success to enhance salt tolerance; however, their performance is yet to be evaluated under realistic field conditions. Regulatory short non‐coding RNAs (rsRNAs) are emerging as next‐generation candidates for engineering salt tolerance in crops. In view of this, the present review provides a comprehensive analysis of a decade's worth of functional studies on non‐coding RNAs involved in salt tolerance. Further, we have integrated this knowledge of rsRNA‐mediated regulation with the current paradigm of salt tolerance to highlight two regulatory complexes (RCs) for regulating salt tolerance in plants. Finally, a knowledge‐driven roadmap is proposed to judiciously utilize RC component(s) for enhancing salt tolerance in crops.
    Type of Medium: Online Resource
    ISSN: 0031-9317 , 1399-3054
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 208872-1
    detail.hit.zdb_id: 2020837-6
    SSG: 12
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  • 3
    Online Resource
    Online Resource
    IP Innovative Publication Pvt Ltd ; 2023
    In:  The Journal of Dental Panacea Vol. 5, No. 1 ( 2023-4-28), p. 13-16
    In: The Journal of Dental Panacea, IP Innovative Publication Pvt Ltd, Vol. 5, No. 1 ( 2023-4-28), p. 13-16
    Abstract: Now a days most commonly used material to treat the defects in the bone after trauma or after any pathology are bone grafts. Bone grafting is a procedure which is performed surgically to join any defect which is surrounding the bone or for the union of the bone. It was found that the graft material which are allogenic in nature as well as other bioactive synthetic substitutes of the bone graft material shows good integration with the remaining bone. To increase the chances of acceptance of these allogenic bone graft materials and others synthetic bioactive graft materials addition of different growth factors for e.g. such as bone morphogenic proteins, platelet rich plasma, platelet rich fibrin have been considered very well. Bone is found to be the second commonly transplanted tissue after the blood. There are various methods present in the treatment of the bone defects such as guided regeneration of bone, use of stem cells and bone grafts, but bone graft shows promising results in the terms of maintaining the normal outline structure of the bone, bone grafts helps in maintaining the aesthetic restoration, helps in eliminating the space or defect which is surrounding the bone due to trauma or due to any pathological condition, helps in providing the width or height for the ease of placement of implant in the oral cavity.
    Type of Medium: Online Resource
    ISSN: 2348-8727
    Language: Unknown
    Publisher: IP Innovative Publication Pvt Ltd
    Publication Date: 2023
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  • 4
    Online Resource
    Online Resource
    Diva Enterprises Private Limited ; 2020
    In:  Baba Farid University Dental Journal Vol. 10, No. 2 ( 2020), p. 72-74
    In: Baba Farid University Dental Journal, Diva Enterprises Private Limited, Vol. 10, No. 2 ( 2020), p. 72-74
    Type of Medium: Online Resource
    ISSN: 0976-8181 , 2230-7273
    Language: English
    Publisher: Diva Enterprises Private Limited
    Publication Date: 2020
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  • 5
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2022
    In:  Vegetos Vol. 35, No. 4 ( 2022-04-06), p. 942-952
    In: Vegetos, Springer Science and Business Media LLC, Vol. 35, No. 4 ( 2022-04-06), p. 942-952
    Type of Medium: Online Resource
    ISSN: 2229-4473
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2022
    detail.hit.zdb_id: 2632294-8
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  • 6
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2017
    In:  Indian Journal of Clinical Biochemistry Vol. 32, No. 2 ( 2017-6), p. 179-185
    In: Indian Journal of Clinical Biochemistry, Springer Science and Business Media LLC, Vol. 32, No. 2 ( 2017-6), p. 179-185
    Type of Medium: Online Resource
    ISSN: 0970-1915 , 0974-0422
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2017
    detail.hit.zdb_id: 2166866-8
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  • 7
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2010
    In:  Cancer Prevention Research Vol. 3, No. 12_Supplement ( 2010-12-01), p. A37-A37
    In: Cancer Prevention Research, American Association for Cancer Research (AACR), Vol. 3, No. 12_Supplement ( 2010-12-01), p. A37-A37
    Abstract: Background: Cyclooxygenase (COX)-2 inhibitor, celecoxib and n-3 poly unsaturated fatty acid (PUFA) rich fish oil has been reported to have a synergistic chemopreventive effect on colon and breast cancer in animal models and this effect may be mediated through alteration in apoptosis and cell cycle. Therefore, the present study was designed to understand the mechanism of action of this combinatorial strategy in 7,12-Dimethylbenz(a) anthracene (DMBA) induced mammary carcinogenesis. Study Design: Female Wistar rats were distributed into six groups: group-1 (vehicle treated), group-2 (DMBA treated), group-3 (20mg/kg body weight celecoxib + DMBA), group-4 (0.5 ml fish oil + DMBA), group-5 (20 mg/kg body weight celecoxib+0.5 ml fish oil) and group-6 (20 mg/kg body weight celecoxib+0.5 ml fish oil + DMBA). The animals were pretreated with the respective dose regimens orally for one week prior to the DMBA (15mg) dose. The animals were subsequently maintained for 90 days and then sacrificed. The levels of reactive oxygen species (ROS) by 2’,7’-dichlorofluorescein diacetate (DCFH-DA), intracellular Ca2+ by fluo-3-penta-acetoxymethylester (fluo-3-AM) dye, p53 by monoclonal antibody and mitochondrial membrane potential (MMP) by 5,5,6,6-tetrachloro-1,1,3,3-tetraethylbenzamidazolo-carbocyanin iodide (JC-1) dye were estimated in isolated mammary epithelial cells. Results: A significant increase in ROS, intracellular calcium and p53 levels and a decrease in MMP were observed in DMBA treated rats as compared to control animals. There was a significant decrease in p53, intracellular calcium and ROS generation on pretreatment with either celecoxib, fish oil or combination dosage of celecoxib and fish oil in DMBA treated animals with respect to only DMBA treated animals (group 2) with a comparatively marked alteration in combination dose regimen. However, an increase in MMP was observed in fish oil and the combination dosage regimen with respect to DMBA treated animals. Fish oil treatment in comparison to celecoxib in DMBA treated animals led to a significant increase in calcium, ROS and MMP levels. To conclude a synergistic effect of celecoxib and fish oil was observed in intracellular calcium, ROS and p53 levels in DMBA treated animals which may be responsible for the better chemopreventive efficacy of the combinatorial regimen. Citation Information: Cancer Prev Res 2010;3(12 Suppl):A37.
    Type of Medium: Online Resource
    ISSN: 1940-6207 , 1940-6215
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2010
    detail.hit.zdb_id: 2422346-3
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  • 8
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2010
    In:  Cancer Prevention Research Vol. 3, No. 12_Supplement ( 2010-12-01), p. B52-B52
    In: Cancer Prevention Research, American Association for Cancer Research (AACR), Vol. 3, No. 12_Supplement ( 2010-12-01), p. B52-B52
    Abstract: Aim: Cyclooxygenase (COX)-2 enzymes plays an important role in the progression and metastasis of cancer. COX −2 inhibition by non steroidal anti inflammatory drugs (NSAID) is a useful approach for cancer prevention but has side effects. On the other hand, n-3 polyunsaturated fatty acids (PUFA) also have a cancer chemopreventive effect mediated by COX-2 inhibition. Therefore, the present study was designed to investigate the chemopreventive effect of combined dosage of n-3 PUFA rich fish oil and celecoxib, a COX-2 inhibitor in the initiation phase of experimental mammary carcinogenesis. Study Design: Female Wistar rats were distributed into six groups: group-1 (vehicle treated), group-2 (DMBA treated), group-3 (20mg/kg body weight celecoxib), group-4 (0.5 ml fish oil), group-5 (20 mg/kg body weight celecoxib+0.5 ml fish oil) and group-6 (20 mg/kg body weight celecoxib+0.5 ml fish oil). The treatment was given for seven days and on 8th day animals in all groups except group 1 and 5 received an oral dose of 15mg of DMBA (7, 12-Dimethylbenz (a) anthracene) and sacrificed after 90 days. Histopathology was done for morphological examination of the tissue specimens. Apoptosis was measured by using M30 cytodeath monoclonal antibody and Caspase-3 activity and cell cycle analysis by propidium iodide (PI) staining was performed in isolated mammary epithelial cells. Results: In the animals treated with DMBA, the mammary tissue showed the features of ductal hyperplasia. Treatment with combination dosages of celecoxib+fish oil+DMBA resulted in a histological profile similar to the normal mammary tissue while obstruction in duct and lobule as well as hyperplastic changes were observed in the mammary tissue of celecoxib or fish oil treated animals. Group 2 animals showed a significant increase in apoptosis with M-30 cytoDEATH and caspase-3 activity. In addition, an increase in cell population in S and G2/M phase with a concomitant decrease in G1 phase cells was observed in carcinogen treated animals. In comparison to DMBA treated animals, a decrease in percentage apoptotic cells was observed in celecoxib or/and fish oil pretreated groups followed by DMBA with the least reduction in combinatorial regimen treated animals. There was no significant difference in the Caspase-3 activity in the DMBA treated animals and celecoxib + fish oil + DMBA treated animals. In the animals treated with combination dosage of celecoxib + fish oil + DMBA, there was a significant increase in apoptosis as compared to animals treated with celecoxib and fish oil alone. The apoptosis in the groups was also significantly increased with respect to control animals (group 1). Conclusion: Though both celecoxib and fish oil showed chemopreventive potential in experimental mammary carcinogenesis, better efficacy was observed with the combinatorial treatment and their synergistic effect may be mediated by the apoptotic pathway. Citation Information: Cancer Prev Res 2010;3(12 Suppl):B52.
    Type of Medium: Online Resource
    ISSN: 1940-6207 , 1940-6215
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2010
    detail.hit.zdb_id: 2422346-3
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  • 9
    Online Resource
    Online Resource
    Wiley ; 2019
    In:  International Journal of Rheumatic Diseases Vol. 22, No. 5 ( 2019-05), p. 946-950
    In: International Journal of Rheumatic Diseases, Wiley, Vol. 22, No. 5 ( 2019-05), p. 946-950
    Abstract: Biologics have emerged as an important modality of treatment in rheumatic diseases and have allowed the rheumatologist to explore varied therapeutic uses of these drugs. Rituximab, a monoclonal antibody against CD 20 receptor is an important member of the biologic armamentarium for the treatment of various refractory autoimmune inflammatory rheumatic diseases. The drug is now widely used in systemic lupus erythematosus for several complications which are refractory to conventional therapy. Although relatively safe, the post‐marketing surveillance of rituximab has revealed a few rare but important adverse reactions. Cytopenia including neutropenia following rituximab, has been vastly reported as a late event ( 〉 4 weeks), but a few cases of early onset neutropenia ( EON ) and thrombocytopenia are also found in the literature. We describe a case of a 35‐year‐old woman with refractory lupus nephritis who developed asymptomatic EON and thrombocytopenia following rituximab infusion. The neutropenia responded well to granulocyte colony‐stimulating factor treatment and the platelets spontaneously recovered. This case report is aimed at highlighting the importance of identifying early onset cytopenia following rituximab which may have an important bearing on the final outcome for the patient.
    Type of Medium: Online Resource
    ISSN: 1756-1841 , 1756-185X
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2019
    detail.hit.zdb_id: 2427877-4
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  • 10
    Online Resource
    Online Resource
    Informa UK Limited ; 2021
    In:  Electromagnetic Biology and Medicine Vol. 40, No. 1 ( 2021-01-02), p. 92-102
    In: Electromagnetic Biology and Medicine, Informa UK Limited, Vol. 40, No. 1 ( 2021-01-02), p. 92-102
    Type of Medium: Online Resource
    ISSN: 1536-8378 , 1536-8386
    Language: English
    Publisher: Informa UK Limited
    Publication Date: 2021
    detail.hit.zdb_id: 2588120-6
    SSG: 12
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