Zobrazeno 1 - 10
of 121
pro vyhledávání: '"Jayanta Gupta"'
Autor:
Ian R. Barrows, Matt Devalaraja, Rahul Kakkar, Jing Chen, Jayanta Gupta, Sylvia E. Rosas, Santosh Saraf, Jiang He, Alan Go, Dominic S. Raj, Richard L. Amdur
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 11, Iss 18 (2022)
Background Differences in death rate and cardiovascular disease (CVD) between Black and White patients with chronic kidney disease is attributed to sociocultural factors, comorbidities, genetics, and inflammation. Methods and Results We examined the
Externí odkaz:
https://doaj.org/article/389b5aece39441259e556f3b9f6cdae2
Autor:
Anjali Joshi, Erin B. Punke, Melina Sedano, Bethany Beauchamp, Rima Patel, Cassady Hossenlopp, Ogechika K. Alozie, Jayanta Gupta, Debabrata Mukherjee, Himanshu Garg
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-11 (2017)
Abstract CCR5 is the major co-receptor for HIV and polymorphisms in the CCR5 gene as well as promoter region that alter cell surface expression have been associated with disease progression. We determined the relationship between CCR5 promoter polymo
Externí odkaz:
https://doaj.org/article/d544ef3a989b499d8dde2a45dda0a0a2
Publikováno v:
International Journal of Dentistry, Vol 2019 (2019)
Purpose. To determine and compare OHRQoL (oral-health-related quality of life) using the Geriatric Oral Health Assessment Index (GOHAI-12) and Oral Health Impact Profile (OHIP-14) among patients receiving hemodialysis (HD). Methods. Face-to-face inte
Externí odkaz:
https://doaj.org/article/094835f17d0c46cca8acc993a9b40c87
Autor:
David J. Margolis, Jayanta Gupta
Publikováno v:
Curr Treat Options Allergy
PURPOSE OF REVIEW: Mutations in the Filaggrin gene can cause absent or reduced filaggrin protein, leading to impaired keratinization and skin barrier defect, which produce characteristic phenotypes. In this short review, we report current evidence on
Autor:
Junko Takeshita, Jayanta Gupta, Yaqian Zhu, Ronald Berna, Zelma C. Chiesa Fuxench, David J. Margolis
Publikováno v:
Journal of Allergy and Clinical Immunology. 149:1590-1591
Autor:
Jayanta Gupta, Elizabeth A Dominic, Jeffrey C Fink, Akinlolu O Ojo, Ian R Barrows, Muredach P Reilly, Raymond R Townsend, Marshall M Joffe, Sylvia E Rosas, Melanie Wolman, Samir S Patel, Martin G Keane, Harold I Feldman, John W Kusek, Dominic S Raj, CRIC Study Investigators
Publikováno v:
PLoS ONE, Vol 10, Iss 4, p e0124772 (2015)
Left ventricular hypertrophy (LVH) and myocardial contractile dysfunction are independent predictors of mortality in patients with chronic kidney disease (CKD). The association between inflammatory biomarkers and cardiac geometry has not yet been stu
Externí odkaz:
https://doaj.org/article/1f71762ab0c44da5a4e05072a5be9c4e
Publikováno v:
Personalized Medicine in Psychiatry. :11-18
Autor:
Lisa J Martin, Jayanta Gupta, Soma S S K Jyothula, Melinda Butsch Kovacic, Jocelyn M Biagini Myers, Tia L Patterson, Mark B Ericksen, Hua He, Aaron M Gibson, Tesfaye M Baye, Sushil Amirisetty, Anna M Tsoras, Youbao Sha, N Tony Eissa, Gurjit K Khurana Hershey
Publikováno v:
PLoS ONE, Vol 7, Iss 4, p e33454 (2012)
Rationale and objectiveAutophagy is a cellular process directed at eliminating or recycling cellular proteins. Recently, the autophagy pathway has been implicated in immune dysfunction, the pathogenesis of inflammatory disorders, and response to vira
Externí odkaz:
https://doaj.org/article/387c3faf46704aaca8344c0be9ea39da
Autor:
Tesfaye M Baye, Melinda Butsch Kovacic, Jocelyn M Biagini Myers, Lisa J Martin, Mark Lindsey, Tia L Patterson, Hua He, Mark B Ericksen, Jayanta Gupta, Anna M Tsoras, Andrew Lindsley, Marc E Rothenberg, Marsha Wills-Karp, N Tony Eissa, Larry Borish, Gurjit K Khurana Hershey
Publikováno v:
PLoS ONE, Vol 6, Iss 2, p e16522 (2011)
BackgroundCandidate gene case-control studies have identified several single nucleotide polymorphisms (SNPs) that are associated with asthma susceptibility. Most of these studies have been restricted to evaluations of specific SNPs within a single ge
Externí odkaz:
https://doaj.org/article/ccb79b07379a45bcbabd5246bbd0edd7
Autor:
Melinda Butsch Kovacic, Jocelyn M Biagini Myers, Ning Wang, Lisa J Martin, Mark Lindsey, Mark B Ericksen, Hua He, Tia L Patterson, Tesfaye M Baye, Dara Torgerson, Lindsey A Roth, Jayanta Gupta, Umasundari Sivaprasad, Aaron M Gibson, Anna M Tsoras, Donglei Hu, Celeste Eng, Rocío Chapela, José R Rodríguez-Santana, William Rodríguez-Cintrón, Pedro C Avila, Kenneth Beckman, Max A Seibold, Chris Gignoux, Salma M Musaad, Weiguo Chen, Esteban González Burchard, Gurjit K Khurana Hershey
Publikováno v:
PLoS ONE, Vol 6, Iss 8, p e23714 (2011)
Asthma is a chronic inflammatory disease with a strong genetic predisposition. A major challenge for candidate gene association studies in asthma is the selection of biologically relevant genes.Using epithelial RNA expression arrays, HapMap allele fr
Externí odkaz:
https://doaj.org/article/5f4cc418e1864f3d8f3a32d8a027af35