Zobrazeno 1 - 10
of 154
pro vyhledávání: '"Rajarshi, Pal"'
Autor:
Katsarou, Maria, Zwiebel, Bruce, Chowdhury, Rajarshi Pal, Shames, Murray, Berger, Thomas, Przybyla, Bartos, Bismuth, Jean
Publikováno v:
In Journal of Vascular and Interventional Radiology August 2023 34(8):1345-1352
Publikováno v:
Stem Cell Research, Vol 66, Iss , Pp 103005- (2023)
Externí odkaz:
https://doaj.org/article/fa6996f3721e4358b19fa75cf7de4ef2
Autor:
Harshini Surendran, Lalitha Soundararajan, Vijay Bhaskar Reddy K, Janavi Subramani, Jonathan Stoddard, Rene Reynaga, Wayne Tschetter, Renee C. Ryals, Rajarshi Pal
Publikováno v:
STAR Protocols, Vol 3, Iss 4, Pp 101803- (2022)
Summary: We present an optimized protocol for guided differentiation of retinal pigment epithelium (RPE) cells from human-induced pluripotent stem cells (iPSC). De novo-generated RPE cells are mature, polarized, and mimic the cellular and molecular p
Externí odkaz:
https://doaj.org/article/739d88f68a214239b5c935c68815a807
Autor:
Katsarou, Maria, Zwiebel, Bruce, Vogler, James, Shames, Murray L, Thayer, Angelyn, Chowdhurry, Rajarshi Pal, Money, Samuel R., Bismuth, Jean
Publikováno v:
Journal of Endovascular Therapy; Aug2024, Vol. 31 Issue 4, p668-674, 7p
Autor:
Harshini Surendran, Swapna Nandakumar, Vijay Bhaskar Reddy K, Jonathan Stoddard, Varsha Mohan K, Pramod K. Upadhyay, Trevor J. McGill, Rajarshi Pal
Publikováno v:
Stem Cell Research & Therapy, Vol 12, Iss 1, Pp 1-17 (2021)
Abstract Background Age-related macular degeneration (AMD) is a result of degeneration/damage of the retinal pigment epithelium (RPE) while retinitis pigmentosa (RP), an inherited early-onset disease, results from premature loss of photoreceptors. A
Externí odkaz:
https://doaj.org/article/1113ecd795034c4b90ad8b3bdad8aaf8
Publikováno v:
IEEE Access, Vol 9, Pp 38979-38990 (2021)
Fraudsters often alter handwritten contents in a document in order to achieve illicit purposes. At times, this may result in financial and mental loss to an individual or an organization. Hence, ink analysis is necessary to identify such an alteratio
Externí odkaz:
https://doaj.org/article/cf8c40f532b149cbb63eb0f6e294ca03
Publikováno v:
Stem Cell Research, Vol 45, Iss , Pp - (2020)
Inherited retinal diseases (IRDs) are clinically and genetically heterogenous diseases affecting the neural retina and retinal pigment epithelium resulting in irreversible blindness. Owing to advantages like ease of access for treatment, one eye bein
Externí odkaz:
https://doaj.org/article/769e69675be54b87a03c3a667cc75454
Autor:
Helen Louise May-Simera, Qin Wan, Balendu Shekhar Jha, Juliet Hartford, Vladimir Khristov, Roba Dejene, Justin Chang, Sarita Patnaik, Quanlong Lu, Poulomi Banerjee, Jason Silver, Christine Insinna-Kettenhofen, Dishita Patel, Mostafa Lotfi, May Malicdan, Nathan Hotaling, Arvydas Maminishkis, Rupa Sridharan, Brian Brooks, Kiyoharu Miyagishima, Meral Gunay-Aygun, Rajarshi Pal, Christopher Westlake, Sheldon Miller, Ruchi Sharma, Kapil Bharti
Publikováno v:
Cell Reports, Vol 22, Iss 1, Pp 189-205 (2018)
Summary: Primary cilia are sensory organelles that protrude from the cell membrane. Defects in the primary cilium cause ciliopathy disorders, with retinal degeneration as a prominent phenotype. Here, we demonstrate that the retinal pigment epithelium
Externí odkaz:
https://doaj.org/article/bfaae5556aaf4f70affe565c4099f9ee
Akademický článek
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Autor:
Rajarshi Pal Chowdhury, Luke A. Stegeman, Matthew L. Lund, Dan Fry, Stojan Madzunkov, Amir A. Bahadori
Publikováno v:
Life Sciences in Space Research.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ced3bd0333465439d32cbf3c0f0e3624
https://doi.org/10.1016/j.lssr.2023.04.004
https://doi.org/10.1016/j.lssr.2023.04.004