Zobrazeno 1 - 10
of 768
pro vyhledávání: '"Unnisa A"'
Autor:
Mushtaq Gohar, Hasani Ibrahim W., Al-Daoud Fouad, Unnisa Aziz, Mutair Yahya A., Kabba Samer, Alkanash Yaser
Publikováno v:
Türk Biyokimya Dergisi, Vol 48, Iss 5, Pp 446-458 (2023)
MicroRNAs (miRNAs) are small non-coding molecules that play a pivotal part in brain development and the processes of establishment and maintenance of dendrites and neurite outgrowth by modulating gene expression. Dysregulation of miRNAs has been link
Externí odkaz:
https://doaj.org/article/1ccc7910cc2f46d5aee02248714e2c39
Publikováno v:
Türk Biyokimya Dergisi, Vol 48, Iss 4, Pp 446-450 (2023)
Leukemoid Reaction (LR) signifies leukocytosis characterized by mature neutrophils. The incidence of LR is about 1 % among hospitalized patients. Mucormycosis is a rare, aggressive, fatal fungal infection that afflicts immune-compromised patients. Th
Externí odkaz:
https://doaj.org/article/ff5b1ebd128649bfbb1d0724aaebbf35
Autor:
Yoon, John K., Schindler, Jeffrey W., Loperfido, Mariana, Baricordi, Cristina, DeAndrade, Mark P., Jacobs, Mary E., Treleaven, Christopher, Plasschaert, Robert N., Yan, Aimin, Barese, Cecilia N., Dogan, Yildirim, Chen, Vicky Ping, Fiorini, Claudia, Hull, Fritz, Barbarossa, Luigi, Unnisa, Zeenath, Ivanov, Daniel, Kutner, Robert H., Guda, Swaroopa, Oborski, Christine, Maiwald, Tim, Michaud, Véronique, Rothe, Michael, Schambach, Axel, Pfeifer, Richard, Mason, Chris, Biasco, Luca, van Til, Niek P.
Publikováno v:
In Molecular Therapy 6 November 2024 32(11):3847-3864
Autor:
Unnisa, Sk. Mehatab1, Seereen, Sana1, Lekhana, Jampana1, Archana, Goreti1, Kumar, Annam Hemanth1 hemanthkumarannam925@gmail.com, Nikhil, Soma Mani Santhosh1, Chinnaeswraiah, Maram2
Publikováno v:
International Journal of Pharmaceutical Investigation. Apr-Jun2024, Vol. 14 Issue 2, p371-377. 7p.
Kynurenine pathway alteration in acute pancreatitis and its role as a biomarker of infected necrosis
Autor:
Jakkampudi, Aparna, Sarkar, Priyanka, Unnisa, Misbah, Patil, Aashish, Koutarapu, Chandrakanth, Jaggaiahgari, Shashidhar, Naik, Pragathi, Sarkar, Subhaleena, Prasanna, Ambika, Chintaluri, Sreelekha, Reddy, D. Nageshwar, Beedu, Sashidhar Rao, Talukdar, Rupjyoti
Publikováno v:
In Pancreatology September 2023 23(6):589-600
Publikováno v:
In Materials Today: Proceedings 2023 92 Part 2:490-497
Autor:
Yildirim Dogan, Cecilia N. Barese, Jeffrey W. Schindler, John K. Yoon, Zeenath Unnisa, Swaroopa Guda, Mary E. Jacobs, Christine Oborski, Tim Maiwald, Diana L. Clarke, Axel Schambach, Richard Pfeifer, Claudia Harper, Chris Mason, Niek P. van Til
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 27, Iss , Pp 464-487 (2022)
Pompe disease is a rare genetic neuromuscular disorder caused by acid α-glucosidase (GAA) deficiency resulting in lysosomal glycogen accumulation and progressive myopathy. Enzyme replacement therapy, the current standard of care, penetrates poorly i
Externí odkaz:
https://doaj.org/article/19aee40652b94df1a4979d0e41238f5c
Akademický článek
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Autor:
Dogan, Yildirim, Barese, Cecilia N., Schindler, Jeffrey W., Yoon, John K., Unnisa, Zeenath, Guda, Swaroopa, Jacobs, Mary E., Oborski, Christine, Maiwald, Tim, Clarke, Diana L., Schambach, Axel, Pfeifer, Richard, Harper, Claudia, Mason, Chris, van Til, Niek P.
Publikováno v:
In Molecular Therapy - Methods & Clinical Development 8 December 2022 27:464-487
Autor:
Plasschaert, Robert N., DeAndrade, Mark P., Hull, Fritz, Nguyen, Quoc, Peterson, Tara, Yan, Aimin, Loperfido, Mariana, Baricordi, Cristina, Barbarossa, Luigi, Yoon, John K., Dogan, Yildirim, Unnisa, Zeenath, Schindler, Jeffrey W., van Til, Niek P., Biasco, Luca, Mason, Chris
Publikováno v:
In Molecular Therapy 5 October 2022 30(10):3209-3225