Zobrazeno 1 - 10
of 332
pro vyhledávání: '"Ruchi, Jain"'
Autor:
Casey N. Grun, Ruchi Jain, Maren Schniederberend, Charles B. Shoemaker, Bryce Nelson, Barbara I. Kazmierczak
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-19 (2024)
Abstract The remarkable capacity of bacteria to adapt in response to selective pressures drives antimicrobial resistance. Pseudomonas aeruginosa illustrates this point, establishing chronic infections during which it evolves to survive antimicrobials
Externí odkaz:
https://doaj.org/article/91d8ca830418492ca5ea623789ee28ba
Autor:
Monica Singh, Anannya Dhanwal, Arpita Verma, Linus Augustin, Niti Kumari, Soumyananda Chakraborti, Nisheeth Agarwal, Dharmarajan Sriram, Ruchi Jain Dey
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-20 (2024)
Abstract Tuberculosis (TB) continues to be a global health crisis, necessitating urgent interventions to address drug resistance and improve treatment efficacy. In this study, we validate lumazine synthase (RibH), a vital enzyme in the riboflavin bio
Externí odkaz:
https://doaj.org/article/61ea364cc9ed4e7f88d0c931cdc85686
Publikováno v:
Case Studies in Thermal Engineering, Vol 59, Iss , Pp 104313- (2024)
The present paper deals with the hybrid nano fluid, for this we have used Single and Multi-wall carbon nano tubes along with CuO and Water. The inclined magneto-hydrodynamics is considered along with Hall effect, soret and dufour for the impact on Wi
Externí odkaz:
https://doaj.org/article/c30f16da5f6144518b0ffde645a353b8
Autor:
Alicia A. Bicknell, David W. Reid, Marissa C. Licata, Adriana K. Jones, Yi Min Cheng, Mengying Li, Chiaowen Joyce Hsiao, Christopher S. Pepin, Mihir Metkar, Yevgen Levdansky, Brian R. Fritz, Elizaveta A. Andrianova, Ruchi Jain, Eugene Valkov, Caroline Köhrer, Melissa J. Moore
Publikováno v:
Cell Reports, Vol 43, Iss 4, Pp 114098- (2024)
Summary: Developing an effective mRNA therapeutic often requires maximizing protein output per delivered mRNA molecule. We previously found that coding sequence (CDS) design can substantially affect protein output, with mRNA variants containing more
Externí odkaz:
https://doaj.org/article/7b3fb817ec414bcf9bdcba69344c3e0c
Publikováno v:
Journal of Obstetric Anaesthesia and Critical Care, Vol 14, Iss 1, Pp 91-93 (2024)
Neurofibromatosis (NF1) is a relatively common multi-system genetic disorder. NF1 increases the risk of hypertension, and vasculopathy is a common finding. Extracranial vertebral artery aneurysm, though rare, can rupture and cause fatal hemorrhage. P
Externí odkaz:
https://doaj.org/article/651289d675b94894b2621d611b3f4d4f
Autor:
Beshr Abdulaziz Badla, Mohamed Samer Hanifa, Ruchi Jain, Maha El Naofal, Nour Halabi, Sawsan Yaslam, Sathishkumar Ramaswamy, Alan Taylor, Roudha Alfalasi, Shruti Shenbagam, Hamda Khansaheb, Hanan Al Suwaidi, Norbert Nowotny, Rizwana Popatia, Abdulla Al Khayat, Alawi Alsheikh-Ali, Tom Loney, Laila Mohamed AlDabal, Ahmad Abou Tayoun
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract Studies of genetic factors associated with severe COVID-19 in young adults have been limited in non-Caucasian populations. Here, we clinically characterize a case series of patients with COVID-19, who were otherwise healthy, young adults (N
Externí odkaz:
https://doaj.org/article/308a16b8afe846d1a6b14772359f63a7
Autor:
Lemis Yavuz, Sarmad AlHamdani, Samah Alasrawi, Deena Wafadari, Ali Al-Fraihat, Marwa A. Bebars, Jaidev Nath, Diego Arango, Marco Pallavidino, Ruchi Jain, Sinan Yavuz, Mohamed AlAwadhi, Abdulla Alkhayat, Ahmad Abou Tayoun, Walid Mohammad Abuhammour
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 21, Iss 1, Pp 1-8 (2023)
Abstract Objective This is a comprehensive characteristic study of Kawasaki disease (KD) and Multi system inflammatory syndrome in children (MIS-C) in the Middle East that creates a formula to differentiate between the two. Methods We conducted a des
Externí odkaz:
https://doaj.org/article/02130806d61c4b76bc9fef4c465d99e7
Publikováno v:
Performance Measurement and Metrics, 2022, Vol. 24, Issue 1, pp. 1-11.
Externí odkaz:
http://www.emeraldinsight.com/doi/10.1108/PMM-08-2021-0042
Autor:
Maha El Naofal, Sathishkumar Ramaswamy, Ali Alsarhan, Ahmed Nugud, Fatima Sarfraz, Hiba Janbaz, Alan Taylor, Ruchi Jain, Nour Halabi, Sawsan Yaslam, Roudha Alfalasi, Shruti Shenbagam, Fatma Rabea, Martin Bitzan, Lemis Yavuz, Deena Wafadari, Hamda Abulhoul, Shiva Shankar, Munira Al Maazmi, Ruba Rizk, Zeinab Alloub, Haitham Elbashir, Mohamed O. E. Babiker, Nidheesh Chencheri, Ammar AlBanna, Meshal Sultan, Mohamed El Bitar, Safeena Kherani, Nandu Thalange, Sattar Alshryda, Roberto Di Donato, Christos Tzivinikos, Ibrar Majid, Alexandra F. Freeman, Corina Gonzalez, Arif O. Khan, Hisham Hamdan, Walid Abuhammour, Mohamed AlAwadhi, Abdulla AlKhayat, Alawi Alsheikh-Ali, Ahmad N. Abou Tayoun
Publikováno v:
Genome Medicine, Vol 15, Iss 1, Pp 1-12 (2023)
Abstract Background Rare diseases collectively impose a significant burden on healthcare systems, especially in underserved regions, like the Middle East, which lack access to genomic diagnostic services and the associated personalized management pla
Externí odkaz:
https://doaj.org/article/35ba5f303bf24df8a72a134940d5e4d5
Autor:
Kotwal, Shifa Bushra, Orekondey, Nidhi, Saradadevi, Gargi Prasad, Priyadarshini, Neha, Puppala, Navinchandra V., Bhushan, Mahak, Motamarry, Snehasri, Kumar, Rahul, Mohannath, Gireesha, Dey, Ruchi Jain
Publikováno v:
In Heliyon June 2023 9(6)