Zobrazeno 1 - 10
of 1 479
pro vyhledávání: '"gene-based"'
Essential magnetosome proteins MamI and MamL from magnetotactic bacteria interact in mammalian cells
Autor:
Qin Sun, Liu Yu, Sarah C. Donnelly, Cécile Fradin, R. Terry Thompson, Frank S. Prato, Donna E. Goldhawk
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-16 (2024)
Abstract To detect cellular activities deep within the body using magnetic resonance platforms, magnetosomes are the ideal model of genetically-encoded nanoparticles. These membrane-bound iron biominerals produced by magnetotactic bacteria are highly
Externí odkaz:
https://doaj.org/article/ad88c05c7c07482db8e7d1194db473a0
Autor:
Junichi Iwata, Kenta Nakai
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Externí odkaz:
https://doaj.org/article/96df4e5947cb4df1beea1335c760cb80
Autor:
Kawish, S.M. a, Hilles, Ayah Rebhi b, Sharma, Shwetakshi a, Alam, Meraj a, Alimujiang, Kailibinuer c, Iqbal, Zeenat a, beg, Sarwar a, Mahmood, Syed c, d, e, ⁎, Mirza, Mohd Aamir a, ⁎⁎
Publikováno v:
In Journal of Drug Delivery Science and Technology December 2024 102 Part B
Autor:
Manish K. Pandey, Sunil S. Gangurde, Yaduru Shasidhar, Vinay Sharma, Sandip M. Kale, Aamir W. Khan, Priya Shah, Pushpesh Joshi, Ramesh S. Bhat, Pasupuleti Janila, Sandip K. Bera, Rajeev K. Varshney
Publikováno v:
BMC Plant Biology, Vol 24, Iss 1, Pp 1-16 (2024)
Abstract Background Foliar diseases namely late leaf spot (LLS) and leaf rust (LR) reduce yield and deteriorate fodder quality in groundnut. Also the high oleic acid content has emerged as one of the most important traits for industries and consumers
Externí odkaz:
https://doaj.org/article/b3ca4c43533b4623843e9207c3f08236
Publikováno v:
BMC Microbiology, Vol 24, Iss 1, Pp 1-12 (2024)
Abstract Background Accurate identification of bacterial communities is crucial for research applications, diagnostics, and clinical interventions. Although 16S ribosomal RNA (rRNA) gene sequencing is a widely employed technique for bacterial taxonom
Externí odkaz:
https://doaj.org/article/a2d111cdc1ff4daa970feeae12d15bc8
Autor:
Christina Canavati, Dana Sherill-Rofe, Lara Kamal, Idit Bloch, Fouad Zahdeh, Elad Sharon, Batel Terespolsky, Islam Abu Allan, Grace Rabie, Mariana Kawas, Hanin Kassem, Karen B. Avraham, Paul Renbaum, Ephrat Levy-Lahad, Moien Kanaan, Yuval Tabach
Publikováno v:
Genome Medicine, Vol 16, Iss 1, Pp 1-22 (2024)
Abstract Background Next-generation sequencing (NGS) has significantly transformed the landscape of identifying disease-causing genes associated with genetic disorders. However, a substantial portion of sequenced patients remains undiagnosed. This ma
Externí odkaz:
https://doaj.org/article/7a6f2b28ee0648df98cc0e6225b74bb8
Publikováno v:
HGG Advances, Vol 5, Iss 2, Pp 100283- (2024)
Summary: Integrating results from genome-wide association studies (GWASs) and studies of molecular phenotypes such as gene expressions can improve our understanding of the biological functions of trait-associated variants and can help prioritize cand
Externí odkaz:
https://doaj.org/article/f424261c1e5c45edb69c80cd5ac9b2f0
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
The emergence of new genetic tools has led to the discovery of the genetic bases of many intellectual and developmental disabilities. This creates exciting opportunities for research and treatment development, and a few genetic disorders (e.g., spina
Externí odkaz:
https://doaj.org/article/3f0f12b272f54da3bae1313b3b6c57cd
Autor:
Tianyu Deng, Keanning Li, Lili Du, Mang Liang, Li Qian, Qingqing Xue, Shiyuan Qiu, Lingyang Xu, Lupei Zhang, Xue Gao, Xianyong Lan, Junya Li, Huijiang Gao
Publikováno v:
Animals, Vol 14, Iss 11, p 1695 (2024)
Complex traits are widely considered to be the result of a compound regulation of genes, environmental factors, and genotype-by-environment interaction (G × E). The inclusion of G × E in genome-wide association analyses is essential to understand a
Externí odkaz:
https://doaj.org/article/e1253c5ef77f45fdb9df57ff62c542a7
Autor:
Zilong Geng, Wenjuan Li, Ping Yang, Shasha Zhang, Shuo Wu, Junhao Xiong, Kun Sun, Dan Zhu, Sun Chen, Bing Zhang
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Left ventricular outflow tract obstruction (LVOTO), a major form of outflow tract malformation, accounts for a substantial portion of congenital heart defects (CHDs). Unlike its prevalence, the genetic architecture of LVOTO remains largely unknown. T
Externí odkaz:
https://doaj.org/article/fc0b39da05344417a1fef7a68f74465c