Zobrazeno 1 - 10
of 145
pro vyhledávání: '"Min Htet"'
Publikováno v:
Stem Cell Research, Vol 80, Iss , Pp 103518- (2024)
Marfan syndrome (MFS) is a hereditary condition caused by mutations in the FBN1 gene. Genetic mutations in the FBN1 locus impact the function of the encoded protein, Fibrillin 1, a structural molecule forming microfibrils found in the connective tiss
Externí odkaz:
https://doaj.org/article/ec67769c98ae4e5397141702597cad02
Autor:
Bernardo Bonilauri, Hye Sook Shin, Min Htet, Christopher D. Yan, Ronald M. Witteles, Karim Sallam, Joseph C. Wu
Publikováno v:
Stem Cell Research, Vol 72, Iss , Pp 103215- (2023)
Specific mutations in the TTR gene are responsible for the development of variant (hereditary) ATTR amyloidosis. Here, we generated two human induced pluripotent stem cell (iPSC) lines from patients diagnosed with Transthyretin Cardiac Amyloidosis (A
Externí odkaz:
https://doaj.org/article/abeb6b85e161470981f0c07c10df534a
Autor:
Wenqiang Liu, Wenshu Zeng, Xiaohui Kong, Min Htet, Rebecca Yu, Matthew Wheeler, John W. Day, Joseph C. Wu
Publikováno v:
Stem Cell Research, Vol 72, Iss , Pp 103207- (2023)
Duchenne muscular dystrophy (DMD) is an X-linked recessive disorder that leads to death in early adulthood. Patients with DMD have null mutations leading to loss of functional dystrophin protein. Here we generated two DMD induced pluripotent stem cel
Externí odkaz:
https://doaj.org/article/aa3f872aa7874a50ba5ab5ab8227e0f0
Autor:
John P Gillies, Janice M Reimer, Eva P Karasmanis, Indrajit Lahiri, Zaw Min Htet, Andres E Leschziner, Samara L Reck-Peterson
Publikováno v:
eLife, Vol 11 (2022)
The lissencephaly 1 gene, LIS1, is mutated in patients with the neurodevelopmental disease lissencephaly. The Lis1 protein is conserved from fungi to mammals and is a key regulator of cytoplasmic dynein-1, the major minus-end-directed microtubule mot
Externí odkaz:
https://doaj.org/article/0c338fe5a65746bb99102d46fccf8b0d
Publikováno v:
Journal of Marine Science and Engineering, Vol 10, Iss 8, p 1164 (2022)
Hydrodynamical analysis of the conditions for the occurrence of chaotic ship roll, leading in some cases to the capsizing of the vessel, showed that such conditions are most likely to occur in the zone of the main parametric resonance of the roll whe
Externí odkaz:
https://doaj.org/article/cbb09f90650043d69603ebd175a0d4e5
Autor:
Dziedzom K de Souza, Katherine Gass, Joseph Otchere, Ye Min Htet, Odame Asiedu, Benjamin Marfo, Nana-Kwadwo Biritwum, Daniel A Boakye, Collins S Ahorlu
Publikováno v:
PLoS Neglected Tropical Diseases, Vol 14, Iss 5, p e0008306 (2020)
BACKGROUND:Lymphatic filariasis (LF) is endemic in Ghana, and the country has implemented the GPELF strategy since 2000 with significant progress made in the control of the disease. However, after several years of mass drug administration (MDA) imple
Externí odkaz:
https://doaj.org/article/e0854c3678d043898626ef4fd6dd02c2
Akademický článek
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Publikováno v:
Science advances. 8(51)
The 26
Publikováno v:
Science Advances. 8
The 26 S proteasome recognizes thousands of appropriate protein substrates in eukaryotic cells through attached ubiquitin chains and uses its adenosine triphosphatase (ATPase) motor for mechanical unfolding and translocation into a proteolytic chambe
Autor:
Kirill V. Rozhdestvensky, Zin Min Htet
Publikováno v:
Journal of Marine Science and Application. 20:595-620
This paper discusses mathematical modeling of a ship equipped with energy-saving wing devices. Therewith, the ship is mathematically represented by an elongated hull with high-aspect-ratio wings mounted near its bow and stern. Equations, describing s