Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Ladan Amin"'
Autor:
Ladan Amin, David A. Harris
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-16 (2021)
PrPC, a receptor for Aβ oligomers, blocks polarized elongation of Aβ fibrils by binding to the rapidly growing end of each fibril. PrPC and other receptors may trap Aβ oligomers and protofibrils on the neuronal surface by binding to a common molec
Externí odkaz:
https://doaj.org/article/ac93ade48c874d878eefe4d90fa6d6b1
Autor:
Giulia D'Arrigo, Martina Gabrielli, Federica Scaroni, Paolo Swuec, Ladan Amin, Anna Pegoraro, Elena Adinolfi, Francesco Di Virgilio, Dan Cojoc, Giuseppe Legname, Claudia Verderio
Publikováno v:
Journal of Extracellular Vesicles, Vol 10, Iss 9, Pp n/a-n/a (2021)
Abstract Astrocytes‐derived extracellular vesicles (EVs) are key players in glia‐neuron communication. However, whether EVs interact with neurons at preferential sites and how EVs reach these sites on neurons remains elusive. Using optical manipu
Externí odkaz:
https://doaj.org/article/f0b97afff4c5477aa4aa24818d44f083
Publikováno v:
PLoS ONE, Vol 8, Iss 8, p e73025 (2013)
Mechanical properties such as force generation are fundamental for neuronal motility, development and regeneration. We used optical tweezers to compare the force exerted by growth cones (GCs) of neurons from the Peripheral Nervous System (PNS), such
Externí odkaz:
https://doaj.org/article/f4cffb07be974dfa8c217e4e4af673e9
Publikováno v:
BioTechniques, Vol 60, Iss 1, p 35 (2016)
Extracellular vesicles (EVs) are spherical membrane structures released by most cells. These highly conserved mediators of intercellular communication carry proteins, lipids, and nucleic acids, and transfer these cellular components between cells by
Externí odkaz:
https://doaj.org/article/3b627893aca74247adadbe07966aa1d3
Autor:
Fardad Ejtehadi, Maryam Sadat Serpoosh, Iraj Shahramian, Ladan Aminlari, Ramin Niknam, Gholam Reza Sivandzadeh, Masoud Tahani, Amin Javadifar, Fateme Sharafi, Maryam Moini
Publikováno v:
Caspian Journal of Internal Medicine, Vol 15, Iss 3, Pp 451-458 (2024)
Background: Hepatitis A is a widespread viral infection with significant public health implications. Assessing glucose 6-phosphate dehydrogenase (G6PD) deficiency in hepatitis A patients is essential for various reasons, including prognosis, disease
Externí odkaz:
https://doaj.org/article/4990ec78acf24f0787df7a8e3799ba57
Autor:
Behnam Mohammadi, Inga Zerr, Simone Hornemann, Correia A, Mohsin Shafiq, Markus Glatzel, Hermann C. Altmeppen, Jörg Tatzelt, Michaela Schweizer, Ladan Amin, David A. Harris, Julia Bär, Federica Mazzola, Matthias Schmitz, Berta Puig, Antoine Triller, Adriano Aguzzi, Karl Frontzek, Luca Varani, Da Vela S, Alexander Schwarz, Paul Saftig, Simrika Thapa, Marina Mikhaylova, Luise Linsenmeier, Emiliano Biasini, Sebastian Jung, Sabine Gilch, Dmitri I. Svergun, Markus Damme, Amulya Nidhi Shrivastava, Tania Massignan, Hermann M. Schätzl
The cellular prion protein (PrPC) is a central player in neurodegenerative diseases caused by protein misfolding, such as prion diseases or Alzheimer’s disease (AD). Expression levels of this GPI-anchored glycoprotein, especially at the neuronal ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca422690016c15fad3a8edc49ee043a1
https://doi.org/10.1101/2021.04.19.440495
https://doi.org/10.1101/2021.04.19.440495
Autor:
Mohsin Shafiq, Stefano Da Vela, Ladan Amin, Neelam Younas, David A. Harris, Inga Zerr, Hermann C. Altmeppen, Dmitri Svergun, Markus Glatzel
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1869:119240
The prion protein is a multifunctional protein that exists in at least two different folding states. It is subject to diverse proteolytic processing steps that lead to prion protein fragments some of which are membrane-bound whereas others are solubl
Autor:
David A. Harris, Ladan Amin
Publikováno v:
Alzheimer's & Dementia. 15:P1507-P1508
Publikováno v:
Alzheimer's & Dementia. 15:P1507-P1507
Autor:
Ivana Biljan, Giulia Salzano, Gabriele Giachin, Blaž Zupančič, Giuseppe Legname, Urška Slapšak, Gregor Ilc, Janez Plavec, Romany Abskharon, Ladan Amin
Publikováno v:
The Journal of biological chemistry. 291(42)
The cellular form of the prion protein (PrPC) is a highly conserved glycoprotein mostly expressed in the central and peripheral nervous systems by different cell types in mammals. A misfolded, pathogenic isoform, denoted as prion, is related to a cla