scholarly journals Bladder Organoids and Spheroids: Potential Tools for Normal and Diseased Tissue Modelling

2019 ◽  
Vol 39 (3) ◽  
pp. 1105-1118 ◽  
Author(s):  
IGOR VASYUTIN ◽  
LILLIAN ZERIHUN ◽  
CRISTINA IVAN ◽  
ANTHONY ATALA
Keyword(s):  
2021 ◽  
Author(s):  
Gaia Amaranta Taberna ◽  
Jessica Samogin ◽  
Dante Mantini

AbstractIn the last years, technological advancements for the analysis of electroencephalography (EEG) recordings have permitted to investigate neural activity and connectivity in the human brain with unprecedented precision and reliability. A crucial element for accurate EEG source reconstruction is the construction of a realistic head model, incorporating information on electrode positions and head tissue distribution. In this paper, we introduce MR-TIM, a toolbox for head tissue modelling from structural magnetic resonance (MR) images. The toolbox consists of three modules: 1) image pre-processing – the raw MR image is denoised and prepared for further analyses; 2) tissue probability mapping – template tissue probability maps (TPMs) in individual space are generated from the MR image; 3) tissue segmentation – information from all the TPMs is integrated such that each voxel in the MR image is assigned to a specific tissue. MR-TIM generates highly realistic 3D masks, five of which are associated with brain structures (brain and cerebellar grey matter, brain and cerebellar white matter, and brainstem) and the remaining seven with other head tissues (cerebrospinal fluid, spongy and compact bones, eyes, muscle, fat and skin). Our validation, conducted on MR images collected in healthy volunteers and patients as well as an MR template image from an open-source repository, demonstrates that MR-TIM is more accurate than alternative approaches for whole-head tissue segmentation. We hope that MR-TIM, by yielding an increased precision in head modelling, will contribute to a more widespread use of EEG as a brain imaging technique.


Development ◽  
1984 ◽  
Vol 80 (1) ◽  
pp. 63-74
Author(s):  
Sheilagh M. Boyd ◽  
M. L. Hooper ◽  
A. H. Wyllie

Cell death occurring in embryoid bodies derived from the embryonal carcinoma cell line, PSA4, which undergo cavitation, and in those from the related cell line S2, which do not undergo cavitation, was classified as apoptosis or necrosis by ultrastructural criteria. Both modes of cell death were seen in PSA4 embryoid bodies while apoptosis alone was seen in S2 embryoid bodies. No significant difference was found between PSA4 and S2 embryoid bodies either in apoptotic incidence score or in the spatial distribution of apoptotic events. We therefore conclude that although apoptosis and tissue modelling coexist in PSA4 embryoid bodies, necrosis rather than apoptosis is causally related to formation of the cavity.


PLoS ONE ◽  
2019 ◽  
Vol 14 (6) ◽  
pp. e0218237 ◽  
Author(s):  
Glenn Pauwelyn ◽  
Lise Vlerick ◽  
Robrecht Dockx ◽  
Jeroen Verhoeven ◽  
Andre Dobbeleir ◽  
...  

2018 ◽  
Vol 49 ◽  
pp. 42-48 ◽  
Author(s):  
Cristiana Gomes de Oliveira Dal’Molin ◽  
Lars Keld Nielsen

2018 ◽  
Vol 72 ◽  
pp. 499-511
Author(s):  
Oskar Wojciech Wiśniewski ◽  
Malwina Malinowska ◽  
Magdalena Gibas-Dorna

The data consistently suggests that expansion and activation of beige/brite adipose tissue may possibly serve as a novel cure for obesity and obesity-related complications. Interestingly, besides well-known agents affecting adipocyte transformation, such as cold-induced sympathetic stimulation, the vast majority of biological systems (e.g. cardiovascular, endocrine, immune, musculoskeletal and central nervous system) also play a role in an adipose tissue modelling and maintaining energy homeostasis. Therefore, we decided to describe in detail the browning of the adipose tissue with a wide range of physiological factors associated with this process and to present the significant distinctions between “classical” brown and beige/brite adipocytes. Here, we review the current state of knowledge about browning phenomenon with regard to obesity prevention and/or management.


Sign in / Sign up

Export Citation Format

Share Document