scholarly journals Ferroptosis, a new form of cell death, and its relationships with tumourous diseases

2016 ◽  
Vol 21 (4) ◽  
pp. 648-657 ◽  
Author(s):  
Haitao Yu ◽  
Pengyi Guo ◽  
Xiaozai Xie ◽  
Yi Wang ◽  
Gang Chen
Keyword(s):  
Cell Death ◽  
New Form

A new form of cell death: Parthanatos

2011 ◽  
Vol 32 (9) ◽  
pp. 881-885 ◽  
Author(s):  
Lian-Bang WANG ◽  
Li-Ying ZHANG ◽  
Chun-Hua SHAN
Keyword(s):  
Cell Death ◽  
New Form

Ferroptosis, a new form of cell death defined after radiation exposure

2022 ◽  
pp. 1-9
Author(s):  
Xiaohong Zhang ◽  
Xin Li ◽  
Chunyan Zheng ◽  
Chunzhi Yang ◽  
Rui Zhang ◽  
...  
Keyword(s):  
Cell Death ◽  
Radiation Exposure ◽  
New Form

scholarly journals Ferroptosis, a new form of cell death: opportunities and challenges in cancer

2019 ◽  
Vol 12 (1) ◽  
Author(s):  
Yanhua Mou ◽  
Jun Wang ◽  
Jinchun Wu ◽  
Dan He ◽  
Chunfang Zhang ◽  
...  
Keyword(s):  
Cell Death ◽  
New Form

Autoschizis: a new form of cell death for human ovarian carcinoma cells following ascorbate:menadione treatment

2004 ◽  
Vol 36 (3) ◽  
pp. 197-209 ◽  
Author(s):  
Jacques Gilloteaux ◽  
James M Jamison ◽  
Heather E Lorimer ◽  
David Jarjoura ◽  
Henryk S Taper ◽  
...  
Keyword(s):  
Cell Death ◽  
Ovarian Carcinoma ◽  
Carcinoma Cells ◽  
Ovarian Carcinoma Cells ◽  
Human Ovarian Carcinoma ◽  
New Form ◽  
Human Ovarian Carcinoma Cells

scholarly journals Fenretinide induces a new form of dynamin-dependent cell death in pediatric sarcoma

2020 ◽  
Vol 27 (8) ◽  
pp. 2500-2516
Author(s):  
Eva Brack ◽  
Marco Wachtel ◽  
Anja Wolf ◽  
Andres Kaech ◽  
Urs Ziegler ◽  
...  
Keyword(s):  
Cell Death ◽  
Pediatric Sarcoma ◽  
Dependent Cell ◽  
New Form

Fine Structure of Platelet Interaction with a New Microcrystalline Collagen Preparation

1974 ◽  
Vol 32 ◽  
pp. 58-59
Author(s):  
W. H. Zucker ◽  
R. G. Mason
Keyword(s):  
Fine Structure ◽  
Platelet Aggregation ◽  
Hydrochloric Acid ◽  
Whole Blood ◽  
Platelet Adhesion ◽  
Hemostatic Agent ◽  
Native Collagen ◽  
Fibrillar Morphology ◽  
Clinical Interest ◽  
New Form

Platelet adhesion initiates platelet aggregation and is an important component of the hemostatic process. Since the development of a new form of collagen as a topical hemostatic agent is of both basic and clinical interest, an ultrastructural and hematologic study of the interaction of platelets with the microcrystalline collagen preparation was undertaken.In this study, whole blood anticoagulated with EDTA was used in order to inhibit aggregation and permit study of platelet adhesion to collagen as an isolated event. The microcrystalline collagen was prepared from bovine dermal corium; milling was with sharp blades. The preparation consists of partial hydrochloric acid amine collagen salts and retains much of the fibrillar morphology of native collagen.

DNA nick end labeling: a reliable marker for apoptosis?

1995 ◽  
Vol 53 ◽  
pp. 962-963
Author(s):  
Anne F. Bushnell ◽  
Sarah Webster ◽  
Lynn S. Perlmutter
Keyword(s):  
Cell Death ◽  
Cultured Cells ◽  
Apoptotic Cell ◽  
Morphological Characteristics ◽  
Detection Methods ◽  
Tissue Preparation ◽  
Preparation Methods ◽  
Dna Laddering ◽  
Disease States ◽  
Reliable Marker

Apoptosis, or programmed cell death, is an important mechanism in development and in diverse disease states. The morphological characteristics of apoptosis were first identified using the electron microscope. Since then, DNA laddering on agarose gels was found to correlate well with apoptotic cell death in cultured cells of dissimilar origins. Recently numerous DNA nick end labeling methods have been developed in an attempt to visualize, at the light microscopic level, the apoptotic cells responsible for DNA laddering.The present studies were designed to compare various tissue processing techniques and staining methods to assess the occurrence of apoptosis in post mortem tissue from Alzheimer's diseased (AD) and control human brains by DNA nick end labeling methods. Three tissue preparation methods and two commercial DNA nick end labeling kits were evaluated: the Apoptag kit from Oncor and the Biotin-21 dUTP 3' end labeling kit from Clontech. The detection methods of the two kits differed in that the Oncor kit used digoxigenin dUTP and anti-digoxigenin-peroxidase and the Clontech used biotinylated dUTP and avidinperoxidase. Both used 3-3' diaminobenzidine (DAB) for final color development.

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