scholarly journals Methodology and characterization of an in vitro perfusion model for the mouse ovary

Reproduction ◽  
1995 ◽  
Vol 105 (2) ◽  
pp. 177-183 ◽  
Author(s):  
M. Brannstrom ◽  
S. Flaherty
Keyword(s):  
Mouse Ovary ◽  
In Vitro Perfusion ◽  
Perfusion Model

Blocking of human anti-pig xenoantibodies by soluble GALα1-3GAL and Galα1-2GAL disaccharides; studies in a pig kidney in vitro perfusion model

2000 ◽  
Vol 13 (6) ◽  
pp. 402-412 ◽  
Author(s):  
Stefan Magnusson ◽  
Valeri Strokan ◽  
Johan Mölne ◽  
Kurt Nilsson ◽  
Lennart Rydberg ◽  
...  
Keyword(s):  
In Vitro Perfusion ◽  
Pig Kidney ◽  
Perfusion Model

Blocking of human anti-pig xenoantibodies by soluble GALα1-3GAL and Galα1-2GAL disaccharides; studies in a pig kidney in vitro perfusion model

2000 ◽  
Vol 13 (6) ◽  
pp. 402-412
Author(s):  
Stefan Magnusson ◽  
Valeri Strokan ◽  
Johan Mölne ◽  
Kurt Nilsson ◽  
Lennart Rydberg ◽  
...  
Keyword(s):  
In Vitro Perfusion ◽  
Pig Kidney ◽  
Perfusion Model

Simple and viable in vitro perfusion model for training microvascular anastomoses

Microsurgery ◽  
2004 ◽  
Vol 24 (4) ◽  
pp. 335-338 ◽  
Author(s):  
Kartik G. Krishnan ◽  
Peter Dramm ◽  
Gabriele Schackert
Keyword(s):  
In Vitro Perfusion ◽  
Perfusion Model

Novel in vitro perfusion model to study the interaction between coagulation and blood-borne metastasis

2005 ◽  
Vol 96 (4) ◽  
pp. 700-708 ◽  
Author(s):  
Lakshman R. Sehgal ◽  
Jonathan Wong ◽  
Jie He ◽  
Trisha Wood ◽  
Ippei Takagi ◽  
...  
Keyword(s):  
In Vitro Perfusion ◽  
Perfusion Model

scholarly journals The “Artificial Artery” as In Vitro Perfusion Model

PLoS ONE ◽  
2013 ◽  
Vol 8 (3) ◽  
pp. e57227 ◽  
Author(s):  
Doreen Janke ◽  
Joachim Jankowski ◽  
Marieke Rüth ◽  
Ivo Buschmann ◽  
Horst-Dieter Lemke ◽  
...  
Keyword(s):  
In Vitro Perfusion ◽  
Perfusion Model

Biological and physico-chemical characterization of ultra high diluted Hydrastis canadensis and in vitro studies on mammalian cells

2017 ◽  
Vol 262 (02) ◽  
pp. 2-76
Author(s):  
N Chandrakar ◽  
MK Temgire ◽  
SG Kane ◽  
AK Suresh ◽  
J Bellare
Keyword(s):  
Mammalian Cells ◽  
Chemical Characterization ◽  
In Vitro Studies ◽  
Hydrastis Canadensis ◽  
Physico Chemical

Assays for Phospholipid-Dependent Formation of Thrombin and Xa: A Potential Method for Quantifying Lupus Anticoagulant Activity

1991 ◽  
Vol 66 (04) ◽  
pp. 453-458 ◽  
Author(s):  
John T Brandt
Keyword(s):  
Specific Activity ◽  
Anticoagulant Activity ◽  
Factor Xa ◽  
Clinical Importance ◽  
Potential Method ◽  
Quantitative Expression ◽  
Increased Risk ◽  
Apparent Association

SummaryLupus anticoagulants (LAs) are antibodies which interfere with phospholipid-dependent procoagulant reactions. Their clinical importance is due to their apparent association with an increased risk of thrombo-embolic disease. To date there have been few assays for quantifying the specific activity of these antibodies in vitro and this has hampered attempts to purify and characterize these antibodies. Methods for determining phospholipid-dependent generation of thrombin and factor Xa are described. Isolated IgG fractions from 7 of 9 patients with LAs were found to reproducibly inhibit enzyme generation in these assay systems, permitting quantitative expression of inhibitor activity. Different patterns of inhibitory activity, based on the relative inhibition of thrombin and factor Xa generation, were found, further substantiating the known heterogeneity of these antibodies. These systems may prove helpful in further purification and characterization of LAs.

Characterization of the Original Christmas Disease Mutation (Cysteine 206 → Serine): From Clinical Recognition to Molecular Pathogenesis

1992 ◽  
Vol 67 (01) ◽  
pp. 063-065 ◽  
Author(s):  
Sherryl A M Taylor ◽  
Jacalyn Duffin ◽  
Cherie Cameron ◽  
Jerome Teitel ◽  
Bernadette Garvey ◽  
...  
Keyword(s):  
Nucleotide Substitution ◽  
Novel Mutation ◽  
Factor Ix ◽  
Causative Mutation ◽  
Coding Region ◽  
Body Of Knowledge ◽  
Polymerase Chain ◽  
Splice Junctions

SummaryChristmas disease was first reported as a distinct clinical entity in two manuscripts published in 1952 (1, 2). The eponym associated with this disorder, is the surname of the first patient examined in detail and reported by Biggs and colleagues in a paper describing the clinical and laboratory features of seven affected individuals (3). This patient has severe factor IX coagulant deficiency (less than 0.01 units/ml) and no detectable circulating factor IX antigen (less than 0.01 units/ml). Coding sequence and splice junctions of the factor IX gene from this patient have been amplified in vitro through the polymerase chain reaction (PCR). One nucleotide substitution was identified at nucleotide 30,070 where a guanine was replaced by a cytosine. This mutation alters the amino acid encoded at position 206 in the factor IX protein from cysteine to serine. The non conservative nature of this substitution, the absence of this change in more than 200 previously sequenced factor IX genes and the fact that the remainder of the coding region of this gene was normal, all provide strong circumstantial evidence in favour of this change being the causative mutation in this patient. The molecular characterization of this novel mutation in the index case of Christmas disease, contributes to the rapidly expanding body of knowledge pertaining to Christmas disease pathogenesis.

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