Related Experiment Video
Updated: Feb 7, 2026

Flow-sorting and Exome Sequencing of the Reed-Sternberg Cells of Classical Hodgkin Lymphoma
Published on: June 10, 2017
Carolyn Elaine Reed, MD March 4, 1950-November 16, 2012
1Division of Cardiothoracic Surgery, Medical University of South Carolina, Charleston, South Carolina.
Abstract:
Carolyn Reed, 48th President of The Society of Thoracic Surgeons, was an accomplished surgeon, an outstanding educator, a dedicated investigator, a role model for both women and men in surgery, and a national leader in our specialty of cardiothoracic surgery. She filled all of these roles extremely well, but most important to her was her role as a physician who truly cared about her patients, friends, and colleagues as was apparent in her 2007 Southern Thoracic Surgical Association Presidential Address, "Patient Versus Customer, Technology Versus Touch: Where Has Humanism Gone?"
Related Concept Videos
Cattell's 16 Personality Factors
In contrast, source traits are the...
Dipeptidyl Peptidase 4 Inhibitors
Amides to Amines: LiAlH4 Reduction
Amide reduction requires two equivalents of the reducing agent, acting as a source of hydride ions. As shown in the figure, the reaction is initiated with a nucleophilic attack by the hydride ion at the carbonyl carbon to form a tetrahedral intermediate.
Piaget's Stage 4 of Cognitive Development
Abstract Reasoning and Hypothetical-Deductive Thinking
Unlike the concrete operational...
Nitriles to Amines: LiAlH4 Reduction
As shown below, the mechanism involves three steps. Firstly, the hydride ion acting as a nucleophile attacks the nitrile carbon to form an anion. In the second step, a second equivalent of the hydride ion attacks the anion to...
Acid Halides to Alcohols: LiAlH4 Reduction
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...
![Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F60786.jpg&w=3840&q=50)
