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Proofreading

Proofreading

Synthesis of new DNA molecules starts when DNA polymerase links nucleotides together in a sequence that is complementary to the template DNA strand. DNA polymerase has a higher affinity for the correct base to ensure fidelity in DNA replication. The DNA polymerase furthermore proofreads during replication, using an exonuclease domain that cuts off incorrect nucleotides from the nascent DNA strand.Errors during Replication Are Corrected by the DNA Polymerase EnzymeGenomic DNA is synthesized in...

Proofreading

Proofreading

Synthesis of new DNA molecules starts when DNA polymerase links nucleotides together in a sequence that is complementary to the template DNA strand. DNA polymerase has a higher affinity for the correct base to ensure fidelity in DNA replication. The DNA polymerase furthermore proofreads during replication, using an exonuclease domain that cuts off incorrect nucleotides from the nascent DNA strand.Errors during Replication Are Corrected by the DNA Polymerase EnzymeGenomic DNA is synthesized in...

Termination of Translation

Termination of Translation

The large ribosomal subunit has several important structures essential to translation. These include the peptidyl transferase center (PTC) - which is the site where the peptide bond is formed - and a large, internal, water-filled tube through which the nascent polypeptide moves. This latter structure is called the Peptide Exit Tunnel, and it begins at the PTC and spans the body of the large ribosomal subunit. During translation, as the nascent polypeptide chain is synthesized, it passes through...

Termination of Translation

Termination of Translation

The large ribosomal subunit has several important structures essential to translation. These include the peptidyl transferase center (PTC) - which is the site where the peptide bond is formed - and a large, internal, water-filled tube through which the nascent polypeptide moves. This latter structure is called the Peptide Exit Tunnel, and it begins at the PTC and spans the body of the large ribosomal subunit. During translation, as the nascent polypeptide chain is synthesized, it passes through...

Proofreading

Proofreading

Synthesis of new DNA molecules is carried out by the enzyme DNA polymerase, which adds nucleotides on the daughter strand complementary to the template DNA strand. DNA polymerase has a higher affinity to add the correct base and ensures fidelity during DNA replication. Furthermore, it exhibits proofreading activity during replication, using an exonuclease domain that cuts off incorrect nucleotides from the nascent DNA strand.
Errors During Replication are Corrected by the DNA Polymerase Enzyme

Variance

Variance

The deviations show how spread out the data are about the mean. A positive deviation occurs when the data value exceeds the mean, whereas a negative deviation occurs when the data value is less than the mean. If the deviations are added, the sum is always zero. So one cannot simply add the deviations to get the data spread. By squaring the deviations, the numbers are made positive; thus, their sum will also be positive.The standard deviation measures the spread in the same units as the data.

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Updated: Jul 10, 2026

Molecular Evolution of the Tre Recombinase

Molecular Evolution of the Tre Recombinase

Published on: May 29, 2008

Erratum Erratum エラトゥームエラトゥーム

Science (New York, N.Y.)

|September 12, 1986

まとめ

この記事は,数学者と主要な発見に関する以前のレポートの事実上の誤りを訂正しています. マイケル・フリードマンの所属関係を明らかにし,著名な数学者の誤った綴りのいくつかの名前を訂正している.

科学分野:

数学数学数学数学とは
科学的コミュニケーション科学的コミュニケーション

背景:

前回の記事では,フィールドスメダル受賞者のマイケル・フリードマン (Michael Freedman) の出身が誤って報道されていた.
数名の著名な数学者の名前は,オリジナルの出版物では誤って綴られていた.

研究の目的:

マイケル・フリードマンの学術的地位に関する正確な情報を提供するために.
研究ニュースで言及された数学における重要な人物に対する綴り間違いを訂正するために.

主な方法:

公式の大学記録を通じて学術関係を確認する.
名称のクロスリファレンスは,確立された数学的および科学的データベースとクロスリファレンスを行う.

主要な成果:

マイケル・フリードマン (Michael Freedman) は,南カリフォルニア大学ではなく,カリフォルニア大学サンディエゴ校のチャールズ・リー・パウエル数学教授です.
訂正された綴りには,フィールド (以前のフィールドズ),ネヴァンリンナ (以前のネヴァリンナ/ナヴァンリンナ),キルビー (以前のキルキー),アティヤ (以前のアーリヤ),ストラッセン (以前のストラッセン) が含まれる.

結論:

科学的成果と人材の正確な表現は,研究報告において極めて重要です.

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Development of an Experimental Setup for the Measurement of the Coefficient of Restitution under Vacuum Conditions

Development of an Experimental Setup for the Measurement of the Coefficient of Restitution under Vacuum Conditions

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Published on: September 20, 2024

関連する実験動画

Last Updated: Jul 10, 2026

Molecular Evolution of the Tre Recombinase

Molecular Evolution of the Tre Recombinase

Published on: May 29, 2008

Development of an Experimental Setup for the Measurement of the Coefficient of Restitution under Vacuum Conditions

Development of an Experimental Setup for the Measurement of the Coefficient of Restitution under Vacuum Conditions

Published on: March 29, 2016

Correction of Presbyopia by Monocular Bi-Aspheric Ablation Profile

Published on: September 20, 2024

誤った事実や印刷の訂正は,科学コミュニケーションの誠実さを保ちます.