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Discovery and Mechanism of Highly Efficient Cyclic Cell-Penetrating Peptides
Discovery and Mechanism of Highly Efficient Cyclic Cell-Penetrating Peptides
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Discovery and Mechanism of Highly Efficient Cyclic Cell-Penetrating Peptides

Qian, Ziqing ; Martyna, Agnieszka ; Hard, Ryan L ; Wang, Jiang ; Appiah-Kubi, George ; Coss, Christopher ; Phelps, Mitch A ; Rossman, Jeremy S ; Pei, Dehua

Biochemistry (Easton), 2016-05, Vol.55 (18), p.2601-2612 [Periódico revisado por pares]

United States: American Chemical Society

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2
Retro-inversal of Intracellular Selected β‑Amyloid-Interacting Peptides: Implications for a Novel Alzheimer’s Disease Treatment
Retro-inversal of Intracellular Selected β‑Amyloid-Interacting Peptides: Implications for a Novel Alzheimer’s Disease Treatment
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Retro-inversal of Intracellular Selected β‑Amyloid-Interacting Peptides: Implications for a Novel Alzheimer’s Disease Treatment

Acerra, Nicola ; Kad, Neil M ; Griffith, Douglas A ; Ott, Stanislav ; Crowther, Damian C ; Mason, Jody M

Biochemistry (Easton), 2014-04, Vol.53 (13), p.2101-2111 [Periódico revisado por pares]

United States: American Chemical Society

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3
Development of a Proteolytically Stable Retro-Inverso Peptide Inhibitor of β-Amyloid Oligomerization as a Potential Novel Treatment for Alzheimer’s Disease
Development of a Proteolytically Stable Retro-Inverso Peptide Inhibitor of β-Amyloid Oligomerization as a Potential Novel Treatment for Alzheimer’s Disease
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Development of a Proteolytically Stable Retro-Inverso Peptide Inhibitor of β-Amyloid Oligomerization as a Potential Novel Treatment for Alzheimer’s Disease

Taylor, Mark ; Moore, Susan ; Mayes, Jennifer ; Parkin, Edward ; Beeg, Marten ; Canovi, Mara ; Gobbi, Marco ; Mann, David M. A ; Allsop, David

Biochemistry (Easton), 2010-04, Vol.49 (15), p.3261-3272 [Periódico revisado por pares]

United States: American Chemical Society

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4
N-Methylated Peptide Inhibitors of β-Amyloid Aggregation and Toxicity. Optimization of the Inhibitor Structure
N-Methylated Peptide Inhibitors of β-Amyloid Aggregation and Toxicity. Optimization of the Inhibitor Structure
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N-Methylated Peptide Inhibitors of β-Amyloid Aggregation and Toxicity. Optimization of the Inhibitor Structure

Kokkoni, Nicoleta ; Stott, Kelvin ; Amijee, Hozefa ; Mason, Jody M ; Doig, Andrew J

Biochemistry (Easton), 2006-08, Vol.45 (32), p.9906-9918 [Periódico revisado por pares]

United States: American Chemical Society

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5
An Efficient Method for the Expression and Purification of Aβ(M1–42)
An Efficient Method for the Expression and Purification of Aβ(M1–42)
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An Efficient Method for the Expression and Purification of Aβ(M1–42)

Yoo, Stan ; Zhang, Sheng ; Kreutzer, Adam G ; Nowick, James S

Biochemistry (Easton), 2018-07, Vol.57 (26), p.3861-3866 [Periódico revisado por pares]

United States: American Chemical Society

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6
Relative Antagonism of Mutants of the CGRP Receptor Extracellular Loop 2 Domain (ECL2) Using a Truncated Competitive Antagonist (CGRP8–37): Evidence for the Dual Involvement of ECL2 in the Two-Domain Binding Model
Relative Antagonism of Mutants of the CGRP Receptor Extracellular Loop 2 Domain (ECL2) Using a Truncated Competitive Antagonist (CGRP8–37): Evidence for the Dual Involvement of ECL2 in the Two-Domain Binding Model
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Relative Antagonism of Mutants of the CGRP Receptor Extracellular Loop 2 Domain (ECL2) Using a Truncated Competitive Antagonist (CGRP8–37): Evidence for the Dual Involvement of ECL2 in the Two-Domain Binding Model

Woolley, Michael J ; Simms, John ; Uddin, Sifat ; Poyner, David R ; Conner, Alex C

Biochemistry (Easton), 2017-08, Vol.56 (30), p.3877-3880 [Periódico revisado por pares]

United States: American Chemical Society

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7
Translocating Proline-Rich Peptides from the Antimicrobial Peptide Bactenecin 7
Translocating Proline-Rich Peptides from the Antimicrobial Peptide Bactenecin 7
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Translocating Proline-Rich Peptides from the Antimicrobial Peptide Bactenecin 7

Sadler, Kristen ; Eom, Khee Dong ; Yang, Jin-Long ; Dimitrova, Yoana ; Tam, James P

Biochemistry (Easton), 2002-12, Vol.41 (48), p.14150-14157 [Periódico revisado por pares]

United States: American Chemical Society

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8
Solution State Characterization of Amyloid β-Derived Diffusible Ligands
Solution State Characterization of Amyloid β-Derived Diffusible Ligands
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Solution State Characterization of Amyloid β-Derived Diffusible Ligands

Hepler, Robert W ; Grimm, Karen M ; Nahas, Deborah D ; Breese, Robert ; Dodson, Elizabeth Chen ; Acton, Paul ; Keller, Paul M ; Yeager, Mark ; Wang, Hui ; Shughrue, Paul ; Kinney, Gene ; Joyce, Joseph G

Biochemistry (Easton), 2006-12, Vol.45 (51), p.15157-15167 [Periódico revisado por pares]

United States: American Chemical Society

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9
Aβ(39–42) Modulates Aβ Oligomerization but Not Fibril Formation
Aβ(39–42) Modulates Aβ Oligomerization but Not Fibril Formation
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Aβ(39–42) Modulates Aβ Oligomerization but Not Fibril Formation

Gessel, Megan Murray ; Wu, Chun ; Li, Huiyuan ; Bitan, Gal ; Shea, Joan-Emma ; Bowers, Michael T

Biochemistry (Easton), 2012-01, Vol.51 (1), p.108-117 [Periódico revisado por pares]

United States: American Chemical Society

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10
Enzymatic Cross-Linking of Side Chains Generates a Modified Peptide with Four Hairpin-like Bicyclic Repeats
Enzymatic Cross-Linking of Side Chains Generates a Modified Peptide with Four Hairpin-like Bicyclic Repeats
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Enzymatic Cross-Linking of Side Chains Generates a Modified Peptide with Four Hairpin-like Bicyclic Repeats

Lee, Hyunbin ; Park, Youngseon ; Kim, Seokhee

Biochemistry (Easton), 2017-09, Vol.56 (37), p.4927-4930 [Periódico revisado por pares]

United States: American Chemical Society

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