Kuei-Ying Lin
Overview
Explore the profile of Kuei-Ying Lin including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
15
Citations
239
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Arputharaj E, Huang Y, Singh S, Zhuang C, Lin K, Sudewi S, et al.
J Food Drug Anal
. 2025 Jan;
32(4):520-531.
PMID: 39752864
This study introduces an innovative bio-based sorbent bead crafted by integrating chitosan (CS) biopolymers, Fe(NO3)3 and polydopamine nanoparticles (PDA NPs) via glutaraldehyde crosslinking. The primary focus of this study was...
2.
Lin K, Chen P, Chen S, Huang Y, Chen H
Kaohsiung J Med Sci
. 2018 Aug;
34(7):409-414.
PMID: 30063014
The measurement of serum osmolality, and the calculation of osmolal gap (OG) from a calculated osmolality are widely used in clinical and emergency medicine. In this study, the possible effects...
3.
Tzeng W, Chuang J, Lin L, Cherng C, Lin K, Chen L, et al.
Psychoneuroendocrinology
. 2012 Jul;
38(3):425-37.
PMID: 22832183
The presence of companions can reverse the stressor-induced decrease in neurogenesis in mouse dentate gyrus (DG). In this study, we decided to study the underlying mechanisms of the companions' protective...
4.
Cherng C, Chang C, Su C, Tzeng W, Chuang J, Chen L, et al.
Behav Brain Res
. 2011 Dec;
229(1):106-12.
PMID: 22200498
Unconditioned foot shock followed by restraint in water was used as a stress regimen to induce decreases in neurogenesis in mouse dentate gyrus (DG). Presence of conspecific odors has been...
5.
Lin K, Cherng C, Yang F, Lin L, Lu R, Yu L
Behav Brain Res
. 2011 Feb;
220(1):126-31.
PMID: 21277908
In this study, we decided to use low doses of memantine pretreatment to examine the roles of the immune function in cocaine-supported conditioning. Cocaine-induced conditioned place preference (CPP) was used...
6.
Mackman R, Ray A, Hui H, Zhang L, Birkus G, Boojamra C, et al.
Bioorg Med Chem
. 2010 Apr;
18(10):3606-17.
PMID: 20409721
GS-9148 [(5-(6-amino-purin-9-yl)-4-fluoro-2,5-dihydro-furan-2-yloxymethyl)phosphonic acid] 4 is a novel nucleoside phosphonate HIV-1 reverse transcriptase (RT) inhibitor with a unique resistance profile toward N(t)RTI resistance mutations. To effectively deliver 4 and its active...
7.
Mackman R, Lin K, Boojamra C, Hui H, Douglas J, Grant D, et al.
Bioorg Med Chem Lett
. 2007 Dec;
18(3):1116-9.
PMID: 18082402
Modified purine analogs of GS-9148 [5-(6-amino-purin-9-yl)-4-fluoro-2,5-dihydro-furan-2-yloxymethyl]-phosphonic acid (2'-Fd4AP) were synthesized and their anti-HIV potency evaluated. The antiviral activity of guanosine analog (2'-Fd4GP) was comparable that of to 2'-Fd4AP in MT-2...
8.
Cihlar T, Ray A, Boojamra C, Zhang L, Hui H, Laflamme G, et al.
Antimicrob Agents Chemother
. 2007 Dec;
52(2):655-65.
PMID: 18056282
GS-9148 [(5-(6-amino-purin-9-yl)-4-fluoro-2,5-dihydro-furan-2-yloxymethyl)phosphonic acid] is a novel ribose-modified human immunodeficiency virus type 1 (HIV-1) nucleotide reverse transcriptase (RT) inhibitor (NRTI) selected from a series of nucleoside phosphonate analogs for its favorable...
9.
Ray A, Vela J, Boojamra C, Zhang L, Hui H, Callebaut C, et al.
Antimicrob Agents Chemother
. 2007 Dec;
52(2):648-54.
PMID: 18056281
GS-9131 is a phosphonoamidate prodrug of the novel ribose-modified phosphonate nucleotide analog GS-9148 that demonstrates potent anti-human immunodeficiency virus type 1 (HIV-1) activity and an excellent resistance profile in vitro....
10.
Mackman R, Boojamra C, Prasad V, Zhang L, Lin K, Petrakovsky O, et al.
Bioorg Med Chem Lett
. 2007 Nov;
17(24):6785-9.
PMID: 18029175
A series of nucleoside phosphonate reverse transcriptase (RT) inhibitors have been synthesized and their anti-HIV activity and resistance profiles evaluated. The most potent analog [5-(6-amino-purin-9-yl)-2,5-dihydro-furan-2-yloxymethyl]-phosphonic acid (d4AP) demonstrated a HIV...