WOO YONG BAE

Dr. WOO YONG BAE

orcid

Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2018 in Allergy, Asthma & Immunology Research
Verified
Journal Article
Open access
PDF file
MKMi-Ae Kim
Mi-Ae Kim
DKDong-Kyu Kim
Dong-Kyu Kim
HYHyeon-Jong Yang
Hyeon-Jong Yang
YYYoung Yoo
Young Yoo
YAYoungmin Ahn
Youngmin Ahn
CIClinical Immunology
Clinical Immunology
Kim MA, et al. Allergy Asthma Immunol Res. 2018 Nov;10(6):648-661. https://doi.org/10.4168/aair.2018.10.6.648

1 January 2019 in Yonsei Medical Journal
Verified
Journal Article
Open access
PDF file
MKMinji Kim
Minji Kim
YAYoungmin Ahn
Youngmin Ahn
YYYoung Yoo
Young Yoo
DKDong-Kyu Kim
Dong-Kyu Kim
HYHyeon-Jong Yang
Hyeon-Jong Yang
CIClinical Immunology
Clinical Immunology
Kim M, et al. Yonsei Med J. 2019 Oct;60(10):960-968. https://doi.org/10.3349/ymj.2019.60.10.960

29 March 2016 in Otolaryngology–Head and Neck Surgery
Verified
Journal Article
Closed access
BKBo Young Kim
Bo Young Kim
WBWOO YONG BAE
WOO YONG BAE
DHDae Young Hur
Dae Young Hur
JKJae‐Ryong Kim
Jae‐Ryong Kim
TKTae Kyung Koh
Tae Kyung Koh
GPGa Bin Park
Ga Bin Park

1 February 2014 in Auris Nasus Larynx
Verified
Journal Article
Closed access
WBWOO YONG BAE
WOO YONG BAE
SKSo Hyang Kim
So Hyang Kim
MKMin Young Kang
Min Young Kang
TKTae Kyung Koh
Tae Kyung Koh

1 January 2009 in Korean Journal of Otolaryngology-Head and Neck Surgery
Verified
Journal Article
Closed access
PDF file
TATae-Joo Ahn
Tae-Joo Ahn
WBWOO YONG BAE
WOO YONG BAE
SKSoo-Jin Kim
Soo-Jin Kim
MKMyung-Jin Kang
Myung-Jin Kang

1 January 2014 in Clinical and Experimental Otorhinolaryngology
Verified
Journal Article
Open access
PDF file
TGTae Woo Gu
Tae Woo Gu
WBWOO YONG BAE
WOO YONG BAE
HPHwan Tae Park
Hwan Tae Park
JLJae Hoon Lee
Jae Hoon Lee
MKMin Young Kang
Min Young Kang
YSYoon Kyung Shin
Yoon Kyung Shin
To examine the expression profile of Fas-Fas ligand (FasL) during glutamate (Glu)-induced spiral ganglion cell (SGC) apoptosis. Cultured SGCs were treated with 10-mM, 25-mM, and 50-mM concentrations of Glu and incubated for 24 or 48 hours. The expression intensity of FasL, Fas, caspase 3, and morphology of single SGC were evaluated using immunofluorescence staining. In semiquantitative analysis of the Glu-treated SGC, FasL, and caspase 3 expression intensity were increased with concentration- and time-dependent manner. Fas expression intensity did not change with different concentration at 48 hours. In morphologic analysis of the Glu-treated SGC, number of apoptotic cells were increased with concentration- and time-dependent manner. FasL was expressed in apoptotic SGCs, suggesting that the Fas-FasL signaling pathway may be involved in the Glu-induced apoptosis of dissociated SGCs.